[HTML][HTML] Stem cells in clinical practice: applications and warnings
D Lodi, T Iannitti, B Palmieri - Journal of Experimental & Clinical Cancer …, 2011 - Springer
Stem cells are a relevant source of information about cellular differentiation, molecular
processes and tissue homeostasis, but also one of the most putative biological tools to treat …
processes and tissue homeostasis, but also one of the most putative biological tools to treat …
What has the mdx mouse model of duchenne muscular dystrophy contributed to our understanding of this disease?
J Manning, D O'Malley - Journal of muscle research and cell motility, 2015 - Springer
Duchenne muscular dystrophy (DMD) is a fatal X-chromosome linked recessive disorder
caused by the truncation or deletion of the dystrophin gene. The most widely used animal …
caused by the truncation or deletion of the dystrophin gene. The most widely used animal …
Proteomics profiling of urine reveals specific titin fragments as biomarkers of Duchenne muscular dystrophy
J Rouillon, A Zocevic, T Leger, C Garcia… - Neuromuscular …, 2014 - Elsevier
Diagnosis of muscular dystrophies is currently based on invasive methods requiring muscle
biopsies or blood tests. The aim of the present study was to identify urinary biomarkers as a …
biopsies or blood tests. The aim of the present study was to identify urinary biomarkers as a …
Contribution of oxidative stress to pathology in diaphragm and limb muscles with Duchenne muscular dystrophy
JH Kim, HB Kwak, LDV Thompson… - Journal of muscle research …, 2013 - Springer
Duchenne muscular dystrophy (DMD) is a degenerative skeletal muscle disease that makes
walking and breathing difficult. DMD is caused by an X-linked (Xp21) mutation in the …
walking and breathing difficult. DMD is caused by an X-linked (Xp21) mutation in the …
Cognitive dysfunction in Duchenne muscular dystrophy: a possible role for neuromodulatory immune molecules
MG Rae, D O'Malley - Journal of neurophysiology, 2016 - journals.physiology.org
Duchenne muscular dystrophy (DMD) is an X chromosome-linked disease characterized by
progressive physical disability, immobility, and premature death in affected boys. Underlying …
progressive physical disability, immobility, and premature death in affected boys. Underlying …
Inspiratory pressure‐generating capacity is preserved during ventilatory and non‐ventilatory behaviours in young dystrophic mdx mice despite profound diaphragm …
DP Burns, KH Murphy, EF Lucking… - The Journal of …, 2019 - Wiley Online Library
Key points Respiratory muscle weakness is a major feature of Duchenne muscular
dystrophy (DMD), yet little is known about the neural control of the respiratory muscles in …
dystrophy (DMD), yet little is known about the neural control of the respiratory muscles in …
Psychosocial challenges in family caregiving with children suffering from Duchenne muscular dystrophy
Abstract Families of children with Duchenne muscular dystrophy (DMD) go through
significant challenges in dealing with the condition. Few studies have looked into the …
significant challenges in dealing with the condition. Few studies have looked into the …
[HTML][HTML] Post-natal induction of PGC-1α protects against severe muscle dystrophy independently of utrophin
Background Duchenne muscle dystrophy (DMD) afflicts 1 million boys in the US and has few
effective treatments. Constitutive transgenic expression of the transcriptional coactivator …
effective treatments. Constitutive transgenic expression of the transcriptional coactivator …
Abnormal lipid metabolism in skeletal muscle tissue of patients with muscular dystrophy: In vitro, high-resolution NMR spectroscopy based observation in early phase …
NK Srivastava, R Yadav, S Mukherjee, L Pal… - Magnetic resonance …, 2017 - Elsevier
Purpose Qualitative (assignment of lipid components) and quantitative (quantification of lipid
components) analysis of lipid components were performed in skeletal muscle tissue of …
components) analysis of lipid components were performed in skeletal muscle tissue of …
[HTML][HTML] Mental retardation in Duchenne muscular dystrophy
F Nardes, APQC Araújo, MG Ribeiro - Jornal de pediatria, 2012 - SciELO Brasil
Objective: To survey the medical literature directed to the study of cognitive dysfunction in
patients with Duchenne muscular dystrophy through description of the milestones of …
patients with Duchenne muscular dystrophy through description of the milestones of …