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Human genetics

Showing results (751-760 of 9,569) with videos related to

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Human Genetics|April 22, 2015
Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataractSmriti A Agrawal, Deepti Anand, Archana D Siddam, et al.
Human Genetics|July 25, 2016
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutationsXiaohong R Yang, Melissa Rotunno, Yanzi Xiao, et al.
Human Genetics|May 11, 2021
Causal influences of neuroticism on mental health and cardiovascular diseaseFuquan Zhang, Ancha Baranova, Chao Zhou, et al.
Human Genetics|May 12, 2021
Characterization of intermediate-sized insertions using whole-genome sequencing data and analysis of their functional impact on gene expressionSaeideh Ashouri, Jing Hao Wong, Hidewaki Nakagawa, et al.
Human Genetics|June 6, 2020
Rare variant association testing in the non-coding genomeOzvan Bocher, Emmanuelle Génin
Human Genetics|May 14, 2021
Should we respect parents' views about which results to return from genomic sequencing?D F Vears
Human Genetics|June 4, 2020
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle EastFlavia Palombo, Claudio Graziano, Nadia Al Wardy, et al.
Human Genetics|July 1, 1988
cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31M G Mattei, D Weil, D Pribula-Conway, et al.
Human Genetics|August 2, 2021
Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countriesAbdullah Al Mutery, Mona Mahfood, Jihen Chouchen, et al.
Human Genetics|February 4, 2023
Interpreting variants in genes affected by clonal hematopoiesis in population dataSanna Gudmundsson, Colleen M Carlston, Anne O'Donnell-Luria
Pageof 957

Showing results (751-760 of 9,569) with videos related to

Sort By:
Pageof 957
Human Genetics|April 22, 2015
Compound mouse mutants of bZIP transcription factors Mafg and Mafk reveal a regulatory network of non-crystallin genes associated with cataractSmriti A Agrawal, Deepti Anand, Archana D Siddam, et al.
Human Genetics|July 25, 2016
Multiple rare variants in high-risk pancreatic cancer-related genes may increase risk for pancreatic cancer in a subset of patients with and without germline CDKN2A mutationsXiaohong R Yang, Melissa Rotunno, Yanzi Xiao, et al.
Human Genetics|May 11, 2021
Causal influences of neuroticism on mental health and cardiovascular diseaseFuquan Zhang, Ancha Baranova, Chao Zhou, et al.
Human Genetics|May 12, 2021
Characterization of intermediate-sized insertions using whole-genome sequencing data and analysis of their functional impact on gene expressionSaeideh Ashouri, Jing Hao Wong, Hidewaki Nakagawa, et al.
Human Genetics|June 6, 2020
Rare variant association testing in the non-coding genomeOzvan Bocher, Emmanuelle Génin
Human Genetics|May 14, 2021
Should we respect parents' views about which results to return from genomic sequencing?D F Vears
Human Genetics|June 4, 2020
Autozygosity-driven genetic diagnosis in consanguineous families from Italy and the Greater Middle EastFlavia Palombo, Claudio Graziano, Nadia Al Wardy, et al.
Human Genetics|July 1, 1988
cDNA cloning, expression and mapping of human laminin B2 gene to chromosome 1q31M G Mattei, D Weil, D Pribula-Conway, et al.
Human Genetics|August 2, 2021
Genetic etiology of hereditary hearing loss in the Gulf Cooperation Council countriesAbdullah Al Mutery, Mona Mahfood, Jihen Chouchen, et al.
Human Genetics|February 4, 2023
Interpreting variants in genes affected by clonal hematopoiesis in population dataSanna Gudmundsson, Colleen M Carlston, Anne O'Donnell-Luria
Pageof 957