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Sunitinib inhibits STAT3 phosphorylation in cardiac muscle and prevents cardiomyopathy in the mdx mouse model of Duchenne muscular dystrophy

Human molecular genetics, 2022-07, Vol.31 (14), p.2358-2369

2022

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Vemurafenib improves muscle histopathology in a mouse model of LAMA2-related congenital muscular dystrophy

Disease models & mechanisms, 2023-06, Vol.16 (6)

2023

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A retooled drug that restores ionic balance and cardiac function in dystrophin deficient hearts

International journal of cardiology, 2020-11, Vol.319, p.115-116

2020

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The alpha7 integrin subunit in astrocytes promotes endothelial blood-brain barrier integrity

Development (Cambridge), 2023-03, Vol.150 (6)

2023

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Tetrahydrobiopterin shifts the balance from oxidative stress to NO signalling in Duchenne muscular dystrophy

Acta Physiologica, 2021-07, Vol.232 (3), p.e13675-e13675

2021

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Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy

Proceedings of the National Academy of Sciences - PNAS, 2009-05, Vol.106 (19), p.7991-7996

2009

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Laminin and Integrin in LAMA2-Related Congenital Muscular Dystrophy: From Disease to Therapeutics

Frontiers in molecular neuroscience, 2020-02, Vol.13, p.1-1

2020

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Galectin-1 Protein Therapy Prevents Pathology and Improves Muscle Function in the mdx Mouse Model of Duchenne Muscular Dystrophy

Molecular therapy, 2015-08, Vol.23 (8), p.1285-1297

2015

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Laminin-111 Protein Therapy Reduces Muscle Pathology and Improves Viability of a Mouse Model of Merosin-Deficient Congenital Muscular Dystrophy

The American journal of pathology, 2012-04, Vol.180 (4), p.1593-1602

2012

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A gene therapy approach for the treatment of limb-girdle muscular dystrophy 2C/R5

Molecular therapy. Methods & clinical development, 2023-06, Vol.29, p.160-161

2023

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Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy

Human molecular genetics, 2017-06, Vol.26 (11), p.2018-2033

2017

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Laminin-111 improves muscle repair in a mouse model of merosin-deficient congenital muscular dystrophy

Human molecular genetics, 2014-01, Vol.23 (2), p.383-396

2014

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NMRK2 Gene Is Upregulated in Dilated Cardiomyopathy and Required for Cardiac Function and NAD Levels during Aging

International journal of molecular sciences, 2021-03, Vol.22 (7), p.3534

2021

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Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity

Skeletal muscle, 2020-04, Vol.10 (1), p.8-8, Article 8

2020

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Sunitinib promotes myogenic regeneration and mitigates disease progression in the mdx mouse model of Duchenne muscular dystrophy

Human molecular genetics, 2019-07, Vol.28 (13), p.2120-2132

2019

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Laminin-111 protein therapy enhances muscle regeneration and repair in the GRMD dog model of Duchenne muscular dystrophy

Human molecular genetics, 2019-08, Vol.28 (16), p.2686-2695

2019

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Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy

Human molecular genetics, 2020-08, Vol.29 (13), p.2162-2170

2020

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Mesothelioma cells breaking bad: loss of integrin [alpha]7 promotes cell motility and poor clinical outcomes in patients

The Journal of pathology, 2015-11, Vol.237 (3), p.282

2015

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Mesothelioma cells breaking bad: loss of integrin α7 promotes cell motility and poor clinical outcomes in patients

The Journal of pathology, 2015-11, Vol.237 (3), p.282-284

2015

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Laminin-111 Improves the Anabolic Response to Mechanical Load in Aged Skeletal Muscle

The journals of gerontology. Series A, Biological sciences and medical sciences, 2021-04, Vol.76 (4), p.586-590

2021

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Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice

Journal of applied physiology (1985), 2013-11, Vol.115 (9), p.1388-1392

2013

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Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice

Journal of the American Heart Association, 2022-12, Vol.11 (23), p.e026494-e026494

2022

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Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice

Human molecular genetics, 2012-10, Vol.21 (20), p.4378-4393

2012

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Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin

Human molecular genetics, 2015-04, Vol.24 (7), p.2011-2022

2015

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Activation of AKT signaling promotes cell growth and survival in α7β1 integrin-mediated alleviation of muscular dystrophy

Biochimica et biophysica acta, 2011-04, Vol.1812 (4), p.439-446

2011

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Sunitinib inhibits STAT3 phosphorylation in cardiac muscle and prevents cardiomyopathy in the mdx mouse model of Duchenne muscular dystrophy

Vemurafenib improves muscle histopathology in a mouse model of LAMA2-related congenital muscular dystrophy

A retooled drug that restores ionic balance and cardiac function in dystrophin deficient hearts

The alpha7 integrin subunit in astrocytes promotes endothelial blood-brain barrier integrity

Tetrahydrobiopterin shifts the balance from oxidative stress to NO signalling in Duchenne muscular dystrophy

Laminin-111 protein therapy prevents muscle disease in the mdx mouse model for Duchenne muscular dystrophy

Laminin and Integrin in LAMA2-Related Congenital Muscular Dystrophy: From Disease to Therapeutics

Galectin-1 Protein Therapy Prevents Pathology and Improves Muscle Function in the mdx Mouse Model of Duchenne Muscular Dystrophy

Laminin-111 Protein Therapy Reduces Muscle Pathology and Improves Viability of a Mouse Model of Merosin-Deficient Congenital Muscular Dystrophy

A gene therapy approach for the treatment of limb-girdle muscular dystrophy 2C/R5

Impaired fetal muscle development and JAK-STAT activation mark disease onset and progression in a mouse model for merosin-deficient congenital muscular dystrophy

Laminin-111 improves muscle repair in a mouse model of merosin-deficient congenital muscular dystrophy

NMRK2 Gene Is Upregulated in Dilated Cardiomyopathy and Required for Cardiac Function and NAD Levels during Aging

Transgenic mice expressing tunable levels of DUX4 develop characteristic facioscapulohumeral muscular dystrophy-like pathophysiology ranging in severity

Sunitinib promotes myogenic regeneration and mitigates disease progression in the mdx mouse model of Duchenne muscular dystrophy

Laminin-111 protein therapy enhances muscle regeneration and repair in the GRMD dog model of Duchenne muscular dystrophy

Laminin-111 protein therapy after disease onset slows muscle disease in a mouse model of laminin-α2 related congenital muscular dystrophy

Mesothelioma cells breaking bad: loss of integrin [alpha]7 promotes cell motility and poor clinical outcomes in patients

Mesothelioma cells breaking bad: loss of integrin α7 promotes cell motility and poor clinical outcomes in patients

Laminin-111 Improves the Anabolic Response to Mechanical Load in Aged Skeletal Muscle

Alpha 7 integrin preserves the function of the extensor digitorum longus muscle in dystrophin-null mice

Integrin α7 Mutations Are Associated With Adult-Onset Cardiac Dysfunction in Humans and Mice

Dystrophin and utrophin expression require sarcospan: loss of α7 integrin exacerbates a newly discovered muscle phenotype in sarcospan-null mice

Sarcospan integration into laminin-binding adhesion complexes that ameliorate muscular dystrophy requires utrophin and α7 integrin

Activation of AKT signaling promotes cell growth and survival in α7β1 integrin-mediated alleviation of muscular dystrophy

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