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

Ballmann, Christopher ; Hollinger, Katrin ; Selsby, Joshua T ; Amin, Rajesh ; Quindry, John C

Experimental physiology, 2015-01, Vol.100 (1), p.12 [Periódico revisado por pares]

England

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2
PGC‐1α gene transfer improves muscle function in dystrophic muscle following prolonged disease progress
PGC‐1α gene transfer improves muscle function in dystrophic muscle following prolonged disease progress
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PGC‐1α gene transfer improves muscle function in dystrophic muscle following prolonged disease progress

Hollinger, Katrin ; Selsby, Joshua T.

Experimental physiology, 2015-10, Vol.100 (10), p.1145-1158 [Periódico revisado por pares]

England

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3
Angiotensin‐dependent autonomic dysregulation precedes dilated cardiomyopathy in a mouse model of muscular dystrophy
Angiotensin‐dependent autonomic dysregulation precedes dilated cardiomyopathy in a mouse model of muscular dystrophy
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Angiotensin‐dependent autonomic dysregulation precedes dilated cardiomyopathy in a mouse model of muscular dystrophy

Sabharwal, Rasna ; Weiss, Robert M. ; Zimmerman, Kathy ; Domenig, Oliver ; Cicha, Michael Z. ; Chapleau, Mark W.

Experimental physiology, 2015-07, Vol.100 (7), p.776-795 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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4
Targeted genetic therapies for inherited disorders that affect both cardiac and skeletal muscle
Targeted genetic therapies for inherited disorders that affect both cardiac and skeletal muscle
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Targeted genetic therapies for inherited disorders that affect both cardiac and skeletal muscle

Psaras, Yiangos ; Toepfer, Christopher N.

Experimental physiology, 2024-02, Vol.109 (2), p.175-189 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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5
Advances in genetic therapeutic strategies for Duchenne muscular dystrophy
Advances in genetic therapeutic strategies for Duchenne muscular dystrophy
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Advances in genetic therapeutic strategies for Duchenne muscular dystrophy

Guiraud, Simon ; Chen, Huijia ; Burns, David T. ; Davies, Kay E.

Experimental physiology, 2015-12, Vol.100 (12), p.1458-1467 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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6
Striated muscle activator of Rho signalling (STARS) overexpression in the mdx mouse enhances muscle functional capacity and regulates the actin cytoskeleton and oxidative phosphorylation pathways
Striated muscle activator of Rho signalling (STARS) overexpression in the mdx mouse enhances muscle functional capacity and regulates the actin cytoskeleton and oxidative phosphorylation pathways
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Striated muscle activator of Rho signalling (STARS) overexpression in the mdx mouse enhances muscle functional capacity and regulates the actin cytoskeleton and oxidative phosphorylation pathways

Sadler, Kate J. ; Gatta, Paul A. Della ; Naim, Timur ; Wallace, Marita A. ; Lee, Albert ; Zaw, Thiri ; Lindsay, Angus ; Chung, Roger S. ; Bello, Luca ; Pegoraro, Elena ; Lamon, Séverine ; Lynch, Gordon S. ; Russell, Aaron P.

Experimental physiology, 2021-07, Vol.106 (7), p.1597-1611 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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7
Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy
Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy
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Alterations in Notch signalling in skeletal muscles from mdx and dko dystrophic mice and patients with Duchenne muscular dystrophy

Church, Jarrod E. ; Trieu, Jennifer ; Chee, Annabel ; Naim, Timur ; Gehrig, Stefan M. ; Lamon, Séverine ; Angelini, Corrado ; Russell, Aaron P. ; Lynch, Gordon S.

Experimental physiology, 2014-04, Vol.99 (4), p.675-687 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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8
Progress in therapy for Duchenne muscular dystrophy
Progress in therapy for Duchenne muscular dystrophy
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Progress in therapy for Duchenne muscular dystrophy

Fairclough, Rebecca J. ; Bareja, Akshay ; Davies, Kay E.

Experimental physiology, 2011-11, Vol.96 (11), p.1101-1113 [Periódico revisado por pares]

Oxford, UK: Blackwell Publishing Ltd

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9
Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin system
Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin system
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Autonomic, locomotor and cardiac abnormalities in a mouse model of muscular dystrophy: targeting the renin–angiotensin system

Sabharwal, Rasna ; Chapleau, Mark W.

Experimental physiology, 2014-04, Vol.99 (4), p.627-631 [Periódico revisado por pares]

England: John Wiley & Sons, Inc

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