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dc.contributor.author Lee, Kyoungmin -
dc.contributor.author Kim, Taehyeong -
dc.contributor.author Cheon, M. -
dc.contributor.author Yu, Wookyung -
dc.date.accessioned 2022-10-26T08:30:00Z -
dc.date.available 2022-10-26T08:30:00Z -
dc.date.created 2022-06-16 -
dc.date.issued 2022-04 -
dc.identifier.issn 2045-2322 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/16937 -
dc.description.abstract Repeated cocaine use poses many serious health risks to users. One of the risks is hypoxia and ischemia (HI). To restore the biological system against HI, complex biological mechanisms operate at the gene level. Despite the complexity of biological mechanisms, there are common denominator genes that play pivotal roles in various defense systems. Among these genes, the cAMP response element-binding (Creb) protein contributes not only to various aspects of drug-seeking behavior and drug reward, but also to protective mechanisms. However, it is still unclear which Creb members are key players in the protection of cocaine-induced HI conditions. Herein, using one of the state-of-the-art deep learning methods, the generative adversarial network, we revealed that the OASIS family, one of the Creb family, is a key player in various defense mechanisms such as angiogenesis and unfolded protein response against the HI state by unveiling hidden mRNA expression profiles. Furthermore, we identified mysterious kinases in the OASIS family and are able to explain why the prefrontal cortex and hippocampus are vulnerable to HI at the genetic level. © 2022, The Author(s). -
dc.language English -
dc.publisher Nature Publishing Group -
dc.title Unveiling OASIS family as a key player in hypoxia–ischemia cases induced by cocaine using generative adversarial networks -
dc.type Article -
dc.identifier.doi 10.1038/s41598-022-10772-1 -
dc.identifier.scopusid 2-s2.0-85128864306 -
dc.identifier.bibliographicCitation Scientific Reports, v.12, no.1 -
dc.description.isOpenAccess TRUE -
dc.subject.keywordPlus ENDOPLASMIC-RETICULUM STRESS -
dc.subject.keywordPlus UNFOLDED PROTEIN RESPONSE -
dc.subject.keywordPlus MESSENGER-RNA -
dc.subject.keywordPlus TRANSCRIPTION FACTOR -
dc.subject.keywordPlus MYOCARDIAL-ISCHEMIA -
dc.subject.keywordPlus INDUCIBLE FACTOR -
dc.subject.keywordPlus ER STRESS -
dc.subject.keywordPlus KINASE -
dc.subject.keywordPlus BRAIN -
dc.subject.keywordPlus EXPRESSION -
dc.citation.number 1 -
dc.citation.title Scientific Reports -
dc.citation.volume 12 -
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Department of Brain Sciences Laboratory of Protein Biophysics 1. Journal Articles

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