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Douglas M Fowler

Showing results (111-120 of 127) with videos related to

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Clinical and Translational Science|September 20, 2019
Interrogation of CYP2D6 Structural Variant Alleles Improves the Correlation Between CYP2D6 Genotype and CYP2D6-Mediated Metabolic ActivityRachel Dalton, Seung-Been Lee, Katrina G Claw, et al.
Molecular Systems Biology|December 23, 2017
A framework for exhaustively mapping functional missense variantsJochen Weile, Song Sun, Atina G Cote, et al.
Cell|December 18, 2007
Semen-derived amyloid fibrils drastically enhance HIV infectionJan Münch, Elke Rücker, Ludger Ständker, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Saturation genome editing of <i>BARD1</i> resolves VUS and provides insight into BRCA1-BARD1 tumor suppressionIvan Woo, Silvia Casadei, Matthew W Snyder, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Genetics|September 25, 2024
Deep mutational scanning of CYP2C19 in human cells reveals a substrate specificity-abundance tradeoffGabriel E Boyle, Katherine A Sitko, Jared G Galloway, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Editing stem cell genomes at scale to measure variant effects in diverse cell and genetic contextsShawn Fayer, Riddhiman K Garge, Melissa Hopkins, et al.
Cell|May 13, 2026
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
An integrated, scaled approach to resolve TSC2 variants of uncertain significanceCarina G Biar, Ziyu R Wang, Nathan D Camp, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Saturation Genome Editing reveals the functional impact of RAD51D <i>and</i> XRCC2 variantsSilvia Casadei, Matthew W Snyder, Ivan Woo, et al.
Pageof 13

Showing results (111-120 of 127) with videos related to

Sort By:
Pageof 13
Clinical and Translational Science|September 20, 2019
Interrogation of CYP2D6 Structural Variant Alleles Improves the Correlation Between CYP2D6 Genotype and CYP2D6-Mediated Metabolic ActivityRachel Dalton, Seung-Been Lee, Katrina G Claw, et al.
Molecular Systems Biology|December 23, 2017
A framework for exhaustively mapping functional missense variantsJochen Weile, Song Sun, Atina G Cote, et al.
Cell|December 18, 2007
Semen-derived amyloid fibrils drastically enhance HIV infectionJan Münch, Elke Rücker, Ludger Ständker, et al.
Medrxiv : the Preprint Server for Health Sciences|November 24, 2025
Saturation genome editing of <i>BARD1</i> resolves VUS and provides insight into BRCA1-BARD1 tumor suppressionIvan Woo, Silvia Casadei, Matthew W Snyder, et al.
Biorxiv : the Preprint Server for Biology|July 9, 2025
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Genetics|September 25, 2024
Deep mutational scanning of CYP2C19 in human cells reveals a substrate specificity-abundance tradeoffGabriel E Boyle, Katherine A Sitko, Jared G Galloway, et al.
Medrxiv : the Preprint Server for Health Sciences|November 26, 2025
Editing stem cell genomes at scale to measure variant effects in diverse cell and genetic contextsShawn Fayer, Riddhiman K Garge, Melissa Hopkins, et al.
Cell|May 13, 2026
Image-based, pooled phenotyping reveals multidimensional, disease-specific variant effectsSriram Pendyala, Katie Partington, Nicholas Bradley, et al.
Biorxiv : the Preprint Server for Biology|February 6, 2026
An integrated, scaled approach to resolve TSC2 variants of uncertain significanceCarina G Biar, Ziyu R Wang, Nathan D Camp, et al.
Biorxiv : the Preprint Server for Biology|June 22, 2026
Saturation Genome Editing reveals the functional impact of RAD51D <i>and</i> XRCC2 variantsSilvia Casadei, Matthew W Snyder, Ivan Woo, et al.
Pageof 13