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Results of search for 'au:"WALLACE, D C"', page 5 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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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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81.
Community-based service use among the young, middle, and old old.
[electronic resource]
by
Wallace, D C
Hirst, P K
Producer:
19961104
In:
Public health nursing (Boston, Mass.)
vol. 13
Online resources:
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82.
Research priorities in mental health nursing.
[electronic resource]
by
Pullen, L
Tuck, I
Wallace, D C
Producer:
20000629
In:
Issues in mental health nursing
vol. 20
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83.
Mitochondrial mutations in cancer.
[electronic resource]
by
Brandon, M
Baldi, P
Wallace, D C
Producer:
20060920
In:
Oncogene
vol. 25
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84.
Comparison of mitochondrially synthesized polypeptides of human, mouse, and monkey cell lines by a two-dimensional protease gel system.
[electronic resource]
by
Oliver, N
McCarthy, J
Wallace, D C
Producer:
19850114
In:
Somatic cell and molecular genetics
vol. 10
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85.
Conformational mutations in human mitochondrial DNA.
[electronic resource]
by
Singh, G
Neckelmann, N
Wallace, D C
Producer:
19871019
In:
Nature
vol. 329
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86.
Cytoplasmic transfer of the mtDNA nt 8993 T-->G (ATP6) point mutation associated with Leigh syndrome into mtDNA-less cells demonstrates cosegregation with a decrease in state III respiration and ADP/O ratio.
[electronic resource]
by
Trounce, I
Neill, S
Wallace, D C
Producer:
19941004
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 91
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87.
A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy.
[electronic resource]
by
Singh, G
Lott, M T
Wallace, D C
Producer:
19890615
In:
The New England journal of medicine
vol. 320
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88.
OXBOX, a positive transcriptional element of the heart-skeletal muscle ADP/ATP translocator gene.
[electronic resource]
by
Li, K
Hodge, J A
Wallace, D C
Producer:
19901228
In:
The Journal of biological chemistry
vol. 265
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89.
mtDNA variation, climatic adaptation, degenerative diseases, and longevity.
[electronic resource]
by
Wallace, D C
Ruiz-Pesini, E
Mishmar, D
Producer:
20041008
In:
Cold Spring Harbor symposia on quantitative biology
vol. 68
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90.
Dramatic founder effects in Amerindian mitochondrial DNAs.
[electronic resource]
by
Wallace, D C
Garrison, K
Knowler, W C
Producer:
19851219
In:
American journal of physical anthropology
vol. 68
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91.
Clustering of Caucasian Leber hereditary optic neuropathy patients containing the 11778 or 14484 mutations on an mtDNA lineage.
[electronic resource]
by
Brown, M D
Sun, F
Wallace, D C
Producer:
19970213
In:
American journal of human genetics
vol. 60
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92.
Mouse models of mitochondrial disease, oxidative stress, and senescence.
[electronic resource]
by
Melov, S
Coskun, P E
Wallace, D C
Producer:
19990928
In:
Mutation research
vol. 434
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93.
Different nucleotide changes in the large rRNA gene of the mitochondrial DNA confer chloramphenicol resistance on two human cell lines.
[electronic resource]
by
Blanc, H
Adams, C W
Wallace, D C
Producer:
19820222
In:
Nucleic acids research
vol. 9
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94.
Characterization of mitochondrial DNA in chloramphenicol-resistant interspecific hybrids and a cybrid.
[electronic resource]
by
Giles, R E
Stroynowski, I
Wallace, D C
Producer:
19810224
In:
Somatic cell genetics
vol. 6
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95.
Cytoplasmic transfer of chloramphenicol resistance in human tissue culture cells.
[electronic resource]
by
Wallace, D C
Bunn, C L
Eisenstadt, J M
Producer:
19751220
In:
The Journal of cell biology
vol. 67
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96.
The clinical characteristics of pedigrees of Leber's hereditary optic neuropathy with the 11778 mutation.
[electronic resource]
by
Newman, N J
Lott, M T
Wallace, D C
Producer:
19910628
In:
American journal of ophthalmology
vol. 111
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97.
Mitochondrial DNA in anucleate human blood cells.
[electronic resource]
by
Shuster, R C
Rubenstein, A J
Wallace, D C
Producer:
19881121
In:
Biochemical and biophysical research communications
vol. 155
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98.
Mitotic segregation of cytoplasmic determinants for chloramphenicol resistance in mammalian cells II: Fusions with human cell lines.
[electronic resource]
by
Wallace, D C
Bunn, C L
Eisenstadt, J M
Producer:
19780321
In:
Somatic cell genetics
vol. 3
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99.
Partial deficiency of hypoxanthine-guanine phosphoribosyltransferase: intermediate enzyme deficiency in heterozygote red cells.
[electronic resource]
by
Emmerson, B T
Wallace, D C
Thompson, C J
Producer:
19720407
In:
Annals of internal medicine
vol. 76
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100.
Monosomy of a "G" autosome in a 22-year-old female.
[electronic resource]
by
Cooksley, W G
Firouz-Abadi, A
Wallace, D C
Producer:
19731204
In:
The Medical journal of Australia
vol. 2
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