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Transcriptome analysis of gravitational effects on mouse skeletal muscles under microgravity and artificial 1 g onboard environment

Scientific reports, 2021-04, Vol.11 (1), p.9168-9168, Article 9168

2021

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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

PloS one, 2016-12, Vol.11 (12), p.e0167811-e0167811

2016

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Thiamine treatment preserves cardiac function against ischemia injury via maintaining mitochondrial size and ATP levels

Journal of applied physiology (1985), 2021-01, Vol.130 (1), p.26-35

2021

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Troponin T amino acid mutation (ΔK210) knock-in mice as a neonatal dilated cardiomyopathy model

Pediatric research, 2021-03, Vol.89 (4), p.846-857

2021

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Bodywide skipping of exons 45–55 in dystrophic mdx52 mice by systemic antisense delivery

Proceedings of the National Academy of Sciences - PNAS, 2012-08, Vol.109 (34), p.13763-13768

2012

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Truncated dystrophin ameliorates the dystrophic phenotype of mdx mice by reducing sarcolipin-mediated SERCA inhibition

Biochemical and biophysical research communications, 2018-10, Vol.505 (1), p.51-59

2018

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Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy

Molecular & cellular proteomics, 2020-12, Vol.19 (12), p.2047-2068

2020

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Full-length human dystrophin on human artificial chromosome compensates for mouse dystrophin deficiency in a Duchenne muscular dystrophy mouse model

Scientific reports, 2023-03, Vol.13 (1), p.4360-4360, Article 4360

2023

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Low intensity training of mdx mice reduces carbonylation and increases expression levels of proteins involved in energy metabolism and muscle contraction

Free radical biology & medicine, 2015-05, Vol.82 (4), p.122-136

2015

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Low-Intensity Training and the C5a Complement Antagonist NOX-D21 Rescue the mdx Phenotype through Modulation of Inflammation

The American journal of pathology, 2017-05, Vol.187 (5), p.1147-1161

2017

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Urinary titin is not an early biomarker of skeletal muscle atrophy induced by muscle denervation in mice

PloS one, 2023-08, Vol.18 (8), p.e0289185-e0289185

2023

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Characterization of a novel microRNA, miR-188, elevated in serum of muscular dystrophy dog model

PloS one, 2019-01, Vol.14 (1), p.e0211597

2019

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The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx mice

BMC medicine, 2020-11, Vol.18 (1), p.343-22, Article 343

2020

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Age-Dependent Echocardiographic and Pathologic Findings in a Rat Model with Duchenne Muscular Dystrophy Generated by CRISPR/Cas9 Genome Editing

International Heart Journal, 2020/11/28, Vol.61(6), pp.1279-1284

2020

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Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice

Skeletal muscle, 2017-10, Vol.7 (1), p.23-23, Article 23

2017

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Involvement of Parkin‐mediated mitophagy in the pathogenesis of chronic obstructive pulmonary disease‐related sarcopenia

Journal of cachexia, sarcopenia and muscle, 2022-06, Vol.13 (3), p.1864-1882

2022

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Endogenous Multiple Exon Skipping and Back-Splicing at the DMD Mutation Hotspot

International journal of molecular sciences, 2016-10, Vol.17 (10), p.1722-1722

2016

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Changes in cytosolic Ca2+ dynamics in the sarcoplasmic reticulum associated with the pathology of Duchenne muscular dystrophy

The Journal of Physical Fitness and Sports Medicine, 2016/09/25, Vol.5(4), pp.309-312

2016

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Long-Term Efficacy of Systemic Multiexon Skipping Targeting Dystrophin Exons 45–55 With a Cocktail of Vivo-Morpholinos in Mdx52 Mice

Molecular therapy. Nucleic acids, 2015-02, Vol.4 (2), p.e225-e225, Article e225

2015

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iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin

BMC musculoskeletal disorders, 2020-07, Vol.21 (1), p.479-479, Article 479

2020

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Loss of RNA-Binding Protein Sfpq Causes Long-Gene Transcriptopathy in Skeletal Muscle and Severe Muscle Mass Reduction with Metabolic Myopathy

iScience, 2019-03, Vol.13, p.229-242

2019

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Synthesis of 2′-O-(N-methylcarbamoylethyl) 5-methyl-2-thiouridine and its application to splice-switching oligonucleotides

Bioorganic & medicinal chemistry letters, 2019-01, Vol.29 (2), p.160-163

2019

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Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 mice

PloS one, 2013-07, Vol.8 (7), p.e69194-e69194

2013

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Urinary Titin Is Increased in Patients After Cardiac Surgery

Frontiers in cardiovascular medicine, 2019-02, Vol.6, p.7-7

2019

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Zinc-deficiency induced changes in the distribution of rat white blood cells

Journal of Nutritional Science and Vitaminology, 2009, Vol.55(2), pp.162-169

2009

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Transcriptome analysis of gravitational effects on mouse skeletal muscles under microgravity and artificial 1 g onboard environment

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

Thiamine treatment preserves cardiac function against ischemia injury via maintaining mitochondrial size and ATP levels

Troponin T amino acid mutation (ΔK210) knock-in mice as a neonatal dilated cardiomyopathy model

Bodywide skipping of exons 45–55 in dystrophic mdx52 mice by systemic antisense delivery

Truncated dystrophin ameliorates the dystrophic phenotype of mdx mice by reducing sarcolipin-mediated SERCA inhibition

Mutation-independent Proteomic Signatures of Pathological Progression in Murine Models of Duchenne Muscular Dystrophy

Full-length human dystrophin on human artificial chromosome compensates for mouse dystrophin deficiency in a Duchenne muscular dystrophy mouse model

Low intensity training of mdx mice reduces carbonylation and increases expression levels of proteins involved in energy metabolism and muscle contraction

Low-Intensity Training and the C5a Complement Antagonist NOX-D21 Rescue the mdx Phenotype through Modulation of Inflammation

Urinary titin is not an early biomarker of skeletal muscle atrophy induced by muscle denervation in mice

Characterization of a novel microRNA, miR-188, elevated in serum of muscular dystrophy dog model

The nSMase2/Smpd3 gene modulates the severity of muscular dystrophy and the emotional stress response in mdx mice

Age-Dependent Echocardiographic and Pathologic Findings in a Rat Model with Duchenne Muscular Dystrophy Generated by CRISPR/Cas9 Genome Editing

Treatment with the anti-IL-6 receptor antibody attenuates muscular dystrophy via promoting skeletal muscle regeneration in dystrophin-/utrophin-deficient mice

Involvement of Parkin‐mediated mitophagy in the pathogenesis of chronic obstructive pulmonary disease‐related sarcopenia

Endogenous Multiple Exon Skipping and Back-Splicing at the DMD Mutation Hotspot

Changes in cytosolic Ca2+ dynamics in the sarcoplasmic reticulum associated with the pathology of Duchenne muscular dystrophy

Long-Term Efficacy of Systemic Multiexon Skipping Targeting Dystrophin Exons 45–55 With a Cocktail of Vivo-Morpholinos in Mdx52 Mice

iNOS is not responsible for RyR1 S-nitrosylation in mdx mice with truncated dystrophin

Loss of RNA-Binding Protein Sfpq Causes Long-Gene Transcriptopathy in Skeletal Muscle and Severe Muscle Mass Reduction with Metabolic Myopathy

Synthesis of 2′-O-(N-methylcarbamoylethyl) 5-methyl-2-thiouridine and its application to splice-switching oligonucleotides

Mutation types and aging differently affect revertant fiber expansion in dystrophic mdx and mdx52 mice

Urinary Titin Is Increased in Patients After Cardiac Surgery

Zinc-deficiency induced changes in the distribution of rat white blood cells

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