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scopus(5)
Continent-Wide Decoupling of Y-Chromosomal Genetic Variation from Language and Geography in Native South Americans
ArticleAbstract: Numerous studies of human populations in Europe and Asia have revealed a concordance between their ePalabras claves:Autores:Alechine E., Arroyo-Pardo E., Baeta M., Barletta C., Borjas L., Builes J.J., Corach D., da Silva D.A., Ewart E., Fabricio Gonzalez-Andrade, Fagundes de Carvalho E., Geppert M., Gomes V., González M., Gusmão L., Krawczak M., López-Parra A.M., Martı́nez-Jarreta B., Nagy M., Nothnagel M., Núñez C., Palha T., Ribeiro-dos-Santos A., Roewer L., Sala A., Santos N., Santos S., Toscanini U., Turbón D., Willuweit S., Zweynert S.Fuentes:googlescopusFrequency and clinicopathological associations of K-ras mutations in Venezuelan patients with colo-rectal cancer
ArticleAbstract: Mutations in the K-ras oncogene are common in colo-rectal cancer, which affect the biological behaviPalabras claves:Colo-rectal cancer, K- ras mutations, PrognosticAutores:Borjas L., Cañizales J., Estrada P., Francisco Álvarez-Nava, Rojas J., Rojas-Atencio A.E., Soca L., Soto-Quintana M., Urdaneta K., Zabala W.Fuentes:googlescopusFISH and PCR analysis of the presence of Y-chromosome sequences in a patient with Xq-isochromosome and testicular tissue
ArticleAbstract: Mixed gonadal dysgenesis includes a heterogeneous group of different chromosomal, gonadal, and phenoPalabras claves:FISH, PCR, SRY, Testicular development, Xq-isochromosomeAutores:Borjas L., Francisco Álvarez-Nava, González S., Martínez M.C., Rojas A., Soto-Quintana M.Fuentes:googlescopusNovel mutations identification in exon 4 of LDLR gene in patients with moderate hypercholesterolemia in a venezuelan population
ArticleAbstract: Familial hypercholesterolemia (FH) is an autosomal dominant disease characterized by increase in lowPalabras claves:Coronary artery disease, Familial hypercholesterolemia, Frameshift mutations, LDL-receptor, PCR-SSCPAutores:Arráiz N., Borjas L., Carem Prieto, Mujica E., Reyes F., Reyna-Villasmil N., Rondón N., Solís E., Valmore Bermúdez, Velasco M.Fuentes:googlescopusMolecular analysis of SRY gene in patients with mixed gonadal dysgenesis
ArticleAbstract: Mixed gonadal dysgenesis (MGD) includes a group of heterogeneous conditions consisting of a dysgenetPalabras claves:Direct sequencing, Mixed gonadal dysgenesis, PCR, Sex development, SRY gene, SSCPAutores:Álvarez Z., Barrera H., Borjas L., Francisco Álvarez-Nava, Martínez S., Ortiz R., Revol A., Rojas-Martinez A., Soto-Quintana M.Fuentes:googlescopus