| Year |
Citation |
Score |
| 2023 |
Amorim R, Magalhães CC, Benfeito S, Cagide F, Tavares LC, Santos K, Sardão VA, Datta S, Cortopassi GA, Baldeiras I, Jones JG, Borges F, Oliveira PJ, Teixeira J. Mitochondria dysfunction induced by decyl-TPP mitochondriotropic antioxidant based on caffeic acid AntiOxCIN sensitizes cisplatin lung anticancer therapy due to a remodeling of energy metabolism. Biochemical Pharmacology. 115953. PMID 38036191 DOI: 10.1016/j.bcp.2023.115953 |
0.386 |
|
| 2023 |
Jin LW, Di Lucente J, Ruiz Mendiola U, Suthprasertporn N, Tomilov A, Cortopassi G, Kim K, Ramsey JJ, Maezawa I. The ketone body β-hydroxybutyrate shifts microglial metabolism and suppresses amyloid-β oligomer-induced inflammation in human microglia. Faseb Journal : Official Publication of the Federation of American Societies For Experimental Biology. 37: e23261. PMID 37878335 DOI: 10.1096/fj.202301254R |
0.33 |
|
| 2022 |
Abeti R, Jasoliya M, Al-Mahdawi S, Pook M, Gonzalez-Robles C, Hui CK, Cortopassi G, Giunti P. A Drug Combination Rescues Frataxin-Dependent Neural and Cardiac Pathophysiology in FA Models. Frontiers in Molecular Biosciences. 9: 830650. PMID 35664670 DOI: 10.3389/fmolb.2022.830650 |
0.307 |
|
| 2021 |
De Mario A, Tosatto A, Hill JM, Kriston-Vizi J, Ketteler R, Vecellio Reane D, Cortopassi G, Szabadkai G, Rizzuto R, Mammucari C. Identification and functional validation of FDA-approved positive and negative modulators of the mitochondrial calcium uniporter. Cell Reports. 35: 109275. PMID 34161774 DOI: 10.1016/j.celrep.2021.109275 |
0.323 |
|
| 2021 |
Zhou Z, Hagopian K, López-Domínguez JA, Kim K, Jasoliya M, Roberts MN, Cortopassi GA, Showalter MR, Roberts BS, González-Reyes JA, Baar K, Rutkowsky J, Ramsey JJ. A ketogenic diet impacts markers of mitochondrial mass in a tissue specific manner in aged mice. Aging. 13. PMID 33735837 DOI: 10.18632/aging.202834 |
0.351 |
|
| 2021 |
Hui CK, Dedkova EN, Montgomery C, Cortopassi G. Dimethyl fumarate dose-dependently increases mitochondrial gene expression and function in muscle and brain of Friedreich's ataxia model mice. Human Molecular Genetics. PMID 33432356 DOI: 10.1093/hmg/ddaa282 |
0.353 |
|
| 2021 |
Datta S, Sears T, Cortopassi G, Woolard K, Angelastro JM. Repurposing FDA approved drugs inhibiting mitochondrial function for targeting glioma-stem like cells. Biomedicine & Pharmacotherapy = Biomedecine & Pharmacotherapie. 133: 111058. PMID 33378970 DOI: 10.1016/j.biopha.2020.111058 |
0.38 |
|
| 2019 |
Crakes KR, Santos Rocha C, Grishina I, Hirao LA, Napoli E, Gaulke CA, Fenton A, Datta S, Arredondo J, Marco ML, Sankaran-Walters S, Cortopassi G, Giulivi C, Dandekar S. PPARα-targeted mitochondrial bioenergetics mediate repair of intestinal barriers at the host-microbe intersection during SIV infection. Proceedings of the National Academy of Sciences of the United States of America. PMID 31740620 DOI: 10.1096/Fasebj.2020.34.S1.02382 |
0.336 |
|
| 2019 |
McMackin MZ, Durbin-Johnson B, Napierala M, Napierala JS, Ruiz L, Napoli E, Perlman S, Giulivi C, Cortopassi GA. Potential biomarker identification for Friedreich's ataxia using overlapping gene expression patterns in patient cells and mouse dorsal root ganglion. Plos One. 14: e0223209. PMID 31665133 DOI: 10.1371/journal.pone.0223209 |
0.332 |
|
| 2019 |
Jasoliya M, Sacca F, Sahdeo S, Chedin F, Pane C, Brescia Morra V, Filla A, Pook M, Cortopassi G. Dimethyl fumarate dosing in humans increases frataxin expression: A potential therapy for Friedreich's Ataxia. Plos One. 14: e0217776. PMID 31158268 DOI: 10.1371/Journal.Pone.0217776 |
0.333 |
|
| 2019 |
Sears TK, Datta S, Cortopassi G, Angelastro J, Woolard K. Abstract 3846: Targeting epigenetic dysregulation in isocitrate dehydrogenase mutant glioblastoma Cancer Research. 79: 3846-3846. DOI: 10.1158/1538-7445.Am2019-3846 |
0.318 |
|
| 2018 |
Bulkeley EA, Datta S, Cortopassi GA, Serafini R, Teague S, Varner DD, Meyers SA. Age-related Preferential Effects of Mitochondrial Oxidative Function on Progressive Motility and Decline of Mitochondrial Respiratory Capacity in Stallion Spermatozoa Journal of Equine Veterinary Science. 66: 35. DOI: 10.1016/J.Jevs.2018.05.014 |
0.362 |
|
| 2018 |
Cortopassi G. Mitochondria, Nrf2 and mTOR Free Radical Biology and Medicine. 128. DOI: 10.1016/J.Freeradbiomed.2018.10.382 |
0.537 |
|
| 2017 |
Teixeira J, Amorim R, Santos K, Soares P, Datta S, Cortopassi GA, Serafim TL, Sardão VA, Garrido J, Borges F, Oliveira PJ. Disruption of mitochondrial function as mechanism for anti-cancer activity of a novel mitochondriotropic menadione derivative. Toxicology. PMID 29141199 DOI: 10.1016/j.tox.2017.11.014 |
0.4 |
|
| 2017 |
Yu AK, Datta S, McMackin MZ, Cortopassi GA. Rescue of cell death and inflammation of a mouse model of complex 1-mediated vision loss by repurposed drug molecules. Human Molecular Genetics. PMID 29040550 DOI: 10.1093/hmg/ddx373 |
0.375 |
|
| 2017 |
Hayashi G, Jasoliya M, Saccà F, Pane C, Filla A, Marsili A, Puorro G, Lanzillo R, Brescia Morra V, Cortopassi G. Dimethyl Fumarate Mediates Nrf2-dependent Mitochondrial Biogenesis in Mice and Humans. Human Molecular Genetics. PMID 28460056 DOI: 10.1093/hmg/ddx167 |
0.421 |
|
| 2017 |
Jasoliya MJ, McMackin MZ, Henderson CK, Perlman SL, Cortopassi GA. Frataxin Deficiency Impairs Mitochondrial Biogenesis in Cells, Mice and Humans. Human Molecular Genetics. PMID 28444186 DOI: 10.1093/hmg/ddx141 |
0.426 |
|
| 2016 |
Song L, McMackin M, Nguyen A, Cortopassi G. Parkin deficiency accelerates consequences of mitochondrial DNA deletions and Parkinsonism. Neurobiology of Disease. PMID 28042097 DOI: 10.1016/j.nbd.2016.12.024 |
0.346 |
|
| 2016 |
Song L, Yu A, Murray K, Cortopassi G. Bipolar cell reduction precedes retinal ganglion neuron loss in a complex 1 knockout mouse model. Brain Research. PMID 28027875 DOI: 10.1016/j.brainres.2016.12.019 |
0.374 |
|
| 2016 |
Datta S, Sahdeo S, Gray JA, Morriseau C, Hammock BD, Cortopassi G. A high-throughput screen for mitochondrial function reveals known and novel mitochondrial toxicants in a library of environmental agents. Mitochondrion. PMID 27717841 DOI: 10.1016/J.Mito.2016.10.001 |
0.358 |
|
| 2016 |
Datta S, Tomilov A, Cortopassi G. Identification of small molecules that improve ATP synthesis defects conferred by Leber's hereditary optic neuropathy mutations. Mitochondrion. PMID 27497748 DOI: 10.1016/j.mito.2016.08.002 |
0.403 |
|
| 2016 |
Darr CR, Varner DD, Teague S, Cortopassi GA, Datta S, Meyers SA. Lactate and Pyruvate Are Major Sources of Energy for Stallion Sperm with Dose Effects on Mitochondrial Function, Motility, and ROS Production. Biology of Reproduction. PMID 27335066 DOI: 10.1095/Biolreprod.116.140707 |
0.333 |
|
| 2016 |
Hayashi G, Cortopassi G. Lymphoblast Oxidative Stress Genes as Potential Biomarkers of Disease Severity and Drug Effect in Friedreich's Ataxia. Plos One. 11: e0153574. PMID 27078885 DOI: 10.1371/Journal.Pone.0153574 |
0.333 |
|
| 2016 |
Tomilov A, Tomilova N, Shan Y, Hagopian K, Bettaieb A, Kim K, Pelicci PG, Haj F, Ramsey J, Cortopassi G. The mitochondrial isoform of Shc protein inhibits thiolase and lipid oxidation. The Journal of Biological Chemistry. PMID 27059956 DOI: 10.1074/Jbc.M115.695577 |
0.362 |
|
| 2015 |
Shan Y, Cortopassi G. Mitochondrial Hspa9/Mortalin regulates erythroid differentiation via iron-sulfur cluster assembly. Mitochondrion. PMID 26702583 DOI: 10.1016/j.mito.2015.12.005 |
0.422 |
|
| 2015 |
Hayashi G, Cortopassi G. Oxidative stress in inherited mitochondrial diseases. Free Radical Biology & Medicine. 88: 10-7. PMID 26073122 DOI: 10.1016/j.freeradbiomed.2015.05.039 |
0.318 |
|
| 2015 |
Jin LW, Horiuchi M, Wulff H, Liu XB, Cortopassi GA, Erickson JD, Maezawa I. Dysregulation of glutamine transporter SNAT1 in Rett syndrome microglia: a mechanism for mitochondrial dysfunction and neurotoxicity. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 2516-29. PMID 25673846 DOI: 10.1523/Jneurosci.2778-14.2015 |
0.354 |
|
| 2014 |
Sahdeo S, Scott BD, McMackin MZ, Jasoliya M, Brown B, Wulff H, Perlman SL, Pook MA, Cortopassi GA. Dyclonine rescues frataxin deficiency in animal models and buccal cells of patients with Friedreich's ataxia. Human Molecular Genetics. 23: 6848-62. PMID 25113747 DOI: 10.1093/Hmg/Ddu408 |
0.322 |
|
| 2014 |
Hayashi G, Shen Y, Pedersen TL, Newman JW, Pook M, Cortopassi G. Frataxin deficiency increases cyclooxygenase 2 and prostaglandins in cell and animal models of Friedreich's ataxia. Human Molecular Genetics. 23: 6838-47. PMID 25104852 DOI: 10.1093/Hmg/Ddu407 |
0.407 |
|
| 2014 |
Sahdeo S, Tomilov A, Komachi K, Iwahashi C, Datta S, Hughes O, Hagerman P, Cortopassi G. High-throughput screening of FDA-approved drugs using oxygen biosensor plates reveals secondary mitofunctional effects. Mitochondrion. 17: 116-25. PMID 25034306 DOI: 10.1016/J.Mito.2014.07.002 |
0.367 |
|
| 2013 |
Fash DM, Khdour OM, Sahdeo SJ, Goldschmidt R, Jaruvangsanti J, Dey S, Arce PM, Collin VC, Cortopassi GA, Hecht SM. Effects of alkyl side chain modification of coenzyme Q10 on mitochondrial respiratory chain function and cytoprotection. Bioorganic & Medicinal Chemistry. 21: 2346-54. PMID 23473946 DOI: 10.1016/J.Bmc.2013.01.075 |
0.332 |
|
| 2013 |
Sahdeo S, Cortopassi G. Discovery of modulators of oxygen consumption for use in mitochondrial disease Mitochondrion. 13: 918. DOI: 10.1016/J.Mito.2013.07.053 |
0.431 |
|
| 2012 |
Chen L, Liu T, Tran A, Lu X, Tomilov AA, Davies V, Cortopassi G, Chiamvimonvat N, Bers DM, Votruba M, Knowlton AA. OPA1 mutation and late-onset cardiomyopathy: mitochondrial dysfunction and mtDNA instability. Journal of the American Heart Association. 1: e003012. PMID 23316298 DOI: 10.1161/Jaha.112.003012 |
0.518 |
|
| 2012 |
Song L, Shan Y, Lloyd KC, Cortopassi GA. Mutant Twinkle increases dopaminergic neurodegeneration, mtDNA deletions and modulates Parkin expression. Human Molecular Genetics. 21: 5147-58. PMID 22949510 DOI: 10.1093/hmg/dds365 |
0.311 |
|
| 2012 |
Shan Y, Cortopassi G. HSC20 interacts with frataxin and is involved in iron-sulfur cluster biogenesis and iron homeostasis. Human Molecular Genetics. 21: 1457-69. PMID 22171070 DOI: 10.1093/hmg/ddr582 |
0.332 |
|
| 2012 |
Sahdeo S, Pook M, Napierala M, Sarsero J, Cortopassi G. Re-purposing small-molecule drugs to treat the mitochondrial disease Friedreich's ataxia Mitochondrion. 12: 571-572. DOI: 10.1016/J.Mito.2012.07.056 |
0.417 |
|
| 2011 |
Sahdeo S, Schoenfeld R, Cortopassi G. A high throughput screen for effectors of mitochondrial function Mitochondrion. 11: 641. DOI: 10.1016/J.Mito.2011.03.021 |
0.401 |
|
| 2010 |
Schoenfeld R, Wong A, Silva J, Li M, Itoh A, Horiuchi M, Itoh T, Pleasure D, Cortopassi G. Oligodendroglial differentiation induces mitochondrial genes and inhibition of mitochondrial function represses oligodendroglial differentiation. Mitochondrion. 10: 143-50. PMID 20005986 DOI: 10.1016/J.Mito.2009.12.141 |
0.522 |
|
| 2010 |
Chowanadisai W, Bauerly KA, Tchaparian E, Wong A, Cortopassi GA, Rucker RB. Pyrroloquinoline quinone stimulates mitochondrial biogenesis through cAMP response element-binding protein phosphorylation and increased PGC-1alpha expression. The Journal of Biological Chemistry. 285: 142-52. PMID 19861415 DOI: 10.1074/Jbc.M109.030130 |
0.375 |
|
| 2010 |
Schoenfeld R, Bach A, Cortopassi G. 143 Development of a cell based screening assay for drugs that alter mitochondrial function Mitochondrion. 10: 240. DOI: 10.1016/J.Mito.2009.12.134 |
0.418 |
|
| 2009 |
Silva JM, Wong A, Carelli V, Cortopassi GA. Inhibition of mitochondrial function induces an integrated stress response in oligodendroglia. Neurobiology of Disease. 34: 357-65. PMID 19233273 DOI: 10.1016/j.nbd.2009.02.005 |
0.425 |
|
| 2009 |
Rolo AP, Palmeira CM, Cortopassi GA. Biosensor plates detect mitochondrial physiological regulators and mutations in vivo. Analytical Biochemistry. 385: 176-8. PMID 18950600 DOI: 10.1016/j.ab.2008.10.002 |
0.433 |
|
| 2008 |
Silva JM, Wong A, Cortopassi GA. Mitochondrial inhibition induces PERK‐dependent activation of the unfolded protein response stress pathway in human oligodendroglial cells The Faseb Journal. 22: 303-303. DOI: 10.1096/FASEBJ.22.2_SUPPLEMENT.303 |
0.358 |
|
| 2008 |
Shan Y, Cortopassi G. S12.42 The frataxin-interacting protein grp75 chaperone plays an essential role in mitochondrial Fe/S cluster biogenesis Biochimica Et Biophysica Acta. 1777. DOI: 10.1016/J.Bbabio.2008.05.336 |
0.37 |
|
| 2008 |
Silva J, Cortopassi G. S9.6 lhon mutations and rotenone induce the unfolded protein response in human neural cells Biochimica Et Biophysica Acta. 1777. DOI: 10.1016/J.Bbabio.2008.05.221 |
0.393 |
|
| 2007 |
Prigione A, Cortopassi G. Mitochondrial DNA deletions induce the adenosine monophosphate-activated protein kinase energy stress pathway and result in decreased secretion of some proteins. Aging Cell. 6: 619-30. PMID 17651460 DOI: 10.1111/j.1474-9726.2007.00323.x |
0.394 |
|
| 2007 |
Prigione A, Cortopassi G. Mitochondrial DNA deletions and chloramphenicol treatment stimulate the autophagic transcript ATG12. Autophagy. 3: 377-80. PMID 17457038 |
0.483 |
|
| 2007 |
Shan Y, Napoli E, Cortopassi G. Mitochondrial frataxin interacts with ISD11 of the NFS1/ISCU complex and multiple mitochondrial chaperones. Human Molecular Genetics. 16: 929-41. PMID 17331979 DOI: 10.1093/hmg/ddm038 |
0.388 |
|
| 2007 |
Alemi M, Prigione A, Wong A, Schoenfeld R, DiMauro S, Hirano M, Taroni F, Cortopassi G. Mitochondrial DNA deletions inhibit proteasomal activity and stimulate an autophagic transcript. Free Radical Biology & Medicine. 42: 32-43. PMID 17157191 DOI: 10.1016/j.freeradbiomed.2006.09.014 |
0.398 |
|
| 2007 |
Lu C, Cortopassi G. Frataxin knockdown causes loss of cytoplasmic iron-sulfur cluster functions, redox alterations and induction of heme transcripts. Archives of Biochemistry and Biophysics. 457: 111-22. PMID 17098208 DOI: 10.1016/j.abb.2006.09.010 |
0.353 |
|
| 2006 |
Cortopassi G, Danielson S, Alemi M, Zhan SS, Tong W, Carelli V, Martinuzzi A, Marzuki S, Majamaa K, Wong A. Mitochondrial disease activates transcripts of the unfolded protein response and cell cycle and inhibits vesicular secretion and oligodendrocyte-specific transcripts. Mitochondrion. 6: 161-75. PMID 16815102 DOI: 10.1016/J.Mito.2006.05.002 |
0.71 |
|
| 2006 |
Napoli E, Taroni F, Cortopassi GA. Frataxin, iron-sulfur clusters, heme, ROS, and aging. Antioxidants & Redox Signaling. 8: 506-16. PMID 16677095 DOI: 10.1089/ars.2006.8.506 |
0.414 |
|
| 2006 |
von Wurmb-Schwark N, Cavelier L, Cortopassi GA. A low dose of ethidium bromide leads to an increase of total mitochondrial DNA while higher concentrations induce the mtDNA 4997 deletion in a human neuronal cell line. Mutation Research. 596: 57-63. PMID 16488450 DOI: 10.1016/J.MRFMMM.2005.12.003 |
0.386 |
|
| 2005 |
Schoenfeld RA, Napoli E, Wong A, Zhan S, Reutenauer L, Morin D, Buckpitt AR, Taroni F, Lonnerdal B, Ristow M, Puccio H, Cortopassi GA. Frataxin deficiency alters heme pathway transcripts and decreases mitochondrial heme metabolites in mammalian cells. Human Molecular Genetics. 14: 3787-99. PMID 16239244 DOI: 10.1093/Hmg/Ddi393 |
0.454 |
|
| 2005 |
Danielson SR, Carelli V, Tan G, Martinuzzi A, Schapira AH, Savontaus ML, Cortopassi GA. Isolation of transcriptomal changes attributable to LHON mutations and the cybridization process. Brain : a Journal of Neurology. 128: 1026-37. PMID 15728653 DOI: 10.1093/Brain/Awh447 |
0.707 |
|
| 2003 |
Tan G, Napoli E, Taroni F, Cortopassi G. Decreased expression of genes involved in sulfur amino acid metabolism in frataxin-deficient cells. Human Molecular Genetics. 12: 1699-711. PMID 12837693 |
0.358 |
|
| 2002 |
Wong A, Cortopassi GA. High-throughput measurement of mitochondrial membrane potential in a neural cell line using a fluorescence plate reader. Biochemical and Biophysical Research Communications. 298: 750-4. PMID 12419317 |
0.394 |
|
| 2002 |
Cortopassi GA. A neutral theory predicts multigenic aging and increased concentrations of deleterious mutations on the mitochondrial and Y chromosomes. Free Radical Biology & Medicine. 33: 605-10. PMID 12208346 |
0.391 |
|
| 2002 |
Wong A, Cortopassi G. Reproducible quantitative PCR of mitochondrial and nuclear DNA copy number using the LightCycler. Methods in Molecular Biology (Clifton, N.J.). 197: 129-37. PMID 12013791 DOI: 10.1385/1-59259-284-8:129 |
0.425 |
|
| 2002 |
Wong A, Cavelier L, Collins-Schramm HE, Seldin MF, McGrogan M, Savontaus ML, Cortopassi GA. Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells. Human Molecular Genetics. 11: 431-8. PMID 11854175 DOI: 10.1093/Hmg/11.4.431 |
0.394 |
|
| 2002 |
Danielson SR, Wong A, Carelli V, Martinuzzi A, Schapira AH, Cortopassi GA. Cells bearing mutations causing Leber's hereditary optic neuropathy are sensitized to Fas-Induced apoptosis. The Journal of Biological Chemistry. 277: 5810-5. PMID 11741983 DOI: 10.1074/Jbc.M110119200 |
0.69 |
|
| 2001 |
Tan G, Chen LS, Lonnerdal B, Gellera C, Taroni FA, Cortopassi GA. Frataxin expression rescues mitochondrial dysfunctions in FRDA cells. Human Molecular Genetics. 10: 2099-107. PMID 11590127 DOI: 10.1093/Hmg/10.19.2099 |
0.338 |
|
| 2001 |
Sisemore MF, Zheng J, Yang JC, Thompson DA, Plopper CG, Cortopassi GA, Hammock BD. Cellular characterization of leukotoxin diol-induced mitochondrial dysfunction Archives of Biochemistry and Biophysics. 392: 32-37. PMID 11469791 DOI: 10.1006/Abbi.2001.2434 |
0.44 |
|
| 2001 |
Hutchin TP, Cortopassi GA. Mitochondrial defects and hearing loss. Cellular and Molecular Life Sciences : Cmls. 57: 1927-37. PMID 11215518 DOI: 10.1007/PL00000673 |
0.334 |
|
| 2000 |
Wong A, Yang J, Danielson S, Gellera C, Taroni F, Cortopassi G. Sensitivity of FRDA lymphoblasts to salts of transition metal ions. Antioxidants & Redox Signaling. 2: 461-5. PMID 11229359 DOI: 10.1089/15230860050192233 |
0.678 |
|
| 2000 |
Yang JC, Kahn A, Cortopassi G. Bcl-2 does not inhibit the permeability transition pore in mouse liver mitochondria. Toxicology. 151: 65-72. PMID 11074301 DOI: 10.1016/S0300-483X(00)00298-5 |
0.364 |
|
| 1999 |
Cortopassi GA, Wong A. Mitochondria in organismal aging and degeneration. Biochimica Et Biophysica Acta. 1410: 183-93. PMID 10076026 DOI: 10.1016/S0005-2728(98)00166-2 |
0.414 |
|
| 1999 |
Wong A, Yang J, Cavadini P, Gellera C, Lonnerdal B, Taroni F, Cortopassi G. The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis. Human Molecular Genetics. 8: 425-30. PMID 9949201 DOI: 10.1093/Hmg/8.3.425 |
0.375 |
|
| 1998 |
Goodell S, Cortopassi G. Analysis of oxygen consumption and mitochondrial permeability with age in mice. Mechanisms of Ageing and Development. 101: 245-56. PMID 9622228 DOI: 10.1016/S0047-6374(97)00182-6 |
0.347 |
|
| 1998 |
Yang JC, Cortopassi GA. Induction of the mitochondrial permeability transition causes release of the apoptogenic factor cytochrome c. Free Radical Biology & Medicine. 24: 624-31. PMID 9559874 DOI: 10.1016/S0891-5849(97)00367-5 |
0.371 |
|
| 1997 |
Wong A, Cortopassi G. mtDNA mutations confer cellular sensitivity to oxidant stress that is partially rescued by calcium depletion and cyclosporin A. Biochemical and Biophysical Research Communications. 239: 139-45. PMID 9345284 DOI: 10.1006/BBRC.1997.7443 |
0.379 |
|
| 1997 |
Wallace KB, Eells JT, Madeira VMC, Cortopassi G, Jones DP. Mitochondria-mediated cell injury Fundamental and Applied Toxicology. 38: 23-37. PMID 9268603 DOI: 10.1006/Faat.1997.2320 |
0.405 |
|
| 1997 |
Wang E, Wong A, Cortopassi G. The rate of mitochondrial mutagenesis is faster in mice than humans. Mutation Research. 377: 157-66. PMID 9247611 DOI: 10.1016/S0027-5107(97)00091-2 |
0.34 |
|
| 1997 |
Wallace KB, Eells JT, Madeira VMC, Cortopassi G, Jones DP. Mitochondria-Mediated Cell Injury Toxicological Sciences. 38: 23-37. DOI: 10.1093/Toxsci/38.1.23 |
0.405 |
|
| 1996 |
Murphy AN, Bredesen DE, Cortopassi G, Wang E, Fiskum G. Bcl-2 potentiates the maximal calcium uptake capacity of neural cell mitochondria Proceedings of the National Academy of Sciences of the United States of America. 93: 9893-9898. PMID 8790427 DOI: 10.1073/Pnas.93.18.9893 |
0.333 |
|
| 1996 |
Cortopassi G, Liu Y, Hutchin T. Degeneration of human oncogenes and mitochondrial genes occurs in cells that exhibit age-related pathology. Experimental Gerontology. 31: 253-65. PMID 8706795 DOI: 10.1016/0531-5565(95)00021-6 |
0.387 |
|
| 1996 |
Hutchin TP, Wang E, Bredesen D, Cortopassi GA. A DICHOTOMY OF PROTECTION BY BCL-2 FROM MITOCHONDRIAL POISONS Biochemical Society Transactions. 24: 601S-601S. DOI: 10.1042/BST024601SC |
0.402 |
|
| 1995 |
Hutchin T, Cortopassi G. Mitochondrial DNA haplotype predicts deafness risk American Journal of Medical Genetics. 60: 592-592. PMID 8825904 DOI: 10.1002/Ajmg.1320600623 |
0.428 |
|
| 1995 |
Hutchin T, Cortopassi G. A mitochondrial DNA clone is associated with increased risk for Alzheimer disease. Proceedings of the National Academy of Sciences of the United States of America. 92: 6892-5. PMID 7624338 DOI: 10.1073/PNAS.92.15.6892 |
0.339 |
|
| 1995 |
Cortopassi G, Wang E. Modelling the effects of age-related mtDNA mutation accumulation; complex I deficiency, superoxide and cell death. Biochimica Et Biophysica Acta. 1271: 171-6. PMID 7599205 DOI: 10.1016/0925-4439(95)00025-Y |
0.43 |
|
| 1995 |
Cortopassi G, Liu Y. Genotypic selection of mitochondrial and oncogenic mutations in human tissue suggests mechanisms of age-related pathophysiology. Mutation Research. 338: 151-9. PMID 7565870 DOI: 10.1016/0921-8734(95)00020-7 |
0.389 |
|
| 1994 |
Cortopassi G, Hutchin T. A molecular and cellular hypothesis for aminoglycoside-induced deafness. Hearing Research. 78: 27-30. PMID 7961174 DOI: 10.1016/0378-5955(94)90040-X |
0.322 |
|
| 1993 |
Prezant TR, Agapian JV, Bohlman MC, Bu X, Oztas S, Qiu WQ, Arnos KS, Cortopassi GA, Jaber L, Rotter JI. Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness. Nature Genetics. 4: 289-94. PMID 7689389 DOI: 10.1038/NG0793-289 |
0.415 |
|
| 1992 |
Arnheim N, Cortopassi G. Deleterious mitochondrial DNA mutations accumulate in aging human tissues Mutation Research Dnaging. 275: 157-167. PMID 1383758 DOI: 10.1016/0921-8734(92)90020-P |
0.477 |
|
| 1992 |
Soong NW, Hinton DR, Cortopassi G, Arnheim N. Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain. Nature Genetics. 2: 318-23. PMID 1303287 DOI: 10.1038/Ng1292-318 |
0.357 |
|
| 1990 |
Cortopassi GA, Arnheim N. Detection of a specific mitochondrial DNA deletion in tissues of older humans Nucleic Acids Research. 18: 6927-6933. PMID 2263455 DOI: 10.1093/Nar/18.23.6927 |
0.33 |
|
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