214 related articles for article (PubMed ID: 22257840)
1. Association of primary biliary cirrhosis with variants in the CLEC16A, SOCS1, SPIB and SIAE immunomodulatory genes.
Hirschfield GM; Xie G; Lu E; Sun Y; Juran BD; Chellappa V; Coltescu C; Mason AL; Milkiewicz P; Myers RP; Odin JA; Luketic VA; Bacon B; Bodenheimer H; Liakina V; Vincent C; Levy C; Pillai S; Lazaridis KN; Amos CI; Siminovitch KA
Genes Immun; 2012 Jun; 13(4):328-35. PubMed ID: 22257840
[TBL] [Abstract][Full Text] [Related]
2. Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells.
Leikfoss IS; Keshari PK; Gustavsen MW; Bjølgerud A; Brorson IS; Celius EG; Spurkland A; Bos SD; Harbo HF; Berge T
PLoS One; 2015; 10(7):e0132957. PubMed ID: 26203907
[TBL] [Abstract][Full Text] [Related]
3. Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus.
Leikfoss IS; Mero IL; Dahle MK; Lie BA; Harbo HF; Spurkland A; Berge T
Genes Immun; 2013 Jan; 14(1):62-6. PubMed ID: 23151489
[TBL] [Abstract][Full Text] [Related]
4. Genome-wide association study identifies 12 new susceptibility loci for primary biliary cirrhosis.
Mells GF; Floyd JA; Morley KI; Cordell HJ; Franklin CS; Shin SY; Heneghan MA; Neuberger JM; Donaldson PT; Day DB; Ducker SJ; Muriithi AW; Wheater EF; Hammond CJ; Dawwas MF; ; ; Jones DE; Peltonen L; Alexander GJ; Sandford RN; Anderson CA
Nat Genet; 2011 Mar; 43(4):329-32. PubMed ID: 21399635
[TBL] [Abstract][Full Text] [Related]
5. Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex.
Zuvich RL; Bush WS; McCauley JL; Beecham AH; De Jager PL; ; Ivinson AJ; Compston A; Hafler DA; Hauser SL; Sawcer SJ; Pericak-Vance MA; Barcellos LF; Mortlock DP; Haines JL
Hum Mol Genet; 2011 Sep; 20(17):3517-24. PubMed ID: 21653641
[TBL] [Abstract][Full Text] [Related]
6. M89V Sialic acid Acetyl Esterase (SIAE) and all other non-synonymous common variants of this gene are catalytically normal.
Chellappa V; Taylor KN; Pedrick K; Donado C; Netravali IA; Haider K; Cariappa A; Dalomba NF; Pillai S
PLoS One; 2013; 8(1):e53453. PubMed ID: 23308225
[TBL] [Abstract][Full Text] [Related]
7. Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13.
Tomlinson MJ; Pitsillides A; Pickin R; Mika M; Keene KL; Hou X; Mychaleckyj J; Chen WM; Concannon P; Onengut-Gumuscu S
Diabetes; 2014 Dec; 63(12):4360-8. PubMed ID: 25008175
[TBL] [Abstract][Full Text] [Related]
8. Functionally defective germline variants of sialic acid acetylesterase in autoimmunity.
Surolia I; Pirnie SP; Chellappa V; Taylor KN; Cariappa A; Moya J; Liu H; Bell DW; Driscoll DR; Diederichs S; Haider K; Netravali I; Le S; Elia R; Dow E; Lee A; Freudenberg J; De Jager PL; Chretien Y; Varki A; MacDonald ME; Gillis T; Behrens TW; Bloch D; Collier D; Korzenik J; Podolsky DK; Hafler D; Murali M; Sands B; Stone JH; Gregersen PK; Pillai S
Nature; 2010 Jul; 466(7303):243-7. PubMed ID: 20555325
[TBL] [Abstract][Full Text] [Related]
9. Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.
Skinningsrud B; Husebye ES; Pearce SH; McDonald DO; Brandal K; Wolff AB; Løvås K; Egeland T; Undlien DE
J Clin Endocrinol Metab; 2008 Sep; 93(9):3310-7. PubMed ID: 18593762
[TBL] [Abstract][Full Text] [Related]
10. Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus.
Mero IL; Ban M; Lorentzen ÅR; Smestad C; Celius EG; Sæther H; Saeedi H; Viken MK; Skinningsrud B; Undlien DE; Aarseth J; Myhr KM; Granum S; Spurkland A; Sawcer S; Compston A; Lie BA; Harbo HF
Genes Immun; 2011 Apr; 12(3):191-8. PubMed ID: 21179112
[TBL] [Abstract][Full Text] [Related]
11. A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis.
Vandenbroeck K; Alvarez J; Swaminathan B; Alloza I; Matesanz F; Urcelay E; Comabella M; Alcina A; Fedetz M; Ortiz MA; Izquierdo G; Fernandez O; Rodriguez-Ezpeleta N; Matute C; Caillier S; Arroyo R; Montalban X; Oksenberg JR; Antigüedad A; Aransay A
Genes Immun; 2012 Jan; 13(1):21-8. PubMed ID: 21716315
[TBL] [Abstract][Full Text] [Related]
12. Immunochip analyses identify a novel risk locus for primary biliary cirrhosis at 13q14, multiple independent associations at four established risk loci and epistasis between 1p31 and 7q32 risk variants.
Juran BD; Hirschfield GM; Invernizzi P; Atkinson EJ; Li Y; Xie G; Kosoy R; Ransom M; Sun Y; Bianchi I; Schlicht EM; Lleo A; Coltescu C; Bernuzzi F; Podda M; Lammert C; Shigeta R; Chan LL; Balschun T; Marconi M; Cusi D; Heathcote EJ; Mason AL; Myers RP; Milkiewicz P; Odin JA; Luketic VA; Bacon BR; Bodenheimer HC; Liakina V; Vincent C; Levy C; Franke A; Gregersen PK; Bossa F; Gershwin ME; deAndrade M; Amos CI; ; Lazaridis KN; Seldin MF; Siminovitch KA
Hum Mol Genet; 2012 Dec; 21(23):5209-21. PubMed ID: 22936693
[TBL] [Abstract][Full Text] [Related]
13.
Pandey R; Bakay M; Hakonarson H
Int J Mol Sci; 2023 May; 24(9):. PubMed ID: 37175930
[TBL] [Abstract][Full Text] [Related]
14. NFKB1 and MANBA Confer Disease Susceptibility to Primary Biliary Cholangitis via Independent Putative Primary Functional Variants.
Hitomi Y; Nakatani K; Kojima K; Nishida N; Kawai Y; Kawashima M; Aiba Y; Nagasaki M; Nakamura M; Tokunaga K
Cell Mol Gastroenterol Hepatol; 2019; 7(3):515-532. PubMed ID: 30528300
[TBL] [Abstract][Full Text] [Related]
15.
Sevdali E; Tsitsami E; Tsinti M; Farmaki E; Papadopoulou-Alataki E; Germenis AE; Speletas M
J Immunol Res; 2017; 2017():1514294. PubMed ID: 28900629
[TBL] [Abstract][Full Text] [Related]
16. Association of CLEC16A with human common variable immunodeficiency disorder and role in murine B cells.
Li J; Jørgensen SF; Maggadottir SM; Bakay M; Warnatz K; Glessner J; Pandey R; Salzer U; Schmidt RE; Perez E; Resnick E; Goldacker S; Buchta M; Witte T; Padyukov L; Videm V; Folseraas T; Atschekzei F; Elder JT; Nair RP; Winkelmann J; Gieger C; Nöthen MM; Büning C; Brand S; Sullivan KE; Orange JS; Fevang B; Schreiber S; Lieb W; Aukrust P; Chapel H; Cunningham-Rundles C; Franke A; Karlsen TH; Grimbacher B; Hakonarson H; Hammarström L; Ellinghaus E
Nat Commun; 2015 Apr; 6():6804. PubMed ID: 25891430
[TBL] [Abstract][Full Text] [Related]
17. Functional evaluation of the role of C-type lectin domain family 16A at the chromosome 16p13 locus.
Zouk H; D'Hennezel E; Du X; Ounissi-Benkalha H; Piccirillo CA; Polychronakos C
Clin Exp Immunol; 2014 Mar; 175(3):485-97. PubMed ID: 24237155
[TBL] [Abstract][Full Text] [Related]
18. Dense fine-mapping study identifies new susceptibility loci for primary biliary cirrhosis.
Liu JZ; Almarri MA; Gaffney DJ; Mells GF; Jostins L; Cordell HJ; Ducker SJ; Day DB; Heneghan MA; Neuberger JM; Donaldson PT; Bathgate AJ; Burroughs A; Davies MH; Jones DE; Alexander GJ; Barrett JC; Sandford RN; Anderson CA; ;
Nat Genet; 2012 Oct; 44(10):1137-41. PubMed ID: 22961000
[TBL] [Abstract][Full Text] [Related]
19. The type 1 diabetes candidate gene Dexi does not affect disease risk in the nonobese diabetic mouse model.
Nieves-Bonilla JM; Kiaf B; Schuster C; Kissler S
Genes Immun; 2020 Jan; 21(1):71-77. PubMed ID: 31435002
[TBL] [Abstract][Full Text] [Related]
20. Lack of association between rare mutations of the SIAE gene and rheumatoid arthritis in a Han Chinese population.
Zhang DD; He F; Liu HT; Hao F; Zhu J
Genet Mol Res; 2015 Oct; 14(4):14162-8. PubMed ID: 26535733
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
