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Human genomics

Showing results (621-630 of 1,110) with videos related to

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Human Genomics|May 13, 2023
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human geneM Chograni, H M Alahdal, M Rejili
Human Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.
Human Genomics|November 27, 2012
Association of genome variations in the renin-angiotensin system with physical performanceArgyro Sgourou, Vassilis Fotopoulos, Vassilis Kontos, et al.
Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.
Human Genomics|December 14, 2011
Overview of biological database mapping services for interoperation between different 'omics' datasetsShweta S Chavan, John D Shaughnessy, Ricky D Edmondson
Human Genomics|December 12, 2019
The multi-faceted functioning portrait of LRF/ZBTB7ACaterina Constantinou, Magda Spella, Vasiliki Chondrou, et al.
Human Genomics|January 26, 2019
The association of functional polymorphisms in genes expressed in endothelial cells and smooth muscle cells with the myocardial infarctionYilan Li, Shipeng Wang, Dandan Zhang, et al.
Human Genomics|January 12, 2019
Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary studyDandan Yi, Lei Xu, Jiaqi Luo, et al.
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Human Genomics|December 5, 2019
Genetics and functions of the retinoic acid pathway, with special emphasis on the eyeBrian Thompson, Nicholas Katsanis, Nicholas Apostolopoulos, et al.
Pageof 111

Showing results (621-630 of 1,110) with videos related to

Sort By:
Pageof 111
Human Genomics|May 13, 2023
Autosomal recessive congenital cataract is associated with a novel 4-bp splicing deletion mutation in a novel C10orf71 human geneM Chograni, H M Alahdal, M Rejili
Human Genomics|March 28, 2023
Community data-driven approach to identify pathogenic founder variants for pan-ethnic carrier screening panelsYaron Einhorn, Moshe Einhorn, Alina Kurolap, et al.
Human Genomics|November 27, 2012
Association of genome variations in the renin-angiotensin system with physical performanceArgyro Sgourou, Vassilis Fotopoulos, Vassilis Kontos, et al.
Human Genomics|December 14, 2011
Neurofibromatosis type 1-associated tumours: their somatic mutational spectrum and pathogenesisSebastian Laycock-van Spyk, Nick Thomas, David N Cooper, et al.
Human Genomics|December 14, 2011
Overview of biological database mapping services for interoperation between different 'omics' datasetsShweta S Chavan, John D Shaughnessy, Ricky D Edmondson
Human Genomics|December 12, 2019
The multi-faceted functioning portrait of LRF/ZBTB7ACaterina Constantinou, Magda Spella, Vasiliki Chondrou, et al.
Human Genomics|January 26, 2019
The association of functional polymorphisms in genes expressed in endothelial cells and smooth muscle cells with the myocardial infarctionYilan Li, Shipeng Wang, Dandan Zhang, et al.
Human Genomics|January 12, 2019
Germline TP53 and MSH6 mutations implicated in sporadic triple-negative breast cancer (TNBC): a preliminary studyDandan Yi, Lei Xu, Jiaqi Luo, et al.
Human Genomics|February 2, 2019
A genome-wide association study of mitochondrial DNA copy number in two population-based cohortsAnna L Guyatt, Rebecca R Brennan, Kimberley Burrows, et al.
Human Genomics|December 5, 2019
Genetics and functions of the retinoic acid pathway, with special emphasis on the eyeBrian Thompson, Nicholas Katsanis, Nicholas Apostolopoulos, et al.
Pageof 111