Intron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer

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dc.contributor.authorPalicio, M.
dc.contributor.authorBlanco Guillermo, Ignacio
dc.contributor.authorTórtola, S.
dc.contributor.authorGonzález, I.
dc.contributor.authorMarcuello, Eugenio
dc.contributor.authorBrunet, Joan
dc.contributor.authorGonzalez Aguilera, Juan Jose
dc.contributor.authorPeinado Morales, Miguel Á. (Miguel Ángel)
dc.contributor.authorCapellá, G. (Gabriel)
dc.contributor.authorLluis, Fèlix
dc.date.accessioned2020-01-10T14:35:50Z
dc.date.available2020-01-10T14:35:50Z
dc.date.issued2000-01-18
dc.date.updated2020-01-10T14:35:50Z
dc.description.abstractA polymorphism in hMSH2 gene has been associated with an increased susceptibility to develop colorectal cancer (CRC). Here we show that it is a genetic risk factor for CRC in the Spanish population. However, its presence does not apparently affect hMSH2 function.
dc.format.extent3 p.
dc.format.mimetypeapplication/pdf
dc.identifier.idgrec517203
dc.identifier.issn0007-0920
dc.identifier.pmid10682661
dc.identifier.urihttps://hdl.handle.net/2445/147526
dc.language.isoeng
dc.publisherCancer Research UK
dc.relation.isformatofVersió postprint del document publicat a: https://doi.org/10.1054/bjoc.1999.0959
dc.relation.ispartofBritish Journal of Cancer, 2000, vol. 82, num. 3, p. 535-537
dc.relation.urihttps://doi.org/10.1054/bjoc.1999.0959
dc.rights(c) Palicio, M. et al., 2000
dc.rights.accessRightsinfo:eu-repo/semantics/openAccess
dc.sourceArticles publicats en revistes (Patologia i Terapèutica Experimental)
dc.subject.classificationCàncer colorectal
dc.subject.classificationGenètica humana
dc.subject.classificationEspanya
dc.subject.otherColorectal cancer
dc.subject.otherHuman genetics
dc.subject.otherSpain
dc.titleIntron splice acceptor site polymorphism in the hMSH2 gene in sporadic and familial colorectal cancer
dc.typeinfo:eu-repo/semantics/article
dc.typeinfo:eu-repo/semantics/acceptedVersion

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