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Liu, D. HLA-DRB1 Gene. Encyclopedia. Available online: https://encyclopedia.pub/entry/4096 (accessed on 29 September 2026).
Liu D. HLA-DRB1 Gene. Encyclopedia. Available at: https://encyclopedia.pub/entry/4096. Accessed September 29, 2026.
Liu, Dean. "HLA-DRB1 Gene" Encyclopedia, https://encyclopedia.pub/entry/4096 (accessed September 29, 2026).
Liu, D. (2020, December 23). HLA-DRB1 Gene. In Encyclopedia. https://encyclopedia.pub/entry/4096
Liu, Dean. "HLA-DRB1 Gene." Encyclopedia. Web. 23 December, 2020.
HLA-DRB1 Gene
Edit

Major histocompatibility complex, class II, DR beta 1

genes

References

  1. Alcina A, Abad-Grau Mdel M, Fedetz M, Izquierdo G, Lucas M, Fernández O,Ndagire D, Catalá-Rabasa A, Ruiz A, Gayán J, Delgado C, Arnal C, Matesanz F.Multiple sclerosis risk variant HLA-DRB1*1501 associates with high expression of DRB1 gene in different human populations. PLoS One. 2012;7(1):e29819. doi:10.1371/journal.pone.0029819.
  2. Aly TA, Ide A, Jahromi MM, Barker JM, Fernando MS, Babu SR, Yu L, Miao D,Erlich HA, Fain PR, Barriga KJ, Norris JM, Rewers MJ, Eisenbarth GS. Extremegenetic risk for type 1A diabetes. Proc Natl Acad Sci U S A. 2006 Sep19;103(38):14074-9.
  3. Chinoy H, Lamb JA, Ollier WE, Cooper RG. An update on the immunogenetics ofidiopathic inflammatory myopathies: major histocompatibility complex and beyond. Curr Opin Rheumatol. 2009 Nov;21(6):588-93. doi: 10.1097/BOR.0b013e3283315a22.Review.
  4. Gombos Z, Hermann R, Kiviniemi M, Nejentsev S, Reimand K, Fadeyev V, Peterson P, Uibo R, Ilonen J. Analysis of extended human leukocyte antigen haplotypeassociation with Addison's disease in three populations. Eur J Endocrinol. 2007Dec;157(6):757-61.
  5. Hor H, Kutalik Z, Dauvilliers Y, Valsesia A, Lammers GJ, Donjacour CE, Iranzo A, Santamaria J, Peraita Adrados R, Vicario JL, Overeem S, Arnulf I, Theodorou I,Jennum P, Knudsen S, Bassetti C, Mathis J, Lecendreux M, Mayer G, Geisler P,Benetó A, Petit B, Pfister C, Bürki JV, Didelot G, Billiard M, Ercilla G,Verduijn W, Claas FH, Vollenweider P, Waeber G, Waterworth DM, Mooser V, Heinzer R, Beckmann JS, Bergmann S, Tafti M. Genome-wide association study identifies newHLA class II haplotypes strongly protective against narcolepsy. Nat Genet. 2010Sep;42(9):786-9. doi: 10.1038/ng.647.2011 Apr;43(4):388. Vollenwider, Peter [corrected to Vollenweider, Peter].
  6. Noble JA, Valdes AM. Genetics of the HLA region in the prediction of type 1diabetes. Curr Diab Rep. 2011 Dec;11(6):533-42. doi: 10.1007/s11892-011-0223-x.Review.
  7. Prahalad S, Glass DN. A comprehensive review of the genetics of juvenileidiopathic arthritis. Pediatr Rheumatol Online J. 2008 Jul 21;6:11. doi:10.1186/1546-0096-6-11.
  8. Raychaudhuri S, Sandor C, Stahl EA, Freudenberg J, Lee HS, Jia X, AlfredssonL, Padyukov L, Klareskog L, Worthington J, Siminovitch KA, Bae SC, Plenge RM,Gregersen PK, de Bakker PI. Five amino acids in three HLA proteins explain mostof the association between MHC and seropositive rheumatoid arthritis. Nat Genet. 2012 Jan 29;44(3):291-6. doi: 10.1038/ng.1076.
  9. Rottembourg D, Deal C, Lambert M, Mallone R, Carel JC, Lacroix A,Caillat-Zucman S, le Deist F. 21-Hydroxylase epitopes are targeted by CD8 T cellsin autoimmune Addison's disease. J Autoimmun. 2010 Dec;35(4):309-15. doi:10.1016/j.jaut.2010.07.001.
  10. Skinningsrud B, Lie BA, Lavant E, Carlson JA, Erlich H, Akselsen HE, Gervin K,Wolff AB, Erichsen MM, Løvås K, Husebye ES, Undlien DE. Multiple loci in the HLA complex are associated with Addison's disease. J Clin Endocrinol Metab. 2011Oct;96(10):E1703-8. doi: 10.1210/jc.2011-0645.
  11. Steck AK, Rewers MJ. Genetics of type 1 diabetes. Clin Chem. 2011Feb;57(2):176-85. doi: 10.1373/clinchem.2010.148221.
  12. Viatte S, Plant D, Raychaudhuri S. Genetics and epigenetics of rheumatoidarthritis. Nat Rev Rheumatol. 2013 Mar;9(3):141-53. doi:10.1038/nrrheum.2012.237.
  13. Yu L, Brewer KW, Gates S, Wu A, Wang T, Babu SR, Gottlieb PA, Freed BM, Noble J, Erlich HA, Rewers MJ, Eisenbarth GS. DRB1*04 and DQ alleles: expression of21-hydroxylase autoantibodies and risk of progression to Addison's disease. JClin Endocrinol Metab. 1999 Jan;84(1):328-35.
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