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Gregory M Findlay

Showing results (1-10 of 20) with videos related to

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Human Molecular Genetics|August 2, 2021
Linking genome variants to disease: scalable approaches to test the functional impact of human mutationsGregory M Findlay
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Reducing uncertainty in genetic testing with Saturation Genome EditingPhoebe Dace, Gregory M Findlay
Cell|March 23, 2019
Genomic Medicine-Progress, Pitfalls, and PromiseJay Shendure, Gregory M Findlay, Matthew W Snyder
BMC Biology|November 20, 2019
Concurrent genome and epigenome editing by CRISPR-mediated sequence replacementJes Alexander, Gregory M Findlay, Martin Kircher, et al.
Cell Genomics|March 22, 2025
High-throughput screening of human genetic variants by pooled prime editingMichael Herger, Christina M Kajba, Megan Buckley, et al.
Nature|August 21, 2014
Saturation editing of genomic regions by multiplex homology-directed repairGregory M Findlay, Evan A Boyle, Ronald J Hause, et al.
Science (New York, N.Y.)|May 28, 2016
Whole-organism lineage tracing by combinatorial and cumulative genome editingAaron McKenna, Gregory M Findlay, James A Gagnon, et al.
Nature|June 25, 2013
An siRNA screen for NFAT activation identifies septins as coordinators of store-operated Ca2+ entrySonia Sharma, Ariel Quintana, Gregory M Findlay, et al.
American Journal of Human Genetics|July 18, 2017
CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic DeletionsMolly Gasperini, Gregory M Findlay, Aaron McKenna, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 29, 2011
Dephosphorylation of the nuclear factor of activated T cells (NFAT) transcription factor is regulated by an RNA-protein scaffold complexSonia Sharma, Gregory M Findlay, Hozefa S Bandukwala, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Human Molecular Genetics|August 2, 2021
Linking genome variants to disease: scalable approaches to test the functional impact of human mutationsGregory M Findlay
Medizinische Genetik : Mitteilungsblatt Des Berufsverbandes Medizinische Genetik E.V|June 5, 2024
Reducing uncertainty in genetic testing with Saturation Genome EditingPhoebe Dace, Gregory M Findlay
Cell|March 23, 2019
Genomic Medicine-Progress, Pitfalls, and PromiseJay Shendure, Gregory M Findlay, Matthew W Snyder
BMC Biology|November 20, 2019
Concurrent genome and epigenome editing by CRISPR-mediated sequence replacementJes Alexander, Gregory M Findlay, Martin Kircher, et al.
Cell Genomics|March 22, 2025
High-throughput screening of human genetic variants by pooled prime editingMichael Herger, Christina M Kajba, Megan Buckley, et al.
Nature|August 21, 2014
Saturation editing of genomic regions by multiplex homology-directed repairGregory M Findlay, Evan A Boyle, Ronald J Hause, et al.
Science (New York, N.Y.)|May 28, 2016
Whole-organism lineage tracing by combinatorial and cumulative genome editingAaron McKenna, Gregory M Findlay, James A Gagnon, et al.
Nature|June 25, 2013
An siRNA screen for NFAT activation identifies septins as coordinators of store-operated Ca2+ entrySonia Sharma, Ariel Quintana, Gregory M Findlay, et al.
American Journal of Human Genetics|July 18, 2017
CRISPR/Cas9-Mediated Scanning for Regulatory Elements Required for HPRT1 Expression via Thousands of Large, Programmed Genomic DeletionsMolly Gasperini, Gregory M Findlay, Aaron McKenna, et al.
Proceedings of the National Academy of Sciences of the United States of America|June 29, 2011
Dephosphorylation of the nuclear factor of activated T cells (NFAT) transcription factor is regulated by an RNA-protein scaffold complexSonia Sharma, Gregory M Findlay, Hozefa S Bandukwala, et al.
Pageof 2