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Nature Communications
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August 15, 2023
Treatment of monogenic and digenic dominant genetic hearing loss by CRISPR-Cas9 ribonucleoprotein delivery in vivo
Yong Tao, Veronica Lamas, Wan Du, et al.
Biorxiv : the Preprint Server for Biology
|
November 14, 2023
Small-molecule binding and sensing with a designed protein family
Gyu Rie Lee, Samuel J Pellock, Christoffer Norn, et al.
Journal of the American Chemical Society
|
June 30, 2025
A Molecular Glue Approach to Control the Half-Life of CRISPR-Based Technologies
Vedagopuram Sreekanth, Max Jan, Kevin T Zhao, et al.
Nature Medicine
|
February 16, 2023
Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice
Daniel Reichart, Gregory A Newby, Hiroko Wakimoto, et al.
The Journal of Investigative Dermatology
|
May 19, 2024
Twin Prime Editing Mediated Exon Skipping/Reinsertion for Restored Collagen VII Expression in Recessive Dystrophic Epidermolysis Bullosa
Benjamin J Steinbeck, Xin D Gao, Amber N McElroy, et al.
Genome Biology
|
March 16, 2021
Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression
Pan Gao, Qing Lyu, Amr R Ghanam, et al.
Nature Communications
|
February 7, 2026
A combinatorial synthetic strategy for developing genome-editing protein-delivery agents targeting mouse retina
Jianye Zhang, Rafał Hołubowicz, Roman Smidak, et al.
Cell
|
July 22, 2025
In vivo prime editing rescues alternating hemiplegia of childhood in mice
Alexander A Sousa, Markus Terrey, Holt A Sakai, et al.
Nature Communications
|
May 27, 2025
Multiplex base editing to protect from CD33 directed drugs for immune and gene therapy
Florence Borot, Olivier Humbert, Jeffrey T Ehmsen, et al.
Nature Genetics
|
May 26, 2025
Base editing of trinucleotide repeats that cause Huntington's disease and Friedreich's ataxia reduces somatic repeat expansions in patient cells and in mice
Zaneta Matuszek, Mandana Arbab, Maheswaran Kesavan, et al.
Page
of 33
Search research articles
Search
Showing results (281-290 of 321) with videos related to
Sort By:
Page
of 33
Nature Communications
|
August 15, 2023
Treatment of monogenic and digenic dominant genetic hearing loss by CRISPR-Cas9 ribonucleoprotein delivery in vivo
Yong Tao, Veronica Lamas, Wan Du, et al.
Biorxiv : the Preprint Server for Biology
|
November 14, 2023
Small-molecule binding and sensing with a designed protein family
Gyu Rie Lee, Samuel J Pellock, Christoffer Norn, et al.
Journal of the American Chemical Society
|
June 30, 2025
A Molecular Glue Approach to Control the Half-Life of CRISPR-Based Technologies
Vedagopuram Sreekanth, Max Jan, Kevin T Zhao, et al.
Nature Medicine
|
February 16, 2023
Efficient in vivo genome editing prevents hypertrophic cardiomyopathy in mice
Daniel Reichart, Gregory A Newby, Hiroko Wakimoto, et al.
The Journal of Investigative Dermatology
|
May 19, 2024
Twin Prime Editing Mediated Exon Skipping/Reinsertion for Restored Collagen VII Expression in Recessive Dystrophic Epidermolysis Bullosa
Benjamin J Steinbeck, Xin D Gao, Amber N McElroy, et al.
Genome Biology
|
March 16, 2021
Prime editing in mice reveals the essentiality of a single base in driving tissue-specific gene expression
Pan Gao, Qing Lyu, Amr R Ghanam, et al.
Nature Communications
|
February 7, 2026
A combinatorial synthetic strategy for developing genome-editing protein-delivery agents targeting mouse retina
Jianye Zhang, Rafał Hołubowicz, Roman Smidak, et al.
Cell
|
July 22, 2025
In vivo prime editing rescues alternating hemiplegia of childhood in mice
Alexander A Sousa, Markus Terrey, Holt A Sakai, et al.
Nature Communications
|
May 27, 2025
Multiplex base editing to protect from CD33 directed drugs for immune and gene therapy
Florence Borot, Olivier Humbert, Jeffrey T Ehmsen, et al.
Nature Genetics
|
May 26, 2025
Base editing of trinucleotide repeats that cause Huntington's disease and Friedreich's ataxia reduces somatic repeat expansions in patient cells and in mice
Zaneta Matuszek, Mandana Arbab, Maheswaran Kesavan, et al.
Page
of 33