Cargando…

Association of PTPN22 Haplotypes (−1123G>C/+1858C>T) with Rheumatoid Arthritis in Western Mexican Population

Rheumatoid arthritis (RA) is an autoimmune disease characterized by the presence of antibodies against cyclic citrullinated peptide (anti-CCP), a consequence of the breakdown of immune tolerance. The lymphoid tyrosine phosphatase (Lyp) protein has significant effects on maintenance of peripheral imm...

Descripción completa

Detalles Bibliográficos
Autores principales:	Ruiz-Noa, Yeniley, Padilla-Gutiérrez, Jorge Ramón, Hernández-Bello, Jorge, Palafox-Sánchez, Claudia Azucena, Valle, Yeminia, Oregón-Romero, Edith, Pereira-Suárez, Ana Laura, Bernard-Medina, Ana Guilaisne, Muñoz-Valle, José Francisco
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2017
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5292183/ https://www.ncbi.nlm.nih.gov/pubmed/28210620 http://dx.doi.org/10.1155/2017/8753498

Ejemplares similares

Analysis of PTPN22 −1123 G>C, +788 G>A and +1858 C>T Polymorphisms in Patients with Primary Sjögren’s Syndrome
por: Menchaca-Tapia, Paula Annahi, et al.
Publicado: (2023)

Protein tyrosine phosphatase PTPN22 +1858C/T polymorphism is associated with active vitiligo
por: GARCIA-MELENDEZ, MARTHA ELENA, et al.
Publicado: (2014)

Association between the PTPN22 +1858 C/T polymorphism and psoriatic arthritis
por: Juneblad, Kristina, et al.
Publicado: (2011)

Haplotypes of [‐794(CATT)(5–8)/‐173G>C] MIF gene polymorphisms and its soluble levels in cutaneous squamous cell carcinoma in western Mexican population
por: Guevara‐Gutiérrez, Elizabeth, et al.
Publicado: (2023)

PTPN22 1858 C/T Exon Polymorphism is not Associated with Graves' Disease in Kashmiri population
por: Shehjar, Faheem, et al.
Publicado: (2018)

Susceptibility to type 1 diabetes conferred by the PTPN22 C1858T polymorphism in the Spanish population
por: Santiago, Jose Luis, et al.
Publicado: (2007)

PTPN22 1858C>T gene polymorphism in patients with SLE: association with serological and clinical results
por: Ostanek, Lidia, et al.
Publicado: (2014)

The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease
por: Zaid, Younes, et al.
Publicado: (2018)

The PTPN22 C1858T gene variant is associated with proinsulin in new-onset type 1 diabetes
por: Nielsen, Lotte B, et al.
Publicado: (2011)

Association of PTPN22 1858C/T Polymorphism with Autoimmune Diseases: A Systematic Review and Bayesian Approach
por: Tizaoui, Kalthoum, et al.
Publicado: (2019)

ICOS Gene Polymorphisms (IVS1 + 173 T/C and c. 1624 C/T) in Primary Sjögren’s Syndrome Patients: Analysis of ICOS Expression
por: García-Espinoza, José Antonio, et al.
Publicado: (2022)

The association between PTPN22 C1858T gene polymorphism and type 1 diabetes mellitus: an Indonesian study
por: Rochmah, Nur, et al.
Publicado: (2023)

Association of PTPN22 SNP1858 (rs2476601) and Gene SNP1123 (rs2488457) Polymorphism With Primary Immune Thrombocytopenia Susceptibility: A Meta-Analysis of Case-Control Studies and Trial Sequential Analysis
por: Tian, Haokun, et al.
Publicado: (2022)

PTPN22 1858C>T Polymorphism Distribution in Europe and Association with Rheumatoid Arthritis: Case-Control Study and Meta-Analysis
por: Totaro, Michele Ciro, et al.
Publicado: (2011)

Lack of Association between PTPN22 Gene +1858 C>T Polymorphism and Susceptibility to Generalized Vitiligo in a Turkish Population
por: Akbas, Halit, et al.
Publicado: (2014)

Association of PTPN22-C1858T Polymorphism With Susceptibility to Mycobacterium tuberculosis and Mycobacterium leprae Infection: A Meta-Analysis
por: Li, Shuping, et al.
Publicado: (2021)

Improvement of Lipoplexes With a Sialic Acid Mimetic to Target the C1858T PTPN22 Variant for Immunotherapy in Endocrine Autoimmunity
por: Arena, Andrea, et al.
Publicado: (2022)

Association between the -844 G>A, HindIII C>G, and 4G/5G PAI-1 Polymorphisms and Susceptibility to Multiple Sclerosis in Western Mexican Population
por: Valdés-Alvarado, Emmanuel, et al.
Publicado: (2019)

Role of Toll-Interacting Protein Gene Polymorphisms in Leprosy Mexican Patients
por: Montoya-Buelna, Margarita, et al.
Publicado: (2013)

The Role of PTPN22 C1858T Gene Polymorphism in Diabetes Mellitus Type 1: First Evaluation in Greek Children and Adolescents
por: Giza, Styliani, et al.
Publicado: (2013)

No evidence for association of PTPN22 R620W functional variant C1858T with type 1 diabetes in Asian Indians
por: Baniasadi, V, et al.
Publicado: (2008)

Evaluation of NLRP3 (rs10754558) and PTPN22 (1858C/T) (rs2476601) Functional Polymorphisms in Psoriasis Susceptibility in Egypt
por: ALrefai, Abeer, et al.
Publicado: (2021)

The PTPN22 1858C/T polymorphism is associated with anti-cyclic citrullinated peptide antibody-positive early rheumatoid arthritis in northern Sweden
por: Kokkonen, Heidi, et al.
Publicado: (2007)

Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with unexplained recurrent pregnancy loss: A case-control study
por: Khanbarari, Fateme, et al.
Publicado: (2021)

Correction: The PTPN22 1858C/T polymorphism is associated with anti-cyclic citrullinated peptide antibody-positive early rheumatoid arthritis in northern Sweden
por: Kokkonen, Heidi, et al.
Publicado: (2007)

Preparation and In Vitro Evaluation of RITUXfab-Decorated Lipoplexes to Improve Delivery of siRNA Targeting C1858T PTPN22 Variant in B Lymphocytes
por: Arena, Andrea, et al.
Publicado: (2021)

Altered PTPN22 and IL10 mRNA Expression Is Associated with Disease Activity and Renal Involvement in Systemic Lupus Erythematosus
por: Román-Fernández, Ilce Valeria, et al.
Publicado: (2022)

The PTPN22*C1858T functional polymorphism is associated with susceptibility to inflammatory polyarthritis but neither this nor other variants spanning the gene is associated with disease outcome
por: Naseem, H, et al.
Publicado: (2008)

Expression of ICAM1 and VCAM1 Serum Levels in Rheumatoid Arthritis Clinical Activity. Association with Genetic Polymorphisms
por: Navarro-Hernández, Rosa Elena, et al.
Publicado: (2009)

The -844 G>A PAI-1 Polymorphism Is Associated with Acute Coronary Syndrome in Mexican Population
por: García-González, Ilian Janet, et al.
Publicado: (2015)

High prevalence of autoantibodies to RNA helicase A in Mexican patients with systemic lupus erythematosus
por: Vázquez-Del Mercado, Monica, et al.
Publicado: (2010)

Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population
por: Zhebrun, Daria, et al.
Publicado: (2011)

Association between the −794 (CATT)(5–8) MIF Gene Polymorphism and Susceptibility to Acute Coronary Syndrome in a Western Mexican Population
por: Valdés-Alvarado, Emmanuel, et al.
Publicado: (2014)

Non-Melanoma Skin Cancer: A Genetic Update and Future Perspectives
por: Zambrano-Román, Marianela, et al.
Publicado: (2022)

RAAS: A Convergent Player in Ischemic Heart Failure and Cancer
por: Garcia-Garduño, Texali C., et al.
Publicado: (2021)

APOA1 (-75 G>A and 83 C>T) and APOB (2488 C>T) polymorphisms and their association with myocardial infarction, lipids and apolipoproteins in patients with type 2 diabetes mellitus
por: Casillas, Fidel Antonio, et al.
Publicado: (2021)

Association of soluble CD40 levels with ‐1 C > T CD40 polymorphism and chronic kidney disease in systemic lupus erythematosus
por: Tapia‐Llanos, Raziel, et al.
Publicado: (2019)

Assessment of the E-Selectin rs5361 (561A>C) Polymorphism and Soluble Protein Concentration in Acute Coronary Syndrome: Association with Circulating Levels
por: Sandoval-Pinto, Elena, et al.
Publicado: (2014)

Altered B Cell Homeostasis and Toll-Like Receptor 9-Driven Response in Type 1 Diabetes Carriers of the C1858T PTPN22 Allelic Variant: Implications in the Disease Pathogenesis
por: Gianchecchi, Elena, et al.
Publicado: (2014)

B-cell activating factor receptor expression is associated with germinal center B-cell maintenance
por: Carrillo-Ballesteros, Francisco Josué, et al.
Publicado: (2019)

Cannot write session to /tmp/vufind_sessions/sess_s00hm99bkl467kfaulqnlcksp8