[HTML][HTML] Stem cell therapy for muscular dystrophies

S Biressi, A Filareto, TA Rando - The Journal of Clinical …, 2020 - Am Soc Clin Investig
Muscular dystrophies are a heterogeneous group of genetic diseases, characterized by
progressive degeneration of skeletal and cardiac muscle. Despite the intense investigation …

Clonal isolation of muscle-derived cells capable of enhancing muscle regeneration and bone healing

JY Lee, Z Qu-Petersen, B Cao, S Kimura… - The Journal of cell …, 2000 - rupress.org
Several recent studies suggest the isolation of stem cells in skeletal muscle, but the
functional properties of these muscle-derived stem cells is still unclear. In the present study …

[HTML][HTML] Combination of inflammation-related cytokines promotes long-term muscle stem cell expansion

X Fu, J Xiao, Y Wei, S Li, Y Liu, J Yin, K Sun, H Sun… - Cell research, 2015 - nature.com
Muscle stem cells (MuSCs, satellite cells) are the major contributor to muscle regeneration.
Like most adult stem cells, long-term expansion of MuSCs in vitro is difficult. The in vivo …

Isolation of a slowly adhering cell fraction containing stem cells from murine skeletal muscle by the preplate technique

B Gharaibeh, A Lu, J Tebbets, B Zheng, J Feduska… - Nature protocols, 2008 - nature.com
This protocol details a procedure, known as the modified preplate technique, which is
currently used in our laboratory to isolate muscle cells on the basis of selective adhesion to …

Stem cell-based therapies for Duchenne muscular dystrophy

C Sun, C Serra, G Lee, KR Wagner - Experimental neurology, 2020 - Elsevier
Muscular dystrophies are a group of genetic muscle disorders that cause progressive
muscle weakness and degeneration. Within this group, Duchenne muscular dystrophy …

Dynamics of myoblast transplantation reveal a discrete minority of precursors with stem cell–like properties as the myogenic source

JR Beauchamp, JE Morgan, CN Pagel… - The Journal of cell …, 1999 - rupress.org
Myoblasts, the precursors of skeletal muscle fibers, can be induced to withdraw from the cell
cycle and differentiate in vitro. Recent studies have also identified undifferentiated …

[HTML][HTML] Concordant but varied phenotypes among Duchenne muscular dystrophy patient-specific myoblasts derived using a human iPSC-based model

IY Choi, HT Lim, K Estrellas, J Mula, TV Cohen… - Cell reports, 2016 - cell.com
Duchenne muscular dystrophy (DMD) remains an intractable genetic disease. Althogh there
are several animal models of DMD, there is no human cell model that carries patient-specific …

Development of approaches to improve cell survival in myoblast transfer therapy

Z Qu, L Balkir, JCT Van Deutekom… - The Journal of cell …, 1998 - rupress.org
Myoblast transplantation has been extensively studied as a gene complementation
approach for genetic diseases such as Duchenne Muscular Dystrophy. This approach has …

Functional skeletal muscle regeneration from differentiating embryonic stem cells

R Darabi, K Gehlbach, RM Bachoo, S Kamath… - Nature medicine, 2008 - nature.com
Little progress has been made toward the use of embryonic stem (ES) cells to study and
isolate skeletal muscle progenitors. This is due to the paucity of paraxial mesoderm …

[HTML][HTML] Muscle and cardiac therapeutic strategies for Duchenne muscular dystrophy: past, present, and future

A Łoboda, J Dulak - Pharmacological Reports, 2020 - Springer
Background Duchenne muscular dystrophy (DMD) is a severe X-linked neuromuscular
childhood disorder that causes progressive muscle weakness and degeneration and results …