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Douglas M Fowler

Showing results (71-80 of 127) with videos related to

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Biorxiv : the Preprint Server for Biology|November 24, 2025
Multiplex design and discovery of proximity handles for programmable proteome editingChase C Suiter, Green Ahn, Melodie Chiu, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Not Forgotten: Patient Experiences with Genetic Variant ReclassificationsPankhuri Gupta, Min Seon Park, Eric Y Kao, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2013
Activity-enhancing mutations in an E3 ubiquitin ligase identified by high-throughput mutagenesisLea M Starita, Jonathan N Pruneda, Russell S Lo, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
A complete map of human cytosolic degrons and their relevance for diseaseVasileios Voutsinos, Kristoffer E Johansson, Fia B Larsen, et al.
The Journal of Biological Chemistry|October 21, 2009
N-terminal domains elicit formation of functional Pmel17 amyloid fibrilsBrenda Watt, Guillaume van Niel, Douglas M Fowler, et al.
American Journal of Human Genetics|July 27, 2021
Massively parallel characterization of CYP2C9 variant enzyme activity and abundanceClara J Amorosi, Melissa A Chiasson, Matthew G McDonald, et al.
Science Advances|February 6, 2026
A near-complete map of human cytosolic degrons and their relevance for diseaseVasileios Voutsinos, Kristoffer E Johansson, Fia B Larsen, et al.
Molecular Systems Biology|June 6, 2020
High-throughput, microscope-based sorting to dissect cellular heterogeneityNicholas Hasle, Anthony Cooke, Sanjay Srivatsan, et al.
American Journal of Human Genetics|November 18, 2021
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTENShawn Fayer, Carrie Horton, Jennifer N Dines, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Insights on improving accessibility and usability of functional data to unlock its potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Pageof 13

Showing results (71-80 of 127) with videos related to

Sort By:
Pageof 13
Biorxiv : the Preprint Server for Biology|November 24, 2025
Multiplex design and discovery of proximity handles for programmable proteome editingChase C Suiter, Green Ahn, Melodie Chiu, et al.
Medrxiv : the Preprint Server for Health Sciences|May 25, 2026
Not Forgotten: Patient Experiences with Genetic Variant ReclassificationsPankhuri Gupta, Min Seon Park, Eric Y Kao, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 20, 2013
Activity-enhancing mutations in an E3 ubiquitin ligase identified by high-throughput mutagenesisLea M Starita, Jonathan N Pruneda, Russell S Lo, et al.
Biorxiv : the Preprint Server for Biology|June 4, 2025
A complete map of human cytosolic degrons and their relevance for diseaseVasileios Voutsinos, Kristoffer E Johansson, Fia B Larsen, et al.
The Journal of Biological Chemistry|October 21, 2009
N-terminal domains elicit formation of functional Pmel17 amyloid fibrilsBrenda Watt, Guillaume van Niel, Douglas M Fowler, et al.
American Journal of Human Genetics|July 27, 2021
Massively parallel characterization of CYP2C9 variant enzyme activity and abundanceClara J Amorosi, Melissa A Chiasson, Matthew G McDonald, et al.
Science Advances|February 6, 2026
A near-complete map of human cytosolic degrons and their relevance for diseaseVasileios Voutsinos, Kristoffer E Johansson, Fia B Larsen, et al.
Molecular Systems Biology|June 6, 2020
High-throughput, microscope-based sorting to dissect cellular heterogeneityNicholas Hasle, Anthony Cooke, Sanjay Srivatsan, et al.
American Journal of Human Genetics|November 18, 2021
Closing the gap: Systematic integration of multiplexed functional data resolves variants of uncertain significance in BRCA1, TP53, and PTENShawn Fayer, Carrie Horton, Jennifer N Dines, et al.
Medrxiv : the Preprint Server for Health Sciences|February 20, 2025
Insights on improving accessibility and usability of functional data to unlock its potential for variant interpretationMin Seon Park, Runjun D Kumar, Cristian Ovadiuc, et al.
Pageof 13