PTPN22 Single-Nucleotide Polymorphisms in Iranian Patients with Type 1 Diabetes Mellitus

F Abbasi, S Soltani, A Saghazadeh… - Immunological …, 2017 - Taylor & Francis
Background: PTPN22 plays a crucial role in regulating the function of various cells of the
immune system, particularly T cells. Polymorphisms of the PTPN22 gene have been …

Analysis of PTPN22 C1858T gene polymorphism in cases with type 1 diabetes of Azerbaijan, Northwest Iran

S Almasi, MR Aliparasti, L Yazdchi-Marandi… - Cellular …, 2014 - Elsevier
Abstract Background Type 1 diabetes (T1D) is a T-cell mediated autoimmune multifactorial
disease. The PTPN22 gene encodes an intracellular lymphoid-specific phosphatase (Lyp) …

[HTML][HTML] Association of PTPN22 1858T/T genotype with type 1 diabetes, Graves' disease but not with rheumatoid arthritis in Russian population

D Zhebrun, Y Kudryashova, A Babenko… - Aging (Albany …, 2011 - ncbi.nlm.nih.gov
The protein tyrosine phosphatase nonreceptor 22 gene (PTPN22) is an important negative
regulator of signal transduction through the T-cell receptors (TCR). Recently a single …

The potential role of PTPN-22 C1858T Gene polymorphism in the pathogenesis of Type 1 diabetes in Saudi population

KA Alswat, A Nasr, MS Al Dubayee… - Immunological …, 2018 - Taylor & Francis
Background: Recent investigations have reported an association between protein tyrosine
phosphatase non-receptor type-22 (PTPN-22) gene polymorphism and susceptibility to the …

The 1858T PTPN22 gene variant contributes to a genetic risk of type 1 diabetes in a Ukrainian population

M Fedetz, F Matesanz, A Caro‐Maldonado… - Tissue …, 2006 - Wiley Online Library
The 1858T variant of the protein tyrosine phosphatase gene, PTPN22, is associated with an
increased risk of several autoimmune diseases. The aim of this study has been to …

Further Evidence of a Primary, Causal Association of the PTPN22 620W Variant With Type 1 Diabetes

M Zoledziewska, C Perra, V Orru, L Moi, P Frongia… - Diabetes, 2008 - Am Diabetes Assoc
OBJECTIVE—The minor allele of the nonsynonymous single nucleotide polymorphism
(SNP)+ 1858C> T within the PTPN22 gene is positively associated with type 1 diabetes and …

The association of PTPN22 (rs2476601) and IL2RA (rs11594656) polymorphisms with T1D in Egyptian children

HM Abdelrahman, LM Sherief, DM Abd Elrahman… - Human Immunology, 2016 - Elsevier
Background Type 1 diabetes mellitus (T1D) is a T cell-mediated autoimmune disease
characterized by the destruction of pancreatic β cells. PTPN22 and IL2RA polymorphisms …

Genetic Polymorphism of PTPN22 in Autoimmune Diseases: A Comprehensive Review

K Tizaoui, JI Shin, GH Jeong, JW Yang, S Park, JH Kim… - Medicina, 2022 - mdpi.com
It is known that the etiology and clinical outcomes of autoimmune diseases are associated
with a combination of genetic and environmental factors. In the case of the genetic factor, the …

[HTML][HTML] Genetic association of PTPN22 polymorphisms with Type 1 diabetes in Pakistani children

S Rafaqat, J Manzoor, R Akhter, Z Ishaque… - Journal of King Saud …, 2023 - Elsevier
Objective Type 1 diabetes, a multigenic autoimmune disorder, is caused by the destruction
of pancreatic beta-cells leads to insufficient insulin production and hyperglycemia, resulting …

[HTML][HTML] Association of PTPN22 rs2476601 Polymorphism with rheumatoid arthritis and celiac disease in Khuzestan province, southwestern Iran

Z Abbasi, SRK Nezhad… - Iranian biomedical …, 2017 - ncbi.nlm.nih.gov
Background: Single-nucleotide polymorphism (SNP) rs2476601 within protein tyrosine
phosphatase non-receptor type 22 gene (PTPN22) has been shown to be a risk factor for …