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Cited 6 time in webofscience Cited 5 time in scopus
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dc.contributor.authorHAN, JK-
dc.date.accessioned2016-03-31T14:33:40Z-
dc.date.available2016-03-31T14:33:40Z-
dc.date.created2009-03-18-
dc.date.issued1995-01-17-
dc.identifier.issn0006-291X-
dc.identifier.other1995-OAK-0000009030-
dc.identifier.urihttps://oasis.postech.ac.kr/handle/2014.oak/21862-
dc.description.abstractEvidence suggests that a transient increase in intracellular calcium ([Ca2+](i)) is an important modulator during the cell division cycle in early embryos. We have recently shown that inhibition of Ins(1,4,5)P-3-induced Ca2+ release in the cleaving Xenopus embryos greatly lengthens the cell cycle duration. In this report, we have directly measured the changes of Ins(1,4,5)P-3 content during the first two cleavage cycles in the Xenopus embryos. HPLC profiles of cell extracts from dividing embryos show oscillations of inositol polyphosphates throughout the cleavage cycle with a transient production of Ins(1,4,5)P-3 by the time of cleavage furrow completion. In addition, cyclic changes in inositol phospholipids, phosphatidylinositol 4,5-bisphosphate (PIP2) and phosphatidylinositol 4-phosphate (PIP) were detected during the cleavage cycle. These data strongly suggest the involvement of PIP2 turnover and periodic increase in Ins(1,4,5)P-3 triggers [Ca2+](i) transients during the early embryonic cell cycle in the Xenopus. (C) 1995 Academic Press, Inc.-
dc.description.statementofresponsibilityX-
dc.languageEnglish-
dc.publisherACADEMIC PRESS INC JNL-COMP SUBSCRIPT-
dc.relation.isPartOfBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.subjectINTRACELLULAR FREE CALCIUM-
dc.subjectCELL-CYCLE-
dc.subjectLIPID HYDROLYSIS-
dc.subjectCA2+ WAVE-
dc.subjectPHOSPHATES-
dc.subjectMITOSIS-
dc.subjectEGG-
dc.titleOSCILLATION OF INOSITOL POLYPHOSPHATES IN THE EMBRYONIC CLEAVAGE CYCLE OF THE XENOPUS-LAEVIS-
dc.typeArticle-
dc.contributor.college생명과학과-
dc.identifier.doi10.1006/bbrc.1995.1109-
dc.author.googleHAN, JK-
dc.relation.volume206-
dc.relation.issue2-
dc.relation.startpage775-
dc.relation.lastpage780-
dc.contributor.id10138853-
dc.relation.journalBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.relation.indexSCI급, SCOPUS 등재논문-
dc.relation.sciSCI-
dc.collections.nameJournal Papers-
dc.type.rimsART-
dc.identifier.bibliographicCitationBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, v.206, no.2, pp.775 - 780-
dc.identifier.wosidA1995QC11500048-
dc.date.tcdate2019-01-01-
dc.citation.endPage780-
dc.citation.number2-
dc.citation.startPage775-
dc.citation.titleBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS-
dc.citation.volume206-
dc.contributor.affiliatedAuthorHAN, JK-
dc.identifier.scopusid2-s2.0-0028928645-
dc.description.journalClass1-
dc.description.journalClass1-
dc.description.wostc6-
dc.type.docTypeArticle-
dc.subject.keywordPlusINTRACELLULAR FREE CALCIUM-
dc.subject.keywordPlusCELL-CYCLE-
dc.subject.keywordPlusLIPID HYDROLYSIS-
dc.subject.keywordPlusCA2+ WAVE-
dc.subject.keywordPlusPHOSPHATES-
dc.subject.keywordPlusMITOSIS-
dc.subject.keywordPlusEGG-
dc.relation.journalWebOfScienceCategoryBiochemistry & Molecular Biology-
dc.relation.journalWebOfScienceCategoryBiophysics-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaBiochemistry & Molecular Biology-
dc.relation.journalResearchAreaBiophysics-

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한진관HAN, JIN KWAN
Dept of Life Sciences
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