These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

152 related articles for article (PubMed ID: 32076368)

  • 41. A single-nucleotide polymorphism in the gene encoding lymphoid protein tyrosine phosphatase (PTPN22) confers susceptibility to generalised vitiligo.
    Cantón I; Akhtar S; Gavalas NG; Gawkrodger DJ; Blomhoff A; Watson PF; Weetman AP; Kemp EH
    Genes Immun; 2005 Oct; 6(7):584-7. PubMed ID: 16015369
    [TBL] [Abstract][Full Text] [Related]  

  • 42. Lack of association of the rs2476601 PTPN22 gene polymorphism with transplanted kidney function.
    Domański L; Bobrek-Lesiakowska K; Kłoda K; Pawlik A; Safranow K; Kurzawski M; Wiśniewska M; Sulikowski T; Ciechanowski K
    Ann Transplant; 2011; 16(4):63-8. PubMed ID: 22210423
    [TBL] [Abstract][Full Text] [Related]  

  • 43. Protein tyrosine phosphatase nonreceptor type 22 gene polymorphism in alopecia areata: Does it have an association with disease severity?
    Shehata WA; Maraee A; Kamal H; Tayel N; Azmy R
    J Cosmet Dermatol; 2020 Nov; 19(11):3138-3144. PubMed ID: 32281251
    [TBL] [Abstract][Full Text] [Related]  

  • 44. PTPN22 is genetically associated with risk of generalized vitiligo, but CTLA4 is not.
    LaBerge GS; Bennett DC; Fain PR; Spritz RA
    J Invest Dermatol; 2008 Jul; 128(7):1757-62. PubMed ID: 18200060
    [TBL] [Abstract][Full Text] [Related]  

  • 45. C1858T functional variant of PTPN22 gene is not associated with celiac disease genetic predisposition.
    Rueda B; Núñez C; Orozco G; López-Nevot MA; de la Concha EG; Martin J; Urcelay E
    Hum Immunol; 2005 Jul; 66(7):848-52. PubMed ID: 16112033
    [TBL] [Abstract][Full Text] [Related]  

  • 46. Association of PTPN22 rs2476601 and STAT4 rs7574865 polymorphisms with rheumatoid arthritis: A meta-analysis update.
    Elshazli R; Settin A
    Immunobiology; 2015 Aug; 220(8):1012-24. PubMed ID: 25963842
    [TBL] [Abstract][Full Text] [Related]  

  • 47. Gender-specific association of the PTPN22 C1858T polymorphism with achalasia.
    Santiago JL; Martínez A; Benito MS; Ruiz de León A; Mendoza JL; Fernández-Arquero M; Figueredo MA; de la Concha EG; Urcelay E
    Hum Immunol; 2007 Oct; 68(10):867-70. PubMed ID: 17961776
    [TBL] [Abstract][Full Text] [Related]  

  • 48. Association of the PTPN22 R620W polymorphism with anti-topoisomerase I- and anticentromere antibody-positive systemic sclerosis.
    Gourh P; Tan FK; Assassi S; Ahn CW; McNearney TA; Fischbach M; Arnett FC; Mayes MD
    Arthritis Rheum; 2006 Dec; 54(12):3945-53. PubMed ID: 17133608
    [TBL] [Abstract][Full Text] [Related]  

  • 49. Association of PTPN22 rs2476601 and EGFR rs17337023 Gene polymorphisms and rheumatoid arthritis in Zahedan, Southeast Iran.
    Hashemi M; Atabaki M; Daneshvar H; Zakeri Z; Eskandari-Nasab E
    Int J Immunogenet; 2013 Aug; 40(4):299-305. PubMed ID: 23350658
    [TBL] [Abstract][Full Text] [Related]  

  • 50. Effects of PTPN22 C1858T polymorphism on susceptibility and clinical characteristics of British Caucasian rheumatoid arthritis patients.
    Harrison P; Pointon JJ; Farrar C; Brown MA; Wordsworth BP
    Rheumatology (Oxford); 2006 Aug; 45(8):1009-11. PubMed ID: 16490755
    [TBL] [Abstract][Full Text] [Related]  

  • 51. PTPN22 and CTLA-4 gene polymorphisms in resected thymomas and thymus for myasthenia gravis.
    Zheng K; Zhang J; Zhang P; Guo Y
    Thorac Cancer; 2012 Nov; 3(4):307-312. PubMed ID: 28920273
    [TBL] [Abstract][Full Text] [Related]  

  • 52. Association of the single nucleotide polymorphism C1858T of the
    Khanbarari F; Ghasemi N; Vakili M; Samadi M
    Int J Reprod Biomed; 2021 Oct; 19(10):873-880. PubMed ID: 34805727
    [TBL] [Abstract][Full Text] [Related]  

  • 53. Lack of association between the protein tyrosine phosphatase non-receptor 22 (PTPN22)*620W allele and systemic sclerosis in the French Caucasian population.
    Wipff J; Allanore Y; Kahan A; Meyer O; Mouthon L; Guillevin L; Pierlot C; Glikmans E; Bardin T; Boileau C; Cornélis F; Dieudé P
    Ann Rheum Dis; 2006 Sep; 65(9):1230-2. PubMed ID: 16464986
    [TBL] [Abstract][Full Text] [Related]  

  • 54. Association of the single nucleotide polymorphism C1858T of the PTPN22 gene with type 1 diabetes.
    Ladner MB; Bottini N; Valdes AM; Noble JA
    Hum Immunol; 2005 Jan; 66(1):60-4. PubMed ID: 15620463
    [TBL] [Abstract][Full Text] [Related]  

  • 55. Association study of PTPN22 C1858T polymorphism in Trypanosoma cruzi infection.
    Robledo G; González CI; Morillo C; Martín J; González A
    Tissue Antigens; 2007 Mar; 69(3):261-4. PubMed ID: 17493151
    [TBL] [Abstract][Full Text] [Related]  

  • 56. Contribution of the R620W polymorphism of protein tyrosine phosphatase non-receptor 22 to systemic lupus erythematosus in Poland.
    Piotrowski P; Lianeri M; Wudarski M; Lacki JK; Jagodziński PP
    Clin Exp Rheumatol; 2008; 26(6):1099-102. PubMed ID: 19210878
    [TBL] [Abstract][Full Text] [Related]  

  • 57. 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]  

  • 58. Lymphoid tyrosine phosphatase (PTPN22/LYP) variant and Graves' disease in a Polish population: association and gene dose-dependent correlation with age of onset.
    Skórka A; Bednarczuk T; Bar-Andziak E; Nauman J; Ploski R
    Clin Endocrinol (Oxf); 2005 Jun; 62(6):679-82. PubMed ID: 15943829
    [TBL] [Abstract][Full Text] [Related]  

  • 59. The PTPN22 C1858T (R620W) functional polymorphism in inflammatory bowel disease.
    Zaid Y; Senhaji N; Bakhtaoui FZ; Serrano A; Serbati N; Karkouri M; Badre W; Oudghiri M; Martin J; Nadifi S
    BMC Res Notes; 2018 Nov; 11(1):783. PubMed ID: 30384859
    [TBL] [Abstract][Full Text] [Related]  

  • 60. The putative role of the C1858T polymorphism of protein tyrosine phosphatase PTPN22 gene in autoimmunity.
    Gianchecchi E; Palombi M; Fierabracci A
    Autoimmun Rev; 2013 May; 12(7):717-25. PubMed ID: 23261816
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 8.