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Search life-sciences literature (45,103,589 articles, preprints and more)

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LED therapy plus idebenone treatment targeting calcium and mitochondrial signaling pathways in dystrophic muscle cells.
da Silva HNM, Mizobuti DS, Pereira VA, da Rocha GL, da Cruz MV, de Oliveira AG, Silveira LR, Minatel E
Cell Stress Chaperones, 28(6):773-785, 14 Aug 2023
Cited by: 1 article | PMID: 37578579 | PMCID: PMC10746663
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Calcineurin-Dependent Homeostatic Response of C. elegans Muscle Cells upon Prolonged Activation of Acetylcholine Receptors.
Florin F, Bonneau B, Briseño-Roa L, Bessereau JL, Jospin M
Cells, 12(17):2201, 03 Sep 2023
Cited by: 2 articles | PMID: 37681933 | PMCID: PMC10486475
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Modeling Duchenne Muscular Dystrophy Cardiomyopathy with Patients' Induced Pluripotent Stem-Cell-Derived Cardiomyocytes.
Eisen B, Binah O
Int J Mol Sci, 24(10):8657, 12 May 2023
Cited by: 0 articles | PMID: 37240001 | PMCID: PMC10218670
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Histological Methods to Assess Skeletal Muscle Degeneration and Regeneration in Duchenne Muscular Dystrophy.
Dubuisson N, Versele R, Planchon C, Selvais CM, Noel L, Abou-Samra M, Davis-López de Carrizosa MA
Int J Mol Sci, 23(24):16080, 16 Dec 2022
Cited by: 6 articles | PMID: 36555721 | PMCID: PMC9786356
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Modeling neuromuscular diseases in zebrafish.
Singh J, Patten SA
Front Mol Neurosci, 15:1054573, 13 Dec 2022
Cited by: 5 articles | PMID: 36583079 | PMCID: PMC9794147
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Sulfur amino acid supplementation displays therapeutic potential in a C. elegans model of Duchenne muscular dystrophy.
Ellwood RA, Slade L, Lewis J, Torregrossa R, Sudevan S, Piasecki M, Whiteman M, Etheridge T, Szewczyk NJ
Commun Biol, 5(1):1255, 16 Nov 2022
Cited by: 8 articles | PMID: 36385509 | PMCID: PMC9668843
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Taurine Administration Counteracts Aging-Associated Impingement of Skeletal Muscle Regeneration by Reducing Inflammation and Oxidative Stress.
Barbiera A, Sorrentino S, Fard D, Lepore E, Sica G, Dobrowolny G, Tamagnone L, Scicchitano BM
Antioxidants (Basel), 11(5):1016, 21 May 2022
Cited by: 6 articles | PMID: 35624880 | PMCID: PMC9137670
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Skeletal Ryanodine Receptors Are Involved in Impaired Myogenic Differentiation in Duchenne Muscular Dystrophy Patients.
Meyer P, Notarnicola C, Meli AC, Matecki S, Hugon G, Salvador J, Khalil M, Féasson L, Cances C, Cottalorda J, Desguerre I, Cuisset JM, Sabouraud P, Lacampagne A, Chevassus H, Rivier F, Carnac G
Int J Mol Sci, 22(23):12985, 30 Nov 2021
Cited by: 8 articles | PMID: 34884796 | PMCID: PMC8657486
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Alisporivir Improves Mitochondrial Function in Skeletal Muscle of mdx Mice but Suppresses Mitochondrial Dynamics and Biogenesis.
Dubinin MV, Starinets VS, Talanov EY, Mikheeva IB, Belosludtseva NV, Belosludtsev KN
Int J Mol Sci, 22(18):9780, 10 Sep 2021
Cited by: 17 articles | PMID: 34575944 | PMCID: PMC8464657
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Effect of the Non-Immunosuppressive MPT Pore Inhibitor Alisporivir on the Functioning of Heart Mitochondria in Dystrophin-Deficient mdx Mice.
Dubinin MV, Starinets VS, Talanov EY, Mikheeva IB, Belosludtseva NV, Serov DA, Tenkov KS, Belosludtseva EV, Belosludtsev KN
Biomedicines, 9(9):1232, 16 Sep 2021
Cited by: 9 articles | PMID: 34572419 | PMCID: PMC8466941
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Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype.
Ignatieva E, Smolina N, Kostareva A, Dmitrieva R
Int J Mol Sci, 22(14):7349, 08 Jul 2021
Cited by: 9 articles | PMID: 34298968 | PMCID: PMC8307986
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Caenorhabditis elegans as a Model System for Duchenne Muscular Dystrophy.
Ellwood RA, Piasecki M, Szewczyk NJ
Int J Mol Sci, 22(9):4891, 05 May 2021
Cited by: 7 articles | PMID: 34063069 | PMCID: PMC8125261
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Mitochondrial hydrogen sulfide supplementation improves health in the C. elegans Duchenne muscular dystrophy model.
Ellwood RA, Hewitt JE, Torregrossa R, Philp AM, Hardee JP, Hughes S, van de Klashorst D, Gharahdaghi N, Anupom T, Slade L, Deane CS, Cooke M, Etheridge T, Piasecki M, Antebi A, Lynch GS, Philp A, Vanapalli SA, Whiteman M, Szewczyk NJ
Proc Natl Acad Sci U S A, 118(9):e2018342118, 01 Mar 2021
Cited by: 19 articles | PMID: 33627403 | PMCID: PMC7936346
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A novel chemical-combination screen in zebrafish identifies epigenetic small molecule candidates for the treatment of Duchenne muscular dystrophy.
Farr GH, Morris M, Gomez A, Pham T, Kilroy E, Parker EU, Said S, Henry C, Maves L
Skelet Muscle, 10(1):29, 15 Oct 2020
Cited by: 16 articles | PMID: 33059738 | PMCID: PMC7559456
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Abnormal NFAT5 Physiology in Duchenne Muscular Dystrophy Fibroblasts as a Putative Explanation for the Permanent Fibrosis Formation in Duchenne Muscular Dystrophy.
Herbelet S, De Paepe B, De Bleecker JL
Int J Mol Sci, 21(21):E7888, 24 Oct 2020
Cited by: 5 articles | PMID: 33114289 | PMCID: PMC7660673
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A child with duchenne muscular dystrophy: A case report of a rare diagnosis among Africans.
Nassoro DD, Torres L, Marando R, Mboma L, Mushi S, Habakkuk Mwakyula I
Clin Case Rep, 8(12):2654-2660, 18 Aug 2020
Cited by: 3 articles | PMID: 33363799 | PMCID: PMC7752564
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Adenylosuccinic acid therapy ameliorates murine Duchenne Muscular Dystrophy.
Timpani CA, Goodman CA, Stathis CG, White JD, Mamchaoui K, Butler-Browne G, Gueven N, Hayes A, Rybalka E
Sci Rep, 10(1):1125, 24 Jan 2020
Cited by: 18 articles | PMID: 31980663 | PMCID: PMC6981178
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Tamoxifen in Duchenne muscular dystrophy (TAMDMD): study protocol for a multicenter, randomized, placebo-controlled, double-blind phase 3 trial.
Nagy S, Hafner P, Schmidt S, Rubino-Nacht D, Schädelin S, Bieri O, Fischer D
Trials, 20(1):637, 21 Nov 2019
Cited by: 16 articles | PMID: 31752977 | PMCID: PMC6869203
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Variable cytoplasmic actin expression impacts the sensitivity of different dystrophin-deficient mdx skeletal muscles to eccentric contraction.
Lindsay A, Southern WM, McCourt PM, Larson AA, Hodges JS, Lowe DA, Ervasti JM
FEBS J, 286(13):2562-2576, 11 Apr 2019
Cited by: 8 articles | PMID: 30942954 | PMCID: PMC6613979
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Immune myopathy with large histiocyte-related myofiber necrosis.
Pestronk A, Sinha N, Alhumayyd Z, Ly C, Schmidt R, Bucelli R
Neurology, 92(15):e1763-e1772, 20 Mar 2019
Cited by: 4 articles | PMID: 30894448 | PMCID: PMC6511085
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Sarcolemmal Complement Membrane Attack Complex Deposits During Acute Rejection of Myofibers in Nonhuman Primates.
Skuk D, Tremblay JP
J Neuropathol Exp Neurol, 78(1):38-46, 01 Jan 2019
Cited by: 1 article | PMID: 30481300 | PMCID: PMC6289216
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Characterization and Functional Analysis of Extracellular Vesicles and Muscle-Abundant miRNAs (miR-1, miR-133a, and miR-206) in C2C12 Myocytes and mdx Mice.
Matsuzaka Y, Tanihata J, Komaki H, Ishiyama A, Oya Y, Rüegg U, Takeda SI, Hashido K
PLoS One, 11(12):e0167811, 15 Dec 2016
Cited by: 39 articles | PMID: 27977725 | PMCID: PMC5158003
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Pharmacological therapeutics targeting the secondary defects and downstream pathology of Duchenne muscular dystrophy.
Spinazzola JM, Kunkel LM
Expert Opin Orphan Drugs, 4(11):1179-1194, 18 Oct 2016
Cited by: 20 articles | PMID: 28670506 | PMCID: PMC5487007
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Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.
Allen DG, Whitehead NP, Froehner SC
Physiol Rev, 96(1):253-305, 01 Jan 2016
Cited by: 232 articles | PMID: 26676145 | PMCID: PMC4698395
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Cell membrane integrity in myotonic dystrophy type 1: implications for therapy.
González-Barriga A, Kranzen J, Croes HJ, Bijl S, van den Broek WJ, van Kessel ID, van Engelen BG, van Deutekom JC, Wieringa B, Mulders SA, Wansink DG
PLoS One, 10(3):e0121556, 23 Mar 2015
Cited by: 20 articles | PMID: 25799359 | PMCID: PMC4370802
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1-25 of 258 results

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Search life-sciences literature (45,103,589 articles, preprints and more)

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LED therapy plus idebenone treatment targeting calcium and mitochondrial signaling pathways in dystrophic muscle cells.

Calcineurin-Dependent Homeostatic Response of C. elegans Muscle Cells upon Prolonged Activation of Acetylcholine Receptors.

Modeling Duchenne Muscular Dystrophy Cardiomyopathy with Patients' Induced Pluripotent Stem-Cell-Derived Cardiomyocytes.

Histological Methods to Assess Skeletal Muscle Degeneration and Regeneration in Duchenne Muscular Dystrophy.

Modeling neuromuscular diseases in zebrafish.

Sulfur amino acid supplementation displays therapeutic potential in a C. elegans model of Duchenne muscular dystrophy.

Taurine Administration Counteracts Aging-Associated Impingement of Skeletal Muscle Regeneration by Reducing Inflammation and Oxidative Stress.

Skeletal Ryanodine Receptors Are Involved in Impaired Myogenic Differentiation in Duchenne Muscular Dystrophy Patients.

Alisporivir Improves Mitochondrial Function in Skeletal Muscle of mdx Mice but Suppresses Mitochondrial Dynamics and Biogenesis.

Effect of the Non-Immunosuppressive MPT Pore Inhibitor Alisporivir on the Functioning of Heart Mitochondria in Dystrophin-Deficient mdx Mice.

Skeletal Muscle Mitochondria Dysfunction in Genetic Neuromuscular Disorders with Cardiac Phenotype.

Caenorhabditis elegans as a Model System for Duchenne Muscular Dystrophy.

Mitochondrial hydrogen sulfide supplementation improves health in the C. elegans Duchenne muscular dystrophy model.

A novel chemical-combination screen in zebrafish identifies epigenetic small molecule candidates for the treatment of Duchenne muscular dystrophy.

Abnormal NFAT5 Physiology in Duchenne Muscular Dystrophy Fibroblasts as a Putative Explanation for the Permanent Fibrosis Formation in Duchenne Muscular Dystrophy.

A child with duchenne muscular dystrophy: A case report of a rare diagnosis among Africans.

Adenylosuccinic acid therapy ameliorates murine Duchenne Muscular Dystrophy.

Tamoxifen in Duchenne muscular dystrophy (TAMDMD): study protocol for a multicenter, randomized, placebo-controlled, double-blind phase 3 trial.

Variable cytoplasmic actin expression impacts the sensitivity of different dystrophin-deficient mdx skeletal muscles to eccentric contraction.

Immune myopathy with large histiocyte-related myofiber necrosis.

Sarcolemmal Complement Membrane Attack Complex Deposits During Acute Rejection of Myofibers in Nonhuman Primates.

Characterization and Functional Analysis of Extracellular Vesicles and Muscle-Abundant miRNAs (miR-1, miR-133a, and miR-206) in C2C12 Myocytes and mdx Mice.

Pharmacological therapeutics targeting the secondary defects and downstream pathology of Duchenne muscular dystrophy.

Absence of Dystrophin Disrupts Skeletal Muscle Signaling: Roles of Ca2+, Reactive Oxygen Species, and Nitric Oxide in the Development of Muscular Dystrophy.

Cell membrane integrity in myotonic dystrophy type 1: implications for therapy.

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