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Plos One|January 16, 2014
Global pharmacogenomics: distribution of CYP3A5 polymorphisms and phenotypes in the Brazilian populationGuilherme Suarez-Kurtz, Daniela D Vargens, Ana Beatriz Santoro, et al.
Human Mutation|June 4, 2015
Rapid Detection of Rare Deleterious Variants by Next Generation Sequencing with Optional Microarray SNP Genotype DataChristopher M Watson, Laura A Crinnion, Juliana Gurgel-Gianetti, et al.
Plos One|April 2, 2009
The MHC gene region of murine hosts influences the differential tissue tropism of infecting Trypanosoma cruzi strainsJorge M Freitas, Luciana O Andrade, Simone F Pires, et al.
Plos One|October 21, 2014
Distribution of CYP2D6 alleles and phenotypes in the Brazilian populationDeise C Friedrich, Júlia P Genro, Vinicius A Sortica, et al.
Genetics and Molecular Research : GMR|June 19, 2007
Analysis of DNA polymerase activity in vitro using non-radioactive primer extension assay in an automated DNA sequencerD O Lopes, C G Regis-da-Silva, A Machado-Silva, et al.
Laboratory Investigation; a Journal of Technical Methods and Pathology|September 29, 2020
Assessing the utility of long-read nanopore sequencing for rapid and efficient characterization of mobile element insertionsChristopher M Watson, Laura A Crinnion, Helen Lindsay, et al.
The Pharmacogenomics Journal|December 22, 2010
Global pharmacogenomics: Impact of population diversity on the distribution of polymorphisms in the CYP2C cluster among BraziliansG Suarez-Kurtz, J P Genro, M O de Moraes, et al.
Genetics and Molecular Research : GMR|July 5, 2006
Relationship of the methylenetetrahydrofolate reductase C677T polymorphism with microsatellite instability and promoter hypermethylation in sporadic colorectal cancerAlessandra D Clarizia, Luciana Bastos-Rodrigues, Heloísa B Pena, et al.
Basic & Clinical Pharmacology & Toxicology|December 6, 2011
Influence of genomic ancestry on the distribution of SLCO1B1, SLCO1B3 and ABCB1 gene polymorphisms among BraziliansVinicius de A Sortica, Elida B Ojopi, Júlia P Genro, et al.
Genetics and Molecular Biology|August 26, 2016
1p13.2 deletion displays clinical features overlapping Noonan syndrome, likely related to NRAS gene haploinsufficiencyNatália Duarte Linhares, Maíra Cristina Menezes Freire, Raony Guimarães Corrêa do Carmo Lisboa Cardenas, et al.
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