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Academic Journal

Cell Therapy Strategies on Duchenne Muscular Dystrophy: A Systematic Review of Clinical Applications.

  • Authors : Akat A; Life Park Hospital, Cellular and Biological Products Manufacturing Center, Ragıp Kenan Sok. No:8, Ortakoy, 99010, Nicosia (Lefkosa), Cyprus. .; Karaöz E

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/metabolism

  • Source: Stem cell reviews and reports [Stem Cell Rev Rep] 2024 Jan; Vol. 20 (1), pp. 138-158. Date of Electronic Publication: 2023 Nov 13.Publisher: Springer Science+Business Media Country of Publication: United States NLM ID: 101752767 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

Selection-free precise gene repair using high-capacity adenovector delivery of advanced prime editing systems rescues dystrophin synthesis in DMD muscle cells.

  • Authors : Wang Q; Leiden University Medical Centre, Department of Cell and Chemical Biology, Einthovenweg 20, 2333 ZC Leiden, The Netherlands.; Capelletti S

Subjects: Dystrophin*/Dystrophin*/Dystrophin*/genetics ; Dystrophin*/Dystrophin*/Dystrophin*/metabolism ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics

  • Source: Nucleic acids research [Nucleic Acids Res] 2024 Mar 21; Vol. 52 (5), pp. 2740-2757.Publisher: Oxford University Press Country of Publication: England NLM ID: 0411011 Publication Model: Print Cited Medium: Internet ISSN:

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Academic Journal

Comprehensive analysis of genomic complexity in the 5' end coding region of the DMD gene in patients of exons 1-2 duplications based on long-read sequencing.

  • Authors : Shen J; State Key Laboratory of Reproductive Medicine and Offspring Health, Clinical Center of Reproductive Medicine, First Affiliated Hospital, Nanjing Medical University, Jiangsu Province, Nanjing, 210029, China. .; Ding T

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/diagnosis; Humans

  • Source: BMC genomics [BMC Genomics] 2024 Mar 19; Vol. 25 (1), pp. 292. Date of Electronic Publication: 2024 Mar 19.Publisher: BioMed Central Country of Publication: England NLM ID: 100965258 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2164

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Academic Journal

LEDT and Idebenone treatment modulate autophagy and improve regenerative capacity in the dystrophic muscle through an AMPK-pathway.

  • Authors : Silva HNMD; Department of Structural and Functional Biology, Institute of Biology, University of Campinas, Campinas, Brazil.; Fernandes EM

Subjects: Muscle, Skeletal*/Muscle, Skeletal*/Muscle, Skeletal*/metabolism ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/drug therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/metabolism

  • Source: PloS one [PLoS One] 2024 Mar 18; Vol. 19 (3), pp. e0300006. Date of Electronic Publication: 2024 Mar 18 (Print Publication: 2024).Publisher: Public Library of Science Country of Publication: United States NLM ID: 101285081 Publication Model: eCollection Cited Medium: Internet

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Editorial & Opinion

Skipping, Steroids, and Genes: The First 7 Therapies for Duchenne Muscular Dystrophy.

  • Authors : Kang PB; From the Greg Marzolf Jr. Muscular Dystrophy Center, Department of Neurology, and Institute for Translational Neuroscience, University of Minnesota, Minneapolis.

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/drug therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics; Humans

  • Source: Neurology [Neurology] 2024 Mar 12; Vol. 102 (5), pp. e209210. Date of Electronic Publication: 2024 Feb 09.Publisher: Lippincott Williams & Wilkins Country of Publication: United States NLM ID: 0401060 Publication Model: Print-Electronic Cited Medium:

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Academic Journal

fhl2b mediates extraocular muscle protection in zebrafish models of muscular dystrophies and its ectopic expression ameliorates affected body muscles.

  • Authors : Dennhag N; Department of Medical and Translational Biology, Umeå University, Umeå, Sweden.; Department of Clinical Sciences, Ophthalmology, Umeå University, Umeå, Sweden.

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/metabolism ; Oculomotor Muscles*/Oculomotor Muscles*/Oculomotor Muscles*/metabolism

  • Source: Nature communications [Nat Commun] 2024 Mar 02; Vol. 15 (1), pp. 1950. Date of Electronic Publication: 2024 Mar 02.Publisher: Nature Pub. Group Country of Publication: England NLM ID: 101528555 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

[Characteristics and changes of cardiac injury with age in children of Duchenne muscular dystrophy: a prospective cohort study].

  • Authors : Hu M; Department of Radiology, West China Second Hospital, Sichuan University, Key Laboratory of Obstetric & Gynecologic and Pediatric Diseases and Birth Defect of Ministry of Education, Chengdu 610041, China.; Xu T

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/complications ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/diagnosis ; Cardiomyopathies*/Cardiomyopathies*/Cardiomyopathies*/diagnostic imaging

  • Source: Zhonghua er ke za zhi = Chinese journal of pediatrics [Zhonghua Er Ke Za Zhi] 2024 Mar 02; Vol. 62 (3), pp. 223-230.Publisher: Chinese Medical Association Country of Publication: China NLM ID: 0417427 Publication Model: Print Cited Medium: Print ISSN: 0578-1310

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Report

Association of a novel dystrophin (DMD) genetic nonsense variant in a cat with X-linked muscular dystrophy with a mild clinical course.

  • Authors : Muto H; Otakibashi Animal Hospital, Tokyo, Japan.; Yu Y

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/genetics ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/pathology ; Cat Diseases*/Cat Diseases*/Cat Diseases*/genetics

  • Source: Journal of veterinary internal medicine [J Vet Intern Med] 2024 Mar-Apr; Vol. 38 (2), pp. 1160-1166. Date of Electronic Publication: 2024 Feb 28.Publisher: Wiley Periodicals Country of Publication: United States NLM ID: 8708660 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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Academic Journal

HDAC inhibitors as pharmacological treatment for Duchenne muscular dystrophy: a discovery journey from bench to patients.

  • Authors : Mozzetta C; Institute of Molecular Biology and Pathology (IBPM), National Research Council (CNR) of Italy, Rome, Italy.; Sartorelli V

Subjects: Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/drug therapy ; Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/Muscular Dystrophy, Duchenne*/metabolism; Mice

  • Source: Trends in molecular medicine [Trends Mol Med] 2024 Mar; Vol. 30 (3), pp. 278-294. Date of Electronic Publication: 2024 Feb 26.Publisher: Elsevier Science Ltd Country of Publication: England NLM ID: 100966035 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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  • 1-10 of  19,346 results for ""Muscular Dystrophy, Duchenne""