Arvelige faktorer ved Addisons sykdom
- Prosjektnummer
- 2008089
- Ansvarlig person
- Dag Undlien
- Institusjon
- Oslo universitetssykehus HF
- Prosjektkategori
- Doktorgradsstipend
- Helsekategori
- Inflammatory and Immune System
- Forskningsaktivitet
- 2. Aetiology
CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations.
Genes Immun 2012 Jul;13(5):431-6. Epub 2012 apr 19
PMID: 22513452
Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis.
PLoS One 2012;7(3):e32861. Epub 2012 mar 26
PMID: 22461888
Multiple loci in the HLA complex are associated with Addison's disease.
J Clin Endocrinol Metab 2011 Oct;96(10):E1703-8. Epub 2011 aug 3
PMID: 21816777
Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus.
Genes Immun 2011 Apr;12(3):191-8. Epub 2010 des 23
PMID: 21179112
T cell responses to steroid cytochrome P450 21-hydroxylase in patients with autoimmune primary adrenal insufficiency.
J Clin Endocrinol Metab 2009 Dec;94(12):5117-24. Epub 2009 nov 4
PMID: 19890026
Clinical, immunological, and genetic features of autoimmune primary adrenal insufficiency: observations from a Norwegian registry.
J Clin Endocrinol Metab 2009 Dec;94(12):4882-90. Epub 2009 okt 26
PMID: 19858318
Programmed death ligand 1 (PD-L1) gene variants contribute to autoimmune Addison's disease and Graves' disease susceptibility.
J Clin Endocrinol Metab 2009 Dec;94(12):5139-45. Epub 2009 okt 22
PMID: 19850680
X-linked congenital adrenal hypoplasia with hypogonadotropic hypogonadism caused by an inversion disrupting a conserved noncoding element upstream of the NR0B1 (DAX1) gene.
J Clin Endocrinol Metab 2009 Oct;94(10):4086-93. Epub 2009 sep 22
PMID: 19773398
A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis.
Ann Rheum Dis 2010 Aug;69(8):1471-4. Epub 2009 sep 3
PMID: 19734133
A coding polymorphism in NALP1 confers risk for autoimmune Addison's disease and type 1 diabetes.
Genes Immun 2009 Mar;10(2):120-4. Epub 2008 okt 23
PMID: 18946481
Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.
J Clin Endocrinol Metab 2008 Sep;93(9):3310-7. Epub 2008 jul 1
PMID: 18593762
Mutation screening of PTPN22: association of the 1858T-allele with Addison's disease.
Eur J Hum Genet 2008 Aug;16(8):977-82. Epub 2008 feb 27
PMID: 18301444
PhD
- Disputert:
- desember 2011
- Hovedveileder:
- Dag Undlien
eRapport er utarbeidet av Sølvi Lerfald og Reidar Thorstensen, Regionalt kompetansesenter for klinisk forskning, Helse Vest RHF, og videreutvikles av de fire RHF-ene i fellesskap, med støtte fra Helse Vest IKT
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