2014 - Fellow of the American Association for the Advancement of Science (AAAS)
His primary areas of study are Mitochondrial DNA, Mitochondrion, Molecular biology, Genetics and Apoptosis. His work deals with themes such as Mutation, Mutation, Disease, Ageing and Programmed cell death, which intersect with Mitochondrial DNA. His Mitochondrion study improves the overall literature in Biochemistry.
The concepts of his Molecular biology study are interwoven with issues in Germline mutation, Somatic cell, DNA, Hot start PCR and Polymerase chain reaction. When carried out as part of a general Genetics research project, his work on Phenotype, Ribosome, Gene and Backcrossing is frequently linked to work in Noise-induced hearing loss, therefore connecting diverse disciplines of study. His Apoptosis research is multidisciplinary, incorporating perspectives in Intracellular and Cell biology.
His primary areas of investigation include Mitochondrion, Molecular biology, Mitochondrial DNA, Genetics and Cell biology. His studies in Mitochondrion integrate themes in fields like Apoptosis, Programmed cell death and Mitochondrial disease. Gino A Cortopassi works mostly in the field of Molecular biology, limiting it down to topics relating to Mutant and, in certain cases, Chromosomal translocation.
He works mostly in the field of Mitochondrial DNA, limiting it down to topics relating to Somatic cell and, in certain cases, Carcinogenesis, as a part of the same area of interest. In his research, Dorsal root ganglion and Substantia nigra is intimately related to Neurodegeneration, which falls under the overarching field of Cell biology. His Biochemistry study combines topics in areas such as Endocrinology and Internal medicine.
Pharmacology, Cancer research, Mitochondrion, Inflammation and Internal medicine are his primary areas of study. His Cancer research research also works with subjects such as
He interconnects Epithelium, Toxicity and Cell biology in the investigation of issues within Inflammation. Gino A Cortopassi works mostly in the field of Internal medicine, limiting it down to topics relating to Endocrinology and, in certain cases, Oxidative phosphorylation, Candesartan and Affect. His research integrates issues of Aconitase, Mitochondrial disease, Mitochondrial DNA, Molecular biology and Cytochrome c oxidase in his study of Dimethyl fumarate.
Gino A Cortopassi mainly investigates Mitochondrion, Cell biology, Pharmacology, Inflammation and Cancer cell. His Mitochondrion research includes elements of Ataxia, Gene expression, Gene and Molecular biology. His studies deal with areas such as Epithelium, Gut Epithelium, Immunodeficiency, T cell and Immunity as well as Cell biology.
Gino A Cortopassi combines subjects such as Mechanistic target of rapamycin, Small molecule, In vivo and mTORC2 with his study of Pharmacology. His Inflammation research incorporates elements of NADPH oxidase, Endocrinology, Senescence and Simian immunodeficiency virus. His Cancer cell research is multidisciplinary, relying on both mTORC1, PI3K/AKT/mTOR pathway, In vitro and Caspase 3.
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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness.
T R Prezant;J V Agapian;M C Bohlman;X Bu.
Nature Genetics (1993)
Detection of a specific mitochondrial DNA deletion in tissues of older humans
Gino A. Cortopassi;Norman Arnheim.
Nucleic Acids Research (1990)
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues.
Gino A Cortopassi;D. Shibata;N. W. Soong;N. Arnheim.
Proceedings of the National Academy of Sciences of the United States of America (1992)
A simple method for site-directed mutagenesis using the polymerase chain reaction
Anne Hemsley;Norman Arnheim;Michael Dennis Toney;Gino A Cortopassi.
Nucleic Acids Research (1989)
Bcl-2 potentiates the maximal calcium uptake capacity of neural cell mitochondria
Anne N. Murphy;Dale E. Bredesen;Gino A Cortopassi;Endi Wang.
Proceedings of the National Academy of Sciences of the United States of America (1996)
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
Nay Wei Soong;David R. Hinton;Gino A Cortopassi;Norman Arnheim.
Nature Genetics (1992)
BCL2 translocation frequency rises with age in humans
Yafei Liu;Antonio M. Hernandez;Darryl Shibata;Gino A. Cortopassi.
Proceedings of the National Academy of Sciences of the United States of America (1994)
The Friedreich's Ataxia Mutation Confers Cellular Sensitivity to Oxidant Stress Which Is Rescued by Chelators of Iron and Calcium and Inhibitors of Apoptosis
Alice Wong;Joy Yang;Patrizia Cavadini;Cinzia Gellera.
Human Molecular Genetics (1999)
A molecular basis for human hypersensitivity to aminoglycoside antibiotics.
Tim Hutchin;Ian Haworth;Koichiro Higashi;Nathan Fischel-Ghodsian.
Nucleic Acids Research (1993)
A Ketogenic Diet Extends Longevity and Healthspan in Adult Mice.
Megan N. Roberts;Marita A. Wallace;Alexey A. Tomilov;Zeyu Zhou.
Cell Metabolism (2017)
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