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Journal of Neuromuscular Diseases|January 8, 2019
Report of a TREAT-NMD/World Duchenne Organisation Meeting on Dystrophin Quantification MethodologyAnnemieke Aartsma-Rus, Jennifer Morgan, Pallavi Lonkar, et al.
JCI Insight|January 25, 2019
A recombinant human IgG1 Fc multimer designed to mimic the active fraction of IVIG in autoimmunityXiaoyu Zhang, Jane Owens, Henrik S Olsen, et al.
Molecular Therapy. Methods & Clinical Development|November 11, 2024
Single cell and TCR analysis of immune cells from AAV gene therapy-dosed Duchenne muscular dystrophy patientsMichael R Emami, Mark A Brimble, Alejandro Espinoza, et al.
Journal of Medicinal Chemistry|February 18, 2014
1-(2-Hydroxy-2-methyl-3-phenoxypropanoyl)indoline-4-carbonitrile derivatives as potent and tissue selective androgen receptor modulatorsEugene L Piatnitski Chekler, Rayomond Unwalla, Taukeer A Khan, et al.
The Journal of Pharmacology and Experimental Therapeutics|December 16, 2011
Osteogenic effects of a potent Src-over-Abl-selective kinase inhibitor in the mouseRichard J Murrills, Shoichi Fukayama, Frank Boschelli, et al.
European Heart Journal|August 8, 2024
KCNQ1 suppression-replacement gene therapy in transgenic rabbits with type 1 long QT syndromeSahej Bains, Lucilla Giammarino, Saranda Nimani, et al.
European Heart Journal|August 30, 2025
AAV9-mediated KCNH2 suppression-replacement gene therapy in a transgenic rabbit model of type 1 short QT syndromeSaranda Nimani, Sahej Bains, Nicolò Alerni, et al.
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