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1Academic Journal
المؤلفون: Gregori Font, Josep, Ibañez Lligoña, Marta, Colomer-Castell, Sergi, Campos, Carolina, QUER, JOSEP
المساهمون: Institut Català de la Salut, Gregori J Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei d’Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Ibañez-Lligoña M, Colomer-Castell S, Campos C Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Bellaterra, Spain. Quer J Grup de Recerca de les Malalties Hepàtiques, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Servei Hepatologia, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Instituto de Salud Carlos III, Madrid, Spain. Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Bellaterra, Spain. Departament de Medicina, Universitat Autònoma de Barcelona, Bellaterra, Spain, Vall d'Hebron Barcelona Hospital Campus
المصدر: Scientia
مصطلحات موضوعية: Genètica vírica, Genotip, Genòmica, PHENOMENA AND PROCESSES::Genetic Phenomena::Genetic Variation::Quasispecies, PHENOMENA AND PROCESSES::Genetic Phenomena::Genotype::Haplotypes, ORGANISMS::Viruses, Other subheadings::Other subheadings::Other subheadings::/genetics, DISCIPLINES AND OCCUPATIONS::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genomics::Metagenomics, FENÓMENOS Y PROCESOS::fenómenos genéticos::variación genética::cuasiespecies, FENÓMENOS Y PROCESOS::fenómenos genéticos::genotipo::haplotipos, ORGANISMOS::virus, Otros calificadores::Otros calificadores::Otros calificadores::/genética, DISCIPLINAS Y OCUPACIONES::disciplinas de las ciencias naturales::disciplinas de las ciencias biológicas::biología::genética::genómica::metagenómica
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Relation: Viruses;16(5); https://doi.org/10.3390/v16050710; info:eu-repo/grantAgreement/ES/PEICTI2021-2023/PI22%2F00258; info:eu-repo/grantAgreement/ES/PEICTI2021-2023/FPU21%2F04150; Gregori J, Ibañez-Lligoña M, Colomer-Castell S, Campos C, Quer J. Virus Quasispecies Rarefaction: Subsampling with or without Replacement? Viruses. 2024 Apr 29;16(5):710.; https://hdl.handle.net/11351/11522
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2Academic Journal
المؤلفون: Alvarez Palomo, Belén, Gayoso, Jorge, Raya, Angel, Veiga, Anna, Abad Mendez, Maria, Vidal Pérez, Francisco, Querol Giner, Sergi, Garcia Martínez, Iris
المساهمون: Institut Català de la Salut, Álvarez-Palomo B, Querol S Banc de Sang i Teixits, Barcelona, Spain. Grup d’Enginyeria tissular musculoesquelètica, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. García-Martinez I Banc de Sang i Teixits, Barcelona, Spain. Gayoso J Organización Nacional de Trasplantes, Ministerio de Sanidad, Madrid, Spain. Raya A, Veiga A Programa de Medicina Regenerativa, Institut d’Investigació Biomèdica de Bellvitge. IDIBELL, Hospital Duran i Reynals, L’Hospitalet de Llobregat, Barcelona, Spain. Abad ML Axencia Galega de Sangue, Órganos e Tecidos, Santiago de Compostela, Spain. Vidal F Banc de Sang i Teixits, Barcelona, Spain. Grup de Medicina Transfusional, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. CIBER de Enfermedades Cardiovasculares (CIBERCV), Madrid, Spain, Vall d'Hebron Barcelona Hospital Campus
المصدر: Scientia
مصطلحات موضوعية: Donació d'òrgans i teixits, etc, Cèl·lules mare adultes, ANATOMY::Cells::Stem Cells::Adult Stem Cells::Induced Pluripotent Stem Cells, PHENOMENA AND PROCESSES::Genetic Phenomena::Genotype::Haplotypes, NAMED GROUPS::Persons::Tissue Donors, ANATOMÍA::células::células madre::células madre adultas::células madre pluripotentes inducidas, FENÓMENOS Y PROCESOS::fenómenos genéticos::genotipo::haplotipos, DENOMINACIONES DE GRUPOS::personas::donantes de tejidos
وصف الملف: application/pdf
Relation: Stem Cell Research & Therapy;12; https://doi.org/10.1186/s13287-021-02301-0; info:eu-repo/grantAgreement/ES/PE2013-2016/RTC-2017-6000-1; Álvarez-Palomo B, García-Martinez I, Gayoso J, Raya A, Veiga A, Abad ML, et al. Evaluation of the Spanish population coverage of a prospective HLA haplobank of induced pluripotent stem cells. Stem Cell Res Ther. 2021 Apr 13;12:233.; https://hdl.handle.net/11351/6614; 000640245200001
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3Academic Journal
المؤلفون: Moreno‑Alcázar, Ana, Ribases Haro, Marta, Sanchez Mora, Cristina P, Palomar Martínez, Gloria, Bosch Munso, Rosa M, Ramos-Quiroga, Josep Antoni, Casas Brugué, Miquel
المساهمون: Institut Català de la Salut, Moreno-Alcázar A FIDMAG Research Foundation, Sant Boi de Llobregat, Barcelona, Spain. Centre Forum Research Unit, Institute of Neuropsychiatry and Addictions (INAD), Hospital del Mar, Barcelona, Spain. Institut Hospital del Mar d’Investigacions Mèdiques, Barcelona, Spain. Biomedical Network Research Centre on Mental Health (CIBERSAM), Instituto de Salud Carlos III, Madrid, Spain. Ramos-Quiroga JA, Bosch R, Casas M Biomedical Network Research Centre on Mental Health (CIBERSAM), Instituto de Salud Carlos III, Madrid, Spain. Departament de Psiquiatria i Medicina legal, Universitat Autònoma de Barcelona, Bellaterra, Spain. Unitat de Psiquiatria Genètica, Grup de recerca en Psiquiatria, Salut mental i Addiccions, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari, Barcelona, Spain. Universitat Autònoma de Barcelona, Bellaterra, Spain. Servei de Psiquiatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Ribases M, Sánchez-Mora C Biomedical Network Research Centre on Mental Health (CIBERSAM), Instituto de Salud Carlos III, Madrid, Spain. Unitat de Psiquiatria Genètica, Grup de recerca en Psiquiatria, Salut mental i Addiccions, Vall d’Hebron Institut de Recerca (VHIR), Barcelona, Spain. Vall d’Hebron Hospital Universitari. Servei de Psiquiatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain. Department of Genetics, Microbiology & Statistics, University of Barcelona, Barcelona, Spain. Palomar G Servei de Psiquiatria, Vall d’Hebron Hospital Universitari, Barcelona, Spain, Vall d'Hebron Barcelona Hospital Campus
المصدر: Scientia
مصطلحات موضوعية: Trastorn per dèficit d'atenció amb hiperactivitat, ADN - Anàlisi, PSYCHIATRY AND PSYCHOLOGY::Mental Disorders::Neurodevelopmental Disorders::Attention Deficit and Disruptive Behavior Disorders::Attention Deficit Disorder with Hyperactivity, PHENOMENA AND PROCESSES::Genetic Phenomena::Genotype::Haplotypes, ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES, AND EQUIPMENT::Investigative Techniques::Genetic Techniques::Genotyping Techniques, PSIQUIATRÍA Y PSICOLOGÍA::trastornos mentales::trastornos del desarrollo neurológico::trastornos conductuales disruptivos y déficit de atención::trastornos de déficit de atención con hiperactividad, FENÓMENOS Y PROCESOS::fenómenos genéticos::genotipo::haplotipos, TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::técnicas de investigación::técnicas genéticas::técnicas de genotipado
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Relation: Scientific Reports;11; https://www.nature.com/articles/s41598-021-81915-z; info:eu-repo/grantAgreement/ES/1PN/2008-2011/PI11%2F01629; info:eu-repo/grantAgreement/ES/2PN/2008-2011/PI11%2F01766; info:eu-repo/grantAgreement/ES/PE2013-2016/PI16%2F01505; info:eu-repo/grantAgreement/ES/PE2013-2016/PI17%2F00289; info:eu-repo/grantAgreement/ES/PE2013-2016/PI18%2F01788; info:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F00394; info:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F00721; info:eu-repo/grantAgreement/ES/PE2017-2020/PI19%2F01224; info:eu-repo/grantAgreement/ES/3PN/2008-2011/CP09%2F00119; info:eu-repo/grantAgreement/ES/PE2017-2020/CPII19%2F00009; info:eu-repo/grantAgreement/ES/PE2013-2016/CD15%2F00199; info:eu-repo/grantAgreement/ES/PE2017-2020/FI20%2F00047; info:eu-repo/grantAgreement/ES/PERIS2016-2020/SLT006%2F17%2F287; info:eu-repo/grantAgreement/ES/PERIS2016-2020/2009SGR211; info:eu-repo/grantAgreement/ES/PERIS2016-2020/2017SGR1461; https://hdl.handle.net/11351/6123
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4Academic Journal
المؤلفون: Roura, Santiago, Rudilla Salvador, Francesc, Enrich Rande, Emma, Campos, Eva, Lupón, Josep, Gastelurrutia, Paloma
المساهمون: Institut Català de la Salut, Roura S ICREC Research Program, Germans Trias i Pujol Health Science Research Institute, Badalona, Spain. CIBER Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain. Rudilla F Histocompatibility and Immunogenetics Laboratory, Blood and Tissue Bank, Barcelona, Spain. Grup en medicina transfusional, Vall d’Hebron Institut de Recerca, Barcelona, Spain. Gastelurrutia P ICREC Research Program, Germans Trias i Pujol Health Science Research Institute, Badalona, Spain. CIBER Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain. Enrich E Histocompatibility and Immunogenetics Laboratory, Blood and Tissue Bank, Barcelona, Spain. Grup en medicina transfusional, Vall d’Hebron Institut de Recerca, Barcelona, Spain. Campos E Histocompatibility and Immunogenetics Laboratory, Blood and Tissue Bank, Barcelona, Spain. Lupón J CIBER Cardiovascular, Instituto de Salud Carlos III, Madrid, Spain. Cardiology Service, Germans Trias i Pujol University Hospital, Badalona, Spain. Department of Medicine, UAB, Barcelona, Spain., Vall d'Hebron Barcelona Hospital Campus
المصدر: Scientia
مصطلحات موضوعية: Insuficiència cardíaca - Aspectes genètics, Teràpia cel·lular, DISEASES::Cardiovascular Diseases::Heart Diseases::Heart Failure, Other subheadings::Other subheadings::Other subheadings::/genetics, ANALYTICAL, DIAGNOSTIC AND THERAPEUTIC TECHNIQUES AND EQUIPMENT::Therapeutics::Biological Therapy::Cell- and Tissue-Based Therapy, PHENOMENA AND PROCESSES::Genetic Phenomena::Genotype::Haplotypes, ENFERMEDADES::enfermedades cardiovasculares::enfermedades cardíacas::insuficiencia cardíaca, Otros calificadores::Otros calificadores::Otros calificadores::/genética, TÉCNICAS Y EQUIPOS ANALÍTICOS, DIAGNÓSTICOS Y TERAPÉUTICOS::terapéutica::terapia biológica::tratamientos basados en células y tejidos, FENÓMENOS Y PROCESOS::fenómenos genéticos::genotipo::haplotipos
وصف الملف: application/pdf
Relation: ESC Heart Failure; Roura S, Rudilla F, Gastelurrutia P, Enrich E, Campos E, Lupón J, et al. Determination of HLA-A, -B, -C, -DRB1 and -DQB1 allele and haplotype frequencies in heart failure patients. ESC Hear Fail. 2019.; https://hdl.handle.net/11351/3819
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5
المؤلفون: Carlos Taxonera, Dolores Martín Arranz, Juan Luis Mendoza, José Lázaro Pérez-Calle, Fernando Bermejo, Concepción Núñez, Virginia Pascual, Javier P. Gisbert, María Gómez-García, Elena Urcelay, Javier Martín, Cristina González-Artacho, Luz Maria Medrano, Antonio López-Sanromán, Manuel Barreiro-de Acosta
المساهمون: [Medrano,LM, Pascual,V, Núñez,C, Urcelay,E] Immunology Department, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain. [Taxonera,C, Mendoza,JL] Gastroenterology Department, Hospital Clínico San Carlos, Instituto de Investigación Sanitaria del Hospital Clínico San Carlos (IdISSC), Madrid, Spain. [González-Artacho,C, Gómez-García,M] Gastroenterology Department, Virgen de las Nieves Hospital, Granada, Spain. [Barreiro-de Acosta,M] Gastroenterology Department, Hospital Clínico Universitario de Santiago de Compostela, Santiago de Compostela, Spain. [Perez-Calle,JL] Gastroenterology Department, Alcorcón Hospital, Madrid, Spain. [Bermejo,F] Gastroenterology Department, Fuenlabrada Hospital, Madrid, Spain. [López-Sanromán,A] Gastroenterology Department, Fuenlabrada Hospital, Madrid, Spain. [Martín Arranz,D] Gastroenterology Department, La Paz Hospital, Madrid, Spain. [Gisber,JP] Gastroenterology Department, Hospital Universitario La Princesa, Instituto de Investigación Sanitaria Princesa (IP), Madrid, Spain. Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBEREHD), Madrid, Spain. [Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, IPBLN-CSIC, Armilla, Granada, Spain., Financial support for the study was provided by Fundación Mutua Madrileña.
المصدر: Mediators of Inflammation
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Mediators of Inflammation, Vol 2015 (2015)مصطلحات موضوعية: Male, Polimorfismo genético, Anatomy::Digestive System::Gastrointestinal Tract::Intestines::Intestine, Large::Colon [Medical Subject Headings], Cell Cycle Proteins, Disease, Anatomy::Digestive System::Gastrointestinal Tract::Intestines::Intestine, Small::Ileum [Medical Subject Headings], Genetic analysis, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Crohn Disease, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Intercellular Signaling Peptides and Proteins::Tumor Necrosis Factors::Tumor Necrosis Factor-alpha [Medical Subject Headings], Genotype, Young adult, Crohn's disease, Marcadores biológicos, Interleukin-11, Humanos, Antirheumatic Agents, Female, Haplotipos, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Interleucina-11, lcsh:RB1-214, medicine.drug, Adult, Article Subject, Adolescent, Colon, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intercellular Signaling Peptides and Proteins::Cytokines::Interleukins::Interleukin-11 [Medical Subject Headings], Immunology, Biology, Young Adult, Íleon, Chemicals and Drugs::Biological Factors::Biological Markers [Medical Subject Headings], lcsh:Pathology, medicine, Calgranulin B, Humans, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Blood Proteins::Immunoproteins::Immunoglobulins::Antibodies::Antibodies, Monoclonal [Medical Subject Headings], Diseases::Digestive System Diseases::Gastrointestinal Diseases::Intestinal Diseases::Inflammatory Bowel Diseases::Crohn Disease [Medical Subject Headings], Calgranulin A, Enfermedad de Crohn, Genotyping, Haplotype, Cell Biology, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Infliximab, Factor de necrosis tumoral alfa, Anticuerpos monoclonales, Clinical Study, Genotipo, Cell Adhesion Molecules
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المؤلفون: Stephens, Camilla, Moreno-Casares, Antonia, López-Nevot, Miguel-Ángel, García-Cortés, Miren, Medina-Cáliz, Inmaculada, Hallal, Hacibe, Soriano, German, Roman, Eva, Ruiz-Cabello, Francisco, Romero-Gómez, Manuel, Lucena, M. Isabel, Andrade, Raúl J., Universitat Autònoma de Barcelona
المساهمون: Instituto de Salud Carlos III, European Commission, Agencia Española de Medicamentos y Productos Sanitarios, Centro de Investigación Biomédica en Red Enfermedades Hepáticas y Digestivas (España), [Stephens,C, García-Cortés,M, Medina-Cáliz,I, Lucena,MI, Andrade,RJ] Unidad de Gestión Clínica de Aparato Digestivo, Servicio de Farmacología Clínica, Instituto de Investigación Biomédica de Málaga, Hospital Universitario Virgen de la Victoria, Universidad de Málaga, CIBERehd, Málaga, Spain. [Moreno-Casares,A, López-Nevot,MA] Unidad de Gestión Clínica de Laboratorio, Departamento de Bioquímica y Biología Molecular III/Inmunología, Instituto de Investigación Biosanitario de Granada, Complejo Hospitalario de Granada, Universidad de Granada, Granada, Spain. [Hallal,H, Ruiz-Cabello,F] Servicio de Aparato Digestivo, Hospital Morales Meseguer, Murcia, Spain. [Soriano,G, Roman,E] Servicio de Gastroenterología, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, CIBERehd, Barcelona, Spain. [Roman,E] Escola Universitària d’Infermeria-Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain. [Romero-Gomez,M] Unidad de Gestión Clínica de Aparato Digestivo Intercentros, Hospitales Universitarios Virgen Macarena-Virgen del Rocio, CIBERehd, Seville, Spain., The present study has been supported by grants of the Instituto de Salud Carlos III co-founded by Fondo Europeo de Desarrollo Regional – FEDER (contract numbers: PI12/00378, SAS-PI-0239/2012, AC-0073-2013) and by the Agencia Española del Medicamento. CIBERehd is funded by Instituto de Salud Carlos III.
المصدر: Frontiers in Pharmacology
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Digital.CSIC. Repositorio Institucional del CSIC
Frontiers in Pharmacology, Vol 7 (2016)مصطلحات موضوعية: 0301 basic medicine, Drug-induced liver injury, Lymphocyte, Chemicals and Drugs::Chemical Actions and Uses::Specialty Uses of Chemicals::Laboratory Chemicals::Ligands [Medical Subject Headings], Epitope, immune response, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], 0302 clinical medicine, Genotype, Pharmacology (medical), Receptor, Amoxicilina, Epítopos, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Pseudogenes [Medical Subject Headings], Original Research, pharmacogenetics, receptor/ligand, education.field_of_study, Diseases::Neoplasms [Medical Subject Headings], Células asesinas naturales, Chemicals and Drugs::Biological Factors::Antigens::Epitopes [Medical Subject Headings], Neoplasias, Humanos, HLA, medicine.anatomical_structure, Chemicals and Drugs::Biological Factors::Antigens::Antigens, Surface::Histocompatibility Antigens::HLA Antigens [Medical Subject Headings], Haplotipos, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation [Medical Subject Headings], Receptor/ligand, drug-induced liver injury, hepatotoxicity, Chemicals and Drugs::Organic Chemicals::Amides::Lactams::beta-Lactams::Clavulanic Acids::Clavulanic Acid [Medical Subject Headings], Population, Human leukocyte antigen, Biology, Variación genética, Subgrupos linfocitarios, 03 medical and health sciences, Seudogenes, Chemicals and Drugs::Organic Chemicals::Amides::Lactams::beta-Lactams::Penicillins::Penicillin G::Ampicillin::Amoxicillin [Medical Subject Headings], Immune system, Ácido clavulánico, Enfermedades autoinmunes, Diseases::Immune System Diseases::Autoimmune Diseases [Medical Subject Headings], medicine, Immune response, education, Ligandos, Pharmacology, Receptores KIR, Diseases::Substance-Related Disorders::Poisoning::Drug-Induced Liver Injury [Medical Subject Headings], Haplotype, lcsh:RM1-950, Hepatotoxicity, drug-induced liver injury,pharmacogenetics, Anatomy::Hemic and Immune Systems::Blood::Blood Cells::Leukocytes::Leukocytes, Mononuclear::Lymphocytes::Lymphocyte Subsets [Medical Subject Headings], 030104 developmental biology, lcsh:Therapeutics. Pharmacology, Antígenos HLA, Anatomy::Cells::Blood Cells::Leukocytes::Leukocytes, Mononuclear::Lymphocytes::Killer Cells, Natural [Medical Subject Headings], Pharmacogenetics, Immunology, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Receptors, Cell Surface::Receptors, Immunologic::Receptors, Natural Killer Cell::Receptors, KIR [Medical Subject Headings], Enfermedad hepática inducida por drogas, Genotipo, 030215 immunology
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المؤلفون: Carmen Belén Lupiañez, María Teresa Villaescusa, Agostinho Carvalho, Jan Springer, Michaela Lackner, José Manuel Sánchez-Maldonado, Luz María Canet, Cristina Cunha, Juana Segura-Catena, Laura Alcazar-Fuoli, Carlos Solano, Luana Fianchi, Livio Pagano, Leonardo Potenza, José María Aguado, Mario Luppi, Manuel Cuenca-Estrella, Cornelia Lass-Flörl, Hermann Einsele, Lourdes Vázquez, PCRAGA Study Group, Rafael Ríos-Tamayo, Jurgen Loeffler, Manuel Jurado, Juan Sainz
المساهمون: Instituto de Salud Carlos III, Ministerio de Ciencia e Innovación (España), FWF Austrian Science Fund, Fundação para a Ciência e Tecnologia (Portugal), Unión Europea. Fondo Europeo de Desarrollo Regional (FEDER/ERDF), Universidade do Minho, PCRAGA StudyGroup, PCRAGA Study Group, [Lupiañez,CB, Sánchez-Maldonado,JM, Canet,LM, Segura-Catena,J, Ríos-Tamayo,R, Jurado,M, Sainz,J] Genomic Oncology Area, GENYO, Center for Genomics and Oncological Research, Pfizer/University of Granada/Andalusian Regional Government,Granada, Spain. [Lupiañez,CB, Sainz,J] Hematology Department, Virgen de las Nieves University Hospital, Granada, Spain. [Villaescusa,M, Vázquez,L] Hematology Department, University Hospital of Salamanca, Salamanca, Spain. [Villaescusa,MT] Hematology Department, Jiménez Díaz Foundation, Madrid, Spain. [Carvalho,A, Cunha,C] Life and Health Sciences Research Institute (ICVS), School of Health Sciences, University of Minho. 6ICVS/3B's - PT Government Associate Laboratory, Braga, Portugal. [Springer,J, Einsele,H, Loeffler,J] Universitätsklinikum Würzburg, Klinik II, Würzburg, Germany. [Lackner,M, Lass-Flörl,C] Division of Hygiene and Medical Microbiology, Medical University of Innsbruck, Innsbruck, Austria. [Alcazar-Fuoli,L: Cuenca-Estrella,M] Mycology Reference Laboratory, Centro Nacional de Microbiología, Instituto de Salud Carlos III, Madrid, Spain. [Solano,C] Hematology Department, Clinic University Hospital of Valencia, Valencia, Spain. [Fianchi,L, Pagano,L] Istituto di Ematologia, Università Cattolica del S. Cuore, Rome, Italy. [Potenza,L, Luppi,M] Istituto di Ematologia, Università Cattolica del S. Cuore, Rome, Italy. Department of Medical and Surgical Sciences, University of Modena and Reggio Emilia, AOU Policlinico, Modena, Italy. [Aguado,JM] Unit of Infectious Diseases, University Hospital 12 de Octubre, Research Institute of Hospital 12 de Octubre (i+12), Madrid., This study was supported by grants PI12/02688 from Fondo de Investigaciones Sanitarias (Instituto de Salud Carlos III, Madrid, Spain), the ERA-NET PathoGenoMics (03159000A, Ministerio de Ciencia e Innovación PIM2010EPA-00756, Madrid, Spain), the Collaborative Research Center / Transregio 124 FungiNet, the Austrian Science Fundation (FWF I-656-B09), the Fundação para a Ciência e Tecnologia (FCT), cofunded by Programa Operacional Regional do Norte (ON.2—O Novo Norte), the Quadro de Referência Estratégico Nacional (QREN) through the Fundo Europeu de Desenvolvimento Regional (FEDER) and the Projeto Estratégico – LA 26 – 2013–2014 (PEst-C/SAU/LA0026/2013). Agostinho Carvalho and Cristina Cunha were supported by the Fundação para a Ciência e Tecnologia (FCT), Portugal (IF/00735/2014 and SFRH/BPD/96176/2013, respectively).The PCRAGA trial was supported by an unrestricted grant from Pfizer. This study was also supported by Astellas Pharma Inc. and a donation from Consuelo González Moreno, an acute myeloid leukemia survivor., Austrian Science Fund, Fundação para a Ciência e a Tecnologia (Portugal), European Regional Development Fund
المصدر: Frontiers in Microbiology
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Frontiers in Microbiology, Vol 7 (2016)
Repisalud
Instituto de Salud Carlos III (ISCIII)مصطلحات موضوعية: 0301 basic medicine, Polimorfismo de nucleótido simple, Medicina Básica [Ciências Médicas], lcsh:QR1-502, Diseases::Bacterial Infections and Mycoses::Mycoses::Hyalohyphomycosis::Aspergillosis [Medical Subject Headings], Genetic Susceptibility, NF kappa B-related genes, lcsh:Microbiology, susceptibility, Diseases::Bacterial Infections and Mycoses::Infection::Opportunistic Infections [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Infecciones oportunistas, Invasive Aspergillosis, NFκB-related genes, genetic polymorphisms, interaction, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility [Medical Subject Headings], Genotype, Chemicals and Drugs::Carbohydrates::Glycosides::Nucleotides [Medical Subject Headings], Original Research, Genetics, education.field_of_study, Phenomena and Processes::Genetic Phenomena::Phenotype::Genetic Markers [Medical Subject Headings], Analytical, Diagnostic and Therapeutic Techniques and Equipment::Surgical Procedures, Operative::Transplantation::Cell Transplantation::Stem Cell Transplantation::Hematopoietic Stem Cell Transplantation [Medical Subject Headings], Humanos, 3. Good health, Nucleótidos, Ciências Médicas::Medicina Básica, Haplotipos, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Trasplante de células madre hematopoyéticas, Microbiology (medical), Marcadores genéticos, nfkb pathway, Population, Single-nucleotide polymorphism, Biology, Microbiology, 03 medical and health sciences, Genetic predisposition, SNP, ddc:610, Allele, education, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Science & Technology, Haplotype, Susceptibilidad a enfermedades, Organisms::Eukaryota::Fungi::Mitosporic Fungi::Aspergillus [Medical Subject Headings], Hematologic Diseases, Settore MED/15 - MALATTIE DEL SANGUE, 030104 developmental biology, Aspergilosis, Genetic marker, Invasive Aspergillosis, genetic polymorphisms, susceptibility, NFκB-related genes, interaction, Immunology, Genotipo, Stem Cell Transplantation
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المؤلفون: Isidoro González-Álvaro, Jesús Tornero, Luis Rodriguez-Rodriguez, A. Olivé, Benjamín Fernández-Gutiérrez, Alba Erra, Núria Palau, Francisco J. Blanco, Inmaculada Ureña-Garnica, Juan D. Cañete, María López-Lasanta, Arnald Alonso, Joan Maymó, Raül Tortosa, Antonio Julià, Hèctor Corominas, Mercedes Alperi-López, Gabriela Ávila, Miriam Almirall, Ana M. Ortiz, Sara Marsal
المساهمون: [Lopez-Lasanta,M, Julià,A, Palau,N, Avila,G, Alonso,A, Tortosa,R, Marsal,S] Vall d’Hebron Hospital Research Institute, Rheumatology Research Group, Barcelona, Spain. [Maymó,J, Almirall,A] Rheumatology Department, Hospital del Mar, Barcelona, Spain. [Fernández-Gutiérrez,F] Rheumatology Department, Hospital Clínico San Carlos, Madrid, Spain. [Ureña-Garnica,I] UGC Reumatología, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Regional Universitario de Málaga, Málaga, Spain. [Blanco,FJ] Rheumatology Department, INIBIC-Hospital Universitario A Coruña, A Coruña, Spain. [Cañete,JD] Rheumatology Department, Hospital Clínic de Barcelona, Barcelona, Spain. [Alperi-López,M] Rheumatology Department, Hospital Universitario Central de Asturias, Oviedo, Spain. [Olivè,A] Rheumatology Department, Hospital Universitari Germans Trias i Pujol, Barcelona, Spain. [Corominas,H] Rheumatology Department, Hospital Moisès Broggi, L´ Hospitalet de Llobregat, Barcelona, Spain. [Tornero,J] Rheumatology Department, Hospital Universitario De Guadalajara, Guadalajara, Spain. [Erra,A]Rheumatology Department, Hospital Sant Rafael, Barcelona, Spain. [Ortiz,A, Gonzalez-Alvaro,I] Rheumatology Department, Hospital Universitario La Princesa, IIS La Princesa, Madrid, Spain., This study was funded by the Spanish Ministry of Economy and Competitiveness (grant numbers PSE-010000-2006-6 and IPT-010000-2010-36).
المصدر: Scopus
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
RUC. Repositorio da Universidade da Coruña
Arthritis Research & Therapy
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madridمصطلحات موضوعية: Linkage disequilibrium, España, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Regression Analysis::Linear Models [Medical Subject Headings], Linkage Disequilibrium, Arthritis, Rheumatoid, Cohort Studies, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, Receptors, Metanálisis como asunto, Medicine, Immunology and Allergy, Halotipos, Modelos lineales, Single nucleotide, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Predisposición genética a la enfermedad, Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium [Medical Subject Headings], Polimorfismo de nucleótido único, Diseases::Musculoskeletal Diseases::Rheumatic Diseases::Arthritis, Rheumatoid [Medical Subject Headings], Articulaciones, Rheumatoid arthritis, Arthritis rheumatoid, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Alelos, Research Article, musculoskeletal diseases, Genotype, Anatomy::Musculoskeletal System::Skeleton::Joints [Medical Subject Headings], Immunology, Estudios de cohortes, Genetic predisposition to disease, Single-nucleotide polymorphism, Artritis reumatoide, Polymorphism, Single Nucleotide, Receptores de interleucina-6, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility::Genetic Predisposition to Disease [Medical Subject Headings], Meta-Analysis as Topic, Rheumatology, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Receptors, Cell Surface::Receptors, Immunologic::Receptors, Cytokine::Receptors, Interleukin::Receptors, Interleukin-6 [Medical Subject Headings], Genetic variation, SNP, Humans, Genetic Predisposition to Disease, Allele, Polymorphism, Allele frequency, Alleles, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], business.industry, Interleukin-6, Haplotype, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Research Design::Meta-Analysis as Topic [Medical Subject Headings], Artritis reumatoide -- Tractament, medicine.disease, Receptors, Interleukin-6, Gene frequency, Frecuencia génica, Haplotypes, Desequilibrio de ligamiento, Spain, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Cohort Studies [Medical Subject Headings], Linear Models, Joints, business, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], Genotipo
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المؤلفون: Marta E. Alarcón-Riquelme, Jesus Benitez, Sonia Cabrera, Andrés Soto-Varela, Juan Manuel Espinosa-Sanchez, Eduardo Martin-Sanz, Nicolas Perez, Gabriel Trinidad, Jose A. Lopez-Escamez, Jesus Fraile, Sofía Santos-Pérez, Manuel Martínez-Bueno, Paz Pérez, Teresa Requena, Elena Sánchez, Angel Batuecas, Ismael Aran
المساهمون: [Cabrera,S, Requena,T, Espinosa-Sanchez,JM, Lopez-Escamez,JA] Otology and Neurotology Group, Department of Genomic Medicine-Centro de Genómica e Investigación Oncológica-Pfizar/Universidad de Granada/Junta de Andalucía (Genyo). [Sanchez,E] Department of Neurology, Icahn School of Medicine at Mount Sinai. [Martinez-Bueno,M, Alarcon-Riquelme,ME] Group of Genetics of Complex Diseases, Department of Genomic Medicine-Centro de Genómica e Investigación Oncológica-Pfizer/Universidad de Granada/Junta de Andalucía (GENYO). [Benitez,J] Department of Otolaryngology, Hospital Universitario de Gran Canaria Dr. Negrin. [Perez,N] Department of Otolaryngology, Clínica Universidad de Navarra. [Trinidad,G] Division of Otoneurology, Department of Otorhinolaryngology, Complejo Hospitalario de Badajoz. [Soto-Varela,A, Santos-Perez,S] Division of Otoneurology, Department of Otorhinolaryngology, Complexo Hospitalario Universitario, Santiago de Compostela. [Martin-Sanz,E] Department of Otolaryngology, Hospital Universitario de Getafe. [Fraile,J] Department of Otolaryngology, Hospital Miguel Servet. [Perez,P] Department of Otorhinolaryngology, Hospital Cabueñes. [Batuecas,A] Department of Otolaryngology, Hospital Universitario Salamanca. [Espinosa-Sanchez,JM] Department of Otorhinolaryngology, Hospital San Agustin. [Aran,I] Department of Otolaryngology, Complexo Hospital de Pontevedra. [Lopez-Escamez,JA] Department of Otoloaryngology, Hospital de Poniente., Research Grants PI09/00920 and PI13/1242 from Instituto de Salud Carlos III by FEDER Funds from the EU. The authors also acknowledge the COST Action BM1306 TINNET which supports part of their networking activities (http://tinnet.tinnitusresearch.net/).
المصدر: PLoS ONE, Vol 9, Iss 11, p e112171 (2014)
PLoS ONE
Dadun. Depósito Académico Digital de la Universidad de Navarra
instname
Zaguán. Repositorio Digital de la Universidad de Zaragozaمصطلحات موضوعية: Male, Linkage disequilibrium, Pathology, Desequilibrio de Ligamiento, Progresión de la Enfermedad, lcsh:Medicine, Otology, NFKB1 gene, Kaplan-Meier Estimate, Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], Linkage Disequilibrium, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Tinnitus, Mediana Edad, Hearing, Estimación de Kaplan-Meier, Medicine and Health Sciences, lcsh:Science, Masculino, Diseases::Otorhinolaryngologic Diseases::Ear Diseases::Labyrinth Diseases::Endolymphatic Hydrops::Meniere Disease [Medical Subject Headings], Multidisciplinary, Femenino, Middle Aged, Diseases::Otorhinolaryngologic Diseases::Ear Diseases::Hearing Disorders::Hearing Loss::Hearing Loss, Sensorineural [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium [Medical Subject Headings], 3. Good health, Humanos, Sensorineural hearing loss, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::DNA-Binding Proteins::NF-kappa B::NF-kappa B p50 Subunit [Medical Subject Headings], Rheumatoid arthritis, Meniere's disease, Disease Progression, Female, Haplotipos, medicine.symptom, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::DNA, Intergenic::Introns [Medical Subject Headings], Alelos, Research Article, medicine.medical_specialty, Hearing loss, Hearing Loss, Sensorineural, Immunology, Predisposición Genética a la Enfermedad, Check Tags::Male [Medical Subject Headings], Single-nucleotide polymorphism, Polymorphism, Single Nucleotide, Autoimmune Diseases, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility::Genetic Predisposition to Disease [Medical Subject Headings], Genetics, medicine, otorhinolaryngologic diseases, Humans, Intrones, Genetic Predisposition to Disease, Alleles, Meniere Disease, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Ankylosing spondylitis, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Progression [Medical Subject Headings], Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Survival Analysis::Kaplan-Meier Estimate [Medical Subject Headings], business.industry, Enfermedad de Meniere, lcsh:R, NF-kappa B p50 Subunit, Biology and Life Sciences, Pérdida Auditiva, medicine.disease, Introns, FN-kappa B, Haplotypes, Otorhinolaryngology, Check Tags::Female [Medical Subject Headings], Genetics of Disease, Diseases::Pathological Conditions, Signs and Symptoms::Signs and Symptoms::Neurologic Manifestations::Sensation Disorders::Hearing Disorders::Hearing Loss [Medical Subject Headings], Clinical Immunology, lcsh:Q, Polimorfismo de Nucleótido Simple, business
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المؤلفون: Ulzurrun, Eugenia, Stephens, Camilla, Ruiz-Cabello, Francisco, Robles-Diaz, Mercedes, Saenz-López, Pablo, Hallal, Hacibe, Soriano, German, Roman, Eva, Fernandez, M. Carmen, Lucena, M. Isabel, Andrade, Raúl J., Universitat Autònoma de Barcelona
المساهمون: [Ulzurrun,E, Stephens,C, Robles-Díaz,M, Lucena,MI, Andrade, RJ] S Farmacología Clínica and UGC de Gastroenterología y Hepatología, Instituto de Investigación Biomédica de Málaga (IBIMA), Hospital Universitario Virgen de la Victoria, Universidad de Málaga, Spain. [Ulzurrun,E, Soriano,G, Román,E, Andrade, RJ] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Barcelona, Spain. [Ruiz-Cabello,F, Sáenz-López,P] Departamento de Bioquímica y Biología Molecular III/Inmunología, Hospital Universitario Virgen de las Nieves, Universidad de Granada, Spain. [Ruiz-Cabello,F] Instituto de Investigación Biosanitario de Granada, Spain. [Hallal,H] Servicio de Aparato Digestivo, Hospital Morales Meseguer, Murcia, Spain. [Soriano,G, Román,E] Servicio de Gastroenterología, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Spain. [Román,E] Escola Universitària d'Infermeria EUI-Sant Pau, Universitat Autònoma de Barcelona, Spain. [Fernández,MC] Unidad de Gestión Clínica de Farmacia, Hospital Torrecárdenas, Almería, Spain., This study was supported, in part, by research grants from the Agencia Española del Medicamento and Fondo de Investigación Sanitaria (PS 09/01384). CIBERehd and Red Genómica del Cáncer are funded by Instituto de Salud Carlos III.
المصدر: PLoS One
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
PLoS ONE
PLoS ONE, Vol 9, Iss 4, p e94675 (2014)
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Digibug. Repositorio Institucional de la Universidad de Granadaمصطلحات موضوعية: Oncology, Gerontology, Male, Linkage disequilibrium, España, lcsh:Medicine, Genome-wide association study, Linkage Disequilibrium, Cohort Studies, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Bilirrubina, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Membrane Transport Proteins::ATP-Binding Cassette Transporters [Medical Subject Headings], Risk Factors, Medicine and Health Sciences, Bile, Young adult, lcsh:Science, Aged, 80 and over, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Multidisciplinary, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Membrane Transport Proteins::ATP-Binding Cassette Transporters::Multidrug Resistance-Associated Proteins [Medical Subject Headings], Multidrug resistance-associated protein 2, Liver Diseases, Homozygote, Clinical Pharmacology, Genomics, ABCB4, Middle Aged, Multidrug Resistance-Associated Protein 2, Research Design, Cohort, Female, Drug therapy, Haplotipos, Chemical and Drug Induced Liver Injury, Multidrug Resistance-Associated Proteins, Alelos, Drug induced hepatotoxicity, Research Article, Adult, medicine.medical_specialty, ATP Binding Cassette Transporter, Subfamily B, Adolescent, Genotype, Clinical Research Design, Polimorfismo Genético, Gastroenterology and Hepatology, Research and Analysis Methods, Young Adult, Pharmacotherapy, Genomic Medicine, Adverse Reactions, Chemicals and Drugs::Biological Factors::Pigments, Biological::Bile Pigments::Bilirubin [Medical Subject Headings], Internal medicine, medicine, Genetics, Humans, Genetic Testing, Variant genotypes, Transportadoras de Casetes de Unión a ATP, Proteínas Asociadas a Resistencia a Múltiples Medicamentos, Genetic Association Studies, Alleles, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Aged, Clinical Genetics, Pharmacology, Evolutionary Biology, Drug metabolism, Polymorphism, Genetic, Enfermedad Hepática Inducida por Drogas, business.industry, Diseases::Substance-Related Disorders::Poisoning::Drug-Induced Liver Injury [Medical Subject Headings], lcsh:R, Personalized Medicine, Correction, Biology and Life Sciences, Human Genetics, Bilirubin, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], Estudios Epidemiológicos, Haplotypes, Spain, Pharmacogenetics, Genetic Polymorphism, lcsh:Q, Clinical Medicine, business, Population Genetics, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies [Medical Subject Headings]
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المؤلفون: Miguel A. González-Gay, María Carmen Cenit, Mario Martínez-Florensa, Carles Tolosa, Noelia Armiger, Ana Suárez, Francisco Hernandez, Elena Carnero-Montoro, Javier Martín, Francisco Lozano, Norberto Ortego-Centeno, Enrique de Ramón, Elena Bosch, Miguel Caballero-Baños, M.T. Arias, José Mario Sabio, Daniel Benitez, Marta Consuegra, Lizette Bonet
المساهمون: Universidad de Cantabria, Universitat de Barcelona, Ministerio de Economía y Competitividad (España), Generalitat de Catalunya, Junta de Andalucía, European Commission, Instituto de Salud Carlos III, [Cenit,MC, Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, Consejo Superior de Investigaciones Científicas (CSIC), Granada, Spain. [Martínez-Florensa,M] ImmunNovative Developments, Barcelona, Spain. [Martínez-Florensa,M, Consuegra,M, Bonet,L, Armiger,N, Benitez,D, Lozano,F] Institut d'Investigacions Biomèdiques August Pi i Sunyer, Barcelona, Spain. [Carnero-Montoro,E, Bosch,L] Institut de Biologia Evolutiva (CSIC-Universitat Pompeu Fabra), Departament de Ciències Experimentals i de la Salut, Parc de Recerca Biomèdica de Barcelona, Barcelona, Spain. [Caballero-Baños,M, Arias,MT, Lozano,F] Department of Immunology, Hospital Clínic de Barcelona, Barcelona, Spain. [Ortego-Centeno,N] Department of Internal Medicine, Hospital Clínico San Cecilio, Granada, Spain. [de Ramón,E] Department of Internal Medicine, Hospital Carlos Haya, Málaga, Spain. [Sabio,JM] Department of Internal Medicine, Hospital Virgen de las Nieves, Granada, Spain. [García–Hernández,FJ] Department of Internal Medicine, Hospital Virgen del Rocío, Seville, Spain. [Tolosa,C] Department of Internal Medicine, Hospital Parc Taulí, Sabadell, Spain. [Suárez,A] Department of Functional Biology, Immunology Area, Faculty of Medicine, University of Oviedo, Oviedo, Spain. [González-Gay,MA] Department of Rheumatology, Hospital Marques de Valdecilla, IFIMAV, Santander, Spain. [Lozano,F] Departament de Biologia Cel•lular, Immunologia i Neurociencies, Facultat de Medicina, Universitat de Barcelona, Barcelona, Spain., This work was supported by grants from the Spanish Ministerio de Economía y Competitividad [SAF2010-19717 to FL, SAF2009-11110 to JM, SAF2011-29239, and BFU2008-01046 to EB], Generalitat de Catalunya [2009SGR00252 to FL, and 2009SGR1101 to EB], Junta de Andalucı´a [CTS-4977], and Instituto de Salud Carlos III and Fondo Europeo de Desarrollo Regional/FEDER [RD12/0009/0004 to JM]
المصدر: PLoS ONE, Vol 9, Iss 11, p e113090 (2014)
RUO. Repositorio Institucional de la Universidad de Oviedo
instname
PLoS One. 2014 Nov 17;9(11):e113090
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)
Recercat. Dipósit de la Recerca de Catalunya
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSIC
Dipòsit Digital de la UB
Universidad de Barcelonaمصطلحات موضوعية: Phenomena and Processes::Immune System Phenomena::Immunity::Autoimmunity [Medical Subject Headings], Diseases::Immune System Diseases::Autoimmune Diseases::Lupus Erythematosus, Systemic::Lupus Nephritis [Medical Subject Headings], T-Lymphocytes, Lymphocyte, Lupus nephritis, Polimorfismo genético, Autoimmunity, Lymphocyte Activation, medicine.disease_cause, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], immune system diseases, Nefritis lúpica, Medicine and Health Sciences, Lupus Erythematosus, Systemic, Immunologia, Lymphocytes, Genetics, Multidisciplinary, Estudios de casos y controles, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies [Medical Subject Headings], Diseases::Immune System Diseases::Autoimmune Diseases::Lupus Erythematosus, Systemic [Medical Subject Headings], Predisposición genética a la enfermedad, Lupus Nephritis, Humanos, medicine.anatomical_structure, Medicine, Haplotipos, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Alelos, Nephritis, Research Article, Genotype, Inflammatory Diseases, T cell, Science, Immunology, Antígenos CD5, Single-nucleotide polymorphism, Autoinmunidad, CD5 Antigens, Limfòcits, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility::Genetic Predisposition to Disease [Medical Subject Headings], Rheumatology, Lupus eritematós sistèmic, Lupus eritematoso sistémico, medicine, Humans, Genetic Predisposition to Disease, Allele, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Alleles, Polymorphism, Genetic, Lupus erythematosus, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Glycoproteins::Membrane Glycoproteins::Antigens, CD58 [Medical Subject Headings], business.industry, Haplotype, Biology and Life Sciences, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Haplotypes, Case-Control Studies, Lupus eritematós, business, Genotipo
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المؤلفون: José Luis García Serrano, María Carmen Cenit, María José del Rio, Miguel Cordero-Coma, Ana Márquez, Marina Begoña Gorroño-Echebarría, Alfredo Adán, Joseba Artaraz, Javier Martín, David Díaz Valle, Manuel Díaz-Llopis, Ricardo Blanco, J. Cañal, Victor Llorenç, Esperanza Pato, Norberto Ortego-Centeno, José Manuel Martín-Villa, Enrique de Ramón, Alejandro Fonollosa
المساهمون: [Márquez,A, Cénit,MC, Martín,J] Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, CSIC, Granada, Spain. [Cordero-Coma,M] Ophthalmology Department, Hospital de León, Spain. [Ortego-Centeno,N] Internal Medicine Department, Hospital Clínico San Cecilio, Granada, Spain. [Adán,A, Llorenç,V] Ophthalmology Department, Hospital Clínic, Barcelona, Spain. [Fonollosa,A, Artaraz,J] Ophthalmology Department, Hospital de Cruces, Bilbao, Spain. [Díaz Valle,D] Ophthalmology Department, Hospital Clínico San Carlos, Madrid, Spain. [Pato,E] Rheumatology Department, Hospital Clínico San Carlos, Madrid, Spain. [Blanco,R] Rheumatology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Cañal,J] Ophthalmology Department, Hospital Marqués de Valdecilla, IFIMAV, Santander, Spain. [Díaz-Llopis,M] Ophthalmology Department, Hospital La Fe, Valencia, Spain.[Ramón,E de] Internal Medicine Department, Hospital Carlos Haya, Málaga, Spain. [Rio,MJ del] Ophthalmology Department, Hospital Carlos Haya, Málaga, Spain. [García Serrano,JL] Ophthalmology Department, Hospital Clínico San Cecilio, Granada, Spain. [Martín-Villa,JM] Immunology Department, Facultad de Medicina, Universidad Complutense de Madrid, Spain. [Gorroño-Echebarría,MB] Ophthalmology Department, Hospital Principe de Asturias, Alcalá de Henares, Spain., Universitat de Barcelona
المصدر: PLoS ONE
Dipòsit Digital de la UB
Universidad de Barcelona
PLoS ONE, Vol 8, Iss 10, p e76777 (2013)
Digital.CSIC. Repositorio Institucional del CSIC
instname
Recercat. Dipósit de la Recerca de Catalunyaمصطلحات موضوعية: Male, Phenomena and Processes::Genetic Phenomena::Phenotype [Medical Subject Headings], Polimorfismo de nucleótido simple, lcsh:Medicine, Interferó, Autoimmunity, Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], medicine.disease_cause, Linkage Disequilibrium, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, Interferon, Diseases::Eye Diseases::Uveal Diseases::Uveitis::Panuveitis::Uveitis, Anterior [Medical Subject Headings], lcsh:Science, Multidisciplinary, Autoimmunitat, Middle Aged, Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium [Medical Subject Headings], Uveitis, Anterior, Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], Modelos logísticos, Phenotype, Diseases::Eye Diseases::Retinal Diseases::Retinal Degeneration::Macular Degeneration::Macular Edema [Medical Subject Headings], Oftalmologia, Interferon Regulatory Factors, Female, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Fenotipo, Uveitis, Research Article, medicine.drug, Adult, Genotype, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intracellular Signaling Peptides and Proteins::Adaptor Proteins, Signal Transducing::Interferon Regulatory Factors [Medical Subject Headings], Check Tags::Male [Medical Subject Headings], Biology, Polymorphism, Single Nucleotide, Macular Edema, Genetic variation, Edema macular, medicine, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], Humans, Genetic Predisposition to Disease, Macular edema, Health Care::Health Care Quality, Access, and Evaluation::Quality of Health Care::Health Care Evaluation Mechanisms::Statistics as Topic::Models, Statistical::Logistic Models [Medical Subject Headings], Alleles, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], lcsh:R, medicine.disease, Uveítis anterior, Ophthalmology, Logistic Models, Factores reguladores del interferón, Haplotypes, Desequilibrio de ligamiento, Check Tags::Female [Medical Subject Headings], Genetic marker, Immunology, lcsh:Q, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], IRF5, Interferon regulatory factors
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المؤلفون: Rafael Arroyo, Bhairavi Swaminathan, Elena Urcelay, David Otaegui, Mª Jesus Pinto-Medel, Antonio Alcina, Koen Vandenbroeck, Alfredo Antigüedad, Fuencisla Matesanz, Miguel Lucas, María García-Barcina, María Fedetz, Oscar Fernandez, Eva Tolosa, Angelica Cuapio, Teresa Órpez, Javier Olascoaga, Miguel A. Ortiz, Iraide Alloza, Jorge R. Oksenberg
المساهمون: [Swaminathan,B, Alloza,I, Vandenbroeck,K] Neurogenomiks Laboratory, University of the Basque Country (UPV/EHU), Leioa, Spain. [Cuapio,A, Tolosa,E] Department of Immunology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany. [Matesanz,F, Alcina,A, Fedetz,M] Instituto de Parasitología y Biomedicina 'López Neyra' Consejo Superior de Investigaciones Científicas (CSIC), Granada, Spain. [García-Barcina,M] Servicio de Genética, Hospital de Basurto, Bilbao, Spain. [Fernández,O] Department of Neurology, Institute of Clinical Neurosciences, Hospital Regional Universitario Carlos Haya, Málaga, Spain. [ Lucas,M] Unidad de Esclerosis Múltiple, Hospital Virgen Macarena, Sevilla, Spain. [Orpez,T, Pinto-Medel,MJ] Research Laboratory, Institute of Clinical Neurosciences, Hospital Regional Universitario Carlos Haya, Málaga, Spain. [Otaegui,D] Área de Neurociencias, Instituto de Investigación Sanitaria Biodonostia, San Sebastián, Spain. [ Olascoaga,J] Servicio de Neurología, Unidad de Esclerosis Múltiple, Hospital Donostia, San Sebastián, Spain. [Urcelay,E, Ortiz,MA] Immunology Department H. Clínico S. Carlos, Instituto de Investigación Sanitaria S. Carlos (IdISSC), Madrid, Spain. [Arroyo,R] Multiple Sclerosis Unit, Neurology Department H. Clínico S. Carlos, Instituto de Investigación Sanitaria S. Carlos (IdISSC), Madrid, Spain. [Oksenberg,JR] Department of Neurology, University of California San Francisco, San Francisco, California, United States of America. [Antigüedad,A] Servicio de Neurología, Hospital de Basurto, Bilbao, Spain. [Vandenbroeck,K] IKERBASQUE, Basque Foundation for Science, Bilbao, Spain, This work was supported from the European Community’s Seventh Framework Programme [FP7/2007–2013] under grant agreement no. 212877 (UEPHA*MS, ref. IT512-10). UEPHA*MS (No 2121877). Ministerio de Ciencia e Innovación - FEDER (SAF2009-11491) and FIS_FEDER (CP10/00526), Junta de Andalucía-FEDER (P07-CVI-02551).
المصدر: Addi. Archivo Digital para la Docencia y la Investigación
instname
PLoS ONE, Vol 8, Iss 4, p e62376 (2013)
Digital.CSIC. Repositorio Institucional del CSIC
PLoS ONEمصطلحات موضوعية: Antigens, Differentiation, T-Lymphocyte, CD4-Positive T-Lymphocytes, Male, BIOCHEMISTRY AND MOLECULAR BIOLOGY, lcsh:Medicine, Genome-wide association study, Polimorfismo genético, CD8-Positive T-Lymphocytes, Lymphocyte Activation, Linkage Disequilibrium, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], 0302 clinical medicine, Health Care::Environment and Public Health::Public Health::Epidemiologic Methods::Epidemiologic Research Design::Genome-Wide Association Study [Medical Subject Headings], Gene Order, Cluster Analysis, Cytotoxic T cell, lcsh:Science, Genetics, 0303 health sciences, Multidisciplinary, Genome-wide association, T Cells, Chromosome Mapping, Genomics, Helper 17 cells, Neurology, AGRICULTURAL AND BIOLOGICAL SCIENCES, Cytokines, Female, Haplotipos, Diseases::Immune System Diseases::Autoimmune Diseases::Autoimmune Diseases of the Nervous System::Demyelinating Autoimmune Diseases, CNS::Multiple Sclerosis [Medical Subject Headings], Research Article, Adult, Multiple Sclerosis, Immune Cells, Immunology, Single-nucleotide polymorphism, Biology, Polymorphism, Single Nucleotide, White People, Autoimmune Diseases, Central-nervous-system, Young Adult, 03 medical and health sciences, Antigen, Antigens, CD, Humans, SNP, Genetic Predisposition to Disease, Protein Interaction Domains and Motifs, 030304 developmental biology, Inflammation, MEDICINE, Haplotype, lcsh:R, Immunity, Timocitos, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], Haplotypes, Genetic Loci, Spain, Esclerosis múltiple, estudio de asociación genómica completa, Genetic Polymorphism, Anatomy::Cells::Thymocytes [Medical Subject Headings], Clinical Immunology, Cytokine secretion, lcsh:Q, Population Genetics, CD8, 030215 immunology, Anti-CD6 monoclonal-antibody
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المؤلفون: F David Carmona, Jose-Ezequiel Martin, Lorenzo Beretta, Carmen P Simeón, Patricia E Carreira, José Luis Callejas, Mónica Fernández-Castro, Luis Sáez-Comet, Emma Beltrán, María Teresa Camps, María Victoria Egurbide, Spanish Scleroderma Group, Paolo Airó, Raffaella Scorza, Claudio Lunardi, Nicolas Hunzelmann, Gabriela Riemekasten, Torsten Witte, Alexander Kreuter, Jörg H W Distler, Rajan Madhok, Paul Shiels, Jacob M van Laar, Carmen Fonseca, Christopher Denton, Ariane Herrick, Jane Worthington, Annemie J Schuerwegh, Madelon C Vonk, Alexandre E Voskuyl, Timothy R D J Radstake, Javier Martín
المساهمون: Rheumatology, CCA - Disease profiling, The Spanish Scleroderma Group, [Carmona,FD, Martín JE] Instituto de Parasitología y Biomedicina López-Neyra, CSIC, Granada, Spain. [ Beretta,L, Scorza,R] Referral Center for Systemic Autoimmune Diseases, Fondazione IRCCS Ca’ Granda Ospedale Maggiore Policlinico di Milano, University of Milan, Italy. [ Carmen,P S] Department of Internal Medicine, Hospital Vall d’Hebron, Barcelona, Spain. [Carreira,P E] Department of Rheumatology, Hospital 12 de Octubre, Madrid, Spain. [Callejas,J.L. ] Department of Internal Medicine, Hospital Clínico San Cecilio, Granada, Spain. [Fernández-Castro,M.] Department of Rheumatology, Hospital Puerta de Hierro Majadahonda, Madrid, Spain. [Sáez-Comet,L] Department of Internal Medicine, Hospital Universitario Miguel Servet, Zaragoza, Spain. [Beltran,E.] Department of Rheumatology, Hospital General Universitario de Valencia, Spain. [Camps,MT.] Department of Internal Medicine, Hospital Carlos Haya, Málaga, Spain. [Egurbide,M.V.] Department of Internal Medicine, Hospital de Cruces, Barakaldo, Spain. [Airo,P.] Servizio di Reumatologia ed Immunologia Clinica Spedali Civili, Brescia, Italy. [Lunardi,C] Department of Medicine, Universita` degli Studi di Verona, Verona, Italy. [Hunzelmann, N] Department of Dermatology, University of Cologne, Cologne, Germany. [Riemekasten,G] Department of Rheumatology and Clinical Immunology, Charite´ University Hospital, Berlin, Germany. [Witte,T] Hannover Medical School, Hannover, Germany. [Kreuter,A] Ruhr University of Bochum, Germany. [Distler,JHW] Department of Internal Medicine 3, Institute for Clinical Immunology, University of Erlangen-Nuremberg, Erlangen, Germany. [Madhok,R, Shiels,P] Centre for Rheumatic Diseases, Glasgow Royal Infirmary, University of Glasgow, United Kingdom. [Van Laar,JM] Institute of Cellular Medicine, Newcastle University, Newcastle, United Kingdom. [Fonseca,C, Denton,C] Centre for Rheumatology, Royal Free and University College Medical School, London, United Kingdom. [Herrick,A, Worthington, J] Arthritis Research UK Epidemiology Unit, University of Manchester, Manchester Academic Health Science Centre, Manchester, United Kingdom. [Schuerwegh,AJ] Department of Rheumatology, Leiden University Medical Center, Leiden, The Netherlands. [Vonk,MC, Radstake,T.R.D] Department of Rheumatology, Radboud University Nijmegen Medical Center, Nijmegen, The Netherlands. [Voskuyl,AE] Department of Rheumatology, VU University Medical Center, Amsterdam, The Netherlands. [Radstake,T.R.D] Department of Rheumatology and Clinical Immunology, University Medical Center Utrecht, The Netherland., 17552, Arthritis Research UK, United Kingdom
المصدر: PLoS ONE, Vol 8, Iss 1, p e54419 (2013)
PLoS One, 8
PLoS One, 8, 1
PLoS ONE, 8(1):e54419. Public Library of Science
Carmona, F D, Martin, J E, Beretta, L, Simeon, C P, Carreira, P E, Callejas, J L, Fernandez-Castro, M, Saez-Comet, L, Beltran, E, Camps, M T, Egurbide, M V, Airo, P, Scorza, R, Lunardi, C, Hunzelmann, N, Riemekasten, G, Witte, T, Kreuter, A, Distler, J H W, Madhok, R, Shiels, P, van Laar, J M, Fonseca, C, Denton, C, Herrick, A, Worthington, J, Schuerwegh, A J, Vonk, M C, Voskuyl, A E, Radstake, T R D J & Martin, J 2013, ' The Systemic Lupus Erythematosus IRF5 Risk Haplotype Is Associated with Systemic Sclerosis ', PLoS ONE, vol. 8, no. 1, e54419 . https://doi.org/10.1371/journal.pone.0054419
PLoS ONEمصطلحات موضوعية: Male, Linkage disequilibrium, Phenomena and Processes::Genetic Phenomena::Phenotype [Medical Subject Headings], Polimorfismo de nucleótido simple, SLE, lcsh:Medicine, Autoimmunity, Genome-wide association study, Linkage Disequilibrium, Scleroderma, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, Named Groups::Persons::Population Groups::Continental Population Groups::European Continental Ancestry Group [Medical Subject Headings], Risk Factors, IRF5, Genetics of the Immune System, Lupus Erythematosus, Systemic, Diseases::Skin and Connective Tissue Diseases::Skin Diseases::Scleroderma, Systemic [Medical Subject Headings], skin and connective tissue diseases, lcsh:Science, Multidisciplinary, Diseases::Immune System Diseases::Autoimmune Diseases::Lupus Erythematosus, Systemic [Medical Subject Headings], Predisposición genética a la enfermedad, Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], Phenotype, Interferon Regulatory Factors, SYSTEMIC SCLEROSIS, Medicine, Evaluation of complex medical interventions Auto-immunity, transplantation and immunotherapy [NCEBP 2], Female, TYPE I INTERFERON, Haplotipos, Research Article, Factores de riesgo, Immunology, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intracellular Signaling Peptides and Proteins::Adaptor Proteins, Signal Transducing::Interferon Regulatory Factors [Medical Subject Headings], Check Tags::Male [Medical Subject Headings], Health Care::Environment and Public Health::Public Health::Epidemiologic Factors::Causality::Risk Factors [Medical Subject Headings], Single-nucleotide polymorphism, Human leukocyte antigen, Biology, Polymorphism, Single Nucleotide, White People, Autoimmune Diseases, Rheumatology, Lupus eritematoso sistémico, Genetics, Humans, Genetic Predisposition to Disease, Grupo de ascendencia continental europea, Allele, Allele frequency, Alleles, Genetic Association Studies, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Scleroderma, Systemic, Haplotype, lcsh:R, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genetic Loci [Medical Subject Headings], Human Genetics, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], Factores reguladores del interferón, Haplotypes, Desequilibrio de ligamiento, Check Tags::Female [Medical Subject Headings], Genetic Loci, Genetics of Disease, Genetic Polymorphism, Clinical Immunology, lcsh:Q, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], Population Genetics
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المؤلفون: Germán Soriano, Camilla Stephens, M.A. López-Nevot, Antonia Moreno-Casares, Manuel Romero-Gómez, M. Isabel Lucena, Francisco Ruiz-Cabello, Raúl J. Andrade, Eugenia Ulzurrun
المساهمون: [Stephens,C, Ulzurrun,E, Lucena,MI, Andrade,RJ] Unidad de Gestión Clínica de Enfermedades Digestivas, Servicio de Farmacología Clínica, Hospital Universitario Virgen de la Victoria. Instituto de Investigación Biomédica de Málaga-IBIMA, Universidad de Málaga, Spain. [López-Nevot,MA, Ruiz-Cabello,F, Moreno-Casares,A] Departamento de Bioquímica y Biología Molecular III/Inmunología, Hospital Universitario Virgen de las Nieves, Universidad de Granada, Spain. [Soriano,G] Servicio de Gastroenterología, Hospital de la Santa Creu i Sant Pau, Universitat Autònoma de Barcelona, Barcelona, Spain. [Romero-Gómez,M] Unidad de Gestión Clínica de Enfermedades Digestivas, Hospital Universitario de Valme, Universidad de Sevilla, Andalucía Tech, Sevilla, Spain. [Stephens,C, Soriano,G, Romero-Gómez,M, Andrade,RJ] Centro de Investigación Biomédica en Red de Enfermedades Hepáticas y Digestivas (CIBERehd), Barcelona, Spain. [Ruiz-Cabello,F] Red Genómica del Cáncer, Madrid, Spain., This study was supported by the research grant Proyecto Excelencia P10-CTS-6470 and by the Agencia Española del Medicamento. CIBERehd and Red Genómica del Cancer are funded by Instituto de Salud Carlos III
المصدر: PLoS One
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
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Digibug. Repositorio Institucional de la Universidad de Granada
PLoS ONE, Vol 8, Iss 7, p e68111 (2013)
PLoS ONEمصطلحات موضوعية: Male, Phenomena and Processes::Genetic Phenomena::Phenotype [Medical Subject Headings], España, lcsh:Medicine, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Glycoproteins::Membrane Glycoproteins::Histocompatibility Antigens Class I::HLA-A Antigens [Medical Subject Headings], Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Probability::Risk::Risk Factors [Medical Subject Headings], Major Histocompatibility Complex, Cohort Studies, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], chemistry.chemical_compound, Damage mechanics, HLA Antigens, Genotype, Pathology, lcsh:Science, Factores de Riesgo, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Liver injury, Antígenos HLA-DR, Multidisciplinary, Combinación Amoxicilina-Clavulanato de Potasio, Antígenos HLA-DQ, Liver Diseases, Phenomena and Processes::Immune System Phenomena::Immunity::Adaptive Immunity [Medical Subject Headings], Antígenos HLA-A, Middle Aged, Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], Phenotype, Anti-Bacterial Agents, Phenotypes, Antibacterianos, Medicine, Female, Haplotipos, Inmunidad Adaptativa, Chemical and Drug Induced Liver Injury, Fenotipo, Amino acid analysis, Research Article, Chemicals and Drugs::Chemical Actions and Uses::Pharmacologic Actions::Therapeutic Uses::Anti-Infective Agents::Anti-Bacterial Agents [Medical Subject Headings], Adult, Drugs and Devices, Genotyping, Clinical Research Design, Bilirubin, Predisposición Genética a la Enfermedad, Gastroenterology and Hepatology, Human leukocyte antigen, Biology, Amoxicillin-Potassium Clavulanate Combination, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Major Histocompatibility Complex::Genes, MHC Class II [Medical Subject Headings], Arginine, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Glycoproteins::Membrane Glycoproteins::Histocompatibility Antigens Class II::HLA-D Antigens::HLA-DR Antigens [Medical Subject Headings], Adverse Reactions, Diagnostic Medicine, medicine, Humans, Cadenas beta de HLA-DR, Genetic Testing, Allele, Genes Clase I del Complejo de Histocompatibilidad (MHC), Genetic Association Studies, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Glycoproteins::Membrane Glycoproteins::Histocompatibility Antigens Class II::HLA-D Antigens::HLA-DR Antigens::HLA-DR beta-Chains [Medical Subject Headings], Alleles, Aged, Clinical Genetics, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Glycoproteins::Membrane Glycoproteins::Histocompatibility Antigens Class II::HLA-D Antigens::HLA-DQ Antigens [Medical Subject Headings], Enfermedad Hepática Inducida por Drogas, Chemicals and Drugs::Organic Chemicals::Amides::Lactams::beta-Lactams::Penicillins::Penicillin G::Ampicillin::Amoxicillin::Amoxicillin-Potassium Clavulanate Combination [Medical Subject Headings], Diseases::Substance-Related Disorders::Poisoning::Drug-Induced Liver Injury [Medical Subject Headings], Histocompatibility Antigens Class I, lcsh:R, Haplotype, Histocompatibility Antigens Class II, Personalized Medicine, medicine.disease, chemistry, Pharmacogenetics, Spain, Immunology, Clinical Immunology, lcsh:Q, Genes Clase II del Complejo de Histocompatibilidad (MHC), Biomarkers, General Pathology, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Major Histocompatibility Complex::Genes, MHC Class I [Medical Subject Headings]
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المؤلفون: Luis Javier Martinez-Gonzalez, José Antonio Lorente Acosta, Juan Carlos Álvarez Merino, José Manuel Cózar Olmo, María Saiz Guinaldo, Maria Jesus Alvarez-Cubero
المساهمون: [Álvarez-Cubero,MJ, Saiz Guinaldo,M, Álvarez Merino,LJ, Lorente Acosta,JA] Laboratory of Genetic Identification, Legal Medicine and Toxicology Department, Facultad de Medicina, Universidad de Granada, Granada, Spain. [Martínez-González,LJ, Álvarez Merino,JC, Lorente Acosta,JA] GENYO (Pfizer-University of Granada-Andalusian Government Centre for Genomics and Oncological Research), Granada, Spain. [Cózar Olmo,JM] Service of Urology, University Hospital Virgen de las Nieves, Granada, Spain.
المصدر: PLoS ONE, Vol 7, Iss 7, p e41201 (2012)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
PLoS ONEمصطلحات موضوعية: Male, Epidemiology, España, lcsh:Medicine, Oportunidad Relativa, Haplogroup, Cohort Studies, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Prostate cancer, Antígeno Prostático Específico, Prostate gland, Genotype, Odds Ratio, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Probability::Odds Ratio [Medical Subject Headings], lcsh:Science, Masculino, Mitocondrias, Anatomy::Cells::Cellular Structures::Intracellular Space::Cytoplasm::Cytoplasmic Structures::Organelles::Mitochondria [Medical Subject Headings], Genetics, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], education.field_of_study, Multidisciplinary, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies [Medical Subject Headings], Insertion mutation, Cancer Risk Factors, Environmental Causes of Cancer, ADN Mitocondrial, Estudios de Casos y Controles, Middle Aged, Mitochondrial DNA, Mitochondria, Humanos, Europe, Oncology, Chemicals and Drugs::Enzymes and Coenzymes::Enzymes::Hydrolases::Peptide Hydrolases::Endopeptidases::Serine Endopeptidases::Kallikreins::Prostate-Specific Antigen [Medical Subject Headings], Genetic Epidemiology, Medicine, Haplotipos, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Cancer Epidemiology, Cancer Screening, Research Article, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Sequence Analysis::Sequence Analysis, DNA [Medical Subject Headings], Clinical Research Design, Genetic Causes of Cancer, Population, Anciano, Polimorfismo Genético, Predisposición Genética a la Enfermedad, Análisis de Secuencia de ADN, Check Tags::Male [Medical Subject Headings], Biology, DNA, Mitochondrial, Health Care::Health Care Quality, Access, and Evaluation::Quality of Health Care::Health Care Evaluation Mechanisms::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies [Medical Subject Headings], Predisposing Conditions and Syndromes, Diseases::Neoplasms::Neoplasms by Site::Urogenital Neoplasms::Genital Neoplasms, Male::Prostatic Neoplasms [Medical Subject Headings], Cancer Genetics, Cancer Detection and Diagnosis, medicine, Humans, Genetic Predisposition to Disease, Named Groups::Persons::Age Groups::Adult::Aged [Medical Subject Headings], education, Aged, Chemicals and Drugs::Nucleic Acids, Nucleotides, and Nucleosides::Nucleic Acids::DNA::DNA, Circular::DNA, Mitochondrial [Medical Subject Headings], Clinical Genetics, Polymorphism, Genetic, Somatic mutation, Haplotype, lcsh:R, Personalized Medicine, Case-control study, Prostatic Neoplasms, Sequence Analysis, DNA, Prostate-Specific Antigen, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Biomarker Epidemiology, Haplotypes, Spain, Case-Control Studies, Mutation, Genetic Polymorphism, Haplogroups, lcsh:Q, Genotipo, Population Genetics, Human mitochondrial DNA haplogroup
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المؤلفون: Félix, Claverie-Martín, Víctor, García-Nieto, Cesar, Loris, Gema, Ariceta, Inmaculada, Nadal, Laura, Espinosa, Ángeles, Fernández-Maseda, Montserrat, Antón-Gamero, Africa, Avila, Álvaro, Madrid, Hilaria, González-Acosta, Elizabeth, Córdoba-Lanus, Fernando, Santos, Marta, Gil-Calvo, Mar, Espino, Elena, García-Martinez, Ana, Sanchez, Rafael, Muley, Mireia, Aguirre Meñica
المساهمون: RenalTube Group., [Claverie-Martín,F, González-Acosta,H, Córdoba-Lanus,E]Unidad de Investigación, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.[García-Nieto,V] Nefrología Pediátrica, Hospital Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain.[Loris,C] Nefrología Pediátrica, Hospital Infantil Miguel Servet, Zaragoza, Spain.[Ariceta,G] Nefrología Pediátrica, Hospital de Cruces, Baracaldo, Spain. [Nadal,I] Nefrología Pediátrica, Hospital Virgen del Camino, Pamplona, Spain.[Espinosa,L] Nefrología Pediátrica, Hospital La Paz, Madrid, Spain. [Fernández-Maseda,A] Nefrología Pediátrica, Hospital Virgen de la Salud, Toledo, Spain. [Antón-Gamero,M, García-Martinez,E] Nefrología Pediátrica, Hospital Reina Sofía, Córdoba, Spain.[Avila,A] Nefrología Pediátrica, Complejo Hospitalario de Jaén, Spain. [Madrid,A] Nefrología Pediátrica, Hospital Vall d’Hebron, Barcelona, Spain.[Santos,F] Nefrología Pediátrica, Hospital Central de Asturias, Oviedo, Spain. [Gil-Calvo,M] Nefrología Pediátrica, Hospital Clínico, Santiago de Compostela, Spain.[Espino,M] Pediatría, Hospital Fundación Alcorcón, Madrid, Spain. [Sanchez,A] Nefrología Pediátrica, Hospital Universitario Virgen del Rocío, Sevilla, Spain. [Muley,R] Nefrología Pediátrica, Hospital 12 de Octubre, Madrid, Spain.
المصدر: PLoS ONE
PLoS ONE, Vol 8, Iss 1, p e53151 (2013)مصطلحات موضوعية: Male, Pathology, Anatomy and Physiology, Heredity, Substitution mutation, DNA Mutational Analysis, Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], medicine.disease_cause, Gastroenterology, Magnesio, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Cohort Studies, Autosomal Recessive, Transplante renal, Reacción en cadena de la polimerasa, Chronic Kidney Disease, Medicine, Hypercalciuria, Magnesium, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Sequence Analysis::Sequence Analysis, DNA::DNA Mutational Analysis [Medical Subject Headings], Child, Phenomena and Processes::Genetic Phenomena::Phenotype::Endophenotypes [Medical Subject Headings], Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Kidney, Mutation, Multidisciplinary, Named Groups::Persons::Age Groups::Child::Child, Preschool [Medical Subject Headings], Pediatric Nephrology, Diseases::Nutritional and Metabolic Diseases::Nutrition Disorders::Malnutrition::Deficiency Diseases::Magnesium Deficiency [Medical Subject Headings], Middle Aged, Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], Mutation detection, Polymerase chain reaction, Nephrocalcinosis, Phenotypes, medicine.anatomical_structure, Phenotype, Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Computational Biology [Medical Subject Headings], Nephrology, Named Groups::Persons::Age Groups::Adolescent [Medical Subject Headings], Child, Preschool, Female, Kidney Diseases, Research Article, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Models, Theoretical::Models, Biological::Models, Genetic [Medical Subject Headings], Adult, medicine.medical_specialty, Named Groups::Persons::Age Groups::Adult::Young Adult [Medical Subject Headings], Adolescent, Science, Diseases::Nutritional and Metabolic Diseases::Metabolic Diseases::Calcium Metabolism Disorders::Calcinosis::Nephrocalcinosis [Medical Subject Headings], Genotypes, Check Tags::Male [Medical Subject Headings], Diseases::Pathological Conditions, Signs and Symptoms::Signs and Symptoms::Urological Manifestations::Hypercalciuria [Medical Subject Headings], Hypomagnesemia, Young Adult, Mutación de sustitución, Genetic Mutation, Internal medicine, Detección de mutaciones, Genetics, Humans, Genetic Predisposition to Disease, Biology, Clinical Genetics, Renal Physiology, Polymorphism, Genetic, Models, Genetic, business.industry, Point mutation, Riñones, Computational Biology, Kidneys, Renal transplantation, Human Genetics, Renal System, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Diseases::Female Urogenital Diseases and Pregnancy Complications::Female Urogenital Diseases::Urologic Diseases::Kidney Diseases::Kidney Diseases, Cystic::Polycystic Kidney Diseases [Medical Subject Headings], Transplantation, Check Tags::Female [Medical Subject Headings], Haplotypes, Spain, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Cohort Studies [Medical Subject Headings], Claudins, Genetics of Disease, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Membrane Proteins::Claudins [Medical Subject Headings], business, Magnesium Deficiency, Rare disease
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المؤلفون: Berta Luzón-Toro, Salud Borrego, Rocío Núñez-Torres, Ana Torroglosa, Guillermo Antiñolo, Raquel M. Fernández, Juan Carlos de Agustín, María Valle Enguix-Riego
المساهمون: [Luzón-Toro,B, Torroglosa,A, Núñez-Torres,R, Enguix-Riego,MV, Fernández,RM, Antiñolo,G, Borrego,S] Department of Genetics, Reproduction and Fetal Medicine. Institute of Biomedicine of Seville (IBIS), University Hospital Virgen del Rocío/CSIC/University of Seville. Centre for Biomedical Network Research on Rare Diseases (CIBERER), Seville, Spain. [de Agustín,JC] Department of Pediatric Surgery, University Hospital Virgen del Rocío, Seville, Spain., This study was funded by the Instituto de Salud Carlos III, Spain (PI1001290) and Consejeria de Innovación Ciencia y Empresa de la Junta de Andalucia (CTS-2590 and CTS-7447). The CIBER de Enfermedades Raras is an initiative of the ISCIII, Spanish Ministry of Science and Innovation
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
PLoS ONE
PLoS ONE, Vol 7, Iss 5, p e36524 (2012)مصطلحات موضوعية: Male, DNA Mutational Analysis, Sistema Nervioso Entérico, Gene Identification and Analysis, Genome-wide association study, Disease, Bioinformatics, Variación Genética, Proto-Oncogene Mas, Biochemistry, Enteric Nervous System, Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, Chlorocebus aethiops, Organisms::Eukaryota::Animals [Medical Subject Headings], Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Sequence Analysis::Sequence Analysis, DNA::DNA Mutational Analysis [Medical Subject Headings], Neurregulina-1, Genetics, Multidisciplinary, biology, Major gene, Penetrance, COS Cells, Medicine, Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Cercopithecidae::Cercopithecinae::Cercopithecus::Cercopithecus aethiops [Medical Subject Headings], Female, Pediatric Gastroenterology, Phenomena and Processes::Genetic Phenomena::Genetic Variation [Medical Subject Headings], Research Article, Colon, Science, Neuregulin-1, Check Tags::Male [Medical Subject Headings], Single-nucleotide polymorphism, Context (language use), Gastroenterology and Hepatology, Enfermedad de Hirschsprung, Polymorphism, Single Nucleotide, Molecular Genetics, Diseases::Digestive System Diseases::Digestive System Abnormalities::Hirschsprung Disease [Medical Subject Headings], Genetic Mutation, mental disorders, Animals, Humans, Hirschsprung Disease, Neuregulin 1, Biology, Gene, Anatomy::Cells::Cells, Cultured::Cell Line::Cell Line, Transformed::COS Cells [Medical Subject Headings], Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Peptides::Intercellular Signaling Peptides and Proteins::Nerve Growth Factors::Neuregulins::Neuregulin-1 [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Population Biology, Genetic Variation, Proteins, Transmembrane Proteins, Check Tags::Female [Medical Subject Headings], Haplotypes, Mutation, Genetics of Disease, biology.protein, Gene Function, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], Population Genetics
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المؤلفون: Guillermo Izquierdo, Javier Gayán, Carmen Arnal, Dorothy Ndagire, Antonio Catalá-Rabasa, Agustín Ruiz, Fuencisla Matesanz, María Fedetz, Concepción Delgado, Miguel Lucas, María M. Abad-Grau, Oscar Fernández, Antonio Alcina
المساهمون: [Alcina, A, Fedetz, M, Ndagire, D, Catalá-Rabasa, A, Matesanz,F] Instituto de Parasitología y Biomedicina ‘López Neyra’, Consejo Superior de Investigaciones Científicas (IPBLN-CSIC), Granada, Spain [Abad-Grau,M del M] Departamento de Lenguajes y Sistemas Informáticos, CITIC, Universidad de Granada, Granada, Spain.[Izquierdo,G, Matesanz,F] Unidad de Esclerosis Múltiple, Hospital Virgen Macarena, Sevilla, Spain.[Lucas,M] Servicio de Biología Molecular, Hospital Virgen Macarena, Sevilla, Spain. [Fernández,O] Servicio de Neurología, Instituto de Neurociencias Clínicas, Hospital Carlos Haya, Málaga, Spain. [Ruiz,A, Gayán,J] Departamento de Genómica Estructural, Neocodex, Sevilla, Spain.[Delgado,C] Centro Regional de Transfusión Sanguínea Granada-Almería, Granada, Spain.[Arnal,C] Servicio de Neurología, Hospital Virgen de las Nieves, Granada, Spain., This work was supported by the Ministerio de Ciencia e Innovación - Fondos Feder [PN-SAF2009-11491 to AA], Junta de Andalucía [P07-CVI-02551 to AA], and Fondo de Investigación Sanitaria [FIS PI081636, CP10/00526 to FM]. MF and DN are holders of a fellowship from Fundación Española de Esclerosis Múltple (FEDEM). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
المصدر: PLoS ONE, Vol 7, Iss 1, p e29819 (2012)
Digibug. Repositorio Institucional de la Universidad de Granada
instname
PLoS ONE
Digital.CSIC. Repositorio Institucional del CSICمصطلحات موضوعية: Male, Genome-wide association study, Linkage Disequilibrium, Inflammatory bowel disease, Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], 0302 clinical medicine, Named Groups::Persons::Population Groups::Continental Population Groups::European Continental Ancestry Group [Medical Subject Headings], Grupo de Ascendencia Continental Europea, Regulación de la Expresión Génica, Masculino, lcsh:Science, 0303 health sciences, Disciplines and Occupations::Natural Science Disciplines::Biological Science Disciplines::Biology::Genetics::Genetics, Population [Medical Subject Headings], Genomics, Humanos, 3. Good health, Neurology, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Models, Statistical::Logistic Models [Medical Subject Headings], Medicine, musculoskeletal diseases, Multiple Sclerosis, Immunology, Quantitative Trait Loci, Predisposición Genética a la Enfermedad, Check Tags::Male [Medical Subject Headings], Locus (genetics), Single-nucleotide polymorphism, Human leukocyte antigen, White People, Multiple sclerosis, 03 medical and health sciences, Chemicals and Drugs::Biological Factors::Antigens::Antigens, Surface::Histocompatibility Antigens::HLA Antigens::HLA-D Antigens::HLA-DQ Antigens::HLA-DQ beta-Chains [Medical Subject Headings], Genetics, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], Humans, Variant genotypes, Biology, Alleles, Haplotype, lcsh:R, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Molecular Epidemiology::Genome-Wide Association Study [Medical Subject Headings], Genetics, Population, Logistic Models, African americans, Esclerosis Múltiple, Check Tags::Female [Medical Subject Headings], lcsh:Q, Estudios de Asociación Genética, Polimorfismo de Nucleótido Simple, Gene expression, 030217 neurology & neurosurgery, Neuroscience, Desequilibrio de Ligamiento, Linkage disequilibrium, Phenomena and Processes::Genetic Phenomena::Genetic Processes::Gene Expression Regulation [Medical Subject Headings], lcsh:Medicine, Genome-wide association studies, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Probability::Risk::Risk Factors [Medical Subject Headings], Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Genetic Association Studies [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Risk Factors, HLA-DQ beta-Chains, Multidisciplinary, Cadenas HLA-DRB1, Adulto, Femenino, Phenomena and Processes::Genetic Phenomena::Genetic Linkage::Linkage Disequilibrium [Medical Subject Headings], Cadenas HLA-DRB5, Chemicals and Drugs::Biological Factors::Antigens::Antigens, Surface::Histocompatibility Antigens::Histocompatibility Antigens Class II::HLA-D Antigens::HLA-DQ Antigens::HLA-DQ beta-Chains [Medical Subject Headings], Female, Haplotipos, Alelos, Diseases::Immune System Diseases::Autoimmune Diseases::Autoimmune Diseases of the Nervous System::Demyelinating Autoimmune Diseases, CNS::Multiple Sclerosis [Medical Subject Headings], Research Article, Adult, Chemicals and Drugs::Biological Factors::Antigens::Antigens, Surface::Histocompatibility Antigens::Histocompatibility Antigens Class II::HLA-D Antigens::HLA-DR Antigens::HLA-DR beta-Chains::HLA-DRB5 Chains [Medical Subject Headings], Polymorphism, Single Nucleotide, Estudio de Asociación del Genoma Completo, Diseases::Pathological Conditions, Signs and Symptoms::Pathologic Processes::Disease Attributes::Disease Susceptibility::Genetic Predisposition to Disease [Medical Subject Headings], Systemic lupus erythematosus, Cadenas beta de HLA-DQ, Modelos Logísticos, Genetic Predisposition to Disease, Genética de Población, Allele, Genetic Association Studies, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], 030304 developmental biology, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Sitios de Carácter Cuantitativo, Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genetic Loci::Quantitative Trait Loci [Medical Subject Headings], Demyelinating Disorders, HLA-DRB5 Chains, Gene Expression Regulation, Haplotypes, Expression quantitative trait loci, Genome-Wide Association Study, HLA-DRB1 Chains
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المؤلفون: Fernando Martinez, Sonsoles Morcillo, Juan Carlos Martín-Escudero, Gemma Rojo, María Teresa Martínez-Larrad, Federico Soriguer, Josep Redon, Manuel Serrano-Ríos, Felipe J. Chaves, Maria L. Mansego, Carina Zabena
المساهمون: [Mansego,ML, Chaves,FJ] Genotyping and Genetic Diagnosis Unit, Fundación de Investigación del Hospital Clínico de Valencia-INCLIVA, Valencia, Spain [Martínez,F, Redon,J] Fundación de Investigación del Hospital Clínico de Valencia- INCLIVA, Hypertension Clinic, Hospital Clínico Universitario, University of Valencia, Valencia, Spain. [Martínez-Larrad,MT, Zabena,C, Serrano-Ríos,M] Hospital Clínico San Carlos, Department of Internal Medicine II, Madrid, Spain. [Rojo,G, Morcillo,S, Soriguer,F] Endocrinology and Nutrition Department, Carlos Haya University Hospital, Málaga, Spain. [Martín-Escudero,JC] Internal Medicine department. Hospital Rio Hortega, University of Valladolid, Valladolid, Spain. [Mansego,ML, Chaves,FJ] Centro de Investigación Biomédica en Red (CIBER) de Diabetes y Enfermedades Metabólicas Asociadas ‘‘CIBERDEM’’, Institute of Health Carlos III, Ministry of Health, Madrid, Spain. [Martínez,F, Redon,J] Centro de Investigación Biomédica en Red (CIBER) de Fisiopatología, Obesidad y Nutrición [CIBEROB (CIBER 03/06)], Institute of Health Carlos III, Ministry of Health, Madrid, Spain. [Martínez-Larrad,MT, Serrano-Ríos,M, Rojo,G, Soriguer,F] Centro de Investigación Biomédica en Red (CIBER) de Diabetes y Enfermedades Metabólicas Asociadas (CIBERDEM), Institute of Health Carlos III, Ministry of Health, Madrid, Spain., Funding: This study was supported by grants SAF2005-02883 from the Interministry Commission of Science and Technology (CICYT), Biomedical Research Centers (CIBER) of Physiopathology, Obesity and Nutrition (CIBEROB), CIBER of Diabetes and Metabolic Diseases (CIBERDEM), Carlos III Health Institute Madrid, the Spanish Health Ministry, GRUPOS 03/101 and 2005/027 from the Valencian Government and European Network of Excellence Ingenious Hypercare (EPSS-037093) from the European Commission, and Biobank grant from the National Health Institute Carlos III FEDER RD09/0076/00132 (Madrid, Spain). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
المصدر: PLoS ONE
PLoS ONE Vol. 7 Issue 3
PLoS ONE, Vol 7, Iss 3, p e31853 (2012)
RODERIC. Repositorio Institucional de la Universitat de Valéncia
instnameمصطلحات موضوعية: Male, Anatomy and Physiology, España, Diabetes Mellitus Tipo 2, Named Groups::Persons::Age Groups::Adult::Middle Aged [Medical Subject Headings], Type 2 diabetes, Resistencia a la Insulina, Variación Genética, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Probability::Risk::Risk Factors [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genotype::Haplotypes [Medical Subject Headings], Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Endocrinology, Polymorphism (computer science), Risk Factors, Análisis de Regresión, Factores de Riesgo, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Genetics, education.field_of_study, Multidisciplinary, Adulto, Middle Aged, Cardiovascular Diseases, Diseases::Nutritional and Metabolic Diseases::Metabolic Diseases::Glucose Metabolism Disorders::Diabetes Mellitus::Diabetes Mellitus, Type 2 [Medical Subject Headings], Regression Analysis, Medicine, Female, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation [Medical Subject Headings], Fatty Acid Binding Protein 3, Research Article, Adult, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Mutation [Medical Subject Headings], Genotype, Science, Population, Check Tags::Male [Medical Subject Headings], Single-nucleotide polymorphism, Endocrine System, Biology, Fatty Acid-Binding Proteins, Polymorphism, Single Nucleotide, Diseases::Nutritional and Metabolic Diseases::Metabolic Diseases::Glucose Metabolism Disorders::Hyperinsulinism::Insulin Resistance [Medical Subject Headings], Insulin resistance, Genetic variation, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], medicine, Humans, Named Groups::Persons::Age Groups::Adult::Aged [Medical Subject Headings], education, Diseases::Cardiovascular Diseases [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Structures::Genome::Genome Components::Genes::Alleles [Medical Subject Headings], Alleles, Aged, Diabetic Endocrinology, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Statistics as Topic::Regression Analysis [Medical Subject Headings], Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], Polymorphism, Genetic, Endocrine Physiology, Haplotype, Genetic Variation, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic [Medical Subject Headings], medicine.disease, Obesity, Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Carrier Proteins::Fatty Acid-Binding Proteins [Medical Subject Headings], Check Tags::Female [Medical Subject Headings], Diabetes Mellitus, Type 2, Haplotypes, Spain, Metabolic Disorders, Mutation, Insulin Resistance, Population Genetics
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