Results 231 to 240 of about 62,588 (334)
Abstract The purpose of this exploratory investigation was to determine if acute post‐exercise skeletal muscle myosin heavy chain fragmentation (MyHCfrag) coincides with alterations in molecular chaperones and proteolytic enzymes, select markers of mammalian target of rapamycin complex 1 (mTORC1) signalling, and/or specific gene expression signatures ...
Dakota R. Tiede +10 more
wiley +1 more source
The aggregate proteome of Caenorhabditis elegans mitochondria implicates shared mechanisms of aging and Alzheimer's disease. [PDF]
Pahal S +5 more
europepmc +1 more source
Glial cells in the heart: Implications for their roles in health and disease
Abstract figure legend Schematic representation of cardiac autonomic ganglia within epicardial fat pads (posterior heart surface shown), containing vagal postganglionic neuron cell bodies, associated fibres, and glia. These ganglia receive cholinergic input from vagal preganglionic neurons and adrenergic input from sympathetic postganglionic neurons ...
Svetlana Mastitskaya +2 more
wiley +1 more source
Form follows function: morphology as a map of mechanisms in neurodegenerative disease pathology. [PDF]
Lee EB.
europepmc +1 more source
Abstract figure legend Mitochondria are highly dynamic organelles that continuously remodel their architecture through coordinated cycles of fusion and fission. This review examines the four key GTPases that orchestrate mitochondrial dynamics in mammals: MFN1, MFN2, OPA1, and DRP1.
Rémi Chaney +4 more
wiley +1 more source
Age-related immune states and PD-1 blockade: mechanisms and strategies for the elderly. [PDF]
Yaguchi T, Chamoto K, Honjo T.
europepmc +1 more source
Adaptive preconditioning in neurological diseases – therapeutic insights from proteostatic perturbations [PDF]
et al,, Urano, Fumihiko
core +1 more source
A Meta‐Analysis to Unveil the Diagnostic Gaps in Anderson–Fabry Disease in Women
ABSTRACT Anderson–Fabry disease (AFD) is an X‐linked lysosomal storage disorder caused by mutations in the GLA gene, leading to deficient α‐galactosidase A activity. Although historically considered a male disease, it is now recognized that heterozygous women can present with a wide range of symptoms. However, diagnosis in women remains challenging, as
L. Lenzini +6 more
wiley +1 more source
Autophagy in proteostasis and aging in Caenorhabditis elegans. [PDF]
Lange CM, Higuchi-Sanabria R, Kumsta C.
europepmc +1 more source
Human Cyclophilins—An Emerging Class of Drug Targets
ABSTRACT Cyclophilins are a family of enzymes with peptidyl‐prolyl isomerase activity found in all cells of all organisms. To date, 17 cyclophilin isoforms have been identified in the human body, participating in diverse biological processes. Consequently, cyclophilins have emerged as promising targets for drug development to address a wide array of ...
Katarina Jurkova +3 more
wiley +1 more source

