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Human Genetics|January 5, 2001
Identification of an intronic regulatory element in the human protein C (PROC) geneM K Shamsher, N A Chuzhanova, B Friedman, et al.
Human Molecular Genetics|July 9, 2009
Elucidation of the complex structure and origin of the human trypsinogen locus triplicationAngélique Chauvin, Jian-Min Chen, Sylvia Quemener, et al.
Stem Cells Translational Medicine|March 22, 2013
Clinical-scale derivation of natural killer cells from human pluripotent stem cells for cancer therapyDavid A Knorr, Zhenya Ni, David Hermanson, et al.
Plos Computational Biology|June 15, 2019
Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genomeKymberleigh A Pagel, Danny Antaki, AoJie Lian, et al.
Microorganisms|January 26, 2024
Metagenomic Characterisation of the Gut Microbiome and Effect of Complementary Feeding on Bifidobacterium spp. in Australian InfantsKimberley Parkin, Debra J Palmer, Valerie Verhasselt, et al.
American Journal of Human Genetics|February 5, 2022
Analysis of missense variants in the human genome reveals widespread gene-specific clustering and improves prediction of pathogenicityMathieu Quinodoz, Virginie G Peter, Katarina Cisarova, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|October 1, 1995
Functional analysis of an unusual length polymorphism in the human antithrombin III (AT3) gene promoterP C Winter, D A Scopes, L P Berg, et al.
Journal of Cystic Fibrosis : Official Journal of the European Cystic Fibrosis Society|May 29, 2007
Detection of two Alu insertions in the CFTR geneJian-Min Chen, Emmanuelle Masson, Milan Macek, et al.
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