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Cell Stem Cell|January 29, 2021
Dissecting ELANE neutropenia pathogenicity by human HSC gene editingShuquan Rao, Yao Yao, Josias Soares de Brito, 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.
Science (New York, N.Y.)|November 21, 2014
Mouse regulatory DNA landscapes reveal global principles of cis-regulatory evolutionJeff Vierstra, Eric Rynes, Richard Sandstrom, 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.
Blood Advances|December 7, 2019
End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settingsAnn T Farrell, Julie Panepinto, Ankit A Desai, et al.
The Journal of Clinical Investigation|September 8, 2020
BCL11A enhancer-edited hematopoietic stem cells persist in rhesus monkeys without toxicitySelami Demirci, Jing Zeng, Yuxuan Wu, et al.
Proceedings of the National Academy of Sciences of the United States of America|December 17, 2014
Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcomaJennifer A Perry, Adam Kiezun, Peter Tonzi, et al.
Biorxiv : the Preprint Server for Biology|June 9, 2023
Gene editing without ex vivo culture evades genotoxicity in human hematopoietic stem cellsJing Zeng, My Anh Nguyen, Pengpeng Liu, et al.
Nature Genetics|November 24, 2020
Common variants in signaling transcription-factor-binding sites drive phenotypic variability in red blood cell traitsAvik Choudhuri, Eirini Trompouki, Brian J Abraham, et al.
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