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 …
childhood disorder that causes progressive muscle weakness and degeneration and results …
[HTML][HTML] Targeting Nrf2 for the treatment of Duchenne muscular dystrophy
Imbalances in redox homeostasis can result in oxidative stress, which is implicated in
various pathological conditions including the fatal neuromuscular disease Duchenne …
various pathological conditions including the fatal neuromuscular disease Duchenne …
Oral administration of plumbagin is beneficial in in vivo models of Duchenne muscular dystrophy through control of redox signaling
D Cervia, S Zecchini, L Pincigher, P Roux-Biejat… - Free Radical Biology …, 2024 - Elsevier
Duchenne muscular dystrophy (DMD) is a progressive muscle-wasting disease. Recently
approved molecular/gene treatments do not solve the downstream inflammation-linked …
approved molecular/gene treatments do not solve the downstream inflammation-linked …
miR-378 influences muscle satellite cells and enhances adipogenic potential of fibro-adipogenic progenitors but does not affect muscle regeneration in the glycerol …
O Mucha, P Podkalicka, M Żukowska, E Pośpiech… - Scientific Reports, 2023 - nature.com
Skeletal muscle regeneration relies on the reciprocal interaction between many types of
cells. Regenerative capacity may be altered in different disorders. In our study, we …
cells. Regenerative capacity may be altered in different disorders. In our study, we …
Proteome Profiling of the Dystrophic mdx Mice Diaphragm
O Mucha, M Myszka, P Podkalicka, B Świderska… - Biomolecules, 2023 - mdpi.com
Mdx mice with a spontaneous mutation in exon 23 of the Dmd gene represent the most
common model to investigate the pathophysiology of Duchenne muscular dystrophy (DMD) …
common model to investigate the pathophysiology of Duchenne muscular dystrophy (DMD) …
Hydrogen sulfide as a therapeutic option for the treatment of Duchenne muscular dystrophy and other muscle-related diseases
K Kaziród, M Myszka, J Dulak, A Łoboda - Cellular and Molecular Life …, 2022 - Springer
Hydrogen sulfide (H2S) has been known for years as a poisoning gas and until recently
evoked mostly negative associations. However, the discovery of its gasotransmitter functions …
evoked mostly negative associations. However, the discovery of its gasotransmitter functions …
Targeting angiogenesis in Duchenne muscular dystrophy
P Podkalicka, O Mucha, J Dulak, A Loboda - Cellular and Molecular Life …, 2019 - Springer
Duchenne muscular dystrophy (DMD) represents one of the most devastating types of
muscular dystrophies which affect boys already at early childhood. Despite the fact that the …
muscular dystrophies which affect boys already at early childhood. Despite the fact that the …
Redox homeostasis in muscular dystrophies
N Mosca, S Petrillo, S Bortolani, M Monforte, E Ricci… - Cells, 2021 - mdpi.com
In recent years, growing evidence has suggested a prominent role of oxidative stress in the
pathophysiology of several early-and adult-onset muscle disorders, although effective …
pathophysiology of several early-and adult-onset muscle disorders, although effective …
[HTML][HTML] Heme oxygenase-1: A potential therapeutic target for improving skeletal muscle atrophy
Q **ao, CC Sun, CF Tang - Experimental Gerontology, 2023 - Elsevier
Skeletal muscle atrophy is a common muscle disease that is directly caused by an
imbalance in protein synthesis and degradation. At the histological level, it is mainly …
imbalance in protein synthesis and degradation. At the histological level, it is mainly …
[HTML][HTML] Sodium hydrosulfide moderately alleviates the hallmark symptoms of Duchenne muscular dystrophy in mdx mice
M Myszka, O Mucha, P Podkalicka… - European Journal of …, 2023 - Elsevier
Duchenne muscular dystrophy (DMD) is an incurable disease caused by mutations in the X-
linked DMD gene that encodes a structural muscle protein, dystrophin. This, in turn, leads to …
linked DMD gene that encodes a structural muscle protein, dystrophin. This, in turn, leads to …