Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2. - Wikidata - wikimedia - TriplyDB

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

http://www.wikidata.org/entity/Q33947872

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Pathogenesis of biliary atresia: defining biology to understand clinical phenotypes Biliary atresia: cellular dynamics and immune dysregulation Identification of a plant isoflavonoid that causes biliary atresia Biliary atresia: will blocking inflammation tame the disease?Association between single nucleotide polymorphisms in the ADD3 gene and susceptibility to biliary atresia.Evidence from human and zebrafish that GPC1 is a biliary atresia susceptibility gene.The toxin biliatresone causes mouse extrahepatic cholangiocyte damage and fibrosis through decreased glutathione and SOX17 Functional polymorphisms in FAS/FASL system increase the risk of neuroblastoma in Chinese population The SNP rs402710 in 5p15.33 is associated with lung cancer risk: a replication study in Chinese population and a meta-analysis Genetic variant in MTRR, but not MTR, is associated with risk of congenital heart disease: an integrated meta-analysis Recent advances in the pathogenesis and management of biliary atresia The Role of ARF6 in Biliary Atresia.Rotavirus Infects Human Biliary Epithelial Cells and Stimulates Secretion of Cytokines IL-6 and IL-8 via MAPK Pathway.The Cholangiopathies.Patient complexity and genotype-phenotype correlations in biliary atresia: a cross-sectional analysis.Lack of HLA predominance and HLA shared epitopes in biliary Atresia Pleiotropic roles of bile acids in metabolism.Clues to the etiology of bile duct injury in biliary atresia Extrahepatic anomalies in infants with biliary atresia: results of a large prospective North American multicenter study.Replication of a GWAS signal in a Caucasian population implicates ADD3 in susceptibility to biliary atresia.Etiology of biliary atresia as a developmental anomaly: recent advances.Changes in epigenetic regulation of CD4+ T lymphocytesin biliary atresia.Association between rs17095355 polymorphism on 10q24 and susceptibility to biliary atresia: a meta-analysis.Cirrhosis in children and adolescents: An overview.Genome-wide association studies in biliary atresia.Trans-ethnic meta-analysis of genome-wide association studies for Hirschsprung disease.Glutathione antioxidant pathway activity and reserve determine toxicity and specificity of the biliary toxin biliatresone in zebrafish.Downregulation of microRNA-145 may contribute to liver fibrosis in biliary atresia by targeting ADD3 Loss of a Candidate Biliary Atresia Susceptibility Gene, add3a, Causes Biliary Developmental Defects in Zebrafish.Association of X-prolyl aminopeptidase 1 rs17095355 polymorphism with biliary atresia in Thai children.Atlas of human diseases influenced by genetic variants with extreme allele frequency differences.Three-dimensional structural analysis reveals a Cdk5-mediated kinase cascade regulating hepatic biliary network branching in zebrafish.Update on investigations pertaining to the pathogenesis of biliary atresia.+276 G/T single nucleotide polymorphism of the adiponectin gene is associated with the susceptibility to biliary atresia.The intragenic epistatic association of ADD3 with biliary atresia in Southern Han Chinese population.Cholangiopathies - Towards a molecular understanding A genome-wide association study identifies a susceptibility locus for biliary atresia on 2p16.1 within the gene EFEMP1 Epistatic Association of CD14 and NOTCH2 Genetic Polymorphisms with Biliary Atresia in a Southern Chinese Population

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P2860

Genome-wide association study identifies a susceptibility locus for biliary atresia on 10q24.2.

http://www.wikidata.org/entity/Q33947872

description

2010 nî lūn-bûn

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2010 թուականի Մայիսին հրատարակուած գիտական յօդուած

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2010年の論文

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2010年論文

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2010年論文

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Genome-wide association study ...... or biliary atresia on 10q24.2.

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Danny Chan

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Elly Sau-Wai Ngan

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Guo Cheng

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Jin-Fa Tou

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Kenneth Cheung

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Kenneth Kak-Yuen Wong

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Kenneth-Jeremy W S Hui

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Long Li

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P2860

PLINK: a tool set for whole-genome association and population-based linkage analyses

Haploview: analysis and visualization of LD and haplotype maps

Expression analysis of the human adducin gene family and evidence of ADD2 beta4 multiple splicing variants

Human kininogen gene is transactivated by the farnesoid X receptor

Immunohistochemical localization of placental leucine aminopeptidase/oxytocinase in normal human placental, fetal and adult tissues

Genome-wide association study identifies NRG1 as a susceptibility locus for Hirschsprung's disease

Common and rare variants in multifactorial susceptibility to common diseases

OpenADAM: an open source genome-wide association data management system for Affymetrix SNP arrays.

The cytoskeleton of digestive epithelia in health and disease.

Protease-activated receptors: the role of cell-surface proteolysis in signalling.

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14

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