Eric A. Schon mainly focuses on Mitochondrial DNA, Molecular biology, Mitochondrion, Genetics and Respiratory chain. His Mitochondrial DNA study incorporates themes from Genome and Cytochrome c oxidase. His biological study spans a wide range of topics, including Messenger RNA, In situ hybridization, Direct repeat, Transthyretin and Mutant.
His Mitochondrion study combines topics in areas such as Allotopic expression, Endoplasmic reticulum, Neurodegeneration and ATP synthase. In his study, Phenotype and Enzyme assay is strongly linked to Pathogenesis, which falls under the umbrella field of Genetics. His work carried out in the field of Respiratory chain brings together such families of science as Non-Mendelian inheritance, Mitochondrial respiratory chain and Mitochondrial disease.
His primary scientific interests are in Mitochondrial DNA, Genetics, Molecular biology, Mitochondrion and Respiratory chain. He has researched Mitochondrial DNA in several fields, including Mutation and Point mutation. His Molecular biology research includes themes of Complementary DNA, Protein subunit, Gene, Biochemistry and Cytochrome c oxidase.
His Mitochondrion research is multidisciplinary, incorporating elements of Oxidative phosphorylation, Endoplasmic reticulum, Neuroscience and ATP synthase. His work focuses on many connections between Respiratory chain and other disciplines, such as Pathology, that overlap with his field of interest in Internal medicine. The concepts of his Human mitochondrial genetics study are interwoven with issues in mitochondrial fusion and DNAJA3.
His scientific interests lie mostly in Mitochondrion, Cell biology, Mitochondrial DNA, Endoplasmic reticulum and Respiratory chain. His Mitochondrion research integrates issues from MFN2, Neuroscience and Neurodegeneration. Eric A. Schon has included themes like Parkin, Cytosol, Gene, Mitochondrial disease and Mitophagy in his Cell biology study.
His Mitochondrial DNA research is classified as research in Genetics. His work on Human mitochondrial genetics, Genome and Cytochrome c oxidase as part of general Genetics research is frequently linked to Axial elongation and Emmetropia, bridging the gap between disciplines. Eric A. Schon interconnects Endocrinology, Internal medicine, Basal, Mitochondrial respiratory chain and Mitochondrial biogenesis in the investigation of issues within Respiratory chain.
Eric A. Schon focuses on Mitochondrion, Endoplasmic reticulum, Amyloid precursor protein, Respiratory chain and Cell biology. His work deals with themes such as Neuroscience and MFN2, which intersect with Mitochondrion. Eric A. Schon combines subjects such as Mitochondrial disease and Mitochondrial biogenesis with his study of Respiratory chain.
As part of his studies on Cell biology, he often connects relevant subjects like Molecular biology. As a part of the same scientific family, Eric A. Schon mostly works in the field of Molecular biology, focusing on Cytoplasmic hybrid and, on occasion, Autophagy. His Mitochondrial DNA study incorporates themes from Autophagosome and Mitophagy.
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Guidelines for the use and interpretation of assays for monitoring autophagy (3rd edition)
Daniel J. Klionsky;Kotb Abdelmohsen;Akihisa Abe;Joynal Abedin.
Autophagy (2016)
Mitochondrial respiratory-chain diseases
Salvatore DiMauro;Eric A Schon.
The New England Journal of Medicine (2003)
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.
Neurology (1988)
Human mitochondrial DNA: roles of inherited and somatic mutations
Eric A. Schon;Salvatore DiMauro;Michio Hirano.
Nature Reviews Genetics (2012)
A direct repeat is a hotspot for large-scale deletion of human mitochondrial DNA
Eric A. Schon;Rosario Rizzuto;Carlos T. Moraes;Hirofumi Nakase.
Science (1989)
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.
Carlos T. Moraes;Sara Shanske;Hans Jürgen Tritschler;June R. Aprille.
American Journal of Human Genetics (1991)
Mitochondrial Disorders in the Nervous System
Salvatore DiMauro;Eric A. Schon.
Annual Review of Neuroscience (2008)
Fatal infantile cardioencephalomyopathy with COX deficiency and mutations in SCO2, a COX assembly gene
L C Papadopoulou;C M Sue;M M Davidson;K Tanji.
Nature Genetics (1999)
Depletion of muscle mitochondrial DNA in AIDS patients with zidovudine-induced myopathy
E. Arnaudo;S. Shanske;S. DiMauro;E.A. Schon.
The Lancet (1991)
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