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Keywords: Duchenne muscular dystrophy
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Journal Articles
Dis Model Mech (2022) 15 (3): dmm049291.
Published: 3 March 2022
...Abbe H. Crawford; John C. W. Hildyard; Sophie A. M. Rushing; Dominic J. Wells; Maria Diez-Leon; Richard J. Piercy ABSTRACT Duchenne muscular dystrophy (DMD), a fatal musculoskeletal disease, is associated with neurodevelopmental disorders and cognitive impairment caused by brain dystrophin...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2021) 14 (12): dmm049006.
Published: 16 December 2021
...Chady H. Hakim; Hsiao T. Yang; Matthew J. Burke; James Teixeira; Gregory J. Jenkins; N. Nora Yang; Gang Yao; Dongsheng Duan ABSTRACT Aged dystrophin-null canines are excellent models for studying experimental therapies for Duchenne muscular dystrophy, a lethal muscle disease caused by dystrophin...
Includes: Supplementary data
Journal Articles
Journal Articles
Dis Model Mech (2021) 14 (9): dmm049028.
Published: 21 September 2021
...Amel Saoudi; Faouzi Zarrouki; Catherine Sebrié; Charlotte Izabelle; Aurélie Goyenvalle; Cyrille Vaillend ABSTRACT The exon-52-deleted mdx52 mouse is a critical model of Duchenne muscular dystrophy (DMD), as it features a deletion in a hotspot region of the DMD gene, frequently mutated in patients...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2020) 13 (2): dmm040659.
Published: 10 January 2020
... of Duchenne muscular dystrophy (DMD). Its phenotype is, however, mild, and other mouse models have been explored. The mdx:Cmah −/− mouse carries a human-like mutation in the Cmah gene and has a severe muscle phenotype, but its growth and bone development are unknown. In this study, we compared male mdx...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2020) 13 (2): dmm040840.
Published: 9 December 2019
...Trace L. Stay; Lauren N. Miterko; Marife Arancillo; Tao Lin; Roy V. Sillitoe ABSTRACT Duchenne muscular dystrophy (DMD) is a debilitating and ultimately lethal disease involving progressive muscle degeneration and neurological dysfunction. DMD is caused by mutations in the dystrophin gene, which...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2018) 11 (6): dmm035774.
Published: 13 June 2018
...Dominic J. Wells ABSTRACT Duchenne muscular dystrophy (DMD) is a progressive, fatal, X-linked monogenic muscle disorder caused by mutations in the DMD gene. In order to test treatments for DMD, a range of natural and engineered animal models have been developed, including mice, rats, dogs and pigs...
Journal Articles
Dis Model Mech (2015) 8 (5): 457–466.
Published: 1 May 2015
...Bo Lin; Yang Li; Lu Han; Aaron D. Kaplan; Ying Ao; Spandan Kalra; Glenna C. L. Bett; Randall L. Rasmusson; Chris Denning; Lei Yang ABSTRACT Duchenne muscular dystrophy (DMD) is caused by mutations in the dystrophin gene ( DMD ), and is characterized by progressive weakness in skeletal and cardiac...
Includes: Supplementary data
Journal Articles
Dis Model Mech (2015) 8 (3): 195–213.
Published: 1 March 2015
...Joe W. McGreevy; Chady H. Hakim; Mark A. McIntosh; Dongsheng Duan Duchenne muscular dystrophy (DMD) is a progressive muscle-wasting disorder. It is caused by loss-of-function mutations in the dystrophin gene. Currently, there is no cure. A highly promising therapeutic strategy is to replace...
Includes: Supplementary data