[HTML][HTML] Genetic reduction of the extracellular matrix protein versican attenuates inflammatory cell infiltration and improves contractile function in dystrophic mdx …
There is a persistent, aberrant accumulation of V0/V1 versican in skeletal muscles from
patients with Duchenne muscular dystrophy and in diaphragm muscles from mdx mice …
patients with Duchenne muscular dystrophy and in diaphragm muscles from mdx mice …
[HTML][HTML] Glucocorticoids improve myogenic differentiation in vitro by suppressing the synthesis of versican, a transitional matrix protein overexpressed in dystrophic …
N McRae, L Forgan, B McNeill, A Addinsall… - International journal of …, 2017 - mdpi.com
In Duchenne muscular dystrophy (DMD), a dysregulated extracellular matrix (ECM) directly
exacerbates pathology. Glucocorticoids are beneficial therapeutics in DMD, and have …
exacerbates pathology. Glucocorticoids are beneficial therapeutics in DMD, and have …
[HTML][HTML] Treatment of Dystrophic mdx Mice with an ADAMTS-5 Specific Monoclonal Antibody Increases the Ex Vivo Strength of Isolated Fast Twitch Hindlimb Muscles
AB Addinsall, LG Forgan, NL McRae, RW Kelly… - Biomolecules, 2020 - mdpi.com
Aberrant extracellular matrix synthesis and remodeling contributes to muscle degeneration
and weakness in Duchenne muscular dystrophy (DMD). ADAMTS-5, a secreted …
and weakness in Duchenne muscular dystrophy (DMD). ADAMTS-5, a secreted …
Versican in inflammation and tissue remodeling: the impact on lung disorders
A Andersson-Sjöland, O Hallgren, S Rolandsson… - …, 2015 - academic.oup.com
Versican is a proteoglycan that has many different roles in tissue homeostasis and
inflammation. The biochemical structure comprises four different types of the core protein …
inflammation. The biochemical structure comprises four different types of the core protein …
An anti-ADAMTS1 treatment relieved muscle dysfunction and fibrosis in dystrophic mice
Y Wang, Y Xiao, Y Zheng, L Yang, D Wang - Life Sciences, 2021 - Elsevier
Abstract Duchenne Muscular Dystrophy (DMD) is caused by mutations in the dystrophin
gene, accompanied by aberrant extracellular matrix synthesis and muscle damage …
gene, accompanied by aberrant extracellular matrix synthesis and muscle damage …
Uniform sarcolemmal dystrophin expression is required to prevent extracellular microRNA release and improve dystrophic pathology
TLE van Westering, Y Lomonosova… - Journal of Cachexia …, 2020 - Wiley Online Library
Background Duchenne muscular dystrophy (DMD) is a fatal muscle‐wasting disorder
caused by genetic loss of dystrophin protein. Extracellular microRNAs (ex‐miRNAs) are …
caused by genetic loss of dystrophin protein. Extracellular microRNAs (ex‐miRNAs) are …
[HTML][HTML] Versican processing by a disintegrin-like and metalloproteinase domain with thrombospondin-1 repeats proteinases-5 and-15 facilitates myoblast fusion
Skeletal muscle development and regeneration requires the fusion of myoblasts into
multinucleated myotubes. Because the enzymatic proteolysis of a hyaluronan and versican …
multinucleated myotubes. Because the enzymatic proteolysis of a hyaluronan and versican …
[HTML][HTML] Temporal expression and spatial distribution of the proteoglycan versican during cardiac fibrosis development
A Sasi, A Romaine, PM Erusappan, AO Melleby… - Matrix Biology Plus, 2023 - Elsevier
Cardiac fibrosis is a central pathological feature in several cardiac diseases, but the
underlying molecular players are insufficiently understood. The extracellular matrix …
underlying molecular players are insufficiently understood. The extracellular matrix …
[HTML][HTML] Characterisation of progressive skeletal muscle fibrosis in the Mdx mouse model of duchenne muscular dystrophy: An in vivo and in vitro study
M Giovarelli, F Arnaboldi, S Zecchini… - International Journal of …, 2022 - mdpi.com
Duchenne muscular dystrophy (DMD) is a rare genetic disease leading to progressive
muscle wasting, respiratory failure, and cardiomyopathy. Although muscle fibrosis …
muscle wasting, respiratory failure, and cardiomyopathy. Although muscle fibrosis …
[HTML][HTML] Duchenne muscular dystrophy trajectory in R-DMDdel52 preclinical rat model identifies COMP as biomarker of fibrosis
V Taglietti, K Kefi, I Bronisz-Budzyńska… - Acta Neuropathologica …, 2022 - Springer
Duchenne muscular dystrophy (DMD) is a fatal muscle-wasting disorder caused by
mutations in the Dystrophin gene and for which there is currently no cure. To bridge the gap …
mutations in the Dystrophin gene and for which there is currently no cure. To bridge the gap …