(Q60445325)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23151489%20AND%20SRC:MED&resulttype=core&format=json

17 February 2020

title

Multiple sclerosis-associated single-nucleotide polymorphisms in CLEC16A correlate with reduced SOCS1 and DEXI expression in the thymus (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23151489%20AND%20SRC:MED&resulttype=core&format=json

single-nucleotide polymorphism

17 February 2020

main subject

1 reference

3

1 reference

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17 February 2020

Anne Spurkland

6

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17 February 2020

5

H F Harbo

1 reference

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17 February 2020

author name string

I S Leikfoss

1

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17 February 2020

I-L Mero

2

1 reference

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17 February 2020

B A Lie

4

1 reference

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17 February 2020

T Berge

7

1 reference

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17 February 2020

publication date

15 November 2012

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17 February 2020

1 reference

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17 February 2020

volume

14

1 reference

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17 February 2020

issue

1

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17 February 2020

page(s)

62-66

1 reference

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https://scigraph.springernature.com/pub.10.1038/gene.2012.52

17 February 2020

exact match

0 references

cites work

A genome-wide association study identifies KIAA0350 as a type 1 diabetes gene

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

The expanding genetic overlap between multiple sclerosis and type I diabetes

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https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Robust associations of four new chromosome regions from genome-wide analyses of type 1 diabetes

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https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Specific association of a CLEC16A/KIAA0350 polymorphism with NOD2/CARD15(-) Crohn's disease patients

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Replication of KIAA0350, IL2RA, RPL5 and CD58 as multiple sclerosis susceptibility genes in Australians

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https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Association of IFIH1 and other autoimmunity risk alleles with selective IgA deficiency

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

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

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Exploring the CLEC16A gene reveals a MS-associated variant with correlation to the relative expression of CLEC16A isoforms in thymus

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Risk alleles for multiple sclerosis identified by a genomewide study

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

More CLEC16A gene variants associated with multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

CIITA variation in the presence of HLA-DRB1*1501 increases risk for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

A cytokine gene screen uncovers SOCS1 as genetic risk factor for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Genetic variation in the IL7RA/IL7 pathway increases multiple sclerosis susceptibility

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Replication of CD58 and CLEC16A as genome-wide significant risk genes for multiple sclerosis

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Long-range DNA looping and gene expression analyses identify DEXI as an autoimmune disease candidate gene

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Candidate causal regulatory effects by integration of expression QTLs with complex trait genetic associations

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Multiple common variants for celiac disease influencing immune gene expression

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

MHC2TA is associated with differential MHC molecule expression and susceptibility to rheumatoid arthritis, multiple sclerosis and myocardial infarction

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Complementation cloning of an MHC class II transactivator mutated in hereditary MHC class II deficiency (or bare lymphocyte syndrome)

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Suppressor of cytokine signaling 1 regulates the immune response to infection by a unique inhibition of type I interferon activity

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Cloning of dexamethasone-induced transcript: a novel glucocorticoid-induced gene that is upregulated in emphysema

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Mapping complex disease traits with global gene expression

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Trait-associated SNPs are more likely to be eQTLs: annotation to enhance discovery from GWAS

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Suppressor of cytokine signaling 1 is required for the differentiation of CD4+ T cells.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

SOCS1 negatively regulates the production of Foxp3+ CD4+ T cells in the thymus.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

T-helper 17 cells expand in multiple sclerosis and are inhibited by interferon-beta.

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

SOCS1 is essential for regulatory T cell functions by preventing loss of Foxp3 expression as well as IFN-{gamma} and IL-17A production

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Unraveling the regulatory mechanisms underlying tissue-dependent genetic variation of gene expression

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Glucocorticoids target suppressor of cytokine signaling 1 (SOCS1) and type 1 interferons to regulate Toll-like receptor-induced STAT1 activation

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Antiinflammatory action of glucocorticoids--new mechanisms for old drugs

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

The PTPN22 promoter polymorphism -1123G>C association cannot be distinguished from the 1858C>T association in a Norwegian rheumatoid arthritis material

1 reference

https://api.crossref.org/works/10.1038%2FGENE.2012.52

7 January 2021

Identifiers

DOI

10.1038/GENE.2012.52

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23151489%20AND%20SRC:MED&resulttype=core&format=json

17 February 2020

1 reference