Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/67834
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dc.contributor.authorGallegos-Arreola, M.P.
dc.contributor.authorBatista-Gonzalez, C.M.
dc.contributor.authorDelgado-Lamas, J.L.
dc.contributor.authorFiguera, L.E.
dc.contributor.authorPuebla-Perez, A.M.
dc.contributor.authorArnaud-Lopez, L.
dc.contributor.authorPeralta-Leal, V.
dc.contributor.authorRamirez-Jirano, L.J.
dc.contributor.authorZuniga-Gonzalez, G.M.
dc.date.accessioned2015-11-19T18:52:31Z-
dc.date.available2015-11-19T18:52:31Z-
dc.date.issued2004
dc.identifier.urihttp://hdl.handle.net/20.500.12104/67834-
dc.description.abstractWe studied the role of cytochrome P4501A1 (CYP1A1 Val/Val) genotypes in the etiology of acute lymphoblastic leukemia (ALL) in adult Mexican patients. Distributions of CYP1A1 Val/Val genotypes in peripheral blood DNA samples from 136 healthy controls and 136 adult patients with ALL were evaluated. There was an increased frequency of the CYP1A1 Val/Val genotype among ALL patients, showing a significant association between this genotype and the risk of developing ALL. © 2004 Elsevier Inc. All rights reserved.
dc.titleCytochrome P4501A1 polymorphism is associated with susceptibility to acute lymphoblastic leukemia in adult Mexican patients
dc.typeArticle
dc.identifier.doi10.1016/j.bcmd.2004.07.002
dc.relation.ispartofjournalBlood Cells, Molecules, and Diseases
dc.relation.ispartofvolume33
dc.relation.ispartofissue3
dc.relation.ispartofpage326
dc.relation.ispartofpage329
dc.subject.keywordAcute lymphoblastic leukemia; CYP1A1; Mexican population; Polymorphism
dc.contributor.affiliationGallegos-Arreola, M.P., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico, Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, IMSS Sierra Mojada No. 800, C., Mexico; Batista-González, C.M., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico, Doctorado en Biol. Molecular, Ctro. Univ. de Ciencias de la Salud, Univ. de Guadalajara, Jalisco, Mex., Mexico; Delgado-Lamas, J.L., Servicio de Hematología, Hospital de Especialidades, Ctro. Medico Nac. Occidente, G., Mexico; Figuera, L.E., División de Genética, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico; Puebla-Pérez, A.M., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico; Arnaud-López, L., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico, Doctorado en Genética Humana, Ctro. Univ. de Ciencias de la Salud, Univ. de Guadalajara, Jalisco, Mex., Mexico; Peralta-Leal, V., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico, Doctorado en Genética Humana, Ctro. Univ. de Ciencias de la Salud, Univ. de Guadalajara, Jalisco, Mex., Mexico; Ramírez-Jirano, L.J., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico, Doctorado en Genética Humana, Ctro. Univ. de Ciencias de la Salud, Univ. de Guadalajara, Jalisco, Mex., Mexico; Zúñiga-González, G.M., Div. de Medicina Molecular, Ctro. Invest. Biomedica de Occidente, Guadalajara, Jalisco, México, Mexico
dc.relation.isReferencedByScopus
dc.relation.isReferencedByWOS
dc.identifier.urlhttp://www.scopus.com/inward/record.url?eid=2-s2.0-7544220274&partnerID=40&md5=a49483af5fe4c4af89fd227d318822f5
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