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dc.citation.endPage 1192 -
dc.citation.number 11 -
dc.citation.startPage 1183 -
dc.citation.title GENES & GENOMICS -
dc.citation.volume 39 -
dc.contributor.author Kim, Dong Hee -
dc.contributor.author Gim, Jeong-An -
dc.contributor.author Kim, Kwang Hee -
dc.contributor.author Han, Chang Woo -
dc.contributor.author Jang, Se Bok -
dc.contributor.author Kim, Heui-Soo -
dc.date.accessioned 2023-12-21T21:38:17Z -
dc.date.available 2023-12-21T21:38:17Z -
dc.date.created 2017-11-15 -
dc.date.issued 2017-11 -
dc.description.abstract During primate evolution, the neuronal and cognition-related genes have evolved rapidly. These genes seem to induce neurological illnesses such as Alzheimer's disease (AD). In this study, we analyzed genes APOE, TOMM40, and PICALM known as the risk factors of AD. We performed bioinformatics analyses in relation to evolution, phylogeny, and protein structure for those genes in humans, Neanderthals, chimpanzees, bonobos, gorillas, orangutans, crab-eating monkeys, and rhesus monkeys. Cholesterol-related genes showed relatively rapid evolution toward a lower risk of AD. Neanderthals showed relatively higher polymorphism in genes APOE, TOMM40, and PICALM than humans did. Phylogeny indicated different topologies in the trichotomy of humans, chimpanzees, and gorillas in terms of genes APOE, TOMM40, and PICALM. These results provide to hominin-specific patterns in three genes, and give clues to the modern human-specific traits of AD and shed light on further functional research helping to understand AD. -
dc.identifier.bibliographicCitation GENES & GENOMICS, v.39, no.11, pp.1183 - 1192 -
dc.identifier.doi 10.1007/s13258-017-0584-x -
dc.identifier.issn 1976-9571 -
dc.identifier.scopusid 2-s2.0-85021188768 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/22930 -
dc.identifier.url https://link.springer.com/article/10.1007%2Fs13258-017-0584-x -
dc.identifier.wosid 000413259200002 -
dc.language 영어 -
dc.publisher SPRINGER -
dc.title Alzheimer's disease related genes during primate evolution -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Biochemistry & Molecular Biology; Biotechnology & Applied Microbiology; Genetics & Heredity -
dc.identifier.kciid ART002283841 -
dc.relation.journalResearchArea Biochemistry & Molecular Biology; Biotechnology & Applied Microbiology; Genetics & Heredity -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.description.journalRegisteredClass kci -
dc.subject.keywordAuthor Alzheimer&apos -
dc.subject.keywordAuthor s disease -
dc.subject.keywordAuthor Evolution -
dc.subject.keywordAuthor Hominoid -
dc.subject.keywordAuthor Phylogeny -
dc.subject.keywordAuthor Transposable element -
dc.subject.keywordPlus GENOME-WIDE ASSOCIATION -
dc.subject.keywordPlus ENHANCER-BLOCKING ACTIVITY -
dc.subject.keywordPlus EMBRYONIC STEM-CELLS -
dc.subject.keywordPlus TRANSPOSABLE ELEMENTS -
dc.subject.keywordPlus APOLIPOPROTEIN-E -
dc.subject.keywordPlus CHROMATIN INSULATORS -
dc.subject.keywordPlus TOPOLOGICAL DOMAINS -
dc.subject.keywordPlus SUSCEPTIBILITY LOCI -
dc.subject.keywordPlus CRYSTAL-STRUCTURE -
dc.subject.keywordPlus NERVOUS-SYSTEM -

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