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Twelve loci from HSA10, HSA11 and HSA20 were comparatively FISH-mapped on river buffalo and sheep chromosomes

dc.contributor.authorIannuzzi, L.
dc.contributor.authorGallagher, D. S.
dc.contributor.authorDi Meo, G. P.
dc.contributor.authorSchlapfer, J.
dc.contributor.authorPerucatti, A.
dc.contributor.authorAmarante, MRV
dc.contributor.authorIncarnato, D.
dc.contributor.authorDavis, S. K.
dc.contributor.authorTaylor, J. F.
dc.contributor.authorWomack, J. E.
dc.contributor.institutionCNR
dc.contributor.institutionTexas A&M Univ
dc.contributor.institutionUniv Bern
dc.contributor.institutionUniversidade Estadual Paulista (Unesp)
dc.date.accessioned2014-05-20T13:50:04Z
dc.date.available2014-05-20T13:50:04Z
dc.date.issued2001-01-01
dc.description.abstractTen type I loci from HSA 10 (IL2RA and VIM), HSA11 (HBB and FSHB) and HSA20 (THBD, AVP/OXT, GNAS1, HCK and TOP1) and two domestic cattle type II loci (CSSM30 and BL42) were FISH mapped to R-banded river buffalo (BBU) and sheep (OAR) chromosomes. IL2RA (HSA 10) maps on BBU 14q13 and OAR13q13, VIM (HSA 10) maps on BBU14q15 and OAR13q15, HBB (HSA11) maps on BBU16q25 and OAR15q23, FSHB (HSA11) maps on BBU16q28 and OAR15q26. THBD (HSA20) maps on BBU 14q15 and OAR13q15 while AVP/OXT. GNAS1, HCK, and TOP I (HSA20) as well as CSSM30 and BL42 map on the same large band of BBU 14q22 and OAR13q22. All loci were mapped on the same homologous chromosomes and chromosome bands of the two species, and these results agree with those earlier reported in cattle homologous chromosomes 15 and 13. respectively, confirming the high degree of both banding and physical map similarities among the bovid species. Indirect comparisons between physical maps achieved on bovid chromosomes and those reported on HSA10, HSA11 and HSA20 were performed. Copyright (C) 2001 S. Karger AG, Basel.en
dc.description.affiliationCNR, IABBAM, Lab Anim Cytogenet, I-80147 Naples, Italy
dc.description.affiliationTexas A&M Univ, Dept Anim Sci, College Stn, TX 77843 USA
dc.description.affiliationUniv Bern, Inst Anim Breeding, Bern, Switzerland
dc.description.affiliationUniv Estadual Paulista, Inst Biociencias, Dept Genet, Botucatu, SP, Brazil
dc.description.affiliationTexas A&M Univ, Coll Vet Med, Dept Vet Pathobiol, College Stn, TX 77843 USA
dc.description.affiliationUnespUniv Estadual Paulista, Inst Biociencias, Dept Genet, Botucatu, SP, Brazil
dc.format.extent124-126
dc.identifierhttp://dx.doi.org/10.1159/000056963
dc.identifier.citationCytogenetics and Cell Genetics. Basel: Karger, v. 93, n. 1-2, p. 124-126, 2001.
dc.identifier.doi10.1159/000056963
dc.identifier.issn0301-0171
dc.identifier.lattes5079380279933540
dc.identifier.urihttp://hdl.handle.net/11449/17858
dc.identifier.wosWOS:000170163600027
dc.language.isoeng
dc.publisherKarger
dc.relation.ispartofCytogenetics and Cell Genetics
dc.rights.accessRightsAcesso restrito
dc.sourceWeb of Science
dc.titleTwelve loci from HSA10, HSA11 and HSA20 were comparatively FISH-mapped on river buffalo and sheep chromosomesen
dc.typeArtigo
dcterms.licensehttp://www.karger.com/Services/RightsPermissions
dcterms.rightsHolderKarger
dspace.entity.typePublication
unesp.author.lattes5079380279933540
unesp.author.orcid0000-0002-5929-1223[6]
unesp.campusUniversidade Estadual Paulista (UNESP), Instituto de Biociências, Botucatupt
unesp.departmentGenética - IBBpt

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