Douglas C. Wallace

发表

Marked changes in mitochondrial DNA deletion levels in Alzheimer brains.

M. Beal, D. Wallace, A. McKee, 1994, Genomics.

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

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

Renal amino acid transport in adults with oxidative phosphorylation diseases.

D. Wallace, W. Mitch, J. Shoffner, 1995, Kidney international.

Multi-organ characterization of mitochondrial genomic rearrangements in ad libitum and caloric restricted mice show striking somatic mitochondrial DNA rearrangements with age.

S. Melov, D. Wallace, D. Hinerfeld, 1997, Nucleic acids research.

Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy.

N. Newman, S. Manoukian, D. Wallace, 1992, American journal of ophthalmology.

The Mitochondrial Genome and Human Mitochondrial Diseases

E. Starikovskaya, R. Sukernik, D. Wallace, 2002, Russian Journal of Genetics.

Mitochondrial DNA sequence analysis of four Alzheimer's and Parkinson's disease patients.

D. Wallace, B. Graham, M. F. Cabell, 1996, American journal of medical genetics.

Mitochondrial oxidative phosphorylation defects in parkinson's disease

A. Torroni, D. Wallace, J. Shoffner, 1991, Annals of neurology.

Use of transmitochondrial cybrids to assign a complex I defect to the mitochondrial DNA-encoded NADH dehydrogenase subunit 6 gene mutation at nucleotide pair 14459 that causes Leber hereditary optic neuropathy and dystonia

D. Wallace, M. Brown, J. Shoffner, 1996, Molecular and cellular biology.

Atypical Leber's hereditary optic neuropathy with molecular confirmation.

N. Newman, D. Wallace, M. Lott, 1993, Archives of neurology.