يعرض 1 - 20 نتائج من 34 نتيجة بحث عن '"Proteína tirosina fosfatasa"', وقت الاستعلام: 0.56s تنقيح النتائج
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    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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    Academic Journal
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    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

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    المصدر: Articles publicats en revistes (Patologia i Terapèutica Experimental)

    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

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    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