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Frederick P Roth

Showing results (101-110 of 188) with videos related to

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Development (Cambridge, England)|December 19, 2013
Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafishGabriel Musso, Murat Tasan, Christian Mosimann, et al.
Elife|September 2, 2020
Multiplexed measurement of variant abundance and activity reveals VKOR topology, active site and human variant impactMelissa A Chiasson, Nathan J Rollins, Jason J Stephany, et al.
Biorxiv : the Preprint Server for Biology|December 3, 2025
Systematic and proactive evaluation of AIRE missense variant effectsAnna Axakova, Amund H Berger, Warren van Loggerenberg, et al.
Genome Biology|January 31, 2015
Prioritizing causal disease genes using unbiased genomic featuresRahul C Deo, Gabriel Musso, Murat Tasan, et al.
Genome Biology|July 2, 2023
An Atlas of Variant Effects to understand the genome at nucleotide resolutionDouglas M Fowler, David J Adams, Anna L Gloyn, et al.
The Journal of Biological Chemistry|October 16, 2020
Interrogation of kinase genetic interactions provides a global view of PAK1-mediated signal transduction pathwaysJae-Hong Kim, Yeojin Seo, Myungjin Jo, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Pacybara: Accurate long-read sequencing for barcoded mutagenized allelic librariesJochen Weile, Gabrielle Ferra, Gabriel Boyle, et al.
G3 (Bethesda, Md.)|June 2, 2023
A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collectionBenjamin Weller, Chung-Wen Lin, Oxana Pogoutse, et al.
Bioinformatics (Oxford, England)|April 3, 2024
Pacybara: accurate long-read sequencing for barcoded mutagenized allelic librariesJochen Weile, Gabrielle Ferra, Gabriel Boyle, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|May 6, 2008
Challenges in translating plasma proteomics from bench to bedside: update from the NHLBI Clinical Proteomics ProgramsRobert E Gerszten, Frank Accurso, Gordon R Bernard, et al.
Pageof 19

Showing results (101-110 of 188) with videos related to

Sort By:
Pageof 19
Development (Cambridge, England)|December 19, 2013
Novel cardiovascular gene functions revealed via systematic phenotype prediction in zebrafishGabriel Musso, Murat Tasan, Christian Mosimann, et al.
Elife|September 2, 2020
Multiplexed measurement of variant abundance and activity reveals VKOR topology, active site and human variant impactMelissa A Chiasson, Nathan J Rollins, Jason J Stephany, et al.
Biorxiv : the Preprint Server for Biology|December 3, 2025
Systematic and proactive evaluation of AIRE missense variant effectsAnna Axakova, Amund H Berger, Warren van Loggerenberg, et al.
Genome Biology|January 31, 2015
Prioritizing causal disease genes using unbiased genomic featuresRahul C Deo, Gabriel Musso, Murat Tasan, et al.
Genome Biology|July 2, 2023
An Atlas of Variant Effects to understand the genome at nucleotide resolutionDouglas M Fowler, David J Adams, Anna L Gloyn, et al.
The Journal of Biological Chemistry|October 16, 2020
Interrogation of kinase genetic interactions provides a global view of PAK1-mediated signal transduction pathwaysJae-Hong Kim, Yeojin Seo, Myungjin Jo, et al.
Biorxiv : the Preprint Server for Biology|March 3, 2023
Pacybara: Accurate long-read sequencing for barcoded mutagenized allelic librariesJochen Weile, Gabrielle Ferra, Gabriel Boyle, et al.
G3 (Bethesda, Md.)|June 2, 2023
A resource of human coronavirus protein-coding sequences in a flexible, multipurpose Gateway Entry clone collectionBenjamin Weller, Chung-Wen Lin, Oxana Pogoutse, et al.
Bioinformatics (Oxford, England)|April 3, 2024
Pacybara: accurate long-read sequencing for barcoded mutagenized allelic librariesJochen Weile, Gabrielle Ferra, Gabriel Boyle, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|May 6, 2008
Challenges in translating plasma proteomics from bench to bedside: update from the NHLBI Clinical Proteomics ProgramsRobert E Gerszten, Frank Accurso, Gordon R Bernard, et al.
Pageof 19