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UnknownThe mitochondrial metabolic function of DJ-1 is modulated by 14-3-3β.
Not available
S-EPMC6988861 | biostudies-literature
UnknownAggregation-primed molten globule conformers of the p53 core domain provide potential tools for studying p53C aggregation in cancer.
Not available
S-EPMC6065177 | biostudies-literature
MetabolomicsClenbuterol exerts antidiabetic activity through metabolic reprogramming of skeletal muscle cells
Activation of the sympathetic nervous system causes pronounced metabolic changes that are mediated by multiple adrenergic receptor subtypes. Systemic treatment with β2-adrenergic receptor agonists results in multiple beneficial metabolic effects, including improved glucose homeostasis. To...
2022-08-26 | MTBLS467 | MetaboLights
UnknownAnomalous structural dynamics of minimally frustrated residues in cardiac troponin C triggers hypertrophic cardiomyopathy.
Not available
S-EPMC8171346 | biostudies-literature
UnknownAmide hydrogens reveal a temperature-dependent structural transition that enhances site-II Ca2+-binding affinity in a C-domain mutant of cardiac troponin C.
Not available
S-EPMC5429600 | biostudies-literature
UnknownA Bcl-xL-Drp1 complex regulates synaptic vesicle membrane dynamics during endocytosis.
Not available
S-EPMC3725990 | biostudies-literature
UnknownIdentity, structure, and function of the mitochondrial permeability transition pore: controversies, consensus, recent advances, and future directions.
Not available
S-EPMC10406888 | biostudies-literature
ProteomicsGlycoproteomics identify disease-associated N-glycans and reduced occupancy of glycosylation sites in PMM2-CDG
The routine diagnostic pathway for congenital disorders of glycosylation (CDG) relies on carbohydrate deficient transferrin, a test that incompletely captures defects in N linked glycosylation and may yield false negative results even in classical N glycosylation disorders such as PMM2 CDG. To explo...
ORGANISM(S): Homo sapiens (Human) 
2026-09-28 | PXD080194 | Pride
N‐linked glycosylation Carbohydrate metabolism Glycoproteomics Congenital disorders of glycosylation (cdg) Glycopeptide Glycomics Biomarker Inborn error of metabolism 
UnknownAn uncoupling channel within the c-subunit ring of the F1FO ATP synthase is the mitochondrial permeability transition pore.
Not available
S-EPMC4115574 | biostudies-literature
UnknownGlobal, regional, and national burden of Alzheimer's disease and other dementias, 1990-2016: a systematic analysis for the Global Burden of Disease Study 2016.
Not available
S-EPMC6291454 | biostudies-literature
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