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Human Genetics|January 28, 2014
A novel variant in the 3' UTR of human SCN1A gene from a patient with Dravet syndrome decreases mRNA stability mediated by GAPDH's bindingTao Zeng, Zhao-Fei Dong, Shu-Jing Liu, et al.Human Genetics|June 28, 2014
Host genetics and viral load in primary HIV-1 infection: clear evidence for gene by sex interactionsXuelin Li, Matthew A Price, Dongning He, et al.Human Genetics|July 2, 2014
Population and genomic lessons from genetic analysis of two Indian populationsGarima Juyal, Mayukh Mondal, Pierre Luisi, et al.Human Genetics|May 23, 2014
Amniotic fluid RNA gene expression profiling provides insights into the phenotype of Turner syndromeLauren J Massingham, Kirby L Johnson, Thomas M Scholl, et al.Human Genetics|July 17, 2020
A pooled genome-wide association study identifies pancreatic cancer susceptibility loci on chromosome 19p12 and 19p13.3 in the full-Jewish populationSamantha A Streicher, Alison P Klein, Sara H Olson, et al.Human Genetics|July 31, 2020
Identifying adaptive alleles in the human genome: from selection mapping to functional validationElizabeth A Werren, Obed Garcia, Abigail W BighamHuman Genetics|July 4, 2020
Combi-CRISPR: combination of NHEJ and HDR provides efficient and precise plasmid-based knock-ins in mice and ratsKazuto Yoshimi, Yuichiro Oka, Yoshiki Miyasaka, et al.Human Genetics|April 26, 2021
Geographic variation in the polygenic score of height in JapanMariko Isshiki, Yusuke Watanabe, Jun OhashiHuman Genetics|April 1, 1986
Genetic analysis of human lymphocyte proteins by two-dimensional gel electrophoresis. VIII. Genetic polymorphism of cytosol polypeptide with molecular weight of 20,000I Kondo, S Harada, M Shibasaki, et al.Human Genetics|April 1, 1986
Genetic polymorphism of human complement component C81 in the Japanese populationS Nakamura, O Ohue, K AbePageof 958