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Mouse phenogenomics, toolbox for functional annotation of human genome

DC Field Value Language
dc.contributor.authorKim, Il Yong-
dc.contributor.authorShin, Jae Hoon-
dc.contributor.authorSeong, Je Kyung-
dc.date.accessioned2024-08-08T01:47:34Z-
dc.date.available2024-08-08T01:47:34Z-
dc.date.created2018-01-19-
dc.date.created2018-01-19-
dc.date.issued2010-02-
dc.identifier.citationBMB Reports, Vol.43 No.2, pp.79-90-
dc.identifier.issn1976-6696-
dc.identifier.urihttps://hdl.handle.net/10371/208174-
dc.description.abstractMouse models are crucial for the functional annotation of human genome. Gene modification techniques including gene targeting and gene trap in mouse have provided powerful tools in the form of genetically engineered mice (GEM) for understanding the molecular pathogenesis of human diseases. Several international consortium and programs are under way to deliver mutations in every gene in mouse genome. The information from studying these GEM can be shared through international collaboration. However, there are many limitations in utility because not all human genes are knocked out in mouse and they are not yet phenotypically characterized by standardized ways which is required for sharing and evaluating data from GEM. The recent improvement in mouse genetics has now moved the bottleneck in mouse functional genomics from the production of GEM to the systematic mouse phenotype analysis of GEM. Enhanced, reproducible and comprehensive mouse phenotype analysis has thus emerged as a prerequisite for effectively engaging the phenotyping bottleneck. In this review, cur-rent information on systematic mouse phenotype analysis and an issue-oriented perspective will be provided. [BMB reports 2010; 43(2): 79-90]-
dc.language영어-
dc.publisher생화학분자생물학회-
dc.titleMouse phenogenomics, toolbox for functional annotation of human genome-
dc.typeArticle-
dc.identifier.doi10.5483/BMBRep.2010.43.2.079-
dc.citation.journaltitleBMB Reports-
dc.identifier.wosid000275103000002-
dc.identifier.scopusid2-s2.0-77952473733-
dc.citation.endpage90-
dc.citation.number2-
dc.citation.startpage79-
dc.citation.volume43-
dc.identifier.kciidART001421459-
dc.description.isOpenAccessY-
dc.contributor.affiliatedAuthorSeong, Je Kyung-
dc.type.docTypeReview-
dc.description.journalClass1-
dc.subject.keywordPlusRIKEN BIORESOURCE CENTER-
dc.subject.keywordPlusMUTAGENESIS PROGRAM-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusTRANSGENIC MICE-
dc.subject.keywordPlusHUMAN-DISEASE-
dc.subject.keywordPlusPHENOTYPING RESOURCE-
dc.subject.keywordPlusLABORATORY MOUSE-
dc.subject.keywordPlusDRUG DEVELOPMENT-
dc.subject.keywordPlusMODELS-
dc.subject.keywordPlusSTRAINS-
dc.subject.keywordAuthorFunctional genomics-
dc.subject.keywordAuthorGenetically engineered mouse-
dc.subject.keywordAuthorPhenogenomics-
dc.subject.keywordAuthorPhenotype analysis-
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  • College of Veterinary Medicine
  • Department of Veterinary Medicine
Research Area Metabolic syndrome model construction and omics research, Mouse locomotion and metabolic phenotyping analysis, Study of immune regulatory response in obesity, 대사증후군 모델 구축 및 오믹스 연구, 마우스 운동 및 대사 표현형 분석, 비만에서의 면역 조절 반응 연구

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