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dc.contributor.authorWong, Len_US
dc.contributor.authorLue, MYen_US
dc.contributor.authorChang, CAen_US
dc.contributor.authorLin, YLen_US
dc.contributor.authorChan, ECen_US
dc.date.accessioned2014-12-08T15:02:14Z-
dc.date.available2014-12-08T15:02:14Z-
dc.date.issued1996-11-12en_US
dc.identifier.issn0006-291Xen_US
dc.identifier.urihttp://dx.doi.org/10.1006/bbrc.1996.1686en_US
dc.identifier.urihttp://hdl.handle.net/11536/927-
dc.description.abstractChanges in gene expression patterns in gastric cells infected with Helicobacter pylori were characterized by means of mRNA differential display. Total RNA preparations were extracted from the H. pylori infected gastric cells and paired non-infected cells, and were probed with candidate clones identified after screening up to 6,000 mRNA species. Among them, four clones, 04G-1, 04G-2, 01G-1, and Cppa-2 show significant expression in the infected cells by Northern blot analysis, and they are 199 bp, 196 bp, 228 bp, and 276 bp in length, respectively. Database search revealed that nucleotide sequences of these clones share very low identity with any known sequence. These results indicate that H. pylori can significantly affect gene expression in gastric cells. Furthermore mRNA differential display can be used in pathogenesis studies to identify new genes in gastric cells in response to insults such as H. pylori. (C) 1996 Academic Press, Inc.en_US
dc.language.isoen_USen_US
dc.titleHelicobacter pylori induces gene expression in human gastric cells identified by mRNA differential displayen_US
dc.typeArticleen_US
dc.identifier.doi10.1006/bbrc.1996.1686en_US
dc.identifier.journalBIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONSen_US
dc.citation.volume228en_US
dc.citation.issue2en_US
dc.citation.spage484en_US
dc.citation.epage488en_US
dc.contributor.department生物科技學系zh_TW
dc.contributor.departmentDepartment of Biological Science and Technologyen_US
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