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dc.contributor.author 김경민 -
dc.contributor.author 정창근 -
dc.contributor.author 권민지 -
dc.contributor.author 박정향 -
dc.contributor.author 차인준 -
dc.contributor.author 조재호 -
dc.contributor.author 한명훈 -
dc.contributor.author 박성순 -
dc.contributor.author 김은선 -
dc.contributor.author 고병수 -
dc.contributor.author 이다빈 -
dc.contributor.author 정연진 -
dc.contributor.author Lee, Sung-Bae -
dc.date.accessioned 2021-08-26T05:53:49Z -
dc.date.available 2021-08-26T05:53:49Z -
dc.date.created 2019-07-01 -
dc.date.issued 2019-06-24 -
dc.identifier.uri http://hdl.handle.net/20.500.11750/14411 -
dc.description.abstract For screening drugs or molecules that can modify disease pathophysiology of human disease or conduct drug screening, the use of appropriate in vivo model with low expenditure suitable for large-scale screening is essential. Drosophila Melanogaster, whose genome contain orthologs for 75% of human disease-related genes, offers a quantitative screening platform for assessing both cellular and behavioral defects that are thought to be representative of human diseases like Parkinson’s
disease(PD), Huntington’s disease(HD) or amyotrophic lateral sclerosis(ALS). Here, we present the low cost screening analysis platform available for measuring cellular and behavioral defects in Drosophila. This platform can be adapted for the use of therapeutic target discovery process as an economic and powerful in vivo screening tool for the researchers.
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dc.language English -
dc.publisher 한국분자세포생물학회 초파리분과 -
dc.title Screening platform for assessing cellular and behavioral defects in Drosophila Melanogaster -
dc.type Conference Paper -
dc.identifier.bibliographicCitation 제49회 한국분자세포생물학회 초파리분과 정기 학술대회 -
dc.citation.conferencePlace KO -
dc.citation.conferencePlace 부산 동아대 -
dc.citation.title 제49회 한국분자세포생물학회 초파리분과 정기 학술대회 -
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Department of Brain Sciences Laboratory of Neurodegenerative Diseases and Aging 2. Conference Papers

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