BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

189 related articles for article (PubMed ID: 23559857)

  • 1. Lack of association between the protein tyrosine phosphatase non-receptor type 22 R263Q and R620W functional genetic variants and endogenous non-anterior uveitis.
    Cénit MC; Márquez A; Cordero-Coma M; Fonollosa A; Llorenç V; Artaraz J; Díaz Valle D; Blanco R; Cañal J; Salom D; García Serrano JL; de Ramón E; José del Rio M; Gorroño-Echebarría MB; Martín-Villa JM; Molins B; Ortego-Centeno N; Martín J
    Mol Vis; 2013; 19():638-43. PubMed ID: 23559857
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Genotype analysis of polymorphisms in autoimmune susceptibility genes, CTLA-4 and PTPN22, in an acute anterior uveitis cohort.
    Martin TM; Bye L; Modi N; Stanford MR; Vaughan R; Smith JR; Wade NK; Mackensen F; Suhler EB; Rosenbaum JT; Wallace GR
    Mol Vis; 2009; 15():208-12. PubMed ID: 19180256
    [TBL] [Abstract][Full Text] [Related]  

  • 3. The PTPN22 R263Q polymorphism is a risk factor for rheumatoid arthritis in Caucasian case-control samples.
    Rodríguez-Rodríguez L; Taib WR; Topless R; Steer S; González-Escribano MF; Balsa A; Pascual-Salcedo D; González-Gay MA; Raya E; Fernandez-Gutierrez B; González-Álvaro I; Bottini N; Witte T; Viken MK; Coenen MJ; van Riel PL; Franke B; den Heijer M; Radstake TR; Wordsworth P; Lie BA; Merriman TR; Martín J
    Arthritis Rheum; 2011 Feb; 63(2):365-72. PubMed ID: 21279993
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Analysis of the influence of PTPN22 gene polymorphisms in systemic sclerosis.
    Diaz-Gallo LM; Gourh P; Broen J; Simeon C; Fonollosa V; Ortego-Centeno N; Agarwal S; Vonk MC; Coenen M; Riemekasten G; Hunzelmann N; Hesselstrand R; Tan FK; Reveille JD; Assassi S; García-Hernandez FJ; Carreira P; Camps MT; Fernandez-Nebro A; de la Peña PG; Nearney T; Hilda D; González-Gay MA; Airo P; Beretta L; Scorza R; Herrick A; Worthington J; Pros A; Gómez-Gracia I; Trapiella L; Espinosa G; Castellvi I; Witte T; de Keyser F; Vanthuyne M; Mayes MD; Radstake TR; Arnett FC; Martin J; Rueda B
    Ann Rheum Dis; 2011 Mar; 70(3):454-62. PubMed ID: 21131644
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Differential association of two PTPN22 coding variants with Crohn's disease and ulcerative colitis.
    Diaz-Gallo LM; Espino-Paisán L; Fransen K; Gómez-García M; van Sommeren S; Cardeña C; Rodrigo L; Mendoza JL; Taxonera C; Nieto A; Alcain G; Cueto I; López-Nevot MA; Bottini N; Barclay ML; Crusius JB; van Bodegraven AA; Wijmenga C; Ponsioen CY; Gearry RB; Roberts RL; Weersma RK; Urcelay E; Merriman TR; Alizadeh BZ; Martin J
    Inflamm Bowel Dis; 2011 Nov; 17(11):2287-94. PubMed ID: 21287672
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Identification of the PTPN22 functional variant R620W as susceptibility genetic factor for giant cell arteritis.
    Serrano A; Márquez A; Mackie SL; Carmona FD; Solans R; Miranda-Filloy JA; Hernández-Rodríguez J; Cid MC; Castañeda S; Morado IC; Narváez J; Blanco R; Sopeña B; García-Villanueva MJ; Monfort J; Ortego-Centeno N; Unzurrunzaga A; Marí-Alfonso B; Sánchez Martín J; de Miguel E; Magro C; Raya E; ; ; Braun N; Latus J; Molberg O; Lie BA; Moosig F; Witte T; Morgan AW; González-Gay MA; Martín J
    Ann Rheum Dis; 2013 Nov; 72(11):1882-1886. PubMed ID: 23946333
    [TBL] [Abstract][Full Text] [Related]  

  • 7. The PTPN22 R263Q polymorphism confers protection against systemic lupus erythematosus and rheumatoid arthritis, while PTPN22 R620W confers susceptibility to Graves' disease in a Mexican population.
    López-Cano DJ; Cadena-Sandoval D; Beltrán-Ramírez O; Barbosa-Cobos RE; Sánchez-Muñoz F; Amezcua-Guerra LM; Juárez-Vicuña Y; Aguilera-Cartas MC; Moreno J; Bautista-Olvera J; Valencia-Pacheco G; López-Villanueva RF; Ramírez-Bello J
    Inflamm Res; 2017 Sep; 66(9):775-781. PubMed ID: 28500376
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Association of PTPN22 gene functional variants with development of pulmonary tuberculosis in Moroccan population.
    Lamsyah H; Rueda B; Baassi L; Elaouad R; Bottini N; Sadki K; Martin J
    Tissue Antigens; 2009 Sep; 74(3):228-32. PubMed ID: 19563523
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Role of PTPN22 and CSK gene polymorphisms as predictors of susceptibility and clinical heterogeneity in patients with Henoch-Schönlein purpura (IgA vasculitis).
    López-Mejías R; Genre F; Remuzgo-Martínez S; Pérez BS; Castañeda S; Llorca J; Ortego-Centeno N; Ubilla B; Mijares V; Pina T; Calvo-Río V; Palmou N; Miranda-Filloy JA; Parejo AN; Argila D; Sánchez-Pérez J; Rubio E; Luque ML; Blanco-Madrigal JM; Galíndez-Aguirregoikoa E; Ocejo-Vinyals JG; Martín J; Blanco R; González-Gay MA
    Arthritis Res Ther; 2015 Oct; 17():286. PubMed ID: 26458874
    [TBL] [Abstract][Full Text] [Related]  

  • 10. PTPN22 is not associated with Behçet's disease. Study spanning the complete gene region in the Spanish population and meta-analysis of the functional variant R620W.
    Ortiz-Fernández L; Montes-Cano MA; García-Lozano JR; Conde-Jaldón M; Ortego-Centeno N; González-Leon R; Espinosa G; Graña-Gil G; Sánchez-Bursón J; Juliá MR; Solans R; Blanco R; Barnosi-Marín AC; Fanlo P; Rodríguez Carballeira M; Camps MT; Castañeda S; Martín J; González-Escribano MF
    Clin Exp Rheumatol; 2016; 34(6 Suppl 102):S41-S45. PubMed ID: 27050764
    [TBL] [Abstract][Full Text] [Related]  

  • 11. The PTPN22*R620W polymorphism does not confer genetic susceptibility to antiphospholipid syndrome in the Spanish population.
    Castro-Marrero J; Balada E; Vilardell-Tarrés M; Ordi-Ros J
    Int J Immunogenet; 2011 Dec; 38(6):529-31. PubMed ID: 21923648
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Transethnic associations among immune-mediated diseases and single-nucleotide polymorphisms of the aryl hydrocarbon response gene ARNT and the PTPN22 immune regulatory gene.
    Schurman SH; O'Hanlon TP; McGrath JA; Gruzdev A; Bektas A; Xu H; Garantziotis S; Zeldin DC; Miller FW
    J Autoimmun; 2020 Feb; 107():102363. PubMed ID: 31759816
    [TBL] [Abstract][Full Text] [Related]  

  • 13. The functional PTPN22 C1858T polymorphism confers risk for rheumatoid arthritis in patients from Central Mexico.
    Rincón JF; Cano DL; Morales SJ; Jiménez ML; Cobos RE; Bello JR
    Clin Rheumatol; 2016 Jun; 35(6):1457-62. PubMed ID: 26951256
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Associations of protein tyrosine phosphatase nonreceptor 22 (PTPN22) gene polymorphisms with susceptibility to Graves' disease in a Japanese population.
    Ichimura M; Kaku H; Fukutani T; Koga H; Mukai T; Miyake I; Yamada K; Koda Y; Hiromatsu Y
    Thyroid; 2008 Jun; 18(6):625-30. PubMed ID: 18578611
    [TBL] [Abstract][Full Text] [Related]  

  • 15. No association of PTPN22 R620W gene polymorphism with rheumatic heart disease and systemic lupus erythematosus.
    Aksoy R; Duman T; Keskin O; Düzgün N
    Mol Biol Rep; 2011 Nov; 38(8):5393-6. PubMed ID: 21384170
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Single Nucleotide Polymorphisms of PTPN22 Gene in Iranian Patients with Ulcerative Colitis.
    Sadr M; Moazzami B; Soleimanifar N; Elhamian N; Rezaei A; Ebrahimi Daryani N; Rezaei N
    Fetal Pediatr Pathol; 2019 Feb; 38(1):8-13. PubMed ID: 30636557
    [TBL] [Abstract][Full Text] [Related]  

  • 17. PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus.
    Abbasi F; Soltani S; Saghazadeh A; Soltaninejad E; Rezaei A; Zare Bidoki A; Bahrami T; Amirzargar AA; Rezaei N
    Immunol Invest; 2017 May; 46(4):409-418. PubMed ID: 28375784
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Autoimmunity in primary antibody deficiency is associated with protein tyrosine phosphatase nonreceptor type 22 (PTPN22).
    Chew GY; Sinha U; Gatenby PA; DeMalmanche T; Adelstein S; Garsia R; Hissaria P; French MA; Wilson A; Whittle B; Kirkpatrick P; Riminton DS; Fulcher DA; Cook MC
    J Allergy Clin Immunol; 2013 Apr; 131(4):1130-5, 1135.e1. PubMed ID: 22857794
    [TBL] [Abstract][Full Text] [Related]  

  • 19. The protein tyrosine phosphatase N22 gene is associated with juvenile and adult idiopathic inflammatory myopathy independent of the HLA 8.1 haplotype in British Caucasian patients.
    Chinoy H; Platt H; Lamb JA; Betteridge Z; Gunawardena H; Fertig N; Varsani H; Davidson J; Oddis CV; McHugh NJ; Wedderburn LR; Ollier WE; Cooper RG;
    Arthritis Rheum; 2008 Oct; 58(10):3247-54. PubMed ID: 18821667
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Association of PTPN22 single nucleotide polymorphisms with chronic spontaneous urticaria.
    Sadr M; Khalili N; Mohebbi B; Mosharmovahed B; Afradi P; Rezaei N
    Allergol Immunopathol (Madr); 2021; 49(2):40-45. PubMed ID: 33641292
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 10.