Skeletal muscle atrophy: From mechanisms to treatments
L Yin, N Li, W Jia, N Wang, M Liang, X Yang… - Pharmacological …, 2021 - Elsevier
Skeletal muscle is a crucial tissue for movement, gestural assistance, metabolic
homeostasis, and thermogenesis. It makes up approximately 40% of the total body weight …
homeostasis, and thermogenesis. It makes up approximately 40% of the total body weight …
Ubiquitylomics: An Emerging Approach for Profiling Protein Ubiquitylation in Skeletal Muscle
SO Lord, HE Johnston, RS Samant… - Journal of cachexia …, 2024 - Wiley Online Library
Skeletal muscle is a highly adaptable tissue, finely tuned by various physiological and
pathological factors. Whilst the pivotal role of skeletal muscle in overall health is widely …
pathological factors. Whilst the pivotal role of skeletal muscle in overall health is widely …
[HTML][HTML] The HERC proteins and the nervous system
EM Pérez-Villegas, R Ruiz, S Bachiller… - Seminars in cell & …, 2022 - Elsevier
The HERC protein family is one of three subfamilies of Homologous to E6AP C-terminus
(HECT) E3 ubiquitin ligases. Six HERC genes have been described in humans, two of which …
(HECT) E3 ubiquitin ligases. Six HERC genes have been described in humans, two of which …
Deregulation of SPOP in cancer
H Zhang, X Jin, H Huang - Cancer research, 2023 - AACR
Speckle-type POZ protein (SPOP) is a substrate-binding adaptor of the CULLIN3/RING-box1
E3 ubiquitin ligase complex. SPOP is frequently mutated in prostate and endometrial …
E3 ubiquitin ligase complex. SPOP is frequently mutated in prostate and endometrial …
Upper motor neurons are a target for gene therapy and UCHL1 is necessary and sufficient to improve cellular integrity of diseased upper motor neurons
B Genç, JH Jara, SS Sanchez, AKB Lagrimas… - Gene therapy, 2022 - nature.com
There are no effective cures for upper motor neuron (UMN) diseases, such as amyotrophic
lateral sclerosis (ALS), primary lateral sclerosis, and hereditary spastic paraplegia. Here, we …
lateral sclerosis (ALS), primary lateral sclerosis, and hereditary spastic paraplegia. Here, we …
[HTML][HTML] Cullin-3 intervenes in muscle atrophy in the elderly by mediating the degradation of nAchRs ubiquitination
J Chen, Q Xu, X Wang, Z Xu, X Chen - Experimental Gerontology, 2023 - Elsevier
Sarcopenia involves in the loss of muscle mass associated with aging, which is the major
cause of progressive muscle weakness and deterioration in older adults. Muscle atrophy is a …
cause of progressive muscle weakness and deterioration in older adults. Muscle atrophy is a …
[HTML][HTML] Prenatal skeletal muscle transcriptome analysis reveals novel microRNA-mRNA networks associated with intrauterine growth restriction in pigs
A Ali, E Murani, F Hadlich, X Liu, K Wimmers… - Cells, 2021 - mdpi.com
Intrauterine growth restriction (IUGR) occurs in 15–20% of pig neonates and poses huge
economic losses to the pig industry. IUGR piglets have reduced skeletal muscle growth …
economic losses to the pig industry. IUGR piglets have reduced skeletal muscle growth …
[HTML][HTML] Bap1/SMN axis in Dpp4+ skeletal muscle mesenchymal cells regulates the neuromuscular system
JH Kim, JS Kang, K Yoo, J Jeong, I Park, JH Park… - JCI insight, 2022 - ncbi.nlm.nih.gov
The survival of motor neuron (SMN) protein is a major component of the pre-mRNA splicing
machinery and is required for RNA metabolism. Although SMN has been considered a …
machinery and is required for RNA metabolism. Although SMN has been considered a …
Ovarian tumor deubiquitinase 6A regulates cell proliferation via deubiquitination of nucleolin and caspase‑7
SH Kim, KH Baek - International Journal of Oncology, 2022 - spandidos-publications.com
Most proteins maintain protein homeostasis via post‑translational modifications, including
the ubiquitin‑proteasome system. Deubiquitinating enzymes (DUBs) have essential …
the ubiquitin‑proteasome system. Deubiquitinating enzymes (DUBs) have essential …
Influence of DUX4 Expression in Facioscapulohumeral Muscular Dystrophy and Possible Treatments
Facioscapulohumeral muscular dystrophy (FSHD) represents the third most common form of
muscular dystrophy and is characterized by muscle weakness and atrophy. FSHD is caused …
muscular dystrophy and is characterized by muscle weakness and atrophy. FSHD is caused …