Associated Papers
Signal transduction mechanisms in heme-based globin-coupled oxygen sensors with a focus on a histidine kinase (AfGcHK) and a diguanylate cyclase (YddV or EcDosC).
Vávra J et al.
Biological Chemistry, 2022
Dilated Cardiomyopathy due to the Novel MT-CYB Missense Mutation m.14757T>C.
Zarrouk S et al.
Journal of Medical Cases, 2021
Mitochondrial DNA abnormalities provide mechanistic insight and predict reactive oxygen species-stimulating drug efficacy.
Zaidieh T et al.
Bmc Cancer, 2021
Sigmar1's Molecular, Cellular, and Biological Functions in Regulating Cellular Pathophysiology.
Aishwarya R et al.
Frontiers in Physiology, 2021
Mitochondrial Mutations in Cholestatic Liver Disease with Biliary Atresia.
Koh H et al.
Scientific Reports, 2018
Maternally inherited diabetes is associated with a homoplasmic T10003C mutation in the mitochondrial tRNA(Gly) gene.
Liu H et al.
Mitochondrion, 2015
Maternally transmitted late-onset non-syndromic deafness is associated with the novel heteroplasmic T12201C mutation in the mitochondrial tRNAHis gene.
Yan X et al.
Journal of Medical Genetics, 2011
Failures in mitochondrial tRNAMet and tRNAGln metabolism caused by the novel 4401A>G mutation are involved in essential hypertension in a Han Chinese Family.
Li R et al.
Hypertension (dallas, Tex. : 1979), 2009
Mitochondrial transfer RNAMet 4435A>G mutation is associated with maternally inherited hypertension in a Chinese pedigree.
Liu Y et al.
Hypertension (dallas, Tex. : 1979), 2009
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