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

Subfraction analysis of circulating lipoproteins in a patient with Tangier disease due to a novel ABCA1 mutation.

Clinica chimica acta; international journal of clinical chemistry - 15 Jan 2016

Murano Takeyoshi, Yamaguchi Takashi, Tatsuno Ichiro, Suzuki Masayo, Noike Hirofumi, Takanami Tarou, Yoshida Tomoe, Suzuki Mitsuya, Hashimoto Ryuya, Maeno Takatoshi, Terai Kensuke, Tokuyama Wataru, Hiruta Nobuyuki, Schneider Wolfgang J, Bujo Hideaki

Abstract excerpt

Tangier disease, characterized by low or absent high-density lipoprotein (HDL), is a rare hereditary lipid storage disorder associated with frequent, but not obligatory, severe premature atherosclerosis due to disturbed reverse cholesterol transport from tissues. The reasons for the heterogeneity in atherogenicity in certain dyslipidemias have not been fully elucidated. Here, using high-performance liquid...

Read the complete abstract on PubMed

Topics

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

Share to Adolescent
Share to ATP Binding Cassette Transporter 1

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Chromatography, Gel

Share to Chromatography, High Pressure Liquid

Share to ABCA1 gene

Share to Lipoproteins

Share to Mutation

Share to Tangier Disease

Source

Identifiers

PMID: 26616730
DOI: 10.1016/j.cca.2015.11.021

Genes

ABCA1

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

Subfraction analysis of circulating lipoproteins in a patient with Tangier disease due to a novel ABCA1 mutation.PMID 26616730Read ↗

Tangier disease four decades of research: a reflection of the importance of HDL.Semantic proximity Read ↗

Cellular cholesterol efflux in heterozygotes for Tangier disease is markedly reduced and correlates with high density lipoprotein cholesterol concentration and particle sizeSemantic proximity Read ↗

A novel splicing mutation in the ABCA1 gene, causing Tangier disease and familial HDL deficiency in a large familySemantic proximity Read ↗

Novel mutations of ABCA1 transporter in patients with Tangier disease and familial HDL deficiency.Semantic proximity Read ↗

Tangier disease: epidemiology, pathophysiology, and management.Semantic proximity Read ↗

Tangier disease: still more questions than answers.Semantic proximity Read ↗

A novel ABCA1 variant associated with impaired platelet production contributing to thrombocytopenia in a family with Tangier disease.Semantic proximity Read ↗

Tangier disease and ABCA1.Semantic proximity Read ↗

High density lipoprotein deficiency and foam cell accumulation in mice with targeted disruption of ATP-binding cassette transporter-1.Semantic proximity Read ↗

The gene encoding ATP-binding cassette transporter 1 is mutated in Tangier disease.Semantic proximity Read ↗

Familial HDL deficiency due to ABCA1 gene mutations with or without other genetic lipoprotein disorders.Semantic proximity Read ↗

Transport of lipids from golgi to plasma membrane is defective in tangier disease patients and Abc1-deficient mice.Semantic proximity Read ↗

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