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Showing results (641-650 of 750) with videos related to

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Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Journal of Medical Genetics|August 16, 2015
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotypeIsabelle Perrault, Jan Halbritter, Jonathan D Porath, et al.
Genome Medicine|April 20, 2017
Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burdenZachary R Chalmers, Caitlin F Connelly, David Fabrizio, et al.
The Journal of Infectious Diseases|January 31, 2022
Association of Hyperferritinemia With Distinct Host Response Aberrations in Patients With Community-Acquired PneumoniaXanthe Brands, Tjitske S R van Engelen, Floris M C de Vries, et al.
American Journal of Human Genetics|June 3, 2014
Mutations of CEP83 cause infantile nephronophthisis and intellectual disabilityMarion Failler, Heon Yung Gee, Pauline Krug, et al.
Journal of the American Society of Nephrology : JASN|July 8, 2015
Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE SubjectsMatthew G Sampson, Catherine C Robertson, Sebastian Martini, et al.
JCI Insight|May 20, 2026
Not all reference samples are equal in single-cell transcriptomics of human kidney tissueRajasree Menon, Paul L Kimmel, Edgar A Otto, et al.
Genome Biology|March 13, 2026
Systematic evaluation of single-cell multimodal data integration enhances cell type resolution and discovery of clinically relevant states in complex tissuesMario Acera-Mateos, Xian Adiconis, Jessica-Kanglin Li, et al.
Biorxiv : the Preprint Server for Biology|March 17, 2025
Systematic evaluation of single-cell multimodal data integration for comprehensive human reference atlasMario Acera-Mateos, Xian Adiconis, Jessica-Kanglin Li, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 7, 2013
A high frequency of activating extracellular domain ERBB2 (HER2) mutation in micropapillary urothelial carcinomaJeffrey S Ross, Kai Wang, Laurie M Gay, et al.
Pageof 75

Showing results (641-650 of 750) with videos related to

Sort By:
Pageof 75
Proceedings of the National Academy of Sciences of the United States of America|May 14, 2004
SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexesRainer G Ruf, Pin-Xian Xu, Derek Silvius, et al.
Journal of Medical Genetics|August 16, 2015
IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotypeIsabelle Perrault, Jan Halbritter, Jonathan D Porath, et al.
Genome Medicine|April 20, 2017
Analysis of 100,000 human cancer genomes reveals the landscape of tumor mutational burdenZachary R Chalmers, Caitlin F Connelly, David Fabrizio, et al.
The Journal of Infectious Diseases|January 31, 2022
Association of Hyperferritinemia With Distinct Host Response Aberrations in Patients With Community-Acquired PneumoniaXanthe Brands, Tjitske S R van Engelen, Floris M C de Vries, et al.
American Journal of Human Genetics|June 3, 2014
Mutations of CEP83 cause infantile nephronophthisis and intellectual disabilityMarion Failler, Heon Yung Gee, Pauline Krug, et al.
Journal of the American Society of Nephrology : JASN|July 8, 2015
Integrative Genomics Identifies Novel Associations with APOL1 Risk Genotypes in Black NEPTUNE SubjectsMatthew G Sampson, Catherine C Robertson, Sebastian Martini, et al.
JCI Insight|May 20, 2026
Not all reference samples are equal in single-cell transcriptomics of human kidney tissueRajasree Menon, Paul L Kimmel, Edgar A Otto, et al.
Genome Biology|March 13, 2026
Systematic evaluation of single-cell multimodal data integration enhances cell type resolution and discovery of clinically relevant states in complex tissuesMario Acera-Mateos, Xian Adiconis, Jessica-Kanglin Li, et al.
Biorxiv : the Preprint Server for Biology|March 17, 2025
Systematic evaluation of single-cell multimodal data integration for comprehensive human reference atlasMario Acera-Mateos, Xian Adiconis, Jessica-Kanglin Li, et al.
Clinical Cancer Research : an Official Journal of the American Association for Cancer Research|November 7, 2013
A high frequency of activating extracellular domain ERBB2 (HER2) mutation in micropapillary urothelial carcinomaJeffrey S Ross, Kai Wang, Laurie M Gay, et al.
Pageof 75