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PGC‐1α overexpression increases transcription factor EB nuclear localization and lysosome abundance in dystrophin‐deficient skeletal muscle

Physiological reports, 2020-02, Vol.8 (4), p.e14383-n/a

2020

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Development of rabbit monoclonal antibodies for detection of alpha-dystroglycan in normal and dystrophic tissue

PloS one, 2014-05, Vol.9 (5), p.e97567-e97567

2014

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Development of Novel Micro-dystrophins with Enhanced Functionality

Molecular therapy, 2019-03, Vol.27 (3), p.623-635

2019

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Viral vector-mediated gene therapies

Current opinion in neurology, 2015-10, Vol.28 (5), p.522-527

2015

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PGC‐1α gene transfer rescues dystrophic muscle from advanced disease progression (884.18)

The FASEB journal, 2014-04, Vol.28 (S1), p.n/a

2014

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Rescue of dystrophic skeletal muscle by PGC-1α involves restored expression of dystrophin-associated protein complex components and satellite cell signaling

American journal of physiology. Regulatory, integrative and comparative physiology, 2013-07, Vol.305 (1), p.R13-R23

2013

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PGC‐1α gene transfer improves muscle function in dystrophic muscle following prolonged disease progress

Experimental physiology, 2015-10, Vol.100 (10), p.1145-1158

2015

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Long-term quercetin dietary enrichment decreases muscle injury in mdx mice

Clinical nutrition (Edinburgh, Scotland), 2015-06, Vol.34 (3), p.515-522

2015

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PGC-1[alpha] gene transfer improves muscle function in dystrophic muscle following prolonged disease progress

Experimental physiology, 2015-10, Vol.100 (10), p.1145

2015

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Twelve hours of heat stress induces inflammatory signaling in porcine skeletal muscle

American journal of physiology. Regulatory, integrative and comparative physiology, 2016-06, Vol.310 (11), p.R1288-R1296

2016

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Histological and biochemical outcomes of cardiac pathology in mdx mice with dietary quercetin enrichment

Experimental physiology, 2015-01, Vol.100 (1), p.12

2015

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Histological and biochemical outcomes of cardiac pathology in mdx mice with dietary quercetin enrichment

Experimental physiology, 2015-01, Vol.100 (1), p.12-22

2015

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Effect of chronic quercetin supplementation on dystrophic cardiac pathology in mdx mice (LB672)

The FASEB journal, 2014-04, Vol.28 (S1), p.n/a

2014

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An antisense microwalk reveals critical role of an intronic position linked to a unique long-distance interaction in pre-mRNA splicing

RNA (Cambridge), 2010-06, Vol.16 (6), p.1167-1181

2010

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Porcine Models of Muscular Dystrophy

ILAR journal, 2015-01, Vol.56 (1), p.116-126

2015

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Porcine Models of Muscular Dystrophy 1

ILAR journal, 2015-05, Vol.56 (1), p.116-126

2015

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Porcine Models of Muscular Dystrophy1

ILAR journal, 2015-05, Vol.56 (1), p.116-126

2015

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Dystrophin insufficiency causes selective muscle histopathology and loss of dystrophin-glycoprotein complex assembly in pig skeletal muscle

The FASEB journal, 2014-04, Vol.28 (4), p.1600-1609

2014

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PCG‐1 alpha over‐expression rescues dystrophic muscle by modifying gene expression

The FASEB journal, 2012-04, Vol.26 (S1)

2012

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Dietary quercetin supplementation alleviates disease related muscle injury in dystrophic muscle

The FASEB journal, 2012-04, Vol.26 (S1)

2012

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Dystrophin insufficiency causes a Becker muscular dystrophy‐like phenotype in swine

The FASEB journal, 2013-04, Vol.27 (S1)

2013

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Rescue of dystrophic skeletal muscle by PGC-1? involves restored expression of dystrophin-associated protein complex components and satellite cell signaling

American journal of physiology. Regulatory, integrative and comparative physiology, 2013-07, Vol.305 (1), p.R13

2013

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PGC‐1α over‐expression rescues dystrophin‐deficient skeletal muscle

The FASEB journal, 2011-04, Vol.25 (S1), p.1051.33-1051.33

2011

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Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies

Hollinger, Katrin

2014

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PGC‐1alpha over‐expression alters the proteome of dystrophin deficient skeletal muscle

The FASEB journal, 2011-04, Vol.25 (S1), p.1051.28-1051.28

2011

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Science & Technology
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Life Sciences & Biomedicine
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Animals
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Dystrophin
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Humans
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Clinical Trials
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Duchenne Muscular Dystrophy
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Disease Models, Animal
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Mice
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Muscle, Skeletal - Metabolism
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Muscular Dystrophy, Duchenne - Metabolism
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Physiology
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Dmd
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Male
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Mice, Inbred Mdx
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Muscular Dystrophy, Duchenne - Pathology
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Proteins
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Gene Expression
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Mortality
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Muscle, Skeletal - Pathology
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PGC‐1α overexpression increases transcription factor EB nuclear localization and lysosome abundance in dystrophin‐deficient skeletal muscle

Development of rabbit monoclonal antibodies for detection of alpha-dystroglycan in normal and dystrophic tissue

Development of Novel Micro-dystrophins with Enhanced Functionality

Viral vector-mediated gene therapies

PGC‐1α gene transfer rescues dystrophic muscle from advanced disease progression (884.18)

Rescue of dystrophic skeletal muscle by PGC-1α involves restored expression of dystrophin-associated protein complex components and satellite cell signaling

PGC‐1α gene transfer improves muscle function in dystrophic muscle following prolonged disease progress

Long-term quercetin dietary enrichment decreases muscle injury in mdx mice

PGC-1[alpha] gene transfer improves muscle function in dystrophic muscle following prolonged disease progress

Twelve hours of heat stress induces inflammatory signaling in porcine skeletal muscle

Histological and biochemical outcomes of cardiac pathology in mdx mice with dietary quercetin enrichment

Histological and biochemical outcomes of cardiac pathology in mdx mice with dietary quercetin enrichment

Effect of chronic quercetin supplementation on dystrophic cardiac pathology in mdx mice (LB672)

An antisense microwalk reveals critical role of an intronic position linked to a unique long-distance interaction in pre-mRNA splicing

Porcine Models of Muscular Dystrophy

Porcine Models of Muscular Dystrophy 1

Porcine Models of Muscular Dystrophy1

Dystrophin insufficiency causes selective muscle histopathology and loss of dystrophin-glycoprotein complex assembly in pig skeletal muscle

PCG‐1 alpha over‐expression rescues dystrophic muscle by modifying gene expression

Dietary quercetin supplementation alleviates disease related muscle injury in dystrophic muscle

Dystrophin insufficiency causes a Becker muscular dystrophy‐like phenotype in swine

Rescue of dystrophic skeletal muscle by PGC-1? involves restored expression of dystrophin-associated protein complex components and satellite cell signaling

PGC‐1α over‐expression rescues dystrophin‐deficient skeletal muscle

Evaluating the PGC-1 alpha pathway and a new preclinical model to advance treatment options for dystrophinopathies

PGC‐1alpha over‐expression alters the proteome of dystrophin deficient skeletal muscle

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