Výsledky vyhledávání - Meng, Jinhong

CD133+ cells derived from skeletal muscles of Duchenne muscular dystrophy patients have a compromised myogenic and muscle regenerative capability Autor Meng, Jinhong, Muntoni, Francesco, Morgan, Jennifer

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Effects of Mini-Dystrophin on Dystrophin-Deficient, Human Skeletal Muscle-Derived Cells Autor Meng, Jinhong, Counsell, John, Morgan, Jennifer E.

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Silencing E3 Ubiqutin ligase ITCH as a potential therapy to enhance chemotherapy efficacy in p53 mutant neuroblastoma cells Autor Meng, Jinhong, Tagalakis, Aristides D., Hart, Stephen L.

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The effect of the muscle environment on the regenerative capacity of human skeletal muscle stem cells Autor Meng, Jinhong, Bencze, Maximilien, Asfahani, Rowan, Muntoni, Francesco, Morgan, Jennifer E

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Human Skeletal Muscle–derived CD133(+) Cells Form Functional Satellite Cells After Intramuscular Transplantation in Immunodeficient Host Mice Autor Meng, Jinhong, Chun, Soyon, Asfahani, Rowan, Lochmüller, Hanns, Muntoni, Francesco, Morgan, Jennifer

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Optimized lentiviral vector to restore full-length dystrophin via a cell-mediated approach in a mouse model of Duchenne muscular dystrophy Autor Meng, Jinhong, Moore, Marc, Counsell, John, Muntoni, Francesco, Popplewell, Linda, Morgan, Jennifer

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Contribution of Human Muscle-Derived Cells to Skeletal Muscle Regeneration in Dystrophic Host Mice Autor Meng, Jinhong, Adkin, Carl F., Xu, Shi-wen, Muntoni, Francesco, Morgan, Jennifer E.

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Mouse Regenerating Myofibers Detected as False-Positive Donor Myofibers with Anti-Human Spectrin Autor Rozkalne, Anete, Adkin, Carl, Meng, Jinhong, Lapan, Ariya, Morgan, Jennifer E., Gussoni, Emanuela

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Delivery of large transgene cassettes by foamy virus vector Autor Sweeney, Nathan Paul, Meng, Jinhong, Patterson, Hayley, Morgan, Jennifer E., McClure, Myra

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Restoration of Functional Full-Length Dystrophin After Intramuscular Transplantation of Foamy Virus-Transduced Myoblasts Autor Meng, Jinhong, Sweeney, Nathan Paul, Doreste, Bruno, Muntoni, Francesco, McClure, Myra, Morgan, Jennifer

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Genotype-Phenotype Associations of IL6 and PRG4 With Conjunctival Fibrosis After Glaucoma Surgery Autor Yu-Wai-Man, Cynthia, Tagalakis, Aristides D., Meng, Jinhong, Bouremel, Yann, Lee, Richard M. H., Virasami, Alex, Hart, Stephen L., Khaw, Peng T.

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Lentiviral vectors can be used for full-length dystrophin gene therapy Autor Counsell, John R., Asgarian, Zeinab, Meng, Jinhong, Ferrer, Veronica, Vink, Conrad A., Howe, Steven J., Waddington, Simon N., Thrasher, Adrian J., Muntoni, Francesco, Morgan, Jennifer E., Danos, Olivier

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Lentiviral vectors can be used for full-length dystrophin gene therapy Autor Counsell, John R., Asgarian, Zeinab, Meng, Jinhong, Ferrer, Veronica, Vink, Conrad A., Howe, Steven J., Waddington, Simon N., Thrasher, Adrian J., Muntoni, Francesco, Morgan, Jennifer E., Danos, Olivier

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Necroptosis mediates myofibre death in dystrophin-deficient mice Autor Morgan, Jennifer E., Prola, Alexandre, Mariot, Virginie, Pini, Veronica, Meng, Jinhong, Hourde, Christophe, Dumonceaux, Julie, Conti, Francesco, Relaix, Frederic, Authier, Francois-Jerôme, Tiret, Laurent, Muntoni, Francesco, Bencze, Maximilien

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Publisher Correction: Necroptosis mediates myofibre death in dystrophin-deficient mice Autor Morgan, Jennifer E., Prola, Alexandre, Mariot, Virginie, Pini, Veronica, Meng, Jinhong, Hourde, Christophe, Dumonceaux, Julie, Conti, Francesco, Relaix, Frederic, Authier, Francois-Jerôme, Tiret, Laurent, Muntoni, Francesco, Bencze, Maximilien

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Erratum: Lentiviral vectors can be used for full-length dystrophin gene therapy Autor Counsell, John R., Asgarian, Zeinab, Meng, Jinhong, Ferrer, Veronica, Vink, Conrad A., Howe, Steven J., Waddington, Simon N., Thrasher, Adrian J., Muntoni, Francesco, Morgan, Jennifer E., Danos, Olivier

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Myostatin inhibition in combination with antisense oligonucleotide therapy improves outcomes in spinal muscular atrophy Autor Zhou, Haiyan, Meng, Jinhong, Malerba, Alberto, Catapano, Francesco, Sintusek, Palittiya, Jarmin, Susan, Feng, Lucy, Lu‐Nguyen, Ngoc, Sun, Lianwen, Mariot, Virginie, Dumonceaux, Julie, Morgan, Jennifer E., Gissen, Paul, Dickson, George, Muntoni, Francesco

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Optogenetic modeling of human neuromuscular circuits in Duchenne muscular dystrophy with CRISPR and pharmacological corrections Autor Paredes-Redondo, Amaia, Harley, Peter, Maniati, Eleni, Ryan, David, Louzada, Sandra, Meng, Jinhong, Kowala, Anna, Fu, Beiyuan, Yang, Fengtang, Liu, Pentao, Marino, Silvia, Pourquié, Olivier, Muntoni, Francesco, Wang, Jun, Lieberam, Ivo, Lin, Yung-Yao

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Dystrophin involvement in peripheral circadian SRF signalling Autor Betts, Corinne A, Jagannath, Aarti, van Westering, Tirsa LE, Bowerman, Melissa, Banerjee, Subhashis, Meng, Jinhong, Falzarano, Maria Sofia, Cravo, Lara, McClorey, Graham, Meijboom, Katharina E, Bhomra, Amarjit, Lim, Wooi Fang, Rinaldi, Carlo, Counsell, John R, Chwalenia, Katarzyna, O’Donovan, Elizabeth, Saleh, Amer F, Gait, Michael J, Morgan, Jennifer E, Ferlini, Alessandra, Foster, Russell G, Wood, Matthew JA

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