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NOTE: The following papers are in pdf format, you will
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Hemin rescues adrenodoxin, heme a and cytochrome oxidase
activity in frataxin-deficient oligodendroglioma cells., April 2007
·
Mitochondrial DNA Deletions and
Chloramphenicol Treatment Stimulate the Autophagic Transcript ATG12., April
2007
·
Mitochondrial frataxin interacts with ISD11 of the
Nfs1/ISCU complex and multiple mitochondrial chaperones, March 2007
·
Frataxin knockdown causes loss of cytoplasmic
iron-sulfur cluster functions, redox alterations and induction of heme
transcripts, January 2007
·
Knockdown of frataxin causes loss of
aconitase activity, induction of oxidative stress and induction of heme
transcripts, October 2006
·
Mitochondrial DNA deletions inhibit proteasomal
activity and stimulate an autophagic transcript, May 2006
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Frataxin, Iron–Sulfur Clusters, Heme, ROS, and
Aging, April 2006
·
Frataxin deficiency alters heme pathway transcripts and
decreases mitochondrial heme metabolites in mammalian cells, October 2005
·
Frataxin, iron-sulfur clusters,
heme, ROS and aging, September 2005
·
Isolation of transcriptomal changes
attributable to LHON mutations and the cybridization process, February 2005
·
Decreased expression of genes involved in sulfur
amino acid metabolism in frataxin-deficient cells, May 2003
·
High-throughput measurement of mitochondrial membrane
potential in a neural cell line using a fluorescence plate reader, October
2002
·
A neutral theory predicts multigenic aging
and increased concentrations of deleterious mutations on the mitochondrial and
Y chromosomes, September 2002
·
Fixation of deleterious alleles, evolution and human
aging, May 2002
·
Reproducible quantitative PCR of mitochondrial
and nuclear DNA copy number using the LightCycler, 2002
·
Quantification of human mitochondrial DNA in a real
time PCR, March 2002
·
Differentiation-specific effects of LHON mutations
introduced into neuronal NT2 cells, February 2002
·
Cells bearing mutations causing Leber's hereditary
optic neuropathy are sensitized to Fas-Induced apoptosis, February 2002
·
Frataxin Expression Rescues Mitochondrial
dysfunctions in FRDA cells, July 2001
·
Bcl-2 Does Not Inhibit the Permeability Transition Pore
in Mouse Liver Mitochondria, July 2000
·
Derivation of a Simple Formula
that relates mtDNA mutation frequency to age, September 2000
·
Mitochondria in Organismal Aging and Degeneration,
February 1999
·
dATP Causes Specific Release of Cytochrome C From
Mitochondria, September 1998
·
Analysis of Oxygen Consumption and Mitochondrial
Permeability With Age in Mice, April 1998
·
Induction of the Mitochondrial Permeability
Transition Causes Release of the Apoptogenic Factor CytohromeC,
March 1998
·
mtDNA Mutations Confer Cellular Sensitivity to
Oxidant Stress That is Partially Rescued by Calcium Depletion and Cyclosporin A,
October 1997
·
The Rate of Mitochondrial Mutagenesis is Faster in
Mice Than Humans, July 1997
·
Mutiple Orgins of a Mitochondrial Mutation
Conferring Deafness, March 1997
·
BCL-2 Potentiates the Maximal Calcium Uptake
Capacity of Neural Cell Mitochondria, September 1996
·
Mitochondria and Risk for Deafness, March 1995
·
BCL2 Translocation Frequency Rises With Age in
Human, September 1994
·
Mice With Duplications and Deletions at the Tme
Locus Have Altered MnSOD Activity, September 1994
·
A Molecular Basis for Human Hypersensitivity to
Aminoglycoside Antibiotics, September 1993
·
Mitochondrial Ribosomal RNA Mutation Associated With
Both Antibiotic-Induced and Non-Syndromic Deafness, July 1993
·
Mosaicism for a Specific Somatic Mitochondrial DNA
Mutation in Adult Human Brain, December 1992
·
A Pattern of Accumulation of a Somatic Deletion of
Mitochondrial DNA in Aging Human Tissues, August 1992
·
Detection of a Specific Mitochondrial DNA Deletion
in Tissues of Older Humans, December 1990
Last Updated: January 22, 2008