Takip et
Gino Cortopassi
Gino Cortopassi
Professor of Molecular Biosciences, UC Davis
ucdavis.edu üzerinde doğrulanmış e-posta adresine sahip - Ana Sayfa
Başlık
Alıntı yapanlar
Alıntı yapanlar
Yıl
Mitochondrial ribosomal RNA mutation associated with both antibiotic–induced and non–syndromic deafness
TR Prezant, JV Agapian, MC Bohlman, X Bu, S Öztas, WQ Qiu, KS Arnos, ...
Nature genetics 4 (3), 289-294, 1993
16091993
Detection of a specific mitochondrial DNA deletion in tissues of older humans
GA Cortopassi, N Arnheim
Nucleic acids research 18 (23), 6927-6933, 1990
9751990
A pattern of accumulation of a somatic deletion of mitochondrial DNA in aging human tissues.
GA Cortopassi, D Shibata, NW Soong, N Arnheim
Proceedings of the National Academy of Sciences 89 (16), 7370-7374, 1992
8431992
A simple method for site-directed mutagenesis using the polymerase chain reaction
A Hemsley, N Arnheim, MD Toney, G Cortopassi, DJ Galas
Nucleic acids research 17 (16), 6545-6551, 1989
8211989
Bcl-2 potentiates the maximal calcium uptake capacity of neural cell mitochondria.
AN Murphy, DE Bredesen, G Cortopassi, E Wang, G Fiskum
Proceedings of the National Academy of Sciences 93 (18), 9893-9898, 1996
5211996
Mosaicism for a specific somatic mitochondrial DNA mutation in adult human brain
N Wei Soong, DR Hinton, G Cortopassi, N Arnheim
Nature genetics 2 (4), 318-323, 1992
5121992
A ketogenic diet extends longevity and healthspan in adult mice
MN Roberts, MA Wallace, AA Tomilov, Z Zhou, GR Marcotte, D Tran, ...
Cell metabolism 26 (3), 539-546. e5, 2017
4802017
BCL2 translocation frequency rises with age in humans.
Y LIu, AM Hernandez, D Shibata, GA Cortopassi
Proceedings of the National Academy of Sciences 91 (19), 8910-8914, 1994
4341994
The Friedreich's ataxia mutation confers cellular sensitivity to oxidant stress which is rescued by chelators of iron and calcium and inhibitors of apoptosis
J Yang, P Cavadini, C Gellera, B Lonnerdal, F Taroni, G Cortopassi
Human molecular genetics 8 (3), 425-430, 1999
4211999
A molecular basis for human hypersensitivity of aminoglyscoside antibiotics
T Hutchin, lan Haworth, K Higashi, N Fischel-Ghodsian, M Stoneking, ...
Nucleic acids research 21 (18), 4174-4179, 1993
3351993
Pyrroloquinoline quinone stimulates mitochondrial biogenesis through cAMP response element-binding protein phosphorylation and increased PGC-1α expression
W Chowanadisai, KA Bauerly, E Tchaparian, A Wong, GA Cortopassi, ...
Journal of Biological Chemistry 285 (1), 142-152, 2010
3322010
Mitochondria in organismal aging and degeneration
GA Cortopassi, A Wong
Biochimica et Biophysica Acta (BBA)-Bioenergetics 1410 (2), 183-193, 1999
2721999
Deleterious mitochondrial DNA mutations accumulate in aging human tissues
N Arnheim, G Cortopassi
Mutation Research/DNAging 275 (3-6), 157-167, 1992
2701992
Induction of the mitochondrial permeability transition causes release of the apoptogenic factor cytochrome c
JC Yang, GA Cortopassi
Free Radical Biology and Medicine 24 (4), 624-631, 1998
2641998
A mitochondrial DNA clone is associated with increased risk for Alzheimer disease.
T Hutchin, G Cortopassi
Proceedings of the National Academy of Sciences 92 (15), 6892-6895, 1995
2401995
Genetic basis for susceptibility to noise-induced hearing loss in mice
RR Davis, JK Newlander, XB Ling, GA Cortopassi, EF Krieg, LC Erway
Hearing research 155 (1-2), 82-90, 2001
2142001
Differentiation-specific effects of LHON mutations introduced into neuronal NT2 cells
A Wong, L Cavelier, HE Collins-Schramm, MF Seldin, M McGrogan, ...
Human molecular genetics 11 (4), 431-438, 2002
2122002
OPA 1 Mutation and Late‐Onset Cardiomyopathy: Mitochondrial Dysfunction and mtDNA Instability
L Chen, T Liu, A Tran, X Lu, AA Tomilov, V Davies, G Cortopassi, ...
Journal of the American Heart Association 1 (5), e003012, 2012
2082012
Mitochondria-mediated cell injury
KB Wallace, JT Eells, VMC Madeira, G Cortopassi, DP Jones
Toxicological Sciences 38 (1), 23-37, 1997
1841997
Modelling the effects of age-related mtDNA mutation accumulation; complex I deficiency, superoxide and cell death
G Cortopassi, E Wang
Biochimica et Biophysica Acta (BBA)-Molecular Basis of Disease 1271 (1), 171-176, 1995
1801995
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