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Frontiers in Immunology|January 11, 2021
Modeling MyD88 Deficiency In Vitro Provides New Insights in Its FunctionNils Craig-Mueller, Ruba Hammad, Roland Elling, et al.
Scientific Reports|December 3, 2016
Improved bi-allelic modification of a transcriptionally silent locus in patient-derived iPSC by Cas9 nickaseReto Eggenschwiler, Mohsen Moslem, Mariane Serra Fráguas, et al.
Nature Communications|August 12, 2025
Targeted gene editing and near-universal cDNA insertion of CYBA and CYBB as a treatment for chronic granulomatous diseaseJonas Holst Wolff, Thomas Wisbech Skov, Didde Haslund, et al.
American Journal of Human Genetics|January 31, 2012
Lack of the mitochondrial protein acylglycerol kinase causes Sengers syndromeJohannes A Mayr, Tobias B Haack, Elisabeth Graf, et al.
Medrxiv : the Preprint Server for Health Sciences|April 8, 2024
Data-driven consideration of genetic disorders for global genomic newborn screening programsThomas Minten, Sarah Bick, Sophia Adelson, et al.
Nature Biotechnology|November 28, 2024
Genome editing with the HDR-enhancing DNA-PKcs inhibitor AZD7648 causes large-scale genomic alterationsGrégoire Cullot, Eric J Aird, Moritz F Schlapansky, et al.
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