نتایج جستجو برای: apoe polymorphisms

تعداد نتایج: 75213  

Journal: :Journal of medical genetics 2004
C Aucan A J Walley A V S Hill

A polipoprotein E (apoE) is a protein involved in the transport and metabolism of plasma cholesterol and triglycerides. The apolipoprotein E gene (APOE), located at chromosome 19q13.2, has three major alleles called e2, e3, and e4, defined by two single nucleotide polymorphisms (SNP) located in exon 4 at positions 3937 (T/C) and 4075 (C/T). The corresponding apoE isoforms differ at amino acid p...

2015
Ping Wu Hong-Lei Li Zhi-Jun Liu Qing-Qing Tao Miao Xu Qi-Hao Guo Zhen Hong Yi-Min Sun

OBJECTIVE Apolipoprotein E gene (APOE) polymorphisms contributing to the risk of sporadic Alzheimer's disease (AD) have been identified for decades, but it has not been investigated in large AD samples of Chinese Han population. METHODS We performed a cross-sectional study to explore the effect of APOE polymorphisms on sporadic AD in 875 sporadic AD patients and 1,195 cognitive normal control...

Journal: :Neurobiology of aging 2013
Qiu-Yan Liu Jin-Tai Yu Dan Miao Xiao-Ying Ma Hui-Fu Wang Wei Wang Lan Tan

Both Alzheimer's disease (AD) and progressive supranuclear palsy (PSP) are a class of neurodegenerative diseases associated with the pathologic aggregation of tau protein in the human brain. They share some clinical and pathologic characteristics. A recent genome-wide association study reported several single-nucleotide polymorphisms at the STX6, MOBP, MAPT, and EIF2AK3 in association with PSP....

Journal: :Turkish journal of medical sciences 2015
Gülhan Kaya Esra Gündüz Muradiye Acar Ömer Faruk Hatipoğlu Burcu Acar Atilla Ilhan Mehmet Gündüz

BACKGROUND/AIM Alzheimer disease (AD) is triggered by interactions of multiple genetic and environmental factors. The APOE gene E4 allele is the best-known risk factor for AD, yet it represents a small ratio of genetic factors. According to genome-wide association studies, the BIN1 gene is the second important risk factor for AD, following the APOE gene. We aimed to identify a novel biomarker i...

Journal: :Journal of medical genetics 2003
M A Wozniak E B Faragher J A Todd K A Koram E M Riley R F Itzhaki

Outcome of infection varies greatly among people, and in the case of three very different viruses, it is determined by apolipoprotein E (APOE) genotype. APOE might affect outcome of malaria infection also, since apoE protein and the protozoon (like the viruses) share cell entry mediators (heparan sulphate proteoglycans and/or specific apoE receptors). APOE polymorphisms give rise to protein var...

Journal: :Current opinion in critical care 2005
Ryan J Waters James A R Nicoll

PURPOSE OF REVIEW To examine the evidence for a genetic influence on clinical outcome after a variety of acute neurologic events. RECENT FINDINGS Clinical outcome after brain injury is variable and cannot easily be predicted. It has been proposed that genetic polymorphisms may have an important role in determining outcome from a number of conditions, including acute neurologic events. Apolipo...

2012
Mostafa Saadat

PURPOSE APOLIPOPROTEIN E (APOE, MIM: 107741) has three functionally distinct isoforms of the protein (E2, E3, and E4), encoded by corresponding alleles ε2, ε3, and ε4, which have been well described. Findings from previous studies investigating association between APOE polymorphisms and breast cancer risk have been inconsistent. The present meta-analysis was conducted in order to investigate as...

Journal: :Molecular Vision 2009
Li-Yun Jia Pancy Oi-Sin Tam Sylvia Wai-Yee Chiang Ning Ding Li Jia Chen Gary Hin-Fai Yam Chi-Pui Pang Ning-Li Wang

PURPOSE To evaluate the individual and interactive effects of polymorphisms in the myocilin (MYOC),optineurin (OPTN), WD repeat domain 36 (WDR36), and apolipoprotein E (APOE) genes on primary open-angle glaucoma (POAG) in northern Chinese. METHODS Northern Chinese study subjects, 176 POAG patients and 200 controls, were recruited for screening of the coding exons and splicing regions of MYOC....

2013
Dimitrios Chiras Konstantina Tzika Haris Kokotas Samantha C. Oliveira Maria Grigoriadou Anastasia Kastania Kleanthi Dima Maria Stefaniotou Miltiadis Aspiotis Michael B. Petersen Christos Kroupis George Kitsos

PURPOSE In the Greek population of Epirus, exfoliation syndrome (XFS) and exfoliation glaucoma (XFG) occur at a high prevalence. In this study, we validate a novel lysyl oxidase-like 1 (LOXL1) genotyping method, investigate the previously reported association of LOXL1 with XFS/XFG, and evaluate apolipoprotein E (APOE) and methylenetetrahydrofolate reductase (MTHFR) polymorphisms as genetic risk...

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