Yang Q, Abebe J, Mai M, Rudy G, Kim S, Devinsky O
EMBO J. 2024; 43(17):3733-3751.
PMID: 39039289
PMC: 11377749.
DOI: 10.1038/s44318-024-00158-6.
Kiperman T, Ma K
Int J Mol Sci. 2024; 25(9).
PMID: 38731986
PMC: 11083552.
DOI: 10.3390/ijms25094767.
Florio F, Vencato S, Papa F, Libergoli M, Kheir E, Ghzaiel I
EMBO Mol Med. 2023; 15(12):e17405.
PMID: 37927228
PMC: 10701616.
DOI: 10.15252/emmm.202317405.
Stephenson A, Nicolau S, Vetter T, Dufresne G, Frair E, Sarff J
Mol Ther Methods Clin Dev. 2023; 30:486-499.
PMID: 37706184
PMC: 10495553.
DOI: 10.1016/j.omtm.2023.08.009.
Soussi S, Savchenko L, Rovina D, Iacovoni J, Gottinger A, Vialettes M
Biol Direct. 2023; 18(1):41.
PMID: 37501163
PMC: 10373315.
DOI: 10.1186/s13062-023-00398-2.
Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery.
Hindi S, Petrany M, Greenfeld E, Focke L, Cramer A, Whitt M
Cell. 2023; 186(10):2062-2077.e17.
PMID: 37075755
PMC: 11181154.
DOI: 10.1016/j.cell.2023.03.033.
CRISPR-Editing Therapy for Duchenne Muscular Dystrophy.
Chemello F, Olson E, Bassel-Duby R
Hum Gene Ther. 2023; 34(9-10):379-387.
PMID: 37060194
PMC: 10210224.
DOI: 10.1089/hum.2023.053.
Enveloped viruses pseudotyped with mammalian myogenic cell fusogens target skeletal muscle for gene delivery.
Hindi S, Petrany M, Greenfeld E, Focke L, Cramer A, Whitt M
bioRxiv. 2023; .
PMID: 36993357
PMC: 10055243.
DOI: 10.1101/2023.03.17.533157.
P2 Receptor Signaling in Motor Units in Muscular Dystrophy.
Khairullin A, Grishin S, Ziganshin A
Int J Mol Sci. 2023; 24(2).
PMID: 36675094
PMC: 9865441.
DOI: 10.3390/ijms24021587.
Development of Therapeutic RNA Manipulation for Muscular Dystrophy.
Saifullah , Motohashi N, Tsukahara T, Aoki Y
Front Genome Ed. 2022; 4:863651.
PMID: 35620642
PMC: 9127466.
DOI: 10.3389/fgeed.2022.863651.
CRISPR Therapeutics for Duchenne Muscular Dystrophy.
Erkut E, Yokota T
Int J Mol Sci. 2022; 23(3).
PMID: 35163754
PMC: 8836469.
DOI: 10.3390/ijms23031832.
Toward the correction of muscular dystrophy by gene editing.
Olson E
Proc Natl Acad Sci U S A. 2021; 118(22).
PMID: 34074727
PMC: 8179164.
DOI: 10.1073/pnas.2004840117.
Essential role for InSyn1 in dystroglycan complex integrity and cognitive behaviors in mice.
Uezu A, Hisey E, Kobayashi Y, Gao Y, Bradshaw T, Devlin P
Elife. 2019; 8.
PMID: 31829939
PMC: 6944460.
DOI: 10.7554/eLife.50712.
In vivo non-invasive monitoring of dystrophin correction in a new Duchenne muscular dystrophy reporter mouse.
Amoasii L, Li H, Zhang Y, Min Y, Sanchez-Ortiz E, Shelton J
Nat Commun. 2019; 10(1):4537.
PMID: 31586095
PMC: 6778191.
DOI: 10.1038/s41467-019-12335-x.
Applications of CRISPR/Cas9 for the Treatment of Duchenne Muscular Dystrophy.
Lim K, Yoon C, Yokota T
J Pers Med. 2018; 8(4).
PMID: 30477208
PMC: 6313657.
DOI: 10.3390/jpm8040038.
Improvement of Duchenne muscular dystrophy phenotype following obestatin treatment.
Gonzalez-Sanchez J, Sanchez-Temprano A, Cid-Diaz T, Pabst-Fernandez R, Mosteiro C, Gallego R
J Cachexia Sarcopenia Muscle. 2018; 9(6):1063-1078.
PMID: 30216693
PMC: 6240759.
DOI: 10.1002/jcsm.12338.
Gene editing restores dystrophin expression in a canine model of Duchenne muscular dystrophy.
Amoasii L, Hildyard J, Li H, Sanchez-Ortiz E, Mireault A, Caballero D
Science. 2018; 362(6410):86-91.
PMID: 30166439
PMC: 6205228.
DOI: 10.1126/science.aau1549.
Myoediting: Toward Prevention of Muscular Dystrophy by Therapeutic Genome Editing.
Zhang Y, Long C, Bassel-Duby R, Olson E
Physiol Rev. 2018; 98(3):1205-1240.
PMID: 29717930
PMC: 6335101.
DOI: 10.1152/physrev.00046.2017.
Single-cut genome editing restores dystrophin expression in a new mouse model of muscular dystrophy.
Amoasii L, Long C, Li H, Mireault A, Shelton J, Sanchez-Ortiz E
Sci Transl Med. 2017; 9(418).
PMID: 29187645
PMC: 5749406.
DOI: 10.1126/scitranslmed.aan8081.
RhoA/ROCK inhibition improves the beneficial effects of glucocorticoid treatment in dystrophic muscle: implications for stem cell depletion.
Mu X, Tang Y, Takayama K, Chen W, Lu A, Wang B
Hum Mol Genet. 2017; 26(15):2813-2824.
PMID: 28549178
PMC: 5886088.
DOI: 10.1093/hmg/ddx117.