Cargando…

Evaluation of NLRP3 (rs10754558) and PTPN22 (1858C/T) (rs2476601) Functional Polymorphisms in Psoriasis Susceptibility in Egypt

BACKGROUND: Psoriasis is a complex autoimmune multifactorial disease induced by interaction of environmental and genetic factors. This research aimed to clarify the association of NLRP3 (rs10754558) and PTPN22 (1858C/T) (rs2476601) polymorphisms with susceptibility to psoriasis. METHODS: This case–c...

Descripción completa

Detalles Bibliográficos
Autores principales:	ALrefai, Abeer, Dawood, Ashraf, Shehata, Wafaa, Elhelbawy, Mohammed, Elhelbawy, Nesreen
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Dove 2021
Materias:	Original Research
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8324977/ https://www.ncbi.nlm.nih.gov/pubmed/34345180 http://dx.doi.org/10.2147/TACG.S319065

Ejemplares similares

The Human Genetic Variants CYP2J2 rs2280275 and EPHX2 rs751141 and Risk of Diabetic Nephropathy in Egyptian Type 2 Diabetic Patients
por: Habieb, Mona S, et al.
Publicado: (2020)

rs2476601 in PTPN22 gene in rheumatoid arthritis and periodontitis—a possible interface?
por: Schulz, Susanne, et al.
Publicado: (2020)

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

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)

Association of PTPN22 rs2476601 Polymorphism with Rheumatoid Arthritis and Celiac Disease in Khuzestan Province, Southwestern Iran
por: Abbasi, Zahra, et al.
Publicado: (2017)

The association of PTPN22 rs2476601 polymorphism and CTLA-4 rs231775 polymorphism with LADA risks: a systematic review and meta-analysis
por: Dong, Fang, et al.
Publicado: (2014)

Association between NLRP3 rs10754558 and CARD8 rs2043211 Variants and Susceptibility to Chronic Kidney Disease
por: La Russa, Antonella, et al.
Publicado: (2023)

Association of NLRP3 rs35829419 and rs10754558 Polymorphisms With Risks of Autoimmune Diseases: A Systematic Review and Meta-Analysis
por: Wu, Zubo, et al.
Publicado: (2021)

Impact of NLRP3 gene polymorphisms (rs10754558 and rs10733113) on HPV infection and cervical cancer in southern Chinese population
por: Lu, Qingchun, et al.
Publicado: (2023)

The association between rs2476601 polymorphism in PTPN22 gene and risk of alopecia areata: A meta-analysis of case–control studies
por: Lei, Zi-Xian, et al.
Publicado: (2019)

Associations between inflammasome‐related gene NLRP3 Polymorphisms (rs10754558 and rs35829419) and risk of bladder cancer in a Chinese population
por: Xu, Gang, et al.
Publicado: (2021)

The NLRP3 rs10754558 Polymorphism Is Associated with the Occurrence and Prognosis of Coronary Artery Disease in the Chinese Han Population
por: Zhou, Dong, et al.
Publicado: (2016)

rs2476601 polymorphism in PTPN22 is associated with Crohn’s disease but not with ulcerative colitis: a meta-analysis of 16,838 cases and 13,356 controls
por: Hedjoudje, Abdellah, et al.
Publicado: (2017)

Association between PYTPN22 rs2476601, VEGF rs833070, TNFAIP3 rs6920220 Polymorphisms and Risk for Rheumatoid Arthritis in Early Undifferentiated Arthritis Patients: A Pilot Study
por: Sakalyte, Regina, et al.
Publicado: (2023)

Tumor necrosis factor-α gene promoter −308 and −238 polymorphisms and its serum level in psoriasis
por: Hagag, Magda M., et al.
Publicado: (2021)

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

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

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 Association of Diurnal Blood Glucose Variability With Subclinical Cardiac Disease in Patients With Type 2 Diabetes Mellitus
por: Shehab-Eldin, Walid, et al.
Publicado: (2020)

Circulating microRNA 9-3p and serum endocan as potential biomarkers for hepatitis C virus-related hepatocellular carcinoma
por: Wahb, Amany Mohamed Salah Eldin, et al.
Publicado: (2021)

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)

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)

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

STAT4 rs7574865 G/T and PTPN22 rs2488457 G/C Polymorphisms Influence the Risk of Developing Juvenile Idiopathic Arthritis in Han Chinese Patients
por: Fan, Zhi-Dan, et al.
Publicado: (2015)

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)

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)

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)

Polymorphisms in the PTPN22 region are associated with psoriasis of early onset
por: Smith, RhLl, et al.
Publicado: (2008)

Genetic Polymorphisms of NLRP3 (rs4612666) and CARD8 (rs2043211) in Periodontitis and Cardiovascular Diseases
por: Mahendra, Jaideep, et al.
Publicado: (2021)

Association between cyclin-dependent kinase inhibitor 2B antisense RNA 1 and zinc finger homeobox 3 gene polymorphisms and COVID-19 severity
por: Badr, Eman A., et al.
Publicado: (2023)

Genotype Triad for HOTAIR rs10783618, LINC-ROR rs1942347, and MALAT1 rs3200401 as Molecular Markers in Systemic Lupus Erythematous
por: Ismail, Nesreen M., et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_el9qc7s52qsdnelnke95iaatgu