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

Absence of alpha-1 antitrypsin deficiency alleles (S and Z) in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage.

Stroke - 1 Dec 2004

Yoneyama Taku, Kasuya Hidetoshi, Akagawa Hiroyuki, Onda Hideaki, Nakajima Toshiaki, Hori Tomokatsu, Inoue Ituro, Lee Jung-Chung, Yang Tae-Ki, Kim Chul-Jin

Abstract excerpt

BACKGROUND AND PURPOSE: A possible association has been proposed for the formation of intracranial aneurysm (IA) and deficiency alleles (S and Z) of the alpha1-antitrypsin (AAT) gene. We extensively screened this gene in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage. METHODS: Seven allelic variants, including S and Z alleles, were genotyped by direct sequencing of genomic DNA obtained from...

Read the complete abstract on PubMed

Topics

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

Share to alpha 1-Antitrypsin
Share to Asian People

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Haplotypes

Share to Polymorphism, Single Nucleotide

Share to Subarachnoid Hemorrhage

Source

Identifiers

PMID: 15528457
DOI: 10.1161/01.STR.0000147966.81215.be

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 5 Sept 2026. Manifest publication-graph-cohort-2026-09-05.1.

Source receipt: pubmed, retrieved 5 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Absence of alpha-1 antitrypsin deficiency alleles (S and Z) in Japanese and Korean patients with aneurysmal subarachnoid hemorrhage.PMID 15528457Read ↗

Common variants of the ACE gene and aneurysmal subarachnoid hemorrhage in a Danish population: a case-control study.Semantic proximity Read ↗

The alanine/threonine polymorphism of the alpha-1-antichymotrypsin (SERPINA3) gene and ruptured intracranial aneurysms in the Japanese population.Semantic proximity Read ↗

Polymorphism and plasma levels of apolipoprotein E and the risk of aneurysmal subarachnoid hemorrhage in a Chinese population: a case-control study.Semantic proximity Read ↗

Investigating the Link between Alpha-1 Antitrypsin Deficiency and Abdominal Aortic Aneurysms.Semantic proximity Read ↗

Endothelial nitric oxide gene T-786C polymorphism and subarachnoid hemorrhage in Korean population.Semantic proximity Read ↗

Association of genetic variants with hemorrhagic stroke in Japanese individuals.Semantic proximity Read ↗

Association of renin-angiotensin system genetic polymorphisms and aneurysmal subarachnoid hemorrhage.Semantic proximity Read ↗

Using endothelial nitric oxide synthase gene polymorphisms to identify intracranial aneurysms more prone to rupture in Japanese patients.Semantic proximity Read ↗

Association of SOX17 Gene Polymorphisms and Intracranial Aneurysm: A Case-Control Study and Meta-Analysis.Semantic proximity Read ↗

The relationships between endothelial nitric oxide synthase polymorphisms and the formation of intracranial aneurysms in the Korean population.Semantic proximity Read ↗

Lysyl oxidase family genes polymorphisms and risk of aneurysmal subarachnoid hemorrhage: A case control studySemantic proximity Read ↗

Lack of an association between the angiotensin-converting enzyme insertion/deletion polymorphism and intracranial aneurysms in a Caucasian population in the United States.Semantic proximity Read ↗

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