Biochemical and molecular investigations in respiratory chain deficiencies

1994/07/01 by P. Rustin, Pierre Rustin, Dominique Chrétien +11 · 29 citations
Biochemistry, Genetics and Molecular Biology · Medicine · #Mitochondrial Function and Pathology #Metabolism and Genetic Disorders #Congenital Diaphragmatic Hernia Studies

paper · doi:10.1016/0009-8981(94)90055-8

Cited by

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• Individuals with mutations in XPNPEP3, which encodes a mitochondrial protein, develop a nephronophthisis-like nephropathy. [europepmc]
• Low aerobic mitochondrial energy metabolism in poorly- or undifferentiated neuroblastoma. [europepmc]
• SDHA is a tumor suppressor gene causing paraganglioma. [europepmc]
• Spermidine and resveratrol induce autophagy by distinct pathways converging on the acetylproteome. [europepmc]
• Negative regulation of STAT3 protein-mediated cellular respiration by SIRT1 protein. [europepmc]
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• Cancer metabolism, stemness and tumor recurrence: MCT1 and MCT4 are functional biomarkers of metabolic symbiosis in head and neck cancer. [europepmc]
• Divergent mitochondrial biogenesis responses in human cardiomyopathy. [europepmc]
• Disconnecting mitochondrial content from respiratory chain capacity in PGC-1-deficient skeletal muscle. [europepmc]
• NLRP3 inflammasome is activated in fibromyalgia: the effect of coenzyme Q10. [europepmc]
• Mutations in human lipoyltransferase gene LIPT1 cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. [europepmc]
• Diagnosis and management of mitochondrial disease: a consensus statement from the Mitochondrial Medicine Society. [europepmc]
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• Antimicrobial Susceptibility and Antibacterial Mechanism of Limonene against Listeria monocytogenes . [europepmc]
• Accumulation of amyloid precursor protein C-terminal fragments triggers mitochondrial structure, function, and mitophagy defects in Alzheimer's disease models and human brains. [europepmc]