Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency. - Wikidata - awgldk - TriplyDB

Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.

Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.

http://www.wikidata.org/entity/Q34790983

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A CLEC16A variant confers risk for juvenile idiopathic arthritis and anti-cyclic citrullinated peptide antibody negative rheumatoid arthritis A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus A candidate gene study of CLEC16A does not provide evidence of association with risk for anti-CCP-positive rheumatoid arthritis The expanding genetic overlap between multiple sclerosis and type I diabetes Fine mapping and functional studies of risk variants for type 1 diabetes at chromosome 16p13.13 The role of functionally defective rare germline variants of sialic acid acetylesterase in autoimmune Addison's disease The diabetes susceptibility gene Clec16a regulates mitophagy The novel endosomal membrane protein Ema interacts with the class C Vps-HOPS complex to promote endosomal maturation.Lack of association of the CIITA -168A→G promoter SNP with myasthenia gravis and its role in autoimmunity.Polymorphisms of CLEC16A region and autoimmune thyroid diseases.Recent advances in the genetics of systemic lupus erythematosus.Genome-wide copy number variation (CNV) in patients with autoimmune Addison's disease.Interaction analysis between HLA-DRB1 shared epitope alleles and MHC class II transactivator CIITA gene with regard to risk of rheumatoid arthritis.Clinical implications of shared genetics and pathogenesis in autoimmune diseases.Polymorphisms in the inflammatory genes CIITA, CLEC16A and IFNG influence BMD, bone loss and fracture in elderly women.Haplotype analysis discriminates genetic risk for DR3-associated endocrine autoimmunity and helps define extreme risk for Addison's disease.Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis.Linkage Analysis in Autoimmune Addison's Disease: NFATC1 as a Potential Novel Susceptibility Locus.Multiple Sclerosis Risk Allele in CLEC16A Acts as an Expression Quantitative Trait Locus for CLEC16A and SOCS1 in CD4+ T Cells.Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene Clinical features of hypoadrenocorticism in soft-coated wheaten terrier dogs: 82 cases (1979-2013)Clec16a is Critical for Autolysosome Function and Purkinje Cell Survival Functions of NOD-Like Receptors in Human Diseases.Impact of Month of Birth on the Risk of Development of Autoimmune Addison's Disease Genes involved in type 1 diabetes: an update From Identification to Characterization of the Multiple Sclerosis Susceptibility Gene CLEC16A.The Autoimmunity-Associated Gene CLEC16A Modulates Thymic Epithelial Cell Autophagy and Alters T Cell Selection.Functional evaluation of the role of C-type lectin domain family 16A at the chromosome 16p13 locus.Evaluation of the genetic basis of primary hypoadrenocorticism in Standard Poodles using SNP array genotyping and whole-genome sequencing.MHC class II association study in eight breeds of dog with hypoadrenocorticism.Polymorphisms of the Toll-Like Receptor-3 Gene in Autoimmune Adrenal Failure and Type 1 Diabetes in Polish Patients.Phosphorylation and ubiquitination of degron proximal residues are essential for class II transactivator (CIITA) transactivation and major histocompatibility class II expression.GOP-1 promotes apoptotic cell degradation by activating the small GTPase Rab2 in C. elegans.Polymorphic variants of the IL2RA gene and susceptibility to type 1 diabetes in the Polish population.Common genetic variation in the autoimmune regulator (AIRE) locus is associated with autoimmune Addison's disease in Sweden.Variability in the CIITA gene interacts with HLA in multiple sclerosis CIITA gene variants are associated with rheumatoid arthritis in Scandinavian populations Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients CLEC16A regulates splenocyte and NK cell function in part through MEK signaling

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Polymorphisms in CLEC16A and CIITA at 16p13 are associated with primary adrenal insufficiency.

http://www.wikidata.org/entity/Q34790983

description

2008 nî lūn-bûn

@nan

2008 թուականի Յուլիսին հրատարակուած գիտական յօդուած

@hyw

2008 թվականի հուլիսին հրատարակված գիտական հոդված

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2008年の論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年論文

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2008年论文

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name

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@ast

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@en

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@nl

type

label

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@ast

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@en

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@nl

prefLabel

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@ast

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@en

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@nl

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P1433

The Journal of Clinical Endocrinology and Metabolism

P1476

Polymorphisms in CLEC16A and C ...... primary adrenal insufficiency.

@en

P2093

Anette B Wolff

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Beate Skinningsrud

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David O McDonald

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Eystein S Husebye

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Kristian Løvås

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Kristin Brandal

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Simon H Pearce

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Thore Egeland

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3310-3317

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scholarly article

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10.1210/JC.2008-0821

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9

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93

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2008-07-01T00:00:00Z

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5259210

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18593762

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