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  • 1-10 ل  1,143 نتائج ل ""Muscular Dystrophies""

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Academic Journal

Ribozyme-activated mRNA trans-ligation enables large gene delivery to treat muscular dystrophies.

  • Authors : Lindley SR; Aab Cardiovascular Research Institute, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.; Department of Medicine, University of Rochester School of Medicine and Dentistry, Rochester, NY 14642, USA.

Subjects: Dysferlin*/Dysferlin*/Dysferlin*/genetics ; Genetic Therapy*/Genetic Therapy*/Genetic Therapy*/methods ; Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/therapy

  • Source: Science (New York, N.Y.) [Science] 2024 Nov 15; Vol. 386 (6723), pp. 762-767. Date of Electronic Publication: 2024 Nov 14.Publisher: American Association for the Advancement of Science Country of Publication: United States NLM ID: 0404511 Publication Model: Print-Electronic

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Academic Journal

Ambient floor vibration sensing advances the accessibility of functional gait assessments for children with muscular dystrophies.

Subjects: Vibration* ; Gait*/Gait*/Gait*/physiology ; Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/physiopathology

  • Source: Scientific reports [Sci Rep] 2024 May 11; Vol. 14 (1), pp. 10774. Date of Electronic Publication: 2024 May 11.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

System-level analysis of genes mutated in muscular dystrophies reveals a functional pattern associated with muscle weakness distribution.

  • Authors : Ozisik O; Aix Marseille University, INSERM, MMG, Marseille, France. .; Université Paris Cité, INSERM U976, Paris, France. .

Subjects: Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/genetics ; Mutation* ; Muscle Weakness*/Muscle Weakness*/Muscle Weakness*/genetics

  • Source: Scientific reports [Sci Rep] 2024 May 16; Vol. 14 (1), pp. 11225. Date of Electronic Publication: 2024 May 16.Publisher: Nature Publishing Group Country of Publication: England NLM ID: 101563288 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

A knock down strategy for rapid, generic, and versatile modelling of muscular dystrophies in 3D-tissue-engineered-skeletal muscle.

  • Authors : In 't Groen SLM; Department of Clinical Genetics, Erasmus University Medical Center, Rotterdam, 3015 GE, The Netherlands.; Department of Pediatrics, Erasmus University Medical Center, Rotterdam, 3015 GE, The Netherlands.

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*/pathology

  • Source: Skeletal muscle [Skelet Muscle] 2024 Feb 22; Vol. 14 (1), pp. 3. Date of Electronic Publication: 2024 Feb 22.Publisher: BioMed Central Ltd Country of Publication: England NLM ID: 101561193 Publication Model: Electronic Cited Medium: Internet ISSN:

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Academic Journal

Clinical features, imaging findings and molecular data of limb-girdle muscular dystrophies in a cohort of Chinese patients.

  • Authors : Lin F; Department of Neurology and Institute of Neurology, The First Affiliated Hospital of Fujian Medical University, 20 Cha Zhong Road, Fuzhou, 350005, Fujian, China.; Yang K

Subjects: East Asian People* ; Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/diagnosis; Humans Limb-girdle muscular dystrophy, type 2B; Limb-girdle muscular dystrophy type 2A

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2023 Nov 16; Vol. 18 (1), pp. 356. Date of Electronic Publication: 2023 Nov 16.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Academic Journal

PAX7, a Key for Myogenesis Modulation in Muscular Dystrophies through Multiple Signaling Pathways: A Systematic Review.

  • Authors : Rahman NIA; Centre for Tissue Engineering & Regenerative Medicine, Faculty of Medicine, Universiti Kebangsaan Malaysia Medical Centre, Jalan Yaacob Latif, Cheras, Kuala Lumpur 56000, Malaysia.; Lam CL

Subjects: Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/genetics; Humans ; Muscles

  • Source: International journal of molecular sciences [Int J Mol Sci] 2023 Aug 22; Vol. 24 (17). Date of Electronic Publication: 2023 Aug 22.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Modeling Human Muscular Dystrophies in Zebrafish: Mutant Lines, Transgenic Fluorescent Biosensors, and Phenotyping Assays.

  • Authors : Tesoriero C; Department of Biotechnology, University of Verona, 37134 Verona, Italy.; Greco F

Subjects: Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/genetics ; Muscular Diseases*; Animals

  • Source: International journal of molecular sciences [Int J Mol Sci] 2023 May 05; Vol. 24 (9). Date of Electronic Publication: 2023 May 05.Publisher: MDPI Country of Publication: Switzerland NLM ID: 101092791 Publication Model: Electronic Cited Medium: Internet ISSN: 1422-0067

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Academic Journal

Identification of circulating miRNAs differentially expressed in patients with Limb-girdle, Duchenne or facioscapulohumeral muscular dystrophies.

  • Authors : García-Giménez JL; Center for Biomedical Network Research On Rare Diseases (CIBERER), Institute of Health Carlos III, Valencia, Spain.; INCLIVA Health Research Institute, Valencia, Spain.

Subjects: MicroRNAs*/MicroRNAs*/MicroRNAs*/genetics ; Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/genetics ; Muscular Dystrophy, Facioscapulohumeral*/Muscular Dystrophy, Facioscapulohumeral*/Muscular Dystrophy, Facioscapulohumeral*/genetics

  • Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2022 Dec 27; Vol. 17 (1), pp. 450. Date of Electronic Publication: 2022 Dec 27.Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172

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Academic Journal

A 5-year natural history study in LAMA2-related muscular dystrophy and SELENON-related myopathy: the Extended LAST STRONG study.

  • Authors : de Laat ECM; Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.; Houwen-van Opstal SLS

Subjects: Laminin*/Laminin*/Laminin*/genetics ; Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/genetics ; Muscular Dystrophies*/Muscular Dystrophies*/Muscular Dystrophies*/diagnosis

  • Source: BMC neurology [BMC Neurol] 2024 Oct 23; Vol. 24 (1), pp. 409. Date of Electronic Publication: 2024 Oct 23.Publisher: BioMed Central Country of Publication: England NLM ID: 100968555 Publication Model: Electronic Cited Medium: Internet ISSN: 1471-2377

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Academic Journal

Comprehensive Proteomic Analysis of Dysferlinopathy Unveiling Molecular Mechanisms and Biomarkers Linked to Pathological Progression.

  • Authors : Wang D; Department of Molecular Pathology, Clinical Oncology School of Fujian Medical University, Fujian Cancer Hospital, Fuzhou, China.; Center for Bioinformatics, National Infrastructures for Translational Medicine, Institute of Clinical Medicine and Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Beijing, China.

Subjects: Proteomics* ; Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/pathology ; Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/Muscular Dystrophies, Limb-Girdle*/genetics Dysferlinopathy

  • Source: CNS neuroscience & therapeutics [CNS Neurosci Ther] 2024 Oct; Vol. 30 (10), pp. e70065.Publisher: Wiley-Blackwell Country of Publication: England NLM ID: 101473265 Publication Model: Print Cited Medium: Internet ISSN: 1755-5949

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  • 1-10 ل  1,143 نتائج ل ""Muscular Dystrophies""