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

[Clinical features and gene mutation profiles of patients with chronic hepatitis B and Gilbert's syndrome].

Zhonghua gan zang bing za zhi = Zhonghua ganzangbing zazhi = Chinese journal of hepatology - 1 Jan 2015

Ning Huibin, Li Kuan, Mao Zhongshan, Liu Junping, Xiao Erhui, Kang Yi, Shang Jia

Abstract excerpt

OBJECTIVE: To explore the clinical features and gene mutation profiles of patients with chronic hepatitis B (CHB) and Gilbert's syndrome. METHODS: Thirty-three patients with CHB and Gilbert's syndrome were enrolled in the study. Serum markers of liver function and histological features of disease-related liver injury were assessed by standard methods. Gene mutations were detected by PCR and direct DNA...

Read the complete abstract on PubMed

Topics

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

Share to Exons
Share to Gilbert Disease

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Share to Glucuronosyltransferase

Share to Hepatitis B, Chronic

Share to Mutagenesis, Insertional

Share to Polymerase Chain Reaction

Share to Promoter Regions, Genetic

Share to TATA Box

Source

Open in PubMed Open full text

Identifiers

PMID: 25751380
DOI: 10.3760/cma.j.issn.1007-3418.2015.01.005
PMCID: PMC12769198

Genes

AGA

Variants

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-08.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

[Clinical features and gene mutation profiles of patients with chronic hepatitis B and Gilbert's syndrome].PMID 25751380Read ↗

[Clinical and genetic analyses of UGT1A1 gene from a Chinese family with Gilbert's syndrome].Semantic proximity Read ↗

[Gene mutation pattern of Gilbert's syndrome combined with viral hepatitis and its relationship with the exploration of clinical data].Semantic proximity Read ↗

[Clinical Characteristics and Gene Mutations of Gilbert Syndrome Complicated with Myeloproliferative Neoplasm].Semantic proximity Read ↗

[Analysis of diagnostic value of UGT1A1 gene detection in Gilbert syndrome].Semantic proximity Read ↗

[Gilbert syndrome].Semantic proximity Read ↗

Molecular genetic basis of Gilbert's syndrome.Semantic proximity Read ↗

Impact of UGT1A1 gene variants on total bilirubin levels in Gilbert syndrome patients and in healthy subjects.Semantic proximity Read ↗

[A study of polymorphism in UDP-glucuronosyltransferase 1 (UGT-1A1) promoter gene in Korean patients with Gilbert's syndrome].Semantic proximity Read ↗

Correlation of mutational analysis to clinical features in Taiwanese patients with Gilbert's syndrome.Semantic proximity Read ↗

[Gilbert's syndrome: a clinicogenetic trial].Semantic proximity Read ↗

Differences in UGT1A1 gene mutations and pathological liver changes between Chinese patients with Gilbert syndrome and Crigler-Najjar syndrome type II.Semantic proximity Read ↗

[Gilbert disease and type I and II Crigler-Najjar syndrome due to mutations in the same UGT1A1 gene locus].Semantic proximity Read ↗

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