Douglas C. Wallace

发表

African Origin of Modern Humans in East Asia: A Tale of 12,000 Y Chromosomes

P. Underhill, M. Seielstad, Zhu Chen, 2001, Science.

Mitochondrial DNA‐like sequences in the nucleus (NUMTs): Insights into our African origins and the mechanism of foreign DNA integration

Eduardo Ruiz-Pesini, Marty C. Brandon, Dan Mishmar, 2004, Human mutation.

Mitochondrial DNA and Y Chromosome-Specific Polymorphisms in the Seminole Tribe of Florida

A. Torroni, R. Scozzari, D. Gurley, 1997, European journal of human genetics : EJHG.

Fast capillary electrophoresis‐laser induced fluorescence analysis of ligase chain reaction products: Human mitochondrial DNA point mutations causing Leber's hereditary optic neuropathy

B. Karger, Michael D. Brown, J. Muth, 1996, Electrophoresis.

Classification of European mtDNAs from an analysis of three European populations.

A. Torroni, D. Wallace, R. Scozzari, 1996, Genetics.

Leber’s Hereditary Optic Neuropathy

A. Torroni, D. Wallace, M. Lott, 2022, Güncel Retina Dergisi (Current Retina Journal).

mtDNA diversity in Chukchi and Siberian Eskimos: implications for the genetic history of Ancient Beringia and the peopling of the New World.

R. Sukernik, D. Wallace, T. Schurr, 1998, American journal of human genetics.

Mitochondrial disease in superoxide dismutase 2 mutant mice.

C. Epstein, S. Melov, D. Wallace, 1999, Proceedings of the National Academy of Sciences of the United States of America.

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.

Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.

D. Wallace, M. Brown, F. Sun, 1997, American journal of human genetics.

mtDNA and Y-chromosome polymorphisms in four Native American populations from southern Mexico.

A. Torroni, D. Wallace, O. Semino, 1994, American journal of human genetics.

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 variants can mediate methylation status of inflammation, angiogenesis and signaling genes.

A. Nesburn, D. Wallace, S. Jazwinski, 2015, Human molecular genetics.

Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic.

R. Sukernik, D. Wallace, T. Schurr, 1999, American journal of physical anthropology.

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

B. Crain, M. Gearing, S. Mirra, 1993, Genomics.

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.

Mouse models of mitochondrial disease, oxidative stress, and senescence.

S. Melov, D. Wallace, P. Coskun, 1999, Mutation research.

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

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

Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America.

R. Barrantes, A. Torroni, D. Wallace, 1994, Proceedings of the National Academy of Sciences of the United States of America.

De novo 14484 mitochondrial DNA mutation in monozygotic twins discordant for Leber's hereditary optic neuropathy

N. Newman, G. Meola, D. Wallace, 1997, Neurology.

Mitochondrial oxidative stress in mice lacking the glutathione peroxidase-1 gene.

D. Wallace, B. Cottrell, K. Waymire, 2000, Free radical biology & medicine.

Mitochondrial DNA variation in human evolution and disease.

D. Wallace, M. Lott, M. Brown, 1999, Gene.

Mitochondrial DNA sequence variation in human evolution and disease.

D. Wallace, Douglas C. Wallace, 1994, Proceedings of the National Academy of Sciences of the United States of America.

The human ATP synthase beta subunit gene: sequence analysis, chromosome assignment, and differential expression.

N. Shimizu, S. Minoshima, J. Kudoh, 1989, Genomics.

Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies.

D. Wallace, J. Shoffner, X. Zheng, 1990, Biochimica et biophysica acta.

mtDNA and the origin of Caucasians: identification of ancient Caucasian-specific haplogroups, one of which is prone to a recurrent somatic duplication in the D-loop region.

A. Torroni, D. Wallace, M. Lott, 1994, American journal of human genetics.

Variable genotype of Leber's hereditary optic neuropathy patients.

D. Wallace, M. Lott, A. Voljavec, 1990, American journal of ophthalmology.

Mitochondrial DNA mutations in human degenerative diseases and aging.

D. Wallace, M. Lott, S. Ballinger, 1995, Biochimica et biophysica acta.

A mitochondrial DNA variant, identified in Leber hereditary optic neuropathy patients, which extends the amino acid sequence of cytochrome c oxidase subunit I.

A. Torroni, D. Wallace, M. Lott, 1992, American journal of human genetics.

The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.

N. Newman, D. Wallace, M. Lott, 1991, American journal of ophthalmology.

Subacute necrotizing encephalopathy

D. A. Koontz, P. Fernhoff, N. Newman, 1992, Neurology.

Mitochondrial DNA in anucleate human blood cells.

D. Wallace, R. Shuster, Douglas C. Wallace, 1988, Biochemical and biophysical research communications.

Mitochondrial DNA mutations and neuromuscular disease.

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

Insulin resistance associated with maternally inherited diabetes and deafness.

D. Wallace, J. Shoffner, D. Koontz, 1996, Metabolism: clinical and experimental.

ARL2 and BART enter mitochondria and bind the adenine nucleotide transporter.

D. Wallace, R. Kahn, J. Shern, 2002, Molecular biology of the cell.

Molecular and bioenergetic differences between cells with African versus European inherited mitochondrial DNA haplogroups: implications for population susceptibility to diseases.

M. Vawter, A. Nesburn, D. Wallace, 2014, Biochimica et biophysica acta.

Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.

D. Wallace, J. R. Buncic, B. Robinson, 1992, Biochemical medicine and metabolic biology.

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.

Y chromosome polymorphisms in Native American and Siberian populations: identification of Native American Y chromosome haplotypes

R. Sukernik, L. Moore, A. Torroni, 1997, Human Genetics.

Differential structuring of human populations for homologous X and Y microsatellite loci.

K. Kidd, S. Q. Mehdi, A. Torroni, 1997, American journal of human genetics.

Dramatic founder effects in Amerindian mitochondrial DNAs.

W. Knowler, D. Wallace, K. Garrison, 1985, American journal of physical anthropology.

A mitochondrial paradigm for degenerative diseases and ageing.

D. Wallace, Douglas C. Wallace, 2001, Novartis Foundation symposium.

A Case of Sporadic Infantile Histiocytoid Cardiomyopathy Caused by the A8344G (MERRF) Mitochondrial DNA Mutation

D. Wallace, M. Brown, H. Vallance, 2004, Pediatric Cardiology.

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.

Amerindian mitochondrial DNAs have rare Asian mutations at high frequencies, suggesting they derived from four primary maternal lineages.

K. Weiss, W. Knowler, D. Wallace, 1990, American journal of human genetics.

Retinal function and structure in Ant1-deficient mice.

N. Newman, D. Wallace, V. Biousse, 2010, Investigative ophthalmology & visual science.

Mitochondria and Leber's hereditary optic neuropathy.

N. Newman, D. Wallace, Douglas C. Wallace, 1990, American journal of ophthalmology.

Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation.

A. Torroni, D. Wallace, J. A. Hodge, 1992, The Journal of biological chemistry.

Characterization of retinal and blood mitochondrial DNA from age-related macular degeneration patients.

A. Nesburn, D. Wallace, P. Coskun, 2010, Investigative ophthalmology & visual science.

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.

Variable retinal and neurologic manifestations in patients harboring the mitochondrial DNA 8993 mutation.

N. Newman, D. Wallace, J. Shoffner, 1993, Archives of ophthalmology.

Transcriptional control of nuclear genes for the mitochondrial muscle ADP/ATP translocator and the ATP synthase beta subunit. Multiple factors interact with the OXBOX/REBOX promoter sequences.

D. Wallace, A. B. Chung, K. Li, 1992, The Journal of biological chemistry.

Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients

M. Beal, D. Wallace, B. Graham, 1995, Neurology.

Clinical, genetic, and biochemical characterization of a Leber hereditary optic neuropathy family containing both the 11778 and 14484 primary mutations.

Jon C. Allen, Douglas C. Wallace, Michael D. Brown, 2001, American journal of medical genetics.

Combined use of biallelic and microsatellite Y-chromosome polymorphisms to infer affinities among African populations.

A. Torroni, D. Wallace, R. Scozzari, 1999, American journal of human genetics.

Epidemic neuropathy in Cuba not associated with mitochondrial DNA mutations found in Leber's hereditary optic neuropathy patients. Cuba Neuropathy Field Investigation Team.

N. Newman, A. Torroni, D. Wallace, 1994, American journal of ophthalmology.

Mitochondrial DNA in aging and disease.

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

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.