Time-restricted feeding promotes muscle function through purine cycle and AMPK signaling in Drosophila obesity models

C Livelo, Y Guo, F Abou Daya, V Rajasekaran… - Nature …, 2023 - nature.com
Obesity caused by genetic and environmental factors can lead to compromised skeletal
muscle function. Time-restricted feeding (TRF) has been shown to prevent muscle function …

Time-restricted feeding restores muscle function in Drosophila models of obesity and circadian-rhythm disruption

JE Villanueva, C Livelo, AS Trujillo, S Chandran… - Nature …, 2019 - nature.com
Pathological obesity can result from genetic predisposition, obesogenic diet, and circadian
rhythm disruption. Obesity compromises function of muscle, which accounts for a majority of …

Genetic Control of Muscle Diversification and Homeostasis: Insights from Drosophila

P Poovathumkadavil, K Jagla - Cells, 2020 - mdpi.com
In the fruit fly, Drosophila melanogaster, the larval somatic muscles or the adult thoracic flight
and leg muscles are the major voluntary locomotory organs. They share several …

[HTML][HTML] Genetic and Pathophysiological Basis of Cardiac and Skeletal Muscle Laminopathies

S Bhide, S Chandran, NS Rajasekaran, GC Melkani - Genes, 2024 - mdpi.com
Nuclear lamins, a type V intermediate filament, are crucial components of the nuclear
envelope's inner layer, maintaining nuclear integrity and mediating interactions between the …

Global Proteomic Analysis Reveals Alterations in Differentially Expressed Proteins between Cardiopathic Lamin A/C Mutations

CL Anderson, KA Brown, RJ North… - Journal of Proteome …, 2024 - ACS Publications
Lamin A/C (LMNA) is an important component of nuclear lamina. Mutations cause
arrhythmia, heart failure, and sudden cardiac death. While LMNA-associated …

Cdk8/CDK19 promotes mitochondrial fission through Drp1 phosphorylation and can phenotypically suppress pink1 deficiency in Drosophila

JZ Liao, H Chung, C Shih, KKL Wong, D Dutta… - Nature …, 2024 - nature.com
Cdk8 in Drosophila is the orthologue of vertebrate CDK8 and CDK19. These proteins have
been shown to modulate transcriptional control by RNA polymerase II. We found that …

[HTML][HTML] Modulation of muscle redox and protein aggregation rescues lethality caused by mutant lamins

GS Coombs, JL Rios-Monterrosa, S Lai, Q Dai, AC Goll… - Redox biology, 2021 - Elsevier
Mutations in the human LMNA gene cause a collection of diseases called laminopathies,
which includes muscular dystrophy and dilated cardiomyopathy. The LMNA gene encodes …

Creatine and l-carnitine attenuate muscular laminopathy in the LMNA mutation transgenic zebrafish

SW Pan, HD Wang, HY Hsiao, PJ Hsu, YC Tseng… - Scientific Reports, 2024 - nature.com
Abstract Lamin A/C gene (LMNA) mutations contribute to severe striated muscle
laminopathies, affecting cardiac and skeletal muscles, with limited treatment options. In this …

In silico and in Vivo analysis of amino acid substitutions that cause laminopathies

BE Hinz, SG Walker, A Xiong, RA Gogal… - International journal of …, 2021 - mdpi.com
Mutations in the LMNA gene cause diseases called laminopathies. LMNA encodes lamins A
and C, intermediate filaments with multiple roles at the nuclear envelope. LMNA mutations …

Combined transcriptomic and proteomic profiling to unravel osimertinib, CARP-1 functional mimetic (CFM 4.17) formulation and telmisartan combo treatment in …

R Nimma, AK Kalvala, N Patel, SK Surapaneni, L Sun… - Pharmaceutics, 2022 - mdpi.com
The epidermal growth factor receptor (EGFR) is highly expressed in many non-small cell
lung cancers (NSCLC), necessitating the use of EGFR-tyrosine kinase inhibitors (TKIs) as …