Valeria Tiranti
Fondazione IRCCS Istituto Neurologico Carlo Besta(IT)
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Neurological diseases and metabolism, Porphyrin Metabolism and Disorders
Most-Cited Works
- → Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria(2001)880 cited
- → Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation(2005)752 cited
- → Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance(2000)632 cited
- → Genetic diagnosis of Mendelian disorders via RNA sequencing(2017)584 cited
- → Mutations of SURF-1 in Leigh Disease Associated with Cytochrome c Oxidase Deficiency(1998)526 cited
- → MPV17 encodes an inner mitochondrial membrane protein and is mutated in infantile hepatic mitochondrial DNA depletion(2006)416 cited
- → Loss of ETHE1, a mitochondrial dioxygenase, causes fatal sulfide toxicity in ethylmalonic encephalopathy