Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia.

doi:10.1016/j.metabol.2008.07.031

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

Community

Back to search

Article

Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia.

Metabolism: clinical and experimental - 1 Dec 2008

Engler Mary B, Pullinger Clive R, Malloy Mary J, Natanzon Yanina, Kulkarni Medha V, Song James, Eng Celeste, Huuskonen Jaarko, Rivera Christopher, Poon Annie, Bensley Matt, Sehnert Amy, Zellner Christian, Kane John, Aouizerat Bradley E

Abstract excerpt

We previously demonstrated the role of a phospholipid transfer protein (PLTP) gene variation (rs2294213) in determining levels of high-density lipoprotein cholesterol (HDL-C) in hypoalphalipoproteinemia (HypoA). We have now explored the role of PLTP in hyperalphalipoproteinemia (HyperA). The huma...

Read the complete abstract on PubMed

Topics

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

Share to Chlorocebus aethiops

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to COS Cells

Share to Genetic Linkage

Share to Hyperlipoproteinemias

Share to Lipoproteins

Share to Lipoproteins, HDL

Share to Phospholipid Transfer Proteins

Share to Transfection

Source

Open in PubMed Open full text

Identifiers

PMID: 19013296
DOI: 10.1016/j.metabol.2008.07.031
PMCID: PMC2615231

Genes

PLTP

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 2 Sept 2026. Prepared record publication-19013296-2026-09-02.2. Manifest publication-graph-cohort-2026-09-02.2.

Source receipt: PubMed via Helena Literature Corpus, retrieved 2 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Genetic variation in phospholipid transfer protein modulates lipoprotein profiles in hyperalphalipoproteinemia.PMID 19013296Read ↗

Genetic variation of PLTP modulates lipoprotein profiles in hypoalphalipoproteinemia.Semantic proximity Read ↗

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

Genetic and nongenetic sources of variation in phospholipid transfer protein activity.Semantic proximity Read ↗

Resequencing CETP, LIPC and LIPG genes in Thai subjects with hyperalphalipoproteinemia.Semantic proximity Read ↗

Association between the PLTP rs4810479 SNP and Serum Lipid Traits in the Chinese Maonan and Han Populations.Semantic proximity Read ↗

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

Functional characterization of novel variants in the CETP promoter and the LIPC gene in subjects with hyperalphalipoproteinemia.Semantic proximity Read ↗

Structure-function analyses of microsomal triglyceride transfer protein missense mutations in abetalipoproteinemia and hypobetalipoproteinemia subjects.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 ↗

Genetic variation at the phospholipid transfer protein locus affects its activity and high-density lipoprotein size and is a novel marker of cardiovascular disease susceptibility.Semantic proximity Read ↗

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

Serum phospholipid transfer protein activity and genetic variation of the PLTP gene.Semantic proximity Read ↗

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