The role of CD34 expression and cellular fusion in the regeneration capacity of myogenic progenitor cells
RJ Jankowski, BM Deasy, B Cao… - Journal of Cell …, 2002 - journals.biologists.com
Characterization of myogenic subpopulations has traditionally been performed
independently of their functional performance following transplantation. Using the preplate …
independently of their functional performance following transplantation. Using the preplate …
Intramuscular grafts of myoblasts genetically modified to secrete glial cell line-derived neurotrophic factor prevent motoneuron loss and disease progression in a …
MH Mohajeri, DA Figlewicz, MC Bohn - Human gene therapy, 1999 - liebertpub.com
Effects of ex vivo GDNF gene delivery on the degeneration of motoneurons were studied in
the G1H transgenic mouse model of familial ALS carrying a human superoxide dismutase …
the G1H transgenic mouse model of familial ALS carrying a human superoxide dismutase …
Muscle satellite cells: exploring the basic biology to rule them
CF Almeida, SA Fernandes… - Stem cells …, 2016 - Wiley Online Library
Adult skeletal muscle is a postmitotic tissue with an enormous capacity to regenerate upon
injury. This is accomplished by resident stem cells, named satellite cells, which were …
injury. This is accomplished by resident stem cells, named satellite cells, which were …
Three distinct cell populations express extracellular matrix proteins and increase in number during skeletal muscle fibrosis
MA Chapman, K Mukund… - … of Physiology-Cell …, 2017 - journals.physiology.org
Tissue extracellular matrix (ECM) provides structural support and creates unique
environments for resident cells (Bateman JF, Boot-Handford RP, Lamandé SR. Nat Rev …
environments for resident cells (Bateman JF, Boot-Handford RP, Lamandé SR. Nat Rev …
Gene delivery for limb-girdle muscular dystrophy type 2D by isolated limb infusion
JR Mendell, LG Chicoine, SA Al-Zaidy… - Human Gene …, 2019 - liebertpub.com
In a previous limb-girdle muscular dystrophy type 2D (LGMD2D) clinical trial, robust alpha-
sarcoglycan gene expression was confirmed following intramuscular gene (SGCA) transfer …
sarcoglycan gene expression was confirmed following intramuscular gene (SGCA) transfer …
Cell therapy strategies on Duchenne muscular dystrophy: A systematic review of clinical applications
Abstract Duchenne Muscular Dystrophy (DMD) is an inherited genetic disorder
characterized by progressive degeneration of muscle tissue, leading to functional disability …
characterized by progressive degeneration of muscle tissue, leading to functional disability …
Stem cells isolated from human dental pulp and amniotic fluid improve skeletal muscle histopathology in mdx/SCID mice
A Pisciotta, M Riccio, G Carnevale, A Lu… - Stem Cell Research & …, 2015 - Springer
Introduction Duchenne muscular dystrophy (DMD), caused by a lack of the functional
structural protein dystrophin, leads to severe muscle degeneration where the patients are …
structural protein dystrophin, leads to severe muscle degeneration where the patients are …
The mitotic clock in skeletal muscle regeneration, disease and cell mediated gene therapy
V Mouly, A Aamiri, A Bigot, RN Cooper… - Acta physiologica …, 2005 - Wiley Online Library
The regenerative capacity of skeletal muscle will depend on the number of available satellite
cells and their proliferative capacity. We have measured both parameters in ageing, and …
cells and their proliferative capacity. We have measured both parameters in ageing, and …
Muscle-derived cell-mediated ex vivo gene therapy for urological dysfunction
We have tested the feasibility of muscle-based gene therapy and tissue engineering for
urological dysfunction using highly purified muscle-derived cells (MDC) that display stem …
urological dysfunction using highly purified muscle-derived cells (MDC) that display stem …
Muscle‐derived stem cells: potential for muscle regeneration
J Huard, B Cao, Z Qu‐Petersen - Birth Defects Research Part C …, 2003 - Wiley Online Library
Duchenne muscular dystrophy (DMD) is a devastating X‐linked muscle disease
characterized by progressive muscle weakness caused by the lack of dystrophin expression …
characterized by progressive muscle weakness caused by the lack of dystrophin expression …