Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits.

Endocrine journal - 1 Jan 2014

Kitamoto Aya, Kitamoto Takuya, Nakamura Takahiro, Ogawa Yuji, Yoneda Masato, Hyogo Hideyuki, Ochi Hidenori, Mizusawa Seiho, Ueno Takato, Nakao Kazuwa, Sekine Akihiro, Chayama Kazuaki, Nakajima Atsushi, Hotta Kikuko

Abstract excerpt

In several genome-wide association studies, nonalcoholic fatty liver disease and alanine aminotransferase susceptibility variants have been identified in several genes, including LYPLAL1, ZP4, GCKR, HSD17B13, PALLD, PPP1R3B, FDFT1, TRIB1, COL13A1, CPN1, ERLIN1, CWF19L1, EFCAB4B, PZP, and NCAN. To investigate the relationship between these genes and nonalcoholic fatty liver disease in the Japanese population, we...

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Adaptor Proteins, Signal Transducing
Share to Intracellular Signaling Peptides and Proteins

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Lipase

Share to Logistic Models

Share to Metabolic Syndrome

Share to Non-alcoholic Fatty Liver Disease

Share to Severity of Illness Index

Source

Identifiers

PMID: 24785259
DOI: 10.1507/endocrj.ej14-0052

Genes

GCKR
TRIB1
PNPLA3
CPN1
ERLIN1
FDFT1
LYPLAL1
NCAN
PALLD
PZP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Association of polymorphisms in GCKR and TRIB1 with nonalcoholic fatty liver disease and metabolic syndrome traits.PMID 24785259Read ↗

PARVB and HSD17B13 variants are associated with nonalcoholic fatty liver disease in children.Semantic proximity Read ↗

GWAS-Identified Common Variants With Nonalcoholic Fatty Liver Disease in Chinese Children.Semantic proximity Read ↗

Genetic variants associated with metabolic dysfunction-associated fatty liver disease in western China.Semantic proximity Read ↗

Association of Genetic Risk Score With NAFLD in An Ethnically Diverse Cohort.Semantic proximity Read ↗

Genetic variants in GCKR and PNPLA3 confer susceptibility to nonalcoholic fatty liver disease in obese individuals.Semantic proximity Read ↗

Association of patatin-like phospholipase domain-containing protein 3 gene polymorphisms with susceptibility of nonalcoholic fatty liver disease in a Han Chinese population.Semantic proximity Read ↗

Genetic variation in the GCKR gene is associated with non-alcoholic fatty liver disease in Chinese people.Semantic proximity Read ↗

Integrative genetic and liver transcriptomic analyses identify TRIB1AL as a target for steatotic liver disease.Semantic proximity Read ↗

Risk estimation model for nonalcoholic fatty liver disease in the Japanese using multiple genetic markers.Semantic proximity Read ↗

The long non-coding RNA<i>TRIB1AL</i>links metabolic dysfunction-associated steatotic liver disease, cardiometabolic risk and human lifespanSemantic proximity Read ↗

A genetic risk score is associated with hepatic triglyceride content and non-alcoholic steatohepatitis in Mexicans with morbid obesity.Semantic proximity Read ↗

Polymorphism of receptor-type tyrosine-protein phosphatase delta gene in the development of non-alcoholic fatty liver disease.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.