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Proteomic analysis of cloned porcine conceptuses during the implantation period

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dc.contributor.authorKo, Yeoung-Gyu-
dc.contributor.authorPark, Hae-Geum-
dc.contributor.authorYeom, Gyu-Tae-
dc.contributor.authorHwang, Seongsoo-
dc.contributor.authorKim, Hyun-
dc.contributor.authorPark, Soo-Bong-
dc.contributor.authorYang, Bo-Suck-
dc.contributor.authorSong, Young Min-
dc.contributor.authorCho, Jae-Hyeon-
dc.date.accessioned2022-12-27T00:17:43Z-
dc.date.available2022-12-27T00:17:43Z-
dc.date.issued2013-12-
dc.identifier.issn0141-5492-
dc.identifier.issn1573-6776-
dc.identifier.urihttps://scholarworks.gnu.ac.kr/handle/sw.gnu/20318-
dc.description.abstractDifferentially regulated proteins within porcine somatic cell nuclear transfer (SCNT)-derived conceptuses were compared with conceptuses that were derived from natural matings on day 14 of pregnancy. Proteins that were expressed prominently on day 14 were identified in SCNT-derived conceptuses using 2-D PAGE and MALDI-TOF MS. Sixty eight proteins were identified as being differentially regulated in the SCNT-derived conceptuses. Among these, 62 were down-regulated whereas the other six proteins were up-regulated. Glycolytic proteins, such as pyruvate dehydrogenase, malate dehydrogenase and lactate dehydrogenase, were down-regulated in the SCNT-derived conceptuses whereas apoptosis-related genes as annexin V, Hsp60, and lamin A were up-regulated. Thus, apoptosis-related genes are expressed at significantly higher levels in the SCNT-derived conceptuses than in the control conceptuses, whereas metabolism-related genes are significantly reduced.-
dc.format.extent10-
dc.language영어-
dc.language.isoENG-
dc.publisherSPRINGER-
dc.titleProteomic analysis of cloned porcine conceptuses during the implantation period-
dc.typeArticle-
dc.publisher.location네델란드-
dc.identifier.doi10.1007/s10529-013-1315-2-
dc.identifier.scopusid2-s2.0-84887322080-
dc.identifier.wosid000326631100008-
dc.identifier.bibliographicCitationBIOTECHNOLOGY LETTERS, v.35, no.12, pp 2021 - 2030-
dc.citation.titleBIOTECHNOLOGY LETTERS-
dc.citation.volume35-
dc.citation.number12-
dc.citation.startPage2021-
dc.citation.endPage2030-
dc.type.docTypeArticle-
dc.description.isOpenAccessN-
dc.description.journalRegisteredClasssci-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiotechnology & Applied Microbiology-
dc.relation.journalWebOfScienceCategoryBiotechnology & Applied Microbiology-
dc.subject.keywordPlusEXTRAEMBRYONIC TISSUE-
dc.subject.keywordPlusGENE-EXPRESSION-
dc.subject.keywordPlusUP-REGULATION-
dc.subject.keywordPlusIN-VIVO-
dc.subject.keywordPlusCLONING-
dc.subject.keywordPlusAPOPTOSIS-
dc.subject.keywordPlusMODELS-
dc.subject.keywordPlusDEATH-
dc.subject.keywordPlusMICE-
dc.subject.keywordAuthorApoptosis-related genes-
dc.subject.keywordAuthorBirthrate in GM pigs-
dc.subject.keywordAuthorConceptuses-
dc.subject.keywordAuthorEmbryo implantation-
dc.subject.keywordAuthorGestation day 14-
dc.subject.keywordAuthorGM-pigs-
dc.subject.keywordAuthorProteomic analysis in GM-piglet cells-
dc.subject.keywordAuthorSomatic cell nuclear transfer-
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