Cargando…

The Role of PTPN22 C1858T Gene Polymorphism in Diabetes Mellitus Type 1: First Evaluation in Greek Children and Adolescents

Type 1 diabetes mellitus (T1DM) is an autoimmune multifactorial disease. Protein tyrosine phosphatase nonreceptor type 22 (PTPN22) gene encodes lymphoid-specific tyrosine phosphatase (Lyp), an inhibitor of T cell activation. PTPN22 C1858T polymorphism was associated with T1DM in populations of Cauca...

Descripción completa

Detalles Bibliográficos
Autores principales:	Giza, Styliani, Goulas, Antonios, Gbandi, Emmanouela, Effraimidou, Smaragda, Papadopoulou-Alataki, Efimia, Eboriadou, Maria, Galli-Tsinopoulou, Assimina
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Hindawi Publishing Corporation 2013
Materias:	Clinical Study
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3727122/ https://www.ncbi.nlm.nih.gov/pubmed/23936838 http://dx.doi.org/10.1155/2013/721604

Ejemplares similares

Interleukin-1 Receptor-Associated Kinase 4 Deficiency in a Greek Teenager
por: Karananou, Panagiota, et al.
Publicado: (2020)

Micro-RNA Implications in Type-1 Diabetes Mellitus: A Review of Literature
por: Margaritis, Kosmas, et al.
Publicado: (2021)

Coexistence of Autoimmune Thyroiditis and Juvenile Idiopathic Arthritis
por: Sapountzi, Evdoxia, et al.
Publicado: (2023)

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

Testicular microlithiasis in a boy with X-linked adrenal hypoplasia congenita
por: Serbis, Anastasios, et al.
Publicado: (2018)

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

The Role of TLR4 Asp299Gly and TLR4 Thr399Ile Polymorphisms in the Pathogenesis of Urinary Tract Infections: First Evaluation in Infants and Children of Greek Origin
por: Karananou, Panagiota, et al.
Publicado: (2019)

The Prognostic Significance of BRAF Gene Analysis in Children and Adolescents with Papillary Thyroid Carcinoma: A Systematic Review and Meta-Analysis
por: Kotanidou, Eleni P, 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)

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)

Predictive Factors for Pediatric Craniopharyngioma Recurrence: An Extensive Narrative Review
por: Serbis, Anastasios, et al.
Publicado: (2023)

The Effect of Saffron Kozanis (Crocus sativus L.) Supplementation on Weight Management, Glycemic Markers and Lipid Profile in Adolescents with Obesity: A Double-Blinded Randomized Placebo-Controlled Trial
por: Kotanidou, Eleni P., et al.
Publicado: (2023)

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)

Translation and Validation Study of the Hypoglycemia Fear Survey in a Greek Population of Children and Adolescents with Type 1 Diabetes Mellitus and their Parents
por: Kostopoulou, Eirini, et al.
Publicado: (2023)

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 of PTPN22 Haplotypes (−1123G>C/+1858C>T) with Rheumatoid Arthritis in Western Mexican Population
por: Ruiz-Noa, Yeniley, et al.
Publicado: (2017)

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)

Diagnosis, treatment and prevention of type 2 diabetes mellitus in children and adolescents
por: Serbis, Anastasios, et al.
Publicado: (2021)

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)

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)

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)

46,XY Disorder of Sex Development due to 17-Beta Hydroxysteroid Dehydrogenase Type 3 Deficiency in an Infant of Greek Origin
por: Tsinopoulou, Assimina Galli, et al.
Publicado: (2018)

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)

Association of juvenile idiopathic arthritis with PTPN22 rs2476601 is specific to females in a Greek population
por: Goulielmos, G. N., et al.
Publicado: (2016)

Targeted Genotyping of MIS-C Patients Reveals a Potential Alternative Pathway Mediated Complement Dysregulation during COVID-19 Infection
por: Gavriilaki, Eleni, et al.
Publicado: (2022)

Pseudohypoparathyroidism Type 1A with Normocalcaemia, due to the Novel C.389A>G Variant of Exon 5 of the Guanine Nucleotide-Binding Protein, α-Stimulating Gene
por: Kotanidou, Eleni P., et al.
Publicado: (2021)

Juvenile Recurrent Parotitis: The Role of Sialendoscopy
por: Papadopoulou-Alataki, Efimia, et al.
Publicado: (2019)

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)

Identification of Complement-Related Missense Variants in Pediatric Patients with Acute and Post COVID-19 Syndromes
por: Gavriilaki, Eleni, et al.
Publicado: (2021)

Association of PTPN22 1858 single-nucleotide polymorphism with rheumatoid arthritis in a German cohort: higher frequency of the risk allele in male compared to female patients
por: Pierer, Matthias, et al.
Publicado: (2006)

Cannot write session to /tmp/vufind_sessions/sess_3e1ckl13v95lqq00ml07s4fg67