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Cloning leishmania telomeres in yeast by complementation

dc.contributor.authorEspinoza, José
dc.creatorEspinoza, José
dc.date.accessioned2015-06-24T16:45:46Z
dc.date.available2015-06-24T16:45:46Z
dc.date.issued2003-07
dc.identifier.citationEspinoza J. Cloning leishmania telomeres in yeast by complementation. Informe Científico Tecnológico. Volumen 2 (2002) p. 147-149.es_PE
dc.identifier.issn1684-1662
dc.identifier.urihttps://hdl.handle.net/20.500.13054/363
dc.description.abstractLeishmania telemores were cloned in yeast by complementation using a half arm of the yeast artificial chromosome vector pJS97. A single copy marker associated to the telomere (YT2) located 6 kb away from one end of a megabase size chromosome of 1116c8 was cloned by end rescue and DNA sequenced. The sequence of 1479 bp did not show a significant homology with any sequence stored in GenBank. Leishmania telomeres are amenable to be cloned and maintained in yeast, this approach will facilitate the analysis of telomere and subtelomere regions which are usually underrepresented in genomic libraries.es_PE
dc.formatapplication/pdfes_PE
dc.language.isoenges_PE
dc.publisherLima (Perú)es_PE
dc.rightsinfo:eu-repo/semantics/openAccesses_PE
dc.sourceInstituto Peruano de Energía Nucleares_PE
dc.sourceRepositorio Institucional del Instituto Peruano de Energía Nucleares_PE
dc.subjectLeishmania telemoreses_PE
dc.subjectParásitoses_PE
dc.subjectEnfermedad de leishmaniasises_PE
dc.subjectSecuencia de cromosomases_PE
dc.titleCloning leishmania telomeres in yeast by complementationes_PE
dc.typeinfo:eu-repo/semantics/articlees_PE
dc.publisher.countryPEes_PE


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