Carl D. Gajewski

发表

The mtDNA T8993G (NARP) mutation results in an impairment of oxidative phosphorylation that can be improved by antioxidants.

M. Wiedmann, D. Devivo, G. Lenaz, 2004, Human molecular genetics.

Mutated Human SOD1 Causes Dysfunction of Oxidative Phosphorylation in Mitochondria of Transgenic Mice*

M. Beal, M. Kiaei, M. Mattiazzi, 2002, The Journal of Biological Chemistry.

BCL-2 Improves Oxidative Phosphorylation and Modulates Adenine Nucleotide Translocation in Mitochondria of Cells Harboring Mutant mtDNA*

J. Oca-Cossio, M. Woischnik, C. Moraes, 2003, The Journal of Biological Chemistry.

Measurements of ATP in mammalian cells.

Lichuan Yang, M. Mattiazzi, Lichuan Yang, 2002, Methods.

Heterologous mitochondrial DNA recombination in human cells.

William M. Mauck, C. Moraes, G. Lenaz, 2004, Human molecular genetics.

MTG1 codes for a conserved protein required for mitochondrial translation.

S. Ackerman, A. Barrientos, K. J. Barwell, 2003, Molecular biology of the cell.

Respiratory chain supercomplexes set the threshold for respiration defects in human mtDNA mutant cybrids.

G. Lenaz, G. Manfredi, M. D'Aurelio, 2006, Human molecular genetics.

New insights into the bioenergetics of mitochondrial disorders using intracellular ATP reporters.

E. Schon, Lichuan Yang, G. Manfredi, 2003, Molecular biology of the cell.

Mitochondrial DNA from platelets of sporadic ALS patients restores normal respiratory functions in ρ0 cells

M. Beal, M. Cudkowicz, G. Manfredi, 2003, Experimental Neurology.

Further Evidence for Mitochondrial Dysfunction in Progressive Supranuclear Palsy

Russell H. Swerdlow, M. Beal, R. Swerdlow, 2001, Experimental Neurology.

In Vivo Regulation of Oxidative Phosphorylation in Cells Harboring a Stop-codon Mutation in Mitochondrial DNA-encoded Cytochrome c Oxidase Subunit I*

M. Beal, A. Barrientos, G. Manfredi, 2001, The Journal of Biological Chemistry.