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Results of search for 'au:"WALLACE, D C"', page 12 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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Results
221.
Cloning of neuronal mtDNA variants in cultured cells by synaptosome fusion with mtDNA-less cells.
[electronic resource]
by
Trounce, I
Schmiedel, J
Yen, H C
Hosseini, S
Brown, M D
Olson, J J
Wallace, D C
Producer:
20000626
In:
Nucleic acids research
vol. 28
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222.
Optic disk cupping and electrocardiographic abnormalities in an American pedigree with Leber's hereditary optic neuropathy.
[electronic resource]
by
Ortiz, R G
Newman, N J
Manoukian, S V
Diesenhouse, M C
Lott, M T
Wallace, D C
Producer:
19920601
In:
American journal of ophthalmology
vol. 113
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223.
Leber's disease and dystonia: a mitochondrial disease.
[electronic resource]
by
Novotny, E J
Singh, G
Wallace, D C
Dorfman, L J
Louis, A
Sogg, R L
Steinman, L
Producer:
19860917
In:
Neurology
vol. 36
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224.
Oxidative damage to mitochondrial DNA shows marked age-dependent increases in human brain.
[electronic resource]
by
Mecocci, P
MacGarvey, U
Kaufman, A E
Koontz, D
Shoffner, J M
Wallace, D C
Beal, M F
Producer:
19931112
In:
Annals of neurology
vol. 34
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225.
Accumulation of mitochondrial DNA deletions in the malignant prostate of patients of different ages.
[electronic resource]
by
Jessie, B C
Sun, C Q
Irons, H R
Marshall, F F
Wallace, D C
Petros, J A
Producer:
20020225
In:
Experimental gerontology
vol. 37
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226.
Ocular pathology in mitochondrial superoxide dismutase (Sod2)-deficient mice.
[electronic resource]
by
Sandbach, J M
Coscun, P E
Grossniklaus, H E
Kokoszka, J E
Newman, N J
Wallace, D C
Producer:
20010927
In:
Investigative ophthalmology & visual science
vol. 42
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227.
Genetic studies on the Tharu population of Nepal: restriction endonuclease polymorphisms of mitochondrial DNA.
[electronic resource]
by
Brega, A
Gardella, R
Semino, O
Morpurgo, G
Astaldi Ricotti, G B
Wallace, D C
Santachiara Benerecetti, A S
Producer:
19861121
In:
American journal of human genetics
vol. 39
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228.
Mitochondrial DNA polymorphisms in Italy. I. Population data from Sardinia and Rome.
[electronic resource]
by
Brega, A
Scozzari, R
Maccioni, L
Iodice, C
Wallace, D C
Bianco, I
Cao, A
Santachiara Benerecetti, A S
Producer:
19880418
In:
Annals of human genetics
vol. 50
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229.
Ethnic variation in Hpa 1 endonuclease cleavage patterns of human mitochondrial DNA.
[electronic resource]
by
Denaro, M
Blanc, H
Johnson, M J
Chen, K H
Wilmsen, E
Cavalli-Sforza, L L
Wallace, D C
Producer:
19820128
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 78
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230.
Evidence in a lethal infantile mitochondrial disease for a nuclear mutation affecting respiratory complexes I and IV.
[electronic resource]
by
Zheng, X
Shoffner, J M
Lott, M T
Voljavec, A S
Krawiecki, N S
Winn, K
Wallace, D C
Producer:
19891012
In:
Neurology
vol. 39
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231.
Cuban optic neuropathy.
[electronic resource]
by
Newman, N J
Torroni, A
Brown, M D
Lott, M T
Wallace, D C
Philen, R
Roman, G C
Producer:
19950310
In:
Neurology
vol. 45
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232.
Traumatic aortic rupture: recent outcome with regard to neurologic deficit.
[electronic resource]
by
Attar, S
Cardarelli, M G
Downing, S W
Rodriguez, A
Wallace, D C
West, R S
McLaughlin, J S
Producer:
19990525
In:
The Annals of thoracic surgery
vol. 67
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233.
Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA deletion.
[electronic resource]
by
Ballinger, S W
Shoffner, J M
Hedaya, E V
Trounce, I
Polak, M A
Koontz, D A
Wallace, D C
Producer:
19930610
In:
Nature genetics
vol. 1
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234.
Mitochondrial encephalomyopathy associated with a single nucleotide pair deletion in the mitochondrial tRNALeu(UUR) gene.
[electronic resource]
by
Shoffner, J M
Bialer, M G
Pavlakis, S G
Lott, M
Kaufman, A
Dixon, J
Teichberg, S
Wallace, D C
Producer:
19950310
In:
Neurology
vol. 45
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235.
Classification of European mtDNAs from an analysis of three European populations.
[electronic resource]
by
Torroni, A
Huoponen, K
Francalacci, P
Petrozzi, M
Morelli, L
Scozzari, R
Obinu, D
Savontaus, M L
Wallace, D C
Producer:
19970331
In:
Genetics
vol. 144
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236.
Sleep shift dissociates the nocturnal peaks of parathyroid hormone (1-84), nephrogenous cyclic adenosine monophosphate, and prolactin in normal men.
[electronic resource]
by
Logue, F C
Fraser, W D
O'Reilly, D S
Christie, J
Cameron, D A
Wallace, D C
Beastall, G H
Producer:
19920731
In:
The Journal of clinical endocrinology and metabolism
vol. 75
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237.
A multicentre trial of perhexiline maleate, beta-blocker and placebo in angina pectoris.
[electronic resource]
by
Armstrong, M L
Brand, D
Emmett, A J
Hodge, J L
Kellaway, G S
Mestitz, P
Reefman, M
Wallace, D C
Producer:
19750218
In:
The Medical journal of Australia
vol. 2
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238.
Marked increase in mitochondrial DNA deletion levels in the cerebral cortex of Huntington's disease patients.
[electronic resource]
by
Horton, T M
Graham, B H
Corral-Debrinski, M
Shoffner, J M
Kaufman, A E
Beal, M F
Wallace, D C
Producer:
19951201
In:
Neurology
vol. 45
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239.
Nutrition and its role in human evolution.
[electronic resource]
by
James, W P T
Johnson, R J
Speakman, J R
Wallace, D C
Frühbeck, G
Iversen, P O
Stover, P J
Producer:
20200507
In:
Journal of internal medicine
vol. 285
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240.
Novel mitochondrial DNA deletion found in a renal cell carcinoma.
[electronic resource]
by
Horton, T M
Petros, J A
Heddi, A
Shoffner, J
Kaufman, A E
Graham, S D
Gramlich, T
Wallace, D C
Producer:
19961216
In:
Genes, chromosomes & cancer
vol. 15
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