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Items: 1 to 20 of 132

1.

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. doi: 10.1210/jc.2008-0821. Epub 2008 Jul 1.

PMID:
18593762
2.

Autoimmune disease association signals in CIITA and KIAA0350 are not involved in celiac disease susceptibility.

Dema B, Martínez A, Fernández-Arquero M, Maluenda C, Polanco I, Angeles Figueredo M, de la Concha EG, Urcelay E, Núñez C.

Tissue Antigens. 2009 Apr;73(4):326-9. doi: 10.1111/j.1399-0039.2009.01216.x.

PMID:
19317741
3.

Age-dependent variation of genotypes in MHC II transactivator gene (CIITA) in controls and association to type 1 diabetes.

Gyllenberg A, Asad S, Piehl F, Swanberg M, Padyukov L, Van Yserloo B, Rutledge EA, McNeney B, Graham J, Orho-Melander M, Lindholm E, Graff C, Forsell C, Akesson K, Landin-Olsson M, Carlsson A, Forsander G, Ivarsson SA, Larsson H, Lindblad B, Ludvigsson J, Marcus C, Lernmark A, Alfredsson L, Akesson K, Olsson T, Kockum I; Swedish Childhood Diabetes Study Group; Diabetes Incidence in Sweden Study Group; Better Diabetes Diagnosis Study group.

Genes Immun. 2012 Dec;13(8):632-40. doi: 10.1038/gene.2012.44. Epub 2012 Oct 11.

PMID:
23052709
4.

A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis.

Skinningsrud B, Lie BA, Husebye ES, Kvien TK, Førre Ø, Flatø B, Stormyr A, Joner G, Njølstad PR, Egeland T, Undlien DE.

Ann Rheum Dis. 2010 Aug;69(8):1471-4. doi: 10.1136/ard.2009.114934. Epub 2009 Sep 3.

5.

Association of type 1 diabetes with two Loci on 12q13 and 16p13 and the influence coexisting thyroid autoimmunity in Japanese.

Awata T, Kawasaki E, Tanaka S, Ikegami H, Maruyama T, Shimada A, Nakanishi K, Kobayashi T, Iizuka H, Uga M, Kawabata Y, Kanazawa Y, Kurihara S, Osaki M, Katayama S; Japanese Study Group on Type 1 Diabetes Genetics.

J Clin Endocrinol Metab. 2009 Jan;94(1):231-5. doi: 10.1210/jc.2008-0718. Epub 2008 Oct 21.

PMID:
18940880
6.

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 Jul 23;10(7):e0132957. doi: 10.1371/journal.pone.0132957. eCollection 2015.

7.

Polymorphisms of CLEC16A region and autoimmune thyroid diseases.

Muhali FS, Cai TT, Zhu JL, Qin Q, Xu J, He ST, Shi XH, Jiang WJ, Xiao L, Li DF, Zhang JA.

G3 (Bethesda). 2014 Mar 18;4(6):973-7. doi: 10.1534/g3.114.010926.

8.

Polymorphisms in the cytotoxic T lymphocyte antigen-4 gene region confer susceptibility to Addison's disease.

Blomhoff A, Lie BA, Myhre AG, Kemp EH, Weetman AP, Akselsen HE, Huseby ES, Undlien DE.

J Clin Endocrinol Metab. 2004 Jul;89(7):3474-6.

PMID:
15240634
9.

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. doi: 10.1038/gene.2012.52. Epub 2012 Nov 15.

PMID:
23151489
10.

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; International Multiple Sclerosis Genetics Consortium, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Sawcer SJ, Pericak-Vance MA, Barcellos LF, Mortlock DP, Haines JL.

Hum Mol Genet. 2011 Sep 1;20(17):3517-24. doi: 10.1093/hmg/ddr250. Epub 2011 Jun 8.

11.
12.

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. doi: 10.1530/EJE-14-0432. Epub 2014 Sep 23.

PMID:
25249698
13.

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 Mar 10;9(3):e88991. doi: 10.1371/journal.pone.0088991. eCollection 2014. Erratum in: PLoS One. 2014;9(7):e102428.

14.

More CLEC16A gene variants associated with multiple sclerosis.

Nischwitz S, Cepok S, Kroner A, Wolf C, Knop M, Müller-Sarnowski F, Pfister H, Rieckmann P, Hemmer B, Ising M, Uhr M, Bettecken T, Holsboer F, Müller-Myhsok B, Weber F.

Acta Neurol Scand. 2011 Jun;123(6):400-6. doi: 10.1111/j.1600-0404.2010.01421.x. Epub 2010 Sep 16.

PMID:
20849399
15.

Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women.

Swanberg M, McGuigan FE, Ivaska KK, Gerdhem P, Åkesson K.

PLoS One. 2012;7(10):e47964. doi: 10.1371/journal.pone.0047964. Epub 2012 Oct 25.

16.

CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations.

Eike MC, Skinningsrud B, Ronninger M, Stormyr A, Kvien TK, Joner G, Njølstad PR, Førre O, Flatø B, Alfredsson L, Padyukov L, Undlien DE, Lie BA.

Genes Immun. 2012 Jul;13(5):431-6. doi: 10.1038/gene.2012.11. Epub 2012 Apr 19.

PMID:
22513452
17.

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. doi: 10.1038/gene.2010.59. Epub 2010 Dec 23.

PMID:
21179112
18.

A cytotoxic T lymphocyte antigen-4 (CTLA-4) gene polymorphism is associated with autoimmune Addison's disease in English patients.

Kemp EH, Ajjan RA, Husebye ES, Peterson P, Uibo R, Imrie H, Pearce SH, Watson PF, Weetman AP.

Clin Endocrinol (Oxf). 1998 Nov;49(5):609-13.

PMID:
10197076
19.

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. doi: 10.1038/gene.2011.89. Epub 2012 Jan 19.

20.

Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility.

Mitchell AL, Cordell HJ, Soemedi R, Owen K, Skinningsrud B, Wolff AB, Ericksen M, Undlien D, Husebye E, Pearce SH.

J Clin Endocrinol Metab. 2009 Dec;94(12):5139-45. doi: 10.1210/jc.2009-1404. Epub 2009 Oct 22.

PMID:
19850680

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