Duchenne 型肌营养不良症的再生生物标志物

S Guiraud, KE Davies - 中国神经再生研究(英文版), 2019 - sjzsyj.com.cn
Skeletal muscle has an extraordinary capacity to regenerate after injury and trauma. The
muscle repair mechanism is a complex process orchestrated by multiple steps. In …

[HTML][HTML] Regenerative biomarkers for Duchenne muscular dystrophy

S Guiraud, KE Davies - Neural regeneration research, 2019 - journals.lww.com
Skeletal muscle has an extraordinary capacity to regenerate after injury and trauma. The
muscle repair mechanism is a complex process orchestrated by multiple steps. In …

Biomarker development to support the clinical development of utrophin modulators for Duchenne muscular dystrophy therapy

J Tinsley, N Janghra, J Morgan, C Sewry… - Neuromuscular …, 2015 - nmd-journal.com
Utrophin is an autosomal ubiquitously expressed protein, with structural homology to
dystrophin. It is found at the muscle sarcolemma in utero and is progressively replaced by …

Utrophin modulator drugs as potential therapies for Duchenne and Becker muscular dystrophies

P Soblechero‐Martín, A López‐Martínez… - Neuropathology and …, 2021 - Wiley Online Library
Utrophin is an autosomal paralogue of dystrophin, a protein whose deficit causes Duchenne
and Becker muscular dystrophies (DMD/BMD). Utrophin is naturally overexpressed at the …

Mild course in atypical Duchenne muscular dystrophy patients is not caused by utrophin overexpression

M Vainzof, L Feitosa, M Canovas… - Neuromuscular …, 2015 - nmd-journal.com
Utrophin is an autosomal ubiquitously expressed protein, with structural homology to
dystrophin. It is found at the muscle sarcolemma in utero and is progressively replaced by …

A-utrophin up-regulation in mdx skeletal muscle is independent of regeneration

AP Weir, JE Morgan, KE Davies - Neuromuscular Disorders, 2004 - Elsevier
Duchenne muscular dystrophy is a fatal childhood disease caused by mutations that abolish
the expression of dystrophin in muscle. Utrophin is a paralogue of dystrophin and can …

[HTML][HTML] Utrophin correlates with disease severity in Duchenne muscular dystrophy

S Guiraud, K Davies - Med, 2023 - Elsevier
This month in Med, the description of an unusually severely affected DMD patient suffering
from a large deletion in the dystrophin gene confirms that absence of utrophin worsens the …

[HTML][HTML] Correlation of utrophin levels with the dystrophin protein complex and muscle fibre regeneration in Duchenne and Becker muscular dystrophy muscle …

N Janghra, JE Morgan, CA Sewry, FX Wilson… - PloS one, 2016 - journals.plos.org
Duchenne muscular dystrophy is a severe and currently incurable progressive
neuromuscular condition, caused by mutations in the DMD gene that result in the inability to …

GP 103: Biomarker development to support the clinical development of utrophin modulators for Duchenne muscular dystrophy therapy

J Tinsley, N Janghra, F Wilson, C Sewry… - Neuromuscular …, 2014 - nmd-journal.com
The continual expression of utrophin protein by pharmacological maintenance of utrophin
transcription in dystrophin deficient muscle fibres is a potential disease modifying treatment …

Identification of novel therapy-responsive protein biomarkers for Duchenne muscular dystrophy by aptamer-based serum proteomics

A Coenen-Stass, G McClorey, R Manzano… - Neuromuscular …, 2015 - nmd-journal.com
Utrophin is an autosomal ubiquitously expressed protein, with structural homology to
dystrophin. It is found at the muscle sarcolemma in utero and is progressively replaced by …