2023 - Research.com Medicine in Italy Leader Award
2023 - Research.com Genetics in Italy Leader Award
2022 - Research.com Genetics and Molecular Biology in Italy Leader Award
2013 - Grand Prix scientifique de la Fondation NRJ, Institut de France
His primary scientific interests are in Genetics, Mitochondrial DNA, Mitochondrion, Molecular biology and Mutation. His is doing research in Gene, Multiple mitochondrial DNA deletions, Point mutation, Haplotype and Allele, both of which are found in Genetics. His work carried out in the field of Mitochondrion brings together such families of science as Reactive oxygen species and Mitochondrial disease.
His research in Mitochondrial disease intersects with topics in Mitochondrial biogenesis and Pathology. His Molecular biology research also works with subjects such as
Massimo Zeviani focuses on Genetics, Mitochondrial DNA, Mitochondrial disease, Mitochondrion and Molecular biology. His Genetics study frequently links to related topics such as Ataxia. His Mitochondrial DNA research is multidisciplinary, relying on both Respiratory chain, Point mutation and Pathology.
His Mitochondrial disease study combines topics in areas such as Myopathy, Mitochondrial encephalomyopathy, Nuclear gene, Mitochondrial respiratory chain and Mitochondrial biogenesis. His Mitochondrion research incorporates elements of Oxidative phosphorylation, Internal medicine and Endocrinology. In his study, Leigh disease is strongly linked to Cytochrome c oxidase, which falls under the umbrella field of Molecular biology.
The scientist’s investigation covers issues in Mitochondrial disease, Cell biology, Mitochondrion, Mitochondrial DNA and Genetics. He combines subjects such as Phenotype, Disease, Mitochondrial myopathy and Mitochondrial respiratory chain with his study of Mitochondrial disease. Massimo Zeviani studied Mitochondrion and Endocrinology that intersect with Leigh disease.
His Mitochondrial DNA study incorporates themes from Translation and RNase P. Genetics is closely attributed to Ataxia in his research. Massimo Zeviani works mostly in the field of Mutation, limiting it down to topics relating to Molecular biology and, in certain cases, Mitochondrial translation and Mutant.
His primary areas of study are Mitochondrial disease, Mitochondrion, Cell biology, Genetics and Mitochondrial DNA. He has researched Mitochondrial disease in several fields, including Phenotype, Mitochondrial myopathy, Myopathy, Disease and Mitochondrial respiratory chain. His Mitochondrion study combines topics from a wide range of disciplines, such as mitochondrial fusion, Chronic progressive external ophthalmoplegia, Mitochondrial Encephalomyopathies and Parkinsonism.
His studies in Cell biology integrate themes in fields like Autophagy, Mitophagy, Downregulation and upregulation and Programmed cell death. The study of Genetics is intertwined with the study of Molecular biology in a number of ways. His Mitochondrial DNA research integrates issues from Penetrance and Respiratory chain.
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Identification and characterization of a spinal muscular atrophy-determining gene
Suzie Lefebvre;Lydie Bürglen;Sophie Reboullet;Olivier Clermont.
Mitochondrial DNA Deletions in Progressive External Ophthalmoplegia and Kearns-Sayre Syndrome
Carlos T. Moraes;Salvatore Dimauro;Massimo Zeviani;Anne Lombes.
The New England Journal of Medicine (1989)
Deletions of mitochondrial DNA in Kearns‐Sayre syndrome
M. Zeviani;C. T. Moraes;S. DiMauro;H. Nakase.
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.
Johannes N. Spelbrink;Fang Yuan Li;Valeria Tiranti;Kaisu Nikali.
Nature Genetics (2001)
Spastic Paraplegia and OXPHOS Impairment Caused by Mutations in Paraplegin, a Nuclear-Encoded Mitochondrial Metalloprotease
Giorgio Casari;Maurizio De Fusco;Sonia Ciarmatori;Massimo Zeviani.
Oxygen sensing requires mitochondrial ROS but not oxidative phosphorylation
Joslyn K. Brunelle;Eric L. Bell;Nancy M. Quesada;Kristel Vercauteren.
Cell Metabolism (2005)
Massimo Zeviani;Antonella Spinazzola.
An autosomal dominant disorder with multiple deletions of mitochondrial DNA starting at the D-loop region.
Massimo Zeviani;Serenella Servidei;Cinzia Gellera;Enrico Bertini.
Role of Adenine Nucleotide Translocator 1 in mtDNA Maintenance
Jyrki Kaukonen;Jukka K. Juselius;Valeria Tiranti;Aija Kyttälä.
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA
Eric A. Schon;Rosario Rizzuto;Carlos T. Moraes;Hirofumi Nakase.
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