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1Academic Journal
المؤلفون: Enrique Eduardo Sanchez-Castro, Renato LaTorre-Ramírez, Carlos Patricio Padilla Rojas, Frank Lizaraso-Soto, Jorge Calderón Ticona, José Solís Villanueva, Dr, Wilser Andrés García-Quispes, Mónica Yolanda Paredes Anaya
المصدر: Horizonte Médico, Vol 19, Iss 4, Pp 14-19 (2020)
مصطلحات موضوعية: diabetes mellitus tipo 2, proteína tirosina fosfatasa no receptora tipo 1, marcadores genéticos, polimorfismo de nucleótido simple, Medicine
وصف الملف: electronic resource
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2Dissertation/ Thesis
المؤلفون: González Fernández, Lauro
Thesis Advisors: Tapia García, José Antonio, Universidad de Extremadura. Departamento de Fisiología
مصطلحات موضوعية: Espermatozoides, Mamíferos, Proteína tirosina fosfatasa, Spermatozoa, Mammals, Pprotein tyrosine phosphatase, 2401.13 Fisiología Animal, 3104.11 Reproducción, 3109.02 Genética
URL الوصول: http://hdl.handle.net/10662/6920
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3Dissertation/ Thesis
Thesis Advisors: Tapia García, José Antonio, Universidad de Extremadura. Departamento de Fisiología
مصطلحات موضوعية: Espermatozoides, Mamíferos, Proteína tirosina fosfatasa, Spermatozoa, Mammals, Pprotein tyrosine phosphatase, 2401.13 Fisiología Animal, 3104.11 Reproducción, 3109.02 Genética
URL الوصول: http://hdl.handle.net/10662/6920
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4Report
المؤلفون: Duperou Luna, Paulina
المساهمون: Chávez Riveros, Alejandra, Cortés Benítez, Juan Francisco
مصطلحات موضوعية: Proteína Tirosina Fosfatasa 1B, α-glucosidasa, Diabetes mellitus tipo 2, Química Farmacéutica Biológica, Licenciatura
وصف الملف: 1 recurso en línea (44 páginas); application/pdf
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5Academic Journal
المصدر: Articles publicats en revistes (Biomedicina)
مصطلحات موضوعية: Proteïna-tirosina-fosfatasa, Malalties neurodegeneratives, Protein-tyrosine phosphatase, Neurodegenerative Diseases
وصف الملف: 27 p.; application/pdf
Relation: Reproducció del document publicat a: https://doi.org/10.3389/fnsyn.2021.749001; Frontiers In Synaptic Neuroscience, 2021, vol. 13, p. 749001; https://doi.org/10.3389/fnsyn.2021.749001; http://hdl.handle.net/2445/183272; 719412
الاتاحة: http://hdl.handle.net/2445/183272
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6Academic Journal
المؤلفون: Díaz González, Álvaro, Sapena, Victor, Boix i Ferrero, Loreto, Torres, Ferram, Sanduzzi-Zamparelli, Marco, Da Fonseca, Leonardo G., Llarch, Neus, Iserte, Gemma, Guedes, Cassia, Muñoz Martínez, Sergio, Darnell, Anna, Belmonte, Ernest, Rimola, Jordi, Forner, Alejandro, Ayuso Colella, Carmen, Bruix Tudó, Jordi, Reig, María
المصدر: Articles publicats en revistes (Fonaments Clínics)
مصطلحات موضوعية: Hepatologia, Cèl·lules canceroses, Càncer de fetge, Diarrea, Resistència als medicaments, Anàlisi de supervivència (Biometria), Proteïna-tirosina-fosfatasa, Proteïnes quinases, Inhibició, Hepatology, Cancer cells, Liver cancer, Diarrhea, Drug resistance, Survival analysis (Biometry), Protein-tyrosine phosphatase, Protein kinases, Inhibition
وصف الملف: 7 p.; application/pdf
Relation: Reproducció del document publicat a: https://doi.org/10.1002/ueg2.12111; United European Gastroenterology Journal, 2021, vol. 9, num. 9, p. 655-661; https://doi.org/10.1002/ueg2.12111; http://hdl.handle.net/2445/200305; 737102
الاتاحة: http://hdl.handle.net/2445/200305
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7Academic Journal
المؤلفون: Garcia-Forn, Marta, Martínez Torres, Sara, García-Díaz Barriga, Gerardo, Alberch i Vié, Jordi, 1959-, Milà i Recasens, Montserrat, Azkona, Garikoitz, Pérez Navarro, Esther
المصدر: Articles publicats en revistes (Biomedicina)
مصطلحات موضوعية: Corea de Huntington, Mutació (Biologia), Proteïna-tirosina-fosfatasa, Farmacogenètica, Inhibició, Huntington's chorea, Mutation (Biology), Protein-tyrosine phosphatase, Pharmacogenetics, Inhibition
وصف الملف: 10 p.; application/pdf
Relation: Versió postprint del document publicat a: https://doi.org/10.1016/j.nbd.2018.08.024; Neurobiology of Disease, 2018, vol. 120, p. 88-97; https://doi.org/10.1016/j.nbd.2018.08.024; http://hdl.handle.net/2445/184474; 686622
الاتاحة: http://hdl.handle.net/2445/184474
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8Academic Journal
المؤلفون: Cases, Silvia, Saavedra, Ana, Tyebji, Shiraz, Giralt Torroella, Albert, Alberch i Vié, Jordi, 1959-, Pérez Navarro, Esther
المصدر: Articles publicats en revistes (Biomedicina)
مصطلحات موضوعية: Envelliment cerebral, Proteïna-tirosina-fosfatasa, Regulació genètica, Diferències entre sexes, Aging brain, Protein-tyrosine phosphatase, Genetic regulation, Sex differences
وصف الملف: 9 p.; application/pdf
Relation: Versió postprint del document publicat a: https://doi.org/10.1016/j.mcn.2017.11.003; Molecular and Cellular Neuroscience, 2018, vol. 86, p. 41-49; https://doi.org/10.1016/j.mcn.2017.11.003; http://hdl.handle.net/2445/184462; 677768
الاتاحة: http://hdl.handle.net/2445/184462
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9
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10Academic Journal
المساهمون: Grup de Recerca Biomèdica HJ23, Bioquímica i Biotecnologia, Universitat Rovira i Virgili
المصدر: Plos One ; https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0172887 ; https://doi.org/10.1371/journal.pone.0172887
مصطلحات موضوعية: Proteïna-tirosina-fosfatasa, Està en blanc, Biochemistry and technology, Bioquímica y tecnología, Bioquímica i biotecnologia
جغرافية الموضوع: Anglès
Time: 1932-6203
وصف الملف: 1871 kb
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11Academic Journal
المؤلفون: Saavedra, Ana, Puigdellívol Cañadell, Maria del Mar, Tyebji, Shiraz, Kurup, Pradeep, Xu, Jian, Ginés Padrós, Silvia, Alberch i Vié, Jordi, 1959-, Lombroso, Paul J., Pérez Navarro, Esther
المصدر: Articles publicats en revistes (Biomedicina)
مصطلحات موضوعية: Neurones, Proteïnes, Proteïna-tirosina-fosfatasa, Sinapsi, Neurons, Proteins, Protein-tyrosine phosphatase, Synapses
وصف الملف: 13 p.; application/pdf
Relation: Versió postprint del document publicat a: https://doi.org/10.1007/s12035-015-9335-7; Molecular Neurobiology, 2016, vol. 53, num. 6, p. 4261-4273; https://doi.org/10.1007/s12035-015-9335-7; http://hdl.handle.net/2445/184407; 654620
الاتاحة: http://hdl.handle.net/2445/184407
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12Academic Journal
المؤلفون: Xu, Jian, Kurup, Pradeep, Azkona, Garikoitz, Baguley, Tyler D., Saavedra, Ana, Nairn, Angus C., Ellman, Jonathan A., Pérez Navarro, Esther, Lombroso, Paul J.
المصدر: Articles publicats en revistes (Biomedicina)
مصطلحات موضوعية: Malalties neurodegeneratives, Proteïna-tirosina-fosfatasa, Ubiqüitina, Neurodegenerative Diseases, Protein-tyrosine phosphatase, Ubiquitin
وصف الملف: 37 p.; application/pdf
Relation: Versió postprint del document publicat a: https://doi.org/10.1111/jnc.13295; Journal of Neurochemistry, 2016, vol. 136, num. 2, p. 285-294; https://doi.org/10.1111/jnc.13295; http://hdl.handle.net/2445/184556; 708389
الاتاحة: http://hdl.handle.net/2445/184556
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13
المؤلفون: José Solis Villanueva, Renato LaTorre-Ramírez, Jorge Calderón Ticona, Carlos Patricio Padilla Rojas, Mónica Yolanda Paredes Anaya, Wilser Andrés García-Quispes, Frank Lizaraso-Soto, Enrique Eduardo Sanchez-Castro
المصدر: Horizonte Médico, Vol 19, Iss 4, Pp 14-19 (2020)
مصطلحات موضوعية: Genetics, diabetes mellitus tipo 2, Haplotype, lcsh:R, marcadores genéticos, lcsh:Medicine, Single-nucleotide polymorphism, Type 2 diabetes, Biology, medicine.disease, polimorfismo de nucleótido simple, SNP genotyping, Genotype frequency, Genotype, medicine, SNP, Allele, proteína tirosina fosfatasa no receptora tipo 1
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14Academic Journal
المؤلفون: López-Mejías, Raquel, Genre, Fernanda, Remuzgo-Martínez, Sara, Sevilla Pérez, Belén, Castañeda, Santos, Llorca, Javier, Ortego-Centeno, Norberto, Ubilla, Begoña, Mijares, Verónica, Pina, Trinitario, Calvo-Río, Vanesa, Palmou, Natalia, Miranda-Filloy, José A, Navas Parejo, Antonio, Argila, Diego, Sánchez-Pérez, Javier, Rubio, Esteban, León Luque, Manuel, Blanco-Madrigal, Juan María, Galíndez-Aguirregoikoa, Eva, Ocejo-Vinyals, J Gonzalo, Martín, Javier, Blanco, Ricardo, González-Gay, Miguel A
المساهمون: López-Mejías,R, Genre,F, Remuzgo-Martínez,S, Ubilla,B, Mijares,V, Pina,T, Calvo-Río,V, Palmou,N, Blanco,R, González-Gay,MA Epidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain. Sevilla Pérez,B, Ortego-Centeno,N Department of Medicine, Hospital Universitario San Cecilio, Granada, Spain. Castañeda,S Rheumatology Department, Hospital Universitario La Princesa, IIS-Princesa, Madrid, Spain. Llorca,J Epidemiology and Computational Biology Department, School of Medicine, University of Cantabria, and CIBER Epidemiología y Salud Pública (CIBERESP), IDIVAL, Santander, Spain. Miranda-Filloy,JA Division of Rheumatology, Hospital Universitario Lucus Augusti, Lugo, Spain. Navas Parejo,A Nephrology Department, Hospital Universitario San Cecilio, Granada, Spain. Argila,D, Sánchez-Pérez,J Dermatology Department, Hospital Universitario La Princesa, IIS-Princesa, Madrid, Spain. Rubio,E, León Luque,M Rheumatology Department, Hospital Universitario Virgen del Rocío, Sevilla, Spain. Blanco-Madrigal,JM, Galíndez-Aguirregoikoa,E Rheumatology Department, Hospital Universitario de Basurto, Bilbao, Spain. Ocejo-Vinyals,JG Immunology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain. Martín,J Institute of Parasitology and Biomedicine López-Neyra, CSIC, Granada, Spain. González-Gay,MA Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa., This study was supported by a grant from “Fondo de Investigaciones Sanitarias” PI12/00193 (Spain). RLM is a recipient of a Sara Borrell postdoctoral fellowship from the Instituto de Salud Carlos III at the Spanish Ministry of Health (Spain) (CD12/00425). FG and BU are supported by funds from the RETICS Program (RIER) (RD12/0009/0013).
مصطلحات موضوعية: Niño, Femenino, Frecuencia de los genes, Adulto, Predisposición genética a la enfermedad, Genotipo, Humanos, Masculino, Polimorfismo de nucleótido simple, Proteína tirosina fosfatasa no receptora tipo 22, Púrpura de Schoenlein-Henoch, Reacción en cadena en tiempo real de la polimerasa, España, Medical Subject Headings::Named Groups::Persons::Age Groups::Child, Medical Subject Headings::Check Tags::Female, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Gene Frequency, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype, Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans, Medical Subject Headings::Check Tags::Male, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide, Medical Subject Headings::Diseases::Hemic and Lymphatic Diseases::Hematologic Diseases::Blood Coagulation Disorders::Purpura::Purpura, Schoenlein-Henoch, Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Nucleic Acid Amplification Techniques::Polymerase Chain Reaction::Real-Time Polymerase Chain Reaction, Medical Subject Headings::Geographicals::Geographic Locations::Europe::Spain, Medical Subject Headings::Named Groups::Persons::Age Groups::Adult
وصف الملف: application/pdf; application/msword
Relation: https://arthritis-research.biomedcentral.com/articles/10.1186/s13075-015-0796-x#Abs1; López-Mejías R, Genre F, Remuzgo-Martínez S, Pérez BS, Castañeda S, Llorca J, et al. Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis). Arthritis Res. Ther. 2015; 17:286; http://hdl.handle.net/10668/2556; PMC4603645
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15Academic Journal
المؤلفون: Puerta Turrillas, María Luisa de la, Trinidad, Antonio G., Rodríguez, María del Carmen, Pereda, José María de, Sánchez Crespo, Mariano, Bayón Prieto, Yolanda, Alonso, Andrés
مصطلحات موضوعية: Autoinmunidad, Proteína tirosina fosfatasa, 24 Ciencias de la Vida
وصف الملف: application/pdf
Relation: https://journals.plos.org/plosone/article?id=10.1371/journal.pone.0054569; https://doi.org/10.1371/journal.pone.0054569; PLoS ONE, 2013, vol. 8, n. 1, p. e54569; https://uvadoc.uva.es/handle/10324/47495; e54569; PLoS ONE
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16Academic Journal
المؤلفون: Cénit, María Carmen, Márquez, Ana, Cordero-Coma, Miguel, Fonollosa, Alejandro, Llorenç, Victor, Artaraz, Joseba, Díaz Valle, David, Blanco, Ricardo, Cañal, Joaquín, Salom, David, García Serrano, José Luis, Ramón, Enrique de, Rio, María José del, Gorroño-Echebarría, Marina Begoña, Martín-Villa, José Manuel, Molins, Blanca, Ortego-Centeno, Norberto, Martín, Javier
المساهمون: Cénit,MC, Márquez,A, Martín,J Instituto de Parasitología y Biomedicina López-Neyra, IPBLN, CSIC, Granada, Spain. Cordero-Coma,M Ophthalmology Department, Hospital de León, León, Spain. Fonollosa,A, Artaraz,J Ophthalmology Department, Hospital de Cruces, Bilbao, Spain. Llorenç,V Ophthalmology Department, Hospital Clínic, Barcelona, Spain. Díaz Valle, D Ophthalmology 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. Salom,D Ophthalmology Department, Hospital Universitario La Fe, Valencia, Spain. García Serrano,JL Ophthalmology Department, Hospital Clínico San Cecilio, Granada, Spain. Ramon,E de Internal Medicine Department, Hospital Carlos Haya, Málaga, Spain. Rio,MJ del Ophthalmology Department, Hospital Carlos Haya, Málaga, Spain. Gorroño-Echebarría,MB Ophthalmology Department, Hospital Universitario Principe de Asturias, Alcalá de Henares, Spain. Martín-Villa,JM Immunology Department, Facultad de Medicina, Universidad Complutense de Madrid, Spain. Molins,B Instituto de Investigaciones Biomédicas, IDIBAPS, Hospital Clinic, Barcelona, Spain. Ortego-Centeno,N Internal Medicine Department, Hospital Clínico San Cecilio, Granada, Spain.
مصطلحات موضوعية: Alelos, Demografía, Estudios de casos y controles, Estudios de asociación genética, Frecuencia génica, Predisposición genética a la enfermedad, Proteínas mutantes, Polimorfismo de nucleótido único, Proteína tirosina fosfatasa no receptora de tipo 22, Uveítis anterior, España, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Processes::Mutagenesis::Amino Acid Substitution, Medical Subject Headings::Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Epidemiologic Methods::Epidemiologic Study Characteristics as Topic::Epidemiologic Studies::Case-Control Studies, Medical Subject Headings::Health Care::Population Characteristics::Demography, Medical Subject Headings::Check Tags::Female, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Gene Frequency, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Genetic Association Studies, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease, Medical Subject Headings::Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans, Medical Subject Headings::Check Tags::Male, Medical Subject Headings::Named Groups::Persons::Age Groups::Adult::Middle Aged, Medical Subject Headings::Chemicals and Drugs::Amino Acids, Peptides, and Proteins::Proteins::Mutant Proteins, Medical Subject Headings::Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide, and Proteins::Proteins::Intracellular Signaling Peptides and Proteins::Protein Tyrosine Phosphatases, Non-Receptor::Protein Tyrosine Phosphatase
وصف الملف: application/pdf
Relation: http://www.molvis.org/molvis/v19/638/; Cénit MC, Márquez A, Cordero-Coma M, Fonollosa A, Llorenç V, Artaraz J, et al. Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis Mol Vis. 2013; 19:638-43; http://hdl.handle.net/10668/1590; PMC3611931
الاتاحة: http://hdl.handle.net/10668/1590
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17Academic Journal
المؤلفون: Ortiz, Conrad, Caja Puigsubirà, Laia, Bertran Rodríguez, Esther, González Rodríguez, Águeda, Valverde, Ángela M., Fabregat Romero, Isabel, Sancho, Patrícia
المصدر: Articles publicats en revistes (Ciències Fisiològiques)
مصطلحات موضوعية: Proteïna-tirosina-fosfatasa, Factors de creixement, Proteïnes supressores de tumors, Protein-tyrosine phosphatase, Growth factors, Tumor suppressor protein
وصف الملف: 12 p.; application/pdf
Relation: Reproducció del document publicat a: https://doi.org/10.1074/jbc.M111.303958; Journal of Biological Chemistry, 2012, vol. 287, num. 19, p. 15263-15274; https://doi.org/10.1074/jbc.M111.303958; http://hdl.handle.net/2445/181299; 621696
الاتاحة: http://hdl.handle.net/2445/181299
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18Academic Journal
المؤلفون: Martínez Yélamos, Antonio, Saiz Hinarejos, Albert, Sánchez del Valle Díaz, Raquel, Casado Ruiz, Virginia, Ramon Torrell, Josep M. (Josep Maria), Graus Ribas, Francesc, Arbizu Urdiain, Txomin
المصدر: Articles publicats en revistes (Ciències Clíniques)
مصطلحات موضوعية: Líquid cefalorraquidi, Esclerosi múltiple, Proteïna-tirosina-fosfatasa, Cerebrospinal fluid, Multiple sclerosis, Protein-tyrosine phosphatase
وصف الملف: 3 p.; application/pdf
Relation: Reproducció del document publicat a: https://doi.org/10.1212/wnl.57.4.722; Neurology, 2001, vol. 57, num. 4, p. 722-724; https://doi.org/10.1212/wnl.57.4.722; http://hdl.handle.net/2445/157307; 500870
الاتاحة: http://hdl.handle.net/2445/157307
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19Academic Journal
المصدر: Articles publicats en revistes (Patologia i Terapèutica Experimental)
مصطلحات موضوعية: Proteïnes, Proteïna-tirosina-fosfatasa, Metabolisme, Proteins, Protein-tyrosine phosphatase, Metabolism
وصف الملف: 10 p.; application/pdf
Relation: Reproducció del document publicat a: https://www.jbc.org/issue/S0021-9258(20)X6719-6; Journal of Biological Chemistry, 1993, vol. 268, num. 29, p. 22010-22019; http://hdl.handle.net/2445/177648; 087489; 8408058
الاتاحة: http://hdl.handle.net/2445/177648
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20
المؤلفون: J. M. Blanco-Madrigal, Fernanda Genre, Javier Llorca, José A. Miranda-Filloy, Verónica Mijares, Santos Castañeda, Norberto Ortego-Centeno, Diego de Argila, Antonio Navas Parejo, Javier Martín, Belén Sevilla Pérez, Vanesa Calvo-Río, Javier Sánchez-Pérez, J. Gonzalo Ocejo-Vinyals, Miguel A. González-Gay, Natalia Palmou, E. Rubio, Begoña Ubilla, Sara Remuzgo-Martínez, Ricardo Blanco, Trinitario Pina, Manuel León Luque, Raquel López-Mejías, Eva Galíndez-Aguirregoikoa
المساهمون: Universidad de Cantabria, Instituto de Salud Carlos III, Red de Investigación en Inflamación y Enfermedades Reumáticas (España), [López-Mejías,R, Genre,F, Remuzgo-Martínez,S, Ubilla,B, Mijares,V, Pina,T, Calvo-Río,V, Palmou,N, Blanco,R, González-Gay,MA] Epidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, Hospital Universitario Marqués de Valdecilla, IDIVAL, Santander, Spain. [Sevilla Pérez,B, Ortego-Centeno,N] Department of Medicine, Hospital Universitario San Cecilio, Granada, Spain. [Castañeda,S] Rheumatology Department, Hospital Universitario La Princesa, IIS-Princesa, Madrid, Spain. [Llorca,J] Epidemiology and Computational Biology Department, School of Medicine, University of Cantabria, and CIBER Epidemiología y Salud Pública (CIBERESP), IDIVAL, Santander, Spain. [Miranda-Filloy,JA] Division of Rheumatology, Hospital Universitario Lucus Augusti, Lugo, Spain. [Navas Parejo,A] Nephrology Department, Hospital Universitario San Cecilio, Granada, Spain. [Argila,D, Sánchez-Pérez,J] Dermatology Department, Hospital Universitario La Princesa, IIS-Princesa, Madrid, Spain. [Rubio,E, León Luque,M] Rheumatology Department, Hospital Universitario Virgen del Rocío, Sevilla, Spain. [Blanco-Madrigal,JM, Galíndez-Aguirregoikoa,E] Rheumatology Department, Hospital Universitario de Basurto, Bilbao, Spain. [Ocejo-Vinyals,JG] Immunology Department, Hospital Universitario Marqués de Valdecilla, Santander, Spain. [Martín,J] Institute of Parasitology and Biomedicine López-Neyra, CSIC, Granada, Spain. [González-Gay,MA] Cardiovascular Pathophysiology and Genomics Research Unit, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa., This study was supported by a grant from 'Fondo de Investigaciones Sanitarias' PI12/00193 (Spain). RLM is a recipient of a Sara Borrell postdoctoral fellowship from the Instituto de Salud Carlos III at the Spanish Ministry of Health (Spain) (CD12/00425). FG and BU are supported by funds from the RETICS Program (RIER) (RD12/0009/0013).
المصدر: Arthritis Research & Therapy. 2015 Oct 13;17:286
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
Digital.CSIC. Repositorio Institucional del CSIC
instname
Arthritis Research & Therapy
UCrea Repositorio Abierto de la Universidad de Cantabria
Universidad de Cantabria (UC)مصطلحات موضوعية: Male, Henoch-Schonlein purpura, Polimorfismo de nucleótido simple, España, Protein tyrosine phosphatase, CSK Tyrosine-Protein Kinase, Organisms::Eukaryota::Animals::Chordata::Vertebrates::Mammals::Primates::Haplorhini::Catarrhini::Hominidae::Humans [Medical Subject Headings], Gene Frequency, immune system diseases, Diseases::Hemic and Lymphatic Diseases::Hematologic Diseases::Blood Coagulation Disorders::Purpura::Purpura, Schoenlein-Henoch [Medical Subject Headings], hemic and lymphatic diseases, Genotype, Medicine, Immunology and Allergy, Masculino, Child, Geographicals::Geographic Locations::Europe::Spain [Medical Subject Headings], Purpura, Schoenlein-Henoch, Adulto, Femenino, Predisposición genética a la enfermedad, Phenomena and Processes::Genetic Phenomena::Genotype::Genetic Predisposition to Disease [Medical Subject Headings], Humanos, src-Family Kinases, Niño, Proteína tirosina fosfatasa no receptora tipo 22, Female, Phenomena and Processes::Genetic Phenomena::Genotype [Medical Subject Headings], Tyrosine kinase, Research Article, Adult, medicine.medical_specialty, IgA Vasculitis, Immunology, Púrpura de Schoenlein-Henoch, Check Tags::Male [Medical Subject Headings], Real-Time Polymerase Chain Reaction, Polymorphism, Single Nucleotide, PTPN22, Rheumatology, Internal medicine, Named Groups::Persons::Age Groups::Adult [Medical Subject Headings], Humans, Genetic Predisposition to Disease, Allele frequency, Named Groups::Persons::Age Groups::Child [Medical Subject Headings], Frecuencia de los genes, Reacción en cadena en tiempo real de la polimerasa, Phenomena and Processes::Genetic Phenomena::Genetic Variation::Polymorphism, Genetic::Polymorphism, Single Nucleotide [Medical Subject Headings], business.industry, Analytical, Diagnostic and Therapeutic Techniques and Equipment::Investigative Techniques::Genetic Techniques::Nucleic Acid Amplification Techniques::Polymerase Chain Reaction::Real-Time Polymerase Chain Reaction [Medical Subject Headings], Protein Tyrosine Phosphatase, Non-Receptor Type 22, medicine.disease, IgA vasculitis, Check Tags::Female [Medical Subject Headings], Spain, business, Phenomena and Processes::Genetic Phenomena::Gene Frequency [Medical Subject Headings], Genotipo
وصف الملف: application/pdf; application/msword