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Results of search for 'au:"WALLACE, D C"', page 9 of 14
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Authors
Allen, J C
Ballinger, S W
Blanc, H
Brown, M D
Bunn, C L
Chen, Y S
Corral-Debrinski, M
Eisenstadt, J M
Hodge, J A
Jun, A S
Lott, M T
Melov, S
Newman, N J
Schurr, T G
Scozzari, R
Shoffner, J M
Stepien, G
Torroni, A
Voljavec, A S
Wallace, D C
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Animals
Base Sequence
DNA, Mitochondrial
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Haplotypes
Humans
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Mice
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Mitochondria
Molecular Sequence Data
Mutation
Optic Atrophies, Hereditary
Oxidative Phosphorylation
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analysis
genetics
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161.
Nonviability of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.
[electronic resource]
by
Robinson, B H
Petrova-Benedict, R
Buncic, J R
Wallace, D C
Producer:
19921211
In:
Biochemical medicine and metabolic biology
vol. 48
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162.
Coordinate reciprocal trends in glycolytic and mitochondrial transcript accumulations during the in vitro differentiation of human myoblasts.
[electronic resource]
by
Webster, K A
Gunning, P
Hardeman, E
Wallace, D C
Kedes, L
Producer:
19900424
In:
Journal of cellular physiology
vol. 142
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163.
cDNA sequence of a human skeletal muscle ADP/ATP translocator: lack of a leader peptide, divergence from a fibroblast translocator cDNA, and coevolution with mitochondrial DNA genes.
[electronic resource]
by
Neckelmann, N
Li, K
Wade, R P
Shuster, R
Wallace, D C
Producer:
19871209
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 84
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164.
Differential expression of adenine nucleotide translocator isoforms in mammalian tissues and during muscle cell differentiation.
[electronic resource]
by
Stepien, G
Torroni, A
Chung, A B
Hodge, J A
Wallace, D C
Producer:
19920826
In:
The Journal of biological chemistry
vol. 267
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165.
Multiple self-healing squamous epithelioma.
[electronic resource]
by
Ferguson-Smith, M A
Wallace, D C
James, Z H
Renwick, J H
Producer:
19750523
In:
Birth defects original article series
vol. 7
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166.
Targeted delivery of DNA to the mitochondrial compartment via import sequence-conjugated peptide nucleic acid.
[electronic resource]
by
Flierl, A
Jackson, C
Cottrell, B
Murdock, D
Seibel, P
Wallace, D C
Producer:
20040112
In:
Molecular therapy : the journal of the American Society of Gene Therapy
vol. 7
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167.
Adeno-associated virus-mediated gene transfer of the heart/muscle adenine nucleotide translocator (ANT) in mouse.
[electronic resource]
by
Flierl, A
Chen, Y
Coskun, P E
Samulski, R J
Wallace, D C
Producer:
20050705
In:
Gene therapy
vol. 12
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168.
Mitochondrial DNA "clock" for the Amerinds and its implications for timing their entry into North America.
[electronic resource]
by
Torroni, A
Neel, J V
Barrantes, R
Schurr, T G
Wallace, D C
Producer:
19940308
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 91
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169.
Mitochondrial disease in mouse results in increased oxidative stress.
[electronic resource]
by
Esposito, L A
Melov, S
Panov, A
Cottrell, B A
Wallace, D C
Producer:
19990610
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 96
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170.
Mitochondrial oxidative phosphorylation defects in Parkinson's disease.
[electronic resource]
by
Shoffner, J M
Watts, R L
Juncos, J L
Torroni, A
Wallace, D C
Producer:
19911204
In:
Annals of neurology
vol. 30
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171.
Mitochondrial DNA of chloramphenicol-resistant mouse cells contains a single nucleotide change in the region encoding the 3' end of the large ribosomal RNA.
[electronic resource]
by
Blanc, H
Wright, C T
Bibb, M J
Wallace, D C
Clayton, D A
Producer:
19811029
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 78
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172.
Mitochondrial DNA rearrangements in aging human brain and in situ PCR of mtDNA.
[electronic resource]
by
Melov, S
Schneider, J A
Coskun, P E
Bennett, D A
Wallace, D C
Producer:
20000208
In:
Neurobiology of aging
vol. 20
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173.
African, Native American, and European mitochondrial DNAs in Cubans from Pinar del Rio Province and implications for the recent epidemic neuropathy in Cuba. Cuba Neuropathy Field Investigation Team.
[electronic resource]
by
Torroni, A
Brown, M D
Lott, M T
Newman, N J
Wallace, D C
Producer:
19950906
In:
Human mutation
vol. 5
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174.
Genetic epidemiologic methods to screen for matrilineal inheritance in mitochondrial disorders.
[electronic resource]
by
Mili, F
Flanders, W D
Sherman, S L
Go, R C
Wallace, D C
Producer:
19970306
In:
Genetic epidemiology
vol. 13
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175.
Maternally inherited mitochondrial myopathy and myoclonic epilepsy.
[electronic resource]
by
Rosing, H S
Hopkins, L C
Wallace, D C
Epstein, C M
Weidenheim, K
Producer:
19850529
In:
Annals of neurology
vol. 17
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176.
Mitochondrial diabetes revisited.
[electronic resource]
by
Ballinger, S W
Shoffner, J M
Gebhart, S
Koontz, D A
Wallace, D C
Producer:
19941229
In:
Nature genetics
vol. 7
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177.
Analysis of mtDNA variation in African populations reveals the most ancient of all human continent-specific haplogroups.
[electronic resource]
by
Chen, Y S
Torroni, A
Excoffier, L
Santachiara-Benerecetti, A S
Wallace, D C
Producer:
19950815
In:
American journal of human genetics
vol. 57
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178.
Severe achondroplasia: demonstration of probable heterogeneity within this clinical syndrome.
[electronic resource]
by
Wallace, D C
Exton, L A
Pritchard, D A
Leung, Y
Cooke, R A
Producer:
19710111
In:
Journal of medical genetics
vol. 7
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179.
Leber's hereditary optic neuropathy: a model for mitochondrial neurodegenerative diseases.
[electronic resource]
by
Brown, M D
Voljavec, A S
Lott, M T
MacDonald, I
Wallace, D C
Producer:
19920827
In:
FASEB journal : official publication of the Federation of American Societies for Experimental Biology
vol. 6
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180.
Mitochondrial oxidative phosphorylation defects in Parkinson's disease.
[electronic resource]
by
Wallace, D C
Shoffner, J M
Watts, R L
Juncos, J L
Torroni, A
Producer:
19920901
In:
Annals of neurology
vol. 32
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