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Results of search for 'au:"Wakazono, A"'
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Authors
Donlan, M A
Dunbar, G
Fukao, T
Hashimoto, T
Hoganson, G
Horai, T
Hori, T
Kano, M
Katakura, R
Kimura, M
Kinoshita, Y
Kondo, N
Kuwahara, T
Lambert, M
Lee, G W
Masuno, M
Orii, T
Song, X Q
Wakazono, A
Yamaguchi, S
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Topics
Acetyl-CoA C-Acetyltransferase
Acetyl-CoA C-Acyltransferase
Adult
Amino Acid Sequence
Base Sequence
Child
Female
Fibroblasts
Humans
Immunoblotting
Infant
Male
Mitochondria
Molecular Sequence Data
Mutation
Point Mutation
analysis
deficiency
enzymology
genetics
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English
Your search returned 11 results.
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Results
1.
Hemispheric asymmetry of event-related potentials in a patient with callosal disconnection syndrome: a comparison of auditory, visual and somatosensory modalities.
[electronic resource]
by
Satomi, K
Horai, T
Kinoshita, Y
Wakazono, A
Producer:
19950815
In:
Electroencephalography and clinical neurophysiology
vol. 94
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2.
Interstitial deletion of the long arm of chromosome 11: report of a case and review of the literature.
[electronic resource]
by
Wakazono, A
Masuno, M
Yamaguchi, S
Tsubouchi, K
Kondo, N
Orii, T
Producer:
19930202
In:
The Japanese journal of human genetics
vol. 37
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3.
Interstitial deletion of the long arm of chromosome 11 determined by fluorescence in situ hybridization.
[electronic resource]
by
Hori, T
Masuno, M
Wakazono, A
Takahashi, E
Katakura, R
Orii, T
Producer:
19930929
In:
The Japanese journal of human genetics
vol. 38
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4.
Identification of a novel exonic mutation at -13 from 5' splice site causing exon skipping in a girl with mitochondrial acetoacetyl-coenzyme A thiolase deficiency.
[electronic resource]
by
Fukao, T
Yamaguchi, S
Wakazono, A
Orii, T
Hoganson, G
Hashimoto, T
Producer:
19940421
In:
The Journal of clinical investigation
vol. 93
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5.
Biochemical and immunochemical study of seven families with 3-ketothiolase deficiency: diagnosis of heterozygotes using immunochemical determination of the ratio of mitochondrial acetoacetyl-CoA thiolase and 3-ketoacyl-CoA thiolase proteins.
[electronic resource]
by
Yamaguchi, S
Sakai, A
Fukao, T
Wakazono, A
Kuwahara, T
Orii, T
Hashimoto, T
Producer:
19930715
In:
Pediatric research
vol. 33
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6.
Further analysis of mutant thiolase protein in fibroblasts from a Japanese boy with 3-ketothiolase deficiency.
[electronic resource]
by
Yamaguchi, S
Fukao, T
Kano, M
Wakazono, A
Orii, T
Sakura, N
Hashimoto, T
Producer:
19930202
In:
The Tohoku journal of experimental medicine
vol. 167
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7.
Molecular basis of 3-ketothiolase deficiency: detection of gene mutations and expression of mutant cDNAs of mitochondrial acetoacetyl-CoA thiolase.
[electronic resource]
by
Fukao, T
Yamaguchi, S
Wakazono, A
Okamoto, H
Orii, T
Osumi, T
Hashimoto, T
Producer:
19921223
In:
Journal of inherited metabolic disease
vol. 15
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8.
Prenatal diagnosis in a family with mitochondrial acetoacetyl-coenzyme A thiolase deficiency with the use of the polymerase chain reaction followed by the heteroduplex detection method.
[electronic resource]
by
Fukao, T
Wakazono, A
Song, X Q
Yamaguchi, S
Zacharias, R
Donlan, M A
Orii, T
Producer:
19950818
In:
Prenatal diagnosis
vol. 15
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9.
Molecular studies of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in the two original families.
[electronic resource]
by
Fukao, T
Yamaguchi, S
Scriver, C R
Dunbar, G
Wakazono, A
Kano, M
Orii, T
Hashimoto, T
Producer:
19931006
In:
Human mutation
vol. 2
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10.
Practical assay method of cytosolic acetoacetyl-CoA thiolase by rapid release of cytosolic enzymes from cultured lymphocytes using digitonin.
[electronic resource]
by
Watanabe, H
Yamaguchi, S
Kimura, M
Wakazono, A
Song, X Q
Fukao, T
Orii, T
Hashimoto, T
Producer:
19980727
In:
The Tohoku journal of experimental medicine
vol. 184
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11.
Molecular, biochemical, and clinical characterization of mitochondrial acetoacetyl-coenzyme A thiolase deficiency in two further patients.
[electronic resource]
by
Wakazono, A
Fukao, T
Yamaguchi, S
Hori, T
Orii, T
Lambert, M
Mitchell, G A
Lee, G W
Hashimoto, T
Producer:
19950530
In:
Human mutation
vol. 5
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