D C Wallace

发表

Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations.

D. Murdock, D. Wallace, T. Schurr, 1997, Proceedings of the National Academy of Sciences of the United States of America.

Novel mitochondrial DNA deletion found in a renal cell carcinoma

D. Wallace, J. Shoffner, A. Heddi, 1996, Genes, chromosomes & cancer.

Oxidative damage to mitochondrial DNA shows marked age‐dependent increases in human brain

P. Mecocci, M. Beal, D. Wallace, 1993, Annals of neurology.

Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.

D. Wallace, M. Lott, J. Shoffner, 1992, Mutation research.

Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.

D. Wallace, M. Brown, S. Hosseini, 2000, Nucleic acids research.

Mitochondrial biology, degenerative diseases and aging

S. Melov, D. Wallace, M. Lott, 1998, BioFactors.

OXBOX and REBOX, overlapping promoter elements of the mitochondrial F0F1-ATP synthase beta subunit gene. OXBOX/REBOX in the ATPsyn beta promoter.

Y Haraguchi, D. Wallace, A. B. Chung, 1994, The Journal of biological chemistry.

Mitochondrial defects in cardiomyopathy and neuromuscular disease.

D. Wallace, D C Wallace, Douglas C. Wallace, 2000, American heart journal.

Asian affinities and continental radiation of the four founding Native American mtDNAs.

J V Neel, D. G. Smith, A. Torroni, 1993, American journal of human genetics.

Ocular pathology in mitochondrial superoxide dismutase (Sod2)-deficient mice.

N. Newman, H. Grossniklaus, D. Wallace, 2001, Investigative ophthalmology & visual science.

Bioenergetic origins of complexity and disease.

D. Wallace, D C Wallace, Douglas C. Wallace, 2011, Cold Spring Harbor symposia on quantitative biology.

Mitochondrial DNA analysis in Tibet: implications for the origin of the Tibetan population and its adaptation to high altitude.

L. Moore, A. Torroni, D. Wallace, 1994, American journal of physical anthropology.

Report of the committee on human mitochondrial DNA.

D C Wallace, 1990, Cytogenetics and cell genetics.

mtDNA haplogroup X: An ancient link between Europe/Western Asia and North America?

H. Bandelt, A. Torroni, D. Wallace, 1998, American journal of human genetics.

Mitochondrial defects in neurodegenerative disease.

D. Wallace, D C Wallace, 2001, Mental retardation and developmental disabilities research reviews.

Southeast Asian mitochondrial DNA analysis reveals genetic continuity of ancient mongoloid migrations.

A. Torroni, D. Wallace, T. Schurr, 1992, Genetics.

Diseases of the mitochondrial DNA.

D. Wallace, D C Wallace, Douglas C. Wallace, 1992, Annual review of biochemistry.

Mitochondrial DNA in aging and disease.

D. Wallace, D C Wallace, Douglas C. Wallace, 1997, Scientific American.

Maternal germ-line transmission of mutant mtDNAs from embryonic stem cell-derived chimeric mice.

D. Wallace, J. Heckenlively, K. Waymire, 2000, Proceedings of the National Academy of Sciences of the United States of America.

Mitochondria and cancer: Warburg addressed.

D. Wallace, D C Wallace, Douglas C. Wallace, 2005, Cold Spring Harbor symposia on quantitative biology.

mtDNA variation in the South African Kung and Khwe-and their genetic relationships to other African populations.

D. Wallace, Y. Chen, T. Schurr, 2000, American journal of human genetics.

Mitochondrial DNA sequence diversity in bipolar affective disorder.

F J McMahon, Y S Chen, F. McMahon, 2000, The American journal of psychiatry.

Mitochondrial DNA mutations and neuromuscular disease.

D. Wallace, D C Wallace, Douglas C. Wallace, 1989, Trends in genetics : TIG.

A mitochondrial DNA mutation at nucleotide pair 14459 of the NADH dehydrogenase subunit 6 gene associated with maternally inherited Leber hereditary optic neuropathy and dystonia.

D. Wallace, M. Brown, A. Jun, 1994, Proceedings of the National Academy of Sciences of the United States of America.

1994 William Allan Award Address. Mitochondrial DNA variation in human evolution, degenerative disease, and aging.

D. Wallace, D C Wallace, Douglas C. Wallace, 1995, American journal of human genetics.