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Prashant Mali

Showing results (51-60 of 102) with videos related to

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Journal of Visualized Experiments : Jove|January 22, 2019
Investigation of Genetic Dependencies Using CRISPR-Cas9-based Competition AssaysAnagha Deshpande, Bo Rui Chen, Luyi Zhao, et al.
Molecular Therapy. Methods & Clinical Development|May 29, 2020
CRISPR-Cas9 Gene Editing of Hematopoietic Stem Cells from Patients with Friedreich's AtaxiaCeline J Rocca, Joseph N Rainaldi, Jay Sharma, et al.
Stem Cell Reports|September 24, 2021
Programmatic introduction of parenchymal cell types into blood vessel organoidsAmir Dailamy, Udit Parekh, Dhruva Katrekar, et al.
The Journal of Biological Chemistry|January 3, 2023
Whole-genome CRISPR screening identifies PI3K/AKT as a downstream component of the oncogenic GNAQ-focal adhesion kinase signaling circuitryNadia Arang, Simone Lubrano, Damiano Cosimo Rigiracciolo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 9, 2023
RNA editing: Expanding the potential of RNA therapeuticsBrian J Booth, Sami Nourreddine, Dhruva Katrekar, et al.
Nature Biotechnology|August 3, 2013
CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineeringPrashant Mali, John Aach, P Benjamin Stranges, et al.
Science (New York, N.Y.)|January 5, 2013
RNA-guided human genome engineering via Cas9Prashant Mali, Luhan Yang, Kevin M Esvelt, et al.
Plos One|May 11, 2012
The differential formation of the LINC-mediated perinuclear actin cap in pluripotent and somatic cellsShyam B Khatau, Sravanti Kusuma, Donny Hanjaya-Putra, et al.
Nature Biomedical Engineering|July 24, 2019
Immune-orthogonal orthologues of AAV capsids and of Cas9 circumvent the immune response to the administration of gene therapyAna M Moreno, Nathan Palmer, Fernando Alemán, et al.
Nature Biomedical Engineering|August 29, 2019
Author Correction: Immune-orthogonal orthologues of AAV capsids and of Cas9 circumvent the immune response to the administration of gene therapyAna M Moreno, Nathan Palmer, Fernando Alemán, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
Journal of Visualized Experiments : Jove|January 22, 2019
Investigation of Genetic Dependencies Using CRISPR-Cas9-based Competition AssaysAnagha Deshpande, Bo Rui Chen, Luyi Zhao, et al.
Molecular Therapy. Methods & Clinical Development|May 29, 2020
CRISPR-Cas9 Gene Editing of Hematopoietic Stem Cells from Patients with Friedreich's AtaxiaCeline J Rocca, Joseph N Rainaldi, Jay Sharma, et al.
Stem Cell Reports|September 24, 2021
Programmatic introduction of parenchymal cell types into blood vessel organoidsAmir Dailamy, Udit Parekh, Dhruva Katrekar, et al.
The Journal of Biological Chemistry|January 3, 2023
Whole-genome CRISPR screening identifies PI3K/AKT as a downstream component of the oncogenic GNAQ-focal adhesion kinase signaling circuitryNadia Arang, Simone Lubrano, Damiano Cosimo Rigiracciolo, et al.
Molecular Therapy : the Journal of the American Society of Gene Therapy|January 9, 2023
RNA editing: Expanding the potential of RNA therapeuticsBrian J Booth, Sami Nourreddine, Dhruva Katrekar, et al.
Nature Biotechnology|August 3, 2013
CAS9 transcriptional activators for target specificity screening and paired nickases for cooperative genome engineeringPrashant Mali, John Aach, P Benjamin Stranges, et al.
Science (New York, N.Y.)|January 5, 2013
RNA-guided human genome engineering via Cas9Prashant Mali, Luhan Yang, Kevin M Esvelt, et al.
Plos One|May 11, 2012
The differential formation of the LINC-mediated perinuclear actin cap in pluripotent and somatic cellsShyam B Khatau, Sravanti Kusuma, Donny Hanjaya-Putra, et al.
Nature Biomedical Engineering|July 24, 2019
Immune-orthogonal orthologues of AAV capsids and of Cas9 circumvent the immune response to the administration of gene therapyAna M Moreno, Nathan Palmer, Fernando Alemán, et al.
Nature Biomedical Engineering|August 29, 2019
Author Correction: Immune-orthogonal orthologues of AAV capsids and of Cas9 circumvent the immune response to the administration of gene therapyAna M Moreno, Nathan Palmer, Fernando Alemán, et al.
Pageof 11