Pages that link to "Q42950596"
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The following pages link to Mutational hotspots in electron transfer flavoprotein underlie defective folding and function in multiple acyl-CoA dehydrogenase deficiency (Q42950596):
Displaying 10 items.
- Analyzing effects of naturally occurring missense mutations (Q21284966) (← links)
- Human METTL20 methylates lysine residues adjacent to the recognition loop of the electron transfer flavoprotein in mitochondria (Q24300752) (← links)
- Ethylmalonic encephalopathy ETHE1 R163W/R163Q mutations alter protein stability and redox properties of the iron centre. (Q30366542) (← links)
- Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency (Q36040254) (← links)
- Genetic and cellular modifiers of oxidative stress: what can we learn from fatty acid oxidation defects? (Q38160971) (← links)
- Protein Stability, Folding and Misfolding in Human PGK1 Deficiency. (Q38223684) (← links)
- Distinct properties underlie flavin-based electron bifurcation in a novel electron transfer flavoprotein FixAB from Rhodopseudomonas palustris (Q49806528) (← links)
- Adaptive effect of sericin on hepatic mitochondrial conformation through its regulation of apoptosis, autophagy and energy maintenance: a proteomics approach (Q57296283) (← links)
- Experimental and computational evidence on conformational fluctuations as a source of catalytic defects in genetic diseases (Q57578372) (← links)
- Chronic Hypoxia Enhances β-Oxidation-Dependent Electron Transport via Electron Transferring Flavoproteins (Q64246109) (← links)