https://transhumanist.ru/index.php?action=history&feed=atom&title=EXOC3L2 2026-04-09T12:58:54Z История изменений этой страницы в вики MediaWiki 1.43.6 https://transhumanist.ru/index.php?title=EXOC3L2&diff=4723&oldid=prev 2021-04-29T19:31:56Z

<p>Новая страница: «complex component 3-like protein 2 (HBV X-transactivated gene 7 protein) (HBV XAg-transactivated protein 7) [XTP7] ==Publications== {{medline-entry |title=Gene-...»</p> <p><b>Новая страница</b></p><div>complex component 3-like protein 2 (HBV X-transactivated gene 7 protein) (HBV XAg-transactivated protein 7) [XTP7]<br /> <br /> ==Publications==<br /> <br /> {{medline-entry<br /> |title=Gene-based aggregate SNP associations between candidate AD genes and cognitive decline.<br /> |pubmed-url=https://pubmed.ncbi.nlm.nih.gov/27005436<br /> |abstract=Single nucleotide polymorphisms (SNPs) in and near [[ABCA7]], [[BIN1]], [[CASS4]], [[CD2AP]], [[CD33]], [[CELF1]], [[CLU]], complement receptor 1 ([[CR1]]), [[EPHA1]], [[EXOC3L2]], [[FERMT2]], HLA cluster (DRB5-DQA), [[INPP5D]], [[MEF2C]], MS4A cluster (MS4A3-[[MS4A6E]]), [[NME8]], [[PICALM]], [[PTK2B]], [[SLC24A4]], [[SORL1]], and [[ZCWPW1]] have been associated with Alzheimer&#039;s disease (AD) in large meta-analyses. We aimed to determine whether established AD-associated genes are associated with longitudinal cognitive decline by examining aggregate variation across these gene regions. In two single-sex cohorts of older, community-dwelling adults, we examined the association between SNPs in previously implicated gene regions and cognitive decline (age-adjusted person-specific cognitive slopes) using a Sequence Kernel Association Test (SKAT). In regions which showed aggregate significance, we examined the univariate association between individual SNPs in the region and cognitive decline. Only two of the original AD-associated SNPs were significantly associated with cognitive decline in our cohorts. We identified significant aggregate-level associations between cognitive decline and the gene regions [[BIN1]], [[CD33]], [[CELF1]], [[CR1]], HLA cluster, and [[MEF2C]] in the all-female cohort and significant associations with [[ABCA7]], HLA cluster, [[MS4A6E]], [[PICALM]], [[PTK2B]], [[SLC24A4]], and [[SORL1]] in the all-male cohort. We also identified a block of eight correlated SNPs in [[CD33]] and several blocks of correlated SNPs in [[CELF1]] that were significantly associated with cognitive decline in univariate analysis in the all-female cohort. <br /> |mesh-terms=* Aged<br /> * Aging<br /> * Alzheimer Disease<br /> * Cognition Disorders<br /> * DNA<br /> * Female<br /> * Genetic Association Studies<br /> * Genetic Predisposition to Disease<br /> * Humans<br /> * Male<br /> * Polymorphism, Single Nucleotide<br /> |keywords=* Candidate AD genes<br /> * Cognitive decline<br /> * SNP associations<br /> |full-text-url=https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5005889<br /> }}</div>

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