(Q54210124)

26 May 2018

title

Predisposition to Behçet's disease and VKH syndrome by genetic variants of miR-182. (English)

1 reference

26 May 2018

0 references

1

1 reference

26 May 2018

Aize Kijlstra

series ordinal

4

object named as

Aize Kijlstra

1 reference

26 May 2018

Yunjia Liu

2

1 reference

26 May 2018

Lin Bai

series ordinal

3

1 reference

26 May 2018

Peizeng Yang

series ordinal

5

1 reference

26 May 2018

publication date

8 May 2014

1 reference

26 May 2018

Journal of Molecular Medicine

published in

1 reference

26 May 2018

volume

92

1 reference

26 May 2018

issue

9

1 reference

26 May 2018

page(s)

961-967

1 reference

26 May 2018

https://scigraph.springernature.com/pub.10.1007/s00109-014-1159-9

exact match

0 references

cites work

Clinical features of chinese patients with Behçet's disease

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Epidemiology of Behçet disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Clinical characteristics of Vogt-Koyanagi-Harada syndrome in Chinese patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Familial aggregation of Behçet's disease in Turkey

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Gene expression profiling and association studies implicate the neuregulin signaling pathway in Behçet's disease susceptibility

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Interleukin-17 gene polymorphism is associated with Vogt-Koyanagi-Harada syndrome but not with Behçet's disease in a Chinese Han population.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Foxo transcription factors control regulatory T cell development and function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Novel Foxo1-dependent transcriptional programs control T(reg) cell function

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Coordinate regulation of FOXO1 by miR-27a, miR-96, and miR-182 in breast cancer cells

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

The microRNA miR-182 is induced by IL-2 and promotes clonal expansion of activated helper T lymphocytes.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

miR-182 and miR-10a are key regulators of Treg specialisation and stability during Schistosome and Leishmania-associated inflammation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Association of common genetic variation in the FOXO1 gene with beta-cell dysfunction, impaired glucose tolerance, and type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Genetic variants and abnormal processing of pre-miR-182, a circadian clock modulator, in major depression patients with late insomnia.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Investigation of rheumatoid arthritis susceptibility loci in juvenile idiopathic arthritis confirms high degree of overlap

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Association analyses between the genetic polymorphisms of HNF4A and FOXO1 genes and Chinese Han patients with type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Analysis of FOXO1A as a candidate gene for type 2 diabetes

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Revised diagnostic criteria for Vogt-Koyanagi-Harada disease: report of an international committee on nomenclature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

MicroRNAs and autoimmunity.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

MicroRNA in immunity and autoimmunity

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Genome-wide association study identifies variants in the MHC class I, IL10, and IL23R-IL12RB2 regions associated with Behçet's disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Identification of a susceptibility locus in STAT4 for Behçet's disease in Han Chinese in a genome-wide association study

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Genome-wide association analysis identifies new susceptibility loci for Behçet's disease and epistasis between HLA-B*51 and ERAP1

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

MicroRNA (miRNA) transcriptome of mouse retina and identification of a sensory organ-specific miRNA cluster.

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

A genetic variant in pre-miR-27a is associated with a reduced renal cell cancer risk in a Chinese population

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Evaluation of the IL2/IL21, IL2RA and IL2RB genetic variants influence on the endogenous non-anterior uveitis genetic predisposition

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Association of the CTLA-4 gene with Vogt-Koyanagi-Harada syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Single-nucleotide polymorphisms in the IL2RA gene are associated with age at diagnosis in late-onset Finnish type 1 diabetes subjects

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Replication study of multiple sclerosis (MS) susceptibility alleles and correlation of DNA-variants with disease features in a cohort of Austrian MS patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Association of Variants inIL2RAWith Progression of Joint Destruction in Rheumatoid Arthritis

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS00109-014-1159-9

Genetic association between the interleukin-2 receptor-alpha gene and mode of onset of type 1 diabetes in the Japanese population

21 January 2018

1 reference

12 December 2020

Outfoxing Foxo1 with miR-182

1 reference

12 December 2020

MicroRNA-146a and Ets-1 gene polymorphisms in ocular Behcet's disease and Vogt-Koyanagi-Harada syndrome

1 reference

12 December 2020

Diminished frequency and function of CD4+CD25high regulatory T cells associated with active uveitis in Vogt-Koyanagi-Harada syndrome

1 reference

12 December 2020

Hsa-mir-27a genetic variant contributes to gastric cancer susceptibility through affecting miR-27a and target gene expression

1 reference

12 December 2020

IL-23R gene confers susceptibility to Behcet's disease in a Chinese Han population

1 reference

12 December 2020

10.1007/S00109-014-1159-9

Identifiers

DOI

1 reference

26 May 2018

PubMed ID

24801147

1 reference

26 May 2018