Post-natal muscle growth and protein turnover: a narrative review of current understanding

DJ Millward - Nutrition research reviews, 2024 - cambridge.org
A model explaining the dietary-protein-driven post-natal skeletal muscle growth and protein
turnover in the rat is updated, and the mechanisms involved are described, in this narrative …

Therapeutic aspects of cell signaling and communication in Duchenne muscular dystrophy

A Starosta, P Konieczny - Cellular and Molecular Life Sciences, 2021 - Springer
Duchenne muscular dystrophy (DMD) is a devastating chromosome X-linked disease that
manifests predominantly in progressive skeletal muscle wasting and dysfunctions in the …

Long noncoding RNA lncMREF promotes myogenic differentiation and muscle regeneration by interacting with the Smarca5/p300 complex

W Lv, W Jiang, H Luo, Q Tong, X Niu, X Liu… - Nucleic Acids …, 2022 - academic.oup.com
Long noncoding RNAs (lncRNAs) play important roles in the spatial and temporal regulation
of muscle development and regeneration. Nevertheless, the determination of their biological …

Disturbance of calcium homeostasis and myogenesis caused by TET2 deletion in muscle stem cells

H Zhang, S Wang, Q Zhou, Y Liao, W Luo, Z Peng… - Cell Death …, 2022 - nature.com
Skeletal muscle myogenesis is a sophisticated process controlled by genetic and epigenetic
regulators. In animals, one of the key enzymes for the DNA demethylation of 5 …

Rho/SRF inhibitor modulates mitochondrial functions

P Patyal, B Nguyen, X Zhang, G Azhar… - International Journal of …, 2022 - mdpi.com
CCG-1423 is a Rho A pathway inhibitor that has been reported to inhibit Rho/SRF-mediated
transcriptional regulation. Serum response factor and its cofactors, which include ternary …

Determinants of epigenetic resistance to HDAC inhibitors in dystrophic fibro‐adipogenic progenitors

S Consalvi, L Tucciarone, E Macrì, M De Bardi… - EMBO …, 2022 - embopress.org
Pharmacological treatment of Duchenne muscular dystrophy (DMD) with histone
deacetylase inhibitors (HDACi) is currently being tested in clinical trials; however, pre …

An emerging role for epigenetics in cerebral palsy

B Romero, KG Robinson, M Batish… - Journal of Personalized …, 2021 - mdpi.com
Cerebral palsy is a set of common, severe, motor disabilities categorized by a static,
nondegenerative encephalopathy arising in the developing brain and associated with …

Extraocular muscle stem cells exhibit distinct cellular properties associated with non-muscle molecular signatures

DD Girolamo, M Benavente-Diaz, M Murolo… - …, 2024 - journals.biologists.com
Skeletal muscle stem cells (MuSCs) are recognised as functionally heterogeneous. Cranial
MuSCs are reported to have greater proliferative and regenerative capacity when compared …

Dystrophin-and utrophin-based therapeutic approaches for treatment of duchenne muscular dystrophy: a comparative review

S Szwec, Z Kapłucha, JS Chamberlain, P Konieczny - BioDrugs, 2024 - Springer
Duchenne muscular dystrophy is a devastating disease that leads to progressive muscle
loss and premature death. While medical management focuses mostly on symptomatic …

Resolution of fibrosis in mdx dystrophic mouse after oral consumption of N-163 strain of Aureobasidium pullulans produced β-glucan

S Preethy, Y Aoki, K Minegishi, M Iwasaki… - Scientific Reports, 2023 - nature.com
Recent advances in the management of Duchenne muscular dystrophy (DMD), such as
exon skipping and gene therapy, though have reached a clinical stage, the outcome at its …