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UnknownGenome-Wide Analysis and Characterization of the Proline-Rich Extensin-like Receptor Kinases (PERKs) Gene Family Reveals Their Role in Different Developmental Stages and Stress Conditions in Wheat (Triticum aestivum L.).
Not available
S-EPMC8880425 | biostudies-literature
UnknownThe incentive role of media companies' executive compensation system in transformation and upgrading: Evidence from listed media companies in China.
Not available
S-EPMC10259802 | biostudies-literature
ProteomicsMitochondrial mistranslation modulated by metabolic stress causes cardiovascular disease and reduced life-span
Changes in the rate and fidelity of mitochondrial protein synthesis impact the metabolic and physiological roles of mitochondria. Here we explored how environmental stress in the form of a high-fat diet modulates mitochondrial translation using mutant mice with error-prone (Mrps12ep/ep) or hyper-acc...
ORGANISM(S): Mus musculus (Mouse) 
2021-09-10 | PXD024633 | Pride
Mitochondria Mouse Heart 
UnknownAustralian and New Zealand medical students' confidence and preparedness to prescribe.
Not available
S-EPMC12001628 | biostudies-literature
UnknownDevelopment and evaluation of a tool (named Evidence Brief) to communicate allied health research translation.
Not available
S-EPMC12542262 | biostudies-literature
UnknownGenome-Wide Identification and Characterization of the PERK Gene Family in Gossypium hirsutum Reveals Gene Duplication and Functional Divergence.
Not available
S-EPMC6479967 | biostudies-literature
UnknownClimate and atmospheric deposition effects on forest water-use efficiency and nitrogen availability across Britain.
Not available
S-EPMC7381603 | biostudies-literature
UnknownMeasuring growth in research capacity and capability of allied health professionals at a regional Australian public health service: 2011-2023.
Not available
S-EPMC12539124 | biostudies-literature
UnknownPhotoswitchable Inhibitors to Optically Control Specific Kinase Activity.
Not available
S-EPMC12439212 | biostudies-literature
ProteomicsTANGO2 binds crystallin alpha B and its loss causes desminopathy
Mutations in the TANGO2 gene cause an autosomal recessive disorder characterised by developmental delay, stress-induced episodic rhabdomyolysis, and cardiac arrhythmias along with severe metabolic crises. Although TANGO2 mutations result in a well characterised disease pathology, the function of TAN...
ORGANISM(S): Mus musculus (Mouse) Homo sapiens (Human) 
2025-04-22 | PXD056037 | Pride
Human Heart Dia Brain Liver Mouse Tango2 
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