Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A Wolfe

Showing results (1061-1070 of 1,125) with videos related to

Pageof 113
Sort By:
Nature Biotechnology|September 25, 2024
Increasing intracellular dNTP levels improves prime editing efficiencyPengpeng Liu, Karthikeyan Ponnienselvan, Thomas Nyalile, et al.
Nature Medicine|March 27, 2019
Highly efficient therapeutic gene editing of human hematopoietic stem cellsYuxuan Wu, Jing Zeng, Benjamin P Roscoe, et al.
Nature Genetics|June 30, 2019
Rational targeting of a NuRD subcomplex guided by comprehensive in situ mutagenesisFalak Sher, Mir Hossain, Davide Seruggia, et al.
The Journal of Allergy and Clinical Immunology|March 5, 2014
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairmentYu Zhang, Xiaomin Yu, Mie Ichikawa, et al.
Biorxiv : the Preprint Server for Biology|June 5, 2026
Fully Modified SpyCas9 Guide RNAs Enable Robust Genome Editing In Cells and In VivoKim Anh Vu, Han Zhang, Nadia Amrani, et al.
Molecular Genetics and Metabolism|May 28, 2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivityDavid R Adams, Hongjie Yuan, Todd Holyoak, et al.
Journal of Neurogenetics|May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
Molecular Genetics and Metabolism|May 7, 2015
Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchorsChristina Lam, Gretchen A Golas, Mariska Davids, et al.
Blood Advances|November 8, 2019
Genome editing of HBG1 and HBG2 to induce fetal hemoglobinJean-Yves Métais, Phillip A Doerfler, Thiyagaraj Mayuranathan, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Functional gene delivery to and across brain vasculature of systemic AAVs with endothelial-specific tropism in rodents and broad tropism in primatesXinhong Chen, Damien A Wolfe, Dhanesh Sivadasan Bindu, et al.
Pageof 113

Showing results (1061-1070 of 1,125) with videos related to

Sort By:
Pageof 113
Nature Biotechnology|September 25, 2024
Increasing intracellular dNTP levels improves prime editing efficiencyPengpeng Liu, Karthikeyan Ponnienselvan, Thomas Nyalile, et al.
Nature Medicine|March 27, 2019
Highly efficient therapeutic gene editing of human hematopoietic stem cellsYuxuan Wu, Jing Zeng, Benjamin P Roscoe, et al.
Nature Genetics|June 30, 2019
Rational targeting of a NuRD subcomplex guided by comprehensive in situ mutagenesisFalak Sher, Mir Hossain, Davide Seruggia, et al.
The Journal of Allergy and Clinical Immunology|March 5, 2014
Autosomal recessive phosphoglucomutase 3 (PGM3) mutations link glycosylation defects to atopy, immune deficiency, autoimmunity, and neurocognitive impairmentYu Zhang, Xiaomin Yu, Mie Ichikawa, et al.
Biorxiv : the Preprint Server for Biology|June 5, 2026
Fully Modified SpyCas9 Guide RNAs Enable Robust Genome Editing In Cells and In VivoKim Anh Vu, Han Zhang, Nadia Amrani, et al.
Molecular Genetics and Metabolism|May 28, 2014
Three rare diseases in one Sib pair: RAI1, PCK1, GRIN2B mutations associated with Smith-Magenis Syndrome, cytosolic PEPCK deficiency and NMDA receptor glutamate insensitivityDavid R Adams, Hongjie Yuan, Todd Holyoak, et al.
Journal of Neurogenetics|May 10, 2021
Compound heterozygous <i>KCTD7</i> variants in progressive myoclonus epilepsyElizabeth A Burke, Morgan Sturgeon, Diane B Zastrow, et al.
Molecular Genetics and Metabolism|May 7, 2015
Expanding the clinical and molecular characteristics of PIGT-CDG, a disorder of glycosylphosphatidylinositol anchorsChristina Lam, Gretchen A Golas, Mariska Davids, et al.
Blood Advances|November 8, 2019
Genome editing of HBG1 and HBG2 to induce fetal hemoglobinJean-Yves Métais, Phillip A Doerfler, Thiyagaraj Mayuranathan, et al.
Biorxiv : the Preprint Server for Biology|January 30, 2023
Functional gene delivery to and across brain vasculature of systemic AAVs with endothelial-specific tropism in rodents and broad tropism in primatesXinhong Chen, Damien A Wolfe, Dhanesh Sivadasan Bindu, et al.
Pageof 113