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Human genomics

Showing results (811-820 of 1,110) with videos related to

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Human Genomics|December 19, 2022
Identification of a minimum number of genes to predict triple-negative breast cancer subgroups from gene expression profilesLaila Akhouayri, Paola Ostano, Maurizia Mello-Grand, et al.
Human Genomics|December 19, 2022
Preimplantation genetic testing for aneuploidy: challenges in clinical practiceHui Yang, Andrew Thomas DeWan, Mayur M Desai, et al.
Human Genomics|December 2, 2022
Pan-cancer illumination of TRIM gene family reveals immunology regulation and potential therapeutic implicationsYueying Gao, Tao Pan, Gang Xu, et al.
Human Genomics|July 25, 2022
RNA modification-related variants in genomic loci associated with body mass indexJingyun Wu, Mimi Wang, Limin Han, et al.
Human Genomics|July 19, 2022
Genetic etiology and clinical challenges of phenylketonuriaNasser A Elhawary, Imad A AlJahdali, Iman S Abumansour, et al.
Human Genomics|April 21, 2022
Impaired phosphate transport in SLC34A2 variants in patients with pulmonary alveolar microlithiasisÅsa Lina M Jönsson, Nati Hernando, Thomas Knöpfel, et al.
Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.
Human Genomics|July 24, 2010
Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measuresHortensia Moreno-Macias, Isabelle Romieu, Stephanie J London, et al.
Human Genomics|September 18, 2010
Intronic polymorphisms of cytochromes P450Magnus Ingelman-Sundberg, Sarah C Sim
Human Genomics|September 18, 2010
Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotidesDavid N Cooper, Matthew Mort, Peter D Stenson, et al.
Pageof 111

Showing results (811-820 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|December 19, 2022
Identification of a minimum number of genes to predict triple-negative breast cancer subgroups from gene expression profilesLaila Akhouayri, Paola Ostano, Maurizia Mello-Grand, et al.
Human Genomics|December 19, 2022
Preimplantation genetic testing for aneuploidy: challenges in clinical practiceHui Yang, Andrew Thomas DeWan, Mayur M Desai, et al.
Human Genomics|December 2, 2022
Pan-cancer illumination of TRIM gene family reveals immunology regulation and potential therapeutic implicationsYueying Gao, Tao Pan, Gang Xu, et al.
Human Genomics|July 25, 2022
RNA modification-related variants in genomic loci associated with body mass indexJingyun Wu, Mimi Wang, Limin Han, et al.
Human Genomics|July 19, 2022
Genetic etiology and clinical challenges of phenylketonuriaNasser A Elhawary, Imad A AlJahdali, Iman S Abumansour, et al.
Human Genomics|April 21, 2022
Impaired phosphate transport in SLC34A2 variants in patients with pulmonary alveolar microlithiasisÅsa Lina M Jönsson, Nati Hernando, Thomas Knöpfel, et al.
Human Genomics|July 24, 2010
Characterisation of a functional intronic polymorphism in the human growth hormone (GH1) geneDavid S Millar, Martin Horan, Nadia A Chuzhanova, et al.
Human Genomics|July 24, 2010
Gene-environment interaction tests for family studies with quantitative phenotypes: A review and extension to longitudinal measuresHortensia Moreno-Macias, Isabelle Romieu, Stephanie J London, et al.
Human Genomics|September 18, 2010
Intronic polymorphisms of cytochromes P450Magnus Ingelman-Sundberg, Sarah C Sim
Human Genomics|September 18, 2010
Methylation-mediated deamination of 5-methylcytosine appears to give rise to mutations causing human inherited disease in CpNpG trinucleotides, as well as in CpG dinucleotidesDavid N Cooper, Matthew Mort, Peter D Stenson, et al.
Pageof 111