Adding exogenous biglycan or decorin improves tendon formation for equine peritenon and tendon proper cells in vitro

MY Pechanec, TN Boyd, K Baar… - BMC musculoskeletal …, 2020 - Springer
Background Tendon injuries amount to one of the leading causes of career-ending injuries
in horses due to the inability for tendon to completely repair and the high reinjury potential …

Muscle specific kinase protects dystrophic mdx mouse muscles from eccentric contraction‐induced loss of force‐producing capacity

S Trajanovska, J Ban, J Huang… - The Journal of …, 2019 - Wiley Online Library
Key points Adeno‐associated viral vector was used to elevate the expression of muscle
specific kinase (MuSK) and rapsyn (a cytoplasmic MuSK effector protein) in the tibialis …

Muscle repair and regeneration: stem cells, scaffolds, and the contributions of skeletal muscle to amphibian limb regeneration

DJ Milner, JA Cameron - New Perspectives in Regeneration, 2012 - Springer
Skeletal muscle possesses a robust innate capability for repair of tissue damage. Natural
repair of muscle damage is a stepwise process that requires the coordinated activity of a …

Role of proteoglycans and glycosaminoglycans in Duchenne muscular dystrophy

L Carmen, V Maria, JC Morales-Medina… - …, 2019 - academic.oup.com
Duchenne muscular dystrophy (DMD) is an inherited fatal X-linked myogenic disorder with a
prevalence of 1 in 3500 male live births. It affects voluntary muscles, and heart and …

[HTML][HTML] Promising therapeutic approaches of utrophin replacing dystrophin in the treatment of Duchenne muscular dystrophy

R Wu, Y Song, S Wu, Y Chen - Fundamental Research, 2022 - Elsevier
Duchenne muscular dystrophy (DMD) is a serious genetic neuromuscular rare disease that
is prevalent and caused by the mutation/deletion of the X-linked DMD gene that encodes …

Small leucine‐rich proteoglycans (SLRPs): characteristics and function in the intervertebral disc

L Chen, J Liao, E Klineberg… - Journal of Tissue …, 2017 - Wiley Online Library
The intervertebral disc (IVD) is responsible for normal spinal motion and load distribution.
However, degeneration may occur due to age‐and non‐age‐related processes and is …

Impaired muscle spindle function in murine models of muscular dystrophy

L Gerwin, S Rossmanith, C Haupt… - The Journal of …, 2020 - Wiley Online Library
Key points Muscular dystrophy patients suffer from progressive degeneration of skeletal
muscle fibres, sudden spontaneous falls, balance problems, as well as gait and posture …

[HTML][HTML] The era of genomic medicine

K Davies - Clinical medicine, 2013 - Elsevier
It is becoming increasingly clear that genomics is beginning to have a major impact in
guiding diagnoses and treatment of many disorders. As the cost of DNA sequencing …

Pharmacological therapies for muscular dystrophies

H Abdel-Hamid, PR Clemens - Current opinion in neurology, 2012 - journals.lww.com
The field of pharmacological therapies for the muscular dystrophies continues to steadily
advance. It is encouraging that research into new therapies is increasingly exploring …

Identification of decorin derived peptides with a zinc dependent anti-myostatin activity

S Guiraud, L van Wittenberghe, C Georger… - Neuromuscular …, 2012 - Elsevier
Decorin is a member of the small leucine-rich proteoglycan family and it is a component of
the extracellular matrix. Decorin was previously shown to bind different molecules, including …