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

Associations between genetic variants of HSD17B13 and fasting plasma glucose in Chinese children.

Nutrition, metabolism, and cardiovascular diseases : NMCD - 1 Sept 2023

Zhang Ping-Ping, Song Jie-Yun, Li Li, Xu Miao, Wang Hui, Wang Hai-Jun

Abstract excerpt

BACKGROUND AND AIMS: Genetic variants in 17-β hydroxysteroid dehydrogenase 13 (HSD17B13) were demonstrated to protect against NAFLD, which is highly related with insulin resistance and dyslipidemia. However, the effects of NAFLD associated HSD17B13 variants on circulating glucose and lipids have not been adequately investigated in children. This study aimed to investigate associations between single nucleotide...

Read the complete abstract on PubMed

Topics

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

Share to 17-Hydroxysteroid Dehydrogenases
Share to Alanine Transaminase

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Blood Glucose

Share to East Asian People

Share to Fasting

Share to Linear Models

Share to Lipids

Share to Non-alcoholic Fatty Liver Disease

Source

Identifiers

PMID: 37414661
DOI: 10.1016/j.numecd.2023.05.027

Genes

HSD17B13

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

Associations between genetic variants of HSD17B13 and fasting plasma glucose in Chinese children.PMID 37414661Read ↗

Is HSD17B13 Genetic Variant a Protector for Liver Dysfunction? Future Perspective as a Potential Therapeutic TargetSemantic proximity Read ↗

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

Genetic variation of HSD17B13 is associated with an increased risk of lean nonalcoholic fatty liver diseaseSemantic proximity Read ↗

The rs72613567: TA Variant in the Hydroxysteroid 17-beta Dehydrogenase 13 Gene Reduces Liver Damage in Obese Children.Semantic proximity Read ↗

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

Pediatric non-alcoholic fatty liver disease and kidney function: Effect of HSD17B13 variant.Semantic proximity Read ↗

HSD17B13: A Potential Therapeutic Target for NAFLDSemantic proximity Read ↗

Genetic variant rs72613567 of HSD17B13 gene reduces alcohol-related liver disease risk in Chinese Han population.Semantic proximity Read ↗

Variants of 11β-hydroxysteroid dehydrogenase (HSD11B) gene type 1 and 2 in Chinese obese adolescents.Semantic proximity Read ↗

Variants in mitochondrial amidoxime reducing component 1 and hydroxysteroid 17‐beta dehydrogenase 13 reduce severity of nonalcoholic fatty liver disease in children and suppress fibrotic pathways through distinct mechanismsSemantic proximity Read ↗

Genetic Susceptibility to Chronic Liver Disease in Individuals from Pakistan.Semantic proximity Read ↗

Association of HSD11B1 gene polymorphisms with type 2 diabetes and metabolic syndrome in South Indian population.Semantic proximity Read ↗

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