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Results of search for 'au:"WALLACE, D C"', page 8 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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Adult
Aged
Animals
Base Sequence
DNA, Mitochondrial
Female
Haplotypes
Humans
Male
Mice
Middle Aged
Mitochondria
Molecular Sequence Data
Mutation
Optic Atrophies, Hereditary
Oxidative Phosphorylation
Pedigree
analysis
genetics
metabolism
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141.
Hypoxanthine-guanine phosphoribosyltransferase and deutan colour blindness: the relative positions of their loci on the X-chromosome.
[electronic resource]
by
Emmerson, B T
Thompson, L
Wallace, D C
Spence, M A
Producer:
19740726
In:
Advances in experimental medicine and biology
vol. 41
Online resources:
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142.
Complete moles have paternal chromosomes but maternal mitochondrial DNA.
[electronic resource]
by
Wallace, D C
Surti, U
Adams, C W
Szulman, A E
Producer:
19821221
In:
Human genetics
vol. 61
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143.
Expression of monoamine oxidase A and B activities in mouse cybrids and hybrids.
[electronic resource]
by
Hawkins, M
Wallace, D C
Eisenstadt, J M
Breakefield, X O
Producer:
19810623
In:
Life sciences
vol. 28
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144.
The basal cell naevus syndrome. Report of a family with anosmia and a case of hypogonadotrophic hypopituitarism.
[electronic resource]
by
Wallace, D C
Murphy, K J
Kelly, L
Ward, W H
Producer:
19730611
In:
Journal of medical genetics
vol. 10
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145.
Phylogenetic analysis of Leber's hereditary optic neuropathy mitochondrial DNA's indicates multiple independent occurrences of the common mutations.
[electronic resource]
by
Brown, M D
Torroni, A
Reckord, C L
Wallace, D C
Producer:
19960816
In:
Human mutation
vol. 6
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146.
Older Americans Act: implications for nursing.
[electronic resource]
by
Wallace, D C
McGuire, S L
Lee, H T
Sauter, M
Producer:
19991012
In:
Nursing outlook
vol. 47
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147.
A case of sporadic infantile histiocytoid cardiomyopathy caused by the A8344G (MERRF) mitochondrial DNA mutation.
[electronic resource]
by
Vallance, H D
Jeven, G
Wallace, D C
Brown, M D
Producer:
20050204
In:
Pediatric cardiology
vol. 25
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148.
Diseases resulting from mitochondrial DNA point mutations.
[electronic resource]
by
Wallace, D C
Lott, M T
Shoffner, J M
Brown, M D
Producer:
19921022
In:
Journal of inherited metabolic disease
vol. 15
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149.
Selective killing of cells with oxidative defects in galactose medium: a screening test for affected patient fibroblasts.
[electronic resource]
by
Petrova-Benedict, R
Buncic, J R
Wallace, D C
Robinson, B H
Producer:
19930408
In:
Journal of inherited metabolic disease
vol. 15
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150.
Assessment of mitochondrial oxidative phosphorylation in patient muscle biopsies, lymphoblasts, and transmitochondrial cell lines.
[electronic resource]
by
Trounce, I A
Kim, Y L
Jun, A S
Wallace, D C
Producer:
19961226
In:
Methods in enzymology
vol. 264
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151.
Mitochondrial DNA variation in Koryaks and Itel'men: population replacement in the Okhotsk Sea-Bering Sea region during the Neolithic.
[electronic resource]
by
Schurr, T G
Sukernik, R I
Starikovskaya, Y B
Wallace, D C
Producer:
19990325
In:
American journal of physical anthropology
vol. 108
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152.
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.
[electronic resource]
by
Chung, A B
Stepien, G
Haraguchi, Y
Li, K
Wallace, D C
Producer:
19921118
In:
The Journal of biological chemistry
vol. 267
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153.
The use of microcomputers for the quantitation of light intensity patterns using digitized video signals.
[electronic resource]
by
Lott, T J
Yang, J H
Ye, J H
Wallace, D C
Producer:
19890605
In:
Computer applications in the biosciences : CABIOS
vol. 1
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154.
Ancient mtDNA sequences in the human nuclear genome: a potential source of errors in identifying pathogenic mutations.
[electronic resource]
by
Wallace, D C
Stugard, C
Murdock, D
Schurr, T
Brown, M D
Producer:
19980202
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 94
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155.
Expression and sequence analysis of the mouse adenine nucleotide translocase 1 and 2 genes.
[electronic resource]
by
Levy, S E
Chen, Y S
Graham, B H
Wallace, D C
Producer:
20001030
In:
Gene
vol. 254
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156.
Evaluation of procedures for assaying oxidative phosphorylation enzyme activities in mitochondrial myopathy muscle biopsies.
[electronic resource]
by
Zheng, X X
Shoffner, J M
Voljavec, A S
Wallace, D C
Producer:
19901016
In:
Biochimica et biophysica acta
vol. 1019
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157.
Mitochondrial biology, degenerative diseases and aging.
[electronic resource]
by
Wallace, D C
Brown, M D
Melov, S
Graham, B
Lott, M
Producer:
19980624
In:
BioFactors (Oxford, England)
vol. 7
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158.
Up-regulation of nuclear and mitochondrial genes in the skeletal muscle of mice lacking the heart/muscle isoform of the adenine nucleotide translocator.
[electronic resource]
by
Murdock, D G
Boone, B E
Esposito, L A
Wallace, D C
Producer:
19990617
In:
The Journal of biological chemistry
vol. 274
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159.
Use of home and community-based services by elderly black and white females.
[electronic resource]
by
Wallace, D C
Fields, B L
Witucki, J
Boland, C
Tuck, I
Producer:
20000330
In:
Journal of women & aging
vol. 11
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160.
Association of mitochondrial DNA damage with aging and coronary atherosclerotic heart disease.
[electronic resource]
by
Corral-Debrinski, M
Shoffner, J M
Lott, M T
Wallace, D C
Producer:
19921123
In:
Mutation research
vol. 275
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