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Annual Review of Medicine|October 26, 2018
Emerging Genetic Therapy for Sickle Cell DiseaseStuart H Orkin, Daniel E BauerCurrent Opinion in Pediatrics|December 16, 2010
Update on fetal hemoglobin gene regulation in hemoglobinopathiesDaniel E Bauer, Stuart H OrkinMolecular Therapy : the Journal of the American Society of Gene Therapy|October 10, 2021
Editing outside the body: Ex vivo gene-modification for β-hemoglobinopathy cellular therapyTolulope O Rosanwo, Daniel E BauerCurrent Opinion in Genetics & Development|September 17, 2015
Hemoglobin switching's surprise: the versatile transcription factor BCL11A is a master repressor of fetal hemoglobinDaniel E Bauer, Stuart H OrkinMethods in Molecular Biology (Clifton, N.J.)|October 28, 2017
Growing and Genetically Manipulating Human Umbilical Cord Blood-Derived Erythroid Progenitor (HUDEP) Cell LinesDivya S Vinjamur, Daniel E BauerGenome Medicine|March 11, 2021
Editing GWAS: experimental approaches to dissect and exploit disease-associated genetic variationShuquan Rao, Yao Yao, Daniel E BauerNature Communications|January 13, 2023
Assessing and advancing the safety of CRISPR-Cas tools: from DNA to RNA editingJianli Tao, Daniel E Bauer, Roberto ChiarleBlood Cells, Molecules & Diseases|September 13, 2017
Curative approaches for sickle cell disease: A review of allogeneic and autologous strategiesDaniel E Bauer, Christian Brendel, Courtney D FitzhughPediatric Blood & Cancer|July 20, 2023
Bidirectional processes linking social determinants of health and pediatric sickle cell anemia management: A qualitative studyKristin A Long, Ariel O Blakey, Christina M Amaro, et al.Journal of Visualized Experiments : Jove|December 31, 2014
Generation of genomic deletions in mammalian cell lines via CRISPR/Cas9Daniel E Bauer, Matthew C Canver, Stuart H OrkinPageof 13