DC Field | Value | Language |
---|---|---|
dc.contributor.author | Sunhong Kim | - |
dc.contributor.author | Y M Kim | - |
dc.contributor.author | Young Shin Kwak | - |
dc.date.accessioned | 2017-04-19T09:33:56Z | - |
dc.date.available | 2017-04-19T09:33:56Z | - |
dc.date.issued | 2012 | - |
dc.identifier.issn | 0253-6269 | - |
dc.identifier.uri | 10.1007/s12272-012-0900-6 | ko |
dc.identifier.uri | https://oak.kribb.re.kr/handle/201005/10954 | - |
dc.description.abstract | With growing interest in human microbiome for its implication in metabolic disorders, inflammatory diseases, immune disorders and so forth, understanding the biology at the interface of the gut flora and the host becomes very important for identifying novel therapeutic avenues. GPR43 has been deorphanized and the metabolites of microbiome, such as short-chain fatty acids, serve as its natural ligands. There are numerous reports that GPR43 might be a crucial link to the novel therapies for the unmet medical needs and many drug discovery organizations are making their moves in response. | - |
dc.publisher | Pharmaceutical Soc Korea | - |
dc.title | A novel therapeutic target, GPR43: where it stands in drug discovery = 신약 타겟 GPR43 | - |
dc.title.alternative | A novel therapeutic target, GPR43: where it stands in drug discovery | - |
dc.type | Article | - |
dc.citation.title | Archives of Pharmacal Research | - |
dc.citation.number | 9 | - |
dc.citation.endPage | 1509 | - |
dc.citation.startPage | 1505 | - |
dc.citation.volume | 35 | - |
dc.contributor.affiliatedAuthor | Sunhong Kim | - |
dc.contributor.affiliatedAuthor | Young Shin Kwak | - |
dc.contributor.alternativeName | 김선홍 | - |
dc.contributor.alternativeName | 김유미 | - |
dc.contributor.alternativeName | 곽영신 | - |
dc.identifier.bibliographicCitation | Archives of Pharmacal Research, vol. 35, no. 9, pp. 1505-1509 | - |
dc.identifier.doi | 10.1007/s12272-012-0900-6 | - |
dc.description.journalClass | Y | - |
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