165 related articles for article (PubMed ID: 19884265)
21. A common CTLA4 polymorphism confers susceptibility to autoimmune thyroid disease in celiac children.
Tolone C; Cirillo G; Papparella A; Tolone S; Santoro N; Grandone A; Perrone L; del Giudice EM
Dig Liver Dis; 2009 Jun; 41(6):385-9. PubMed ID: 18929517
[TBL] [Abstract][Full Text] [Related]
22. CYP21A2 polymorphisms in patients with autoimmune Addison's disease, and linkage disequilibrium to HLA risk alleles.
Brønstad I; Skinningsrud B; Bratland E; Løvås K; Undlien D; Sverre Husebye E; Wolff AS
Eur J Endocrinol; 2014 Dec; 171(6):743-50. PubMed ID: 25249698
[TBL] [Abstract][Full Text] [Related]
23. CTLA4/CT60 polymorphism is not relevant in susceptibility to autoimmune inflammatory intestinal disorders.
Rueda B; Zhernakova A; López-Nevot MA; Gomez-Garcia M; Ortega E; Piñero A; Correro F; Brieva JA; Nieto A; Koeleman BP; Martín J
Hum Immunol; 2005 Mar; 66(3):321-5. PubMed ID: 15784471
[TBL] [Abstract][Full Text] [Related]
24. The tryptophan 620 allele of the lymphoid tyrosine phosphatase (PTPN22) gene predisposes to autoimmune Addison's disease.
Roycroft M; Fichna M; McDonald D; Owen K; Zurawek M; Gryczyńska M; Januszkiewicz-Lewandowska D; Fichna P; Cordell H; Donaldson P; Nowak J; Pearce S
Clin Endocrinol (Oxf); 2009 Mar; 70(3):358-62. PubMed ID: 18710467
[TBL] [Abstract][Full Text] [Related]
25. [Polymorphism A/G in position +49 of CTLA4 exon 1 in multiple sclerosis in Russians].
Andreevskiĭ TV; Sudomoina MA; Gusev EI; Boĭko AN; Alekseenkov AD; Favorova OO
Mol Biol (Mosk); 2002; 36(4):643-8. PubMed ID: 12173468
[TBL] [Abstract][Full Text] [Related]
26. Interleukin-2 and subunit alpha of its soluble receptor in autoimmune Addison's disease--an association study and expression analysis.
Fichna M; Żurawek M; Bratland E; Husebye ES; Kasperlik-Załuska A; Czarnocka B; Januszkiewicz-Lewandowska D; Nowak J
Autoimmunity; 2015 Mar; 48(2):100-7. PubMed ID: 25347332
[TBL] [Abstract][Full Text] [Related]
27. Association of Cytotoxic T-Lymphocyte Antigen 4 (CTLA4) and Thyroglobulin (TG) Genetic Variants with Autoimmune Hypothyroidism.
Patel H; Mansuri MS; Singh M; Begum R; Shastri M; Misra A
PLoS One; 2016; 11(3):e0149441. PubMed ID: 26963610
[TBL] [Abstract][Full Text] [Related]
28. Association of autoimmune Addison's disease with alleles of STAT4 and GATA3 in European cohorts.
Mitchell AL; Macarthur KD; Gan EH; Baggott LE; Wolff AS; Skinningsrud B; Platt H; Short A; Lobell A; Kämpe O; Bensing S; Betterle C; Kasperlik-Zaluska A; Zurawek M; Fichna M; Kockum I; Nordling Eriksson G; Ekwall O; Wahlberg J; Dahlqvist P; Hulting AL; Penna-Martinez M; Meyer G; Kahles H; Badenhoop K; Hahner S; Quinkler M; Falorni A; Phipps-Green A; Merriman TR; Ollier W; Cordell HJ; Undlien D; Czarnocka B; Husebye E; Pearce SH
PLoS One; 2014; 9(3):e88991. PubMed ID: 24614117
[TBL] [Abstract][Full Text] [Related]
29. Estimated risk for developing autoimmune Addison's disease in patients with adrenal cortex autoantibodies.
Coco G; Dal Pra C; Presotto F; Albergoni MP; Canova C; Pedini B; Zanchetta R; Chen S; Furmaniak J; Rees Smith B; Mantero F; Betterle C
J Clin Endocrinol Metab; 2006 May; 91(5):1637-45. PubMed ID: 16522688
[TBL] [Abstract][Full Text] [Related]
30. Variants of the CTLA4 gene that segregate with autoimmune diseases are not associated with endometriosis.
Viganó P; Lattuada D; Somigliana E; Abbiati A; Candiani M; Di Blasio AM
Mol Hum Reprod; 2005 Oct; 11(10):745-9. PubMed ID: 16373368
[TBL] [Abstract][Full Text] [Related]
31. CTLA-4 as a genetic determinant in autoimmune Addison's disease.
Wolff AS; Mitchell AL; Cordell HJ; Short A; Skinningsrud B; Ollier W; Badenhoop K; Meyer G; Falorni A; Kampe O; Undlien D; Pearce SH; Husebye ES
Genes Immun; 2015 Sep; 16(6):430-6. PubMed ID: 26204230
[TBL] [Abstract][Full Text] [Related]
32. Polymorphisms in the interferon-induced helicase (IFIH1) locus and susceptibility to Addison's disease.
Zurawek M; Fichna M; Januszkiewicz D; Fichna P; Nowak J
Clin Endocrinol (Oxf); 2013 Feb; 78(2):191-6. PubMed ID: 22789000
[TBL] [Abstract][Full Text] [Related]
33. Inherited susceptibility to autoimmune Addison's disease is linked to human leukocyte antigens-DR3 and/or DR4, except when associated with type I autoimmune polyglandular syndrome.
Maclaren NK; Riley WJ
J Clin Endocrinol Metab; 1986 Mar; 62(3):455-9. PubMed ID: 3484749
[TBL] [Abstract][Full Text] [Related]
34. A suggestive association of fuchs heterochromic cyclitis with cytotoxic T cell antigen 4 gene polymorphism.
Spriewald BM; Lefter C; Huber I; Lauer B; Wenkel H
Ophthalmic Res; 2007; 39(2):116-20. PubMed ID: 17287608
[TBL] [Abstract][Full Text] [Related]
35. The role of a nonsynonymous CD226 (DNAX-accessory molecule-1) variant (Gly 307Ser) in isolated Addison's disease and autoimmune polyendocrinopathy type 2 pathogenesis.
Gan EH; Mitchell AL; Macarthur K; Pearce SH
Clin Endocrinol (Oxf); 2011 Aug; 75(2):165-8. PubMed ID: 21521299
[TBL] [Abstract][Full Text] [Related]
36. AIRE variations in Addison's disease and autoimmune polyendocrine syndromes (APS): partial gene deletions contribute to APS I.
Bøe Wolff AS; Oftedal B; Johansson S; Bruland O; Løvås K; Meager A; Pedersen C; Husebye ES; Knappskog PM
Genes Immun; 2008 Mar; 9(2):130-6. PubMed ID: 18200029
[TBL] [Abstract][Full Text] [Related]
37. Association between cytotoxic T-lymphocyte associated protein 4 gene +49 A/G polymorphism and chronic infection with hepatitis B virus: a meta-analysis.
Xu H; Zhao M; He J; Chen Z
J Int Med Res; 2013 Jun; 41(3):559-67. PubMed ID: 23669295
[TBL] [Abstract][Full Text] [Related]
38. A coding variant in NLRP1 is associated with autoimmune Addison's disease.
Zurawek M; Fichna M; Januszkiewicz-Lewandowska D; Gryczyńska M; Fichna P; Nowak J
Hum Immunol; 2010 May; 71(5):530-4. PubMed ID: 20152874
[TBL] [Abstract][Full Text] [Related]
39. A Variant in the BACH2 Gene Is Associated With Susceptibility to Autoimmune Addison's Disease in Humans.
Pazderska A; Oftedal BE; Napier CM; Ainsworth HF; Husebye ES; Cordell HJ; Pearce SH; Mitchell AL
J Clin Endocrinol Metab; 2016 Nov; 101(11):3865-3869. PubMed ID: 27680876
[TBL] [Abstract][Full Text] [Related]
40. Interacting alleles of the coinhibitory immunoreceptor genes cytotoxic T-lymphocyte antigen 4 and programmed cell-death 1 influence risk and features of primary biliary cirrhosis.
Juran BD; Atkinson EJ; Schlicht EM; Fridley BL; Petersen GM; Lazaridis KN
Hepatology; 2008 Feb; 47(2):563-70. PubMed ID: 18041714
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
