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

A novel missense mutation (L296 Q) in cholesteryl ester transfer protein gene related to coronary heart disease.

Acta biochimica et biophysica Sinica - 1 Jan 2004

Zheng Ke-Qin, Zhang Si-Zong, Zhang Li, Huang De-Jia, Liao Lin-Chuan, Hou Yi-Ping

Abstract excerpt

Cholesteryl ester transfer protein (CETP) is a key participant in the reverse transport of cholesterol from the peripheral tissues to the liver. To understand further the role that CETP gene plays in the pathogenesis of coronary heart disease (CHD), the promoter region, all 16 exons and adjacent intronic regions of CETP gene were screened for single nucleotide polymorphisms (SNPs) in 203 CHD patients and 209...

Read the complete abstract on PubMed

Topics

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

Share to Carrier Proteins
Share to Cholesterol

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Cholesterol Ester Transfer Proteins

Share to Cholesterol, LDL

Share to Coronary Disease

Share to Glycoproteins

Share to Mutation, Missense

Share to Sequence Analysis, Protein

Source

Identifiers

PMID: 14732872
DOI: 10.1093/abbs/36.1.33

Genes

CETP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 6 Sept 2026. Manifest publication-graph-cohort-2026-09-06.1.

Source receipt: pubmed, retrieved 6 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A novel missense mutation (L296 Q) in cholesteryl ester transfer protein gene related to coronary heart disease.PMID 14732872Read ↗

Carriers of three polymorphisms of cholesteryl ester transfer protein gene are at increased risk to coronary heart disease in a Chinese population.Semantic proximity Read ↗

A novel nonsense mutation (G181X) in the human cholesteryl ester transfer protein gene in Japanese hyperalphalipoproteinemic subjects.Semantic proximity Read ↗

Protein-Truncating Variants at the Cholesteryl Ester Transfer Protein Gene and Risk for Coronary Heart Disease.Semantic proximity Read ↗

[Study on the association of cholesteryl ester transfer protein gene mutations with the susceptibility to coronary atherosclerotic heart disease].Semantic proximity Read ↗

[Relationship between cholesteryl ester transfer protein gene -629C→A mutations with HDL-C levels and coronary heart disease].Semantic proximity Read ↗

A meta-analytic evaluation of cholesteryl ester transfer protein (CETP) C-629A polymorphism in association with coronary heart disease risk and lipid changes.Semantic proximity Read ↗

[Absence of association of the L296Q polymorphism in the cholesteryl ester transfer protein gene with type 2 diabetes mellitus in Chinese].Semantic proximity Read ↗

Two novel mutations and functional analyses of the CETP and LIPC genes underlying severe hyperalphalipoproteinemia.Semantic proximity Read ↗

A polymorphic site in the 3' untranslated region of the cholesteryl ester transfer protein (CETP) gene is associated with low CETP activity.Semantic proximity Read ↗

A novel mutation in the intron 1 splice donor site of the cholesterol ester transfer protein (CETP) gene as a cause of hyperalphalipoproteinemia.Semantic proximity Read ↗

Relationship between a novel polymorphism of lipoprotein lipase gene and coronary heart disease.Semantic proximity Read ↗

Novel mutations of CETP gene in Italian subjects with hyperalphalipoproteinemia.Semantic proximity Read ↗

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