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Gene Therapy|March 13, 2021
Correction of X-CGD patient HSPCs by targeted CYBB cDNA insertion using CRISPR/Cas9 with 53BP1 inhibition for enhanced homology-directed repairColin L Sweeney, Mara Pavel-Dinu, Uimook Choi, et al.Human Gene Therapy|September 10, 2016
Lentivirus Mediated Correction of Artemis-Deficient Severe Combined ImmunodeficiencyDivya Punwani, Misako Kawahara, Jason Yu, et al.Nature Neuroscience|March 3, 2017
Differentiation of human and murine induced pluripotent stem cells to microglia-like cellsHetal Pandya, Michael J Shen, David M Ichikawa, et al.Proceedings of the National Academy of Sciences of the United States of America|March 6, 2021
Homozygous IL37 mutation associated with infantile inflammatory bowel diseaseZinan Z Zhang, Yu Zhang, Tingyan He, et al.Blood|May 19, 2012
WHIM syndrome caused by a single amino acid substitution in the carboxy-tail of chemokine receptor CXCR4Qian Liu, Haoqian Chen, Teresa Ojode, et al.Blood Advances|January 4, 2018
Gene-edited pseudogene resurrection corrects p47phox-deficient chronic granulomatous diseaseRandall K Merling, Douglas B Kuhns, Colin L Sweeney, et al.Journal of Human Immunity|May 22, 2026
How I Treat: Chronic granulomatous diseaseJennifer W Leiding, Leah H Pettiford, Christopher C Chang, et al.The Journal of Allergy and Clinical Immunology. in Practice|January 16, 2023
Gastrointestinal and Hepatic Manifestations of Chronic Granulomatous DiseaseAlexander H Yang, Brigit Sullivan, Christa S Zerbe, et al.The Journal of Infectious Diseases|July 12, 2012
Serologic reactivity to the emerging pathogen Granulibacter bethesdensisDavid E Greenberg, Adam R Shoffner, Kimberly R Marshall-Batty, et al.Frontiers in Immunology|September 11, 2025
Reliable genetic diagnosis of NCF1 (p47phox)-deficient chronic granulomatous disease using high-throughput sequencingAmy P Hsu, Eric Karlins, Justin Lack, et al.Pageof 19