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 rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among Caucasians

17 Nov 2009

Abstract excerpt

BACKGROUND: In an earlier study, we identified a locus for Moyamoya disease (MMD) on 17q25.3. METHODS: Linkage analysis and fine mapping were conducted for two new families in additional to the previously studied 15 families. Three genes, CARD14, Raptor, and AATK, were selected based on key words, namely, "inflammation", "apoptosis", "proliferation", and "vascular system", for further sequencing. A segregation...

Read the complete abstract on PubMed

Topics

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

Share to Connective tissue disorders research
Share to Moyamoya disease diagnosis and treatment
Share to Neuroinflammation and Neurodegeneration Mechanisms

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Source

Identifiers

PMID: 19921495
DOI: 10.1007/s12199-009-0116-7

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

A rare Asian founder polymorphism of Raptor may explain the high prevalence of Moyamoya disease among East Asians and its low prevalence among CaucasiansPMID 19921495Read ↗

Genome-wide association study identifies novel susceptibilities to adult moyamoya disease.Semantic proximity Read ↗

Novel Susceptibility Loci for Moyamoya Disease Revealed by a Genome-Wide Association Study.Semantic proximity Read ↗

Common genetic polymorphisms in moyamoya and atherosclerotic disease in Europeans.Semantic proximity Read ↗

An Overview of Genetics of Moyamoya: Beyond RNF213 Gene.Semantic proximity Read ↗

Integrative GWAS and snRNA-seq Reveal a Mesenchymal-Like Endothelial Signature in Moyamoya Disease.Semantic proximity Read ↗

Identification of the potential role of S1PR1 in adult moyamoya disease based on multiple bioinformatics analysis and experimental verificationSemantic proximity Read ↗

The Association of the RNF213 p.R4810K Polymorphism with Quasi-Moyamoya Disease and a Review of the Pertinent Literature.Semantic proximity Read ↗

Association of Genetic Variants With Moyamoya Disease in 13 000 Individuals: A Meta-Analysis.Semantic proximity Read ↗

Genetics of Moyamoya disease.Semantic proximity Read ↗

Rare variants of RNF213 and moyamoya/non-moyamoya intracranial artery stenosis/occlusion disease risk: a meta-analysis and systematic review.Semantic proximity Read ↗

Validation and Extension Study Exploring the Role of RNF213 p.R4810K in 2,877 Chinese Moyamoya Disease Patients.Semantic proximity Read ↗

Distribution of moyamoya disease susceptibility polymorphism p.R4810K in RNF213 in East and Southeast Asian populations.Semantic proximity Read ↗

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