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Results of search for 'au:"Robinson, B H."', page 6 of 14
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Authors
Barnes, A D
Blainey, J D
Chun, K
Duncan, A M
Feigenbaum, A
Halperin, M L
Ling, M
MacKay, N
Mailer, C
Merante, F
Naik, R B
Oei, J
Petrova-Benedict, R
ROBINSON, B H
Raha, S
Rees, G D
Robinson, B H
Seyda, A
Sherwood, W G
Taylor, J
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Animals
Base Sequence
Cells, Cultured
Child
DNA
Female
Fibroblasts
Humans
Infant
Male
Mitochondria
Molecular Sequence Data
Pyruvate Dehydrogenase Complex
analysis
chemistry
deficiency
enzymology
genetics
metabolism
pharmacology
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101.
Iron metabolism in the anaemia of chronic renal failure. Effects of dialysis and of parenteral iron.
[electronic resource]
by
Carter, R A
Hawkins, J B
Robinson, B H
Producer:
19690822
In:
British medical journal
vol. 3
Online resources:
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102.
The effects of graded doses of phenoxybenzamine on the vascular and capsular responses of the isolated, blood-perfused dogs spleen to sympathetic nerve stimulation and catecholamines.
[electronic resource]
by
Davies, B N
Robinson, B H
Withrington, P G
Producer:
19700124
In:
Archives internationales de pharmacodynamie et de therapie
vol. 180
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103.
Macrocyclic lactone synthesis by lipases in water-in-oil microemulsions.
[electronic resource]
by
Rees, G D
Robinson, B H
Stephenson, G R
Producer:
19950922
In:
Biochimica et biophysica acta
vol. 1257
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104.
Sequential deletion of C-terminal amino acids of the E(1)alpha component of the pyruvate dehydrogenase (PDH) complex leads to reduced steady-state levels of functional E(1)alpha(2)beta(2) tetramers: implications for patients with PDH deficiency.
[electronic resource]
by
Seyda, A
McEachern, G
Haas, R
Robinson, B H
Producer:
20000623
In:
Human molecular genetics
vol. 9
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105.
Pyruvate dehydrogenase phosphatase deficiency: orphan disease or an under-diagnosed condition?
[electronic resource]
by
Maj, M C
Cameron, J M
Robinson, B H
Producer:
20060721
In:
Molecular and cellular endocrinology
vol. 249
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106.
Brain amino acid abnormalities in pyruvate carboxylase deficiency.
[electronic resource]
by
Perry, T L
Haworth, J C
Robinson, B H
Producer:
19870109
In:
Journal of inherited metabolic disease
vol. 8
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107.
NADH-coenzyme Q reductase (complex I) deficiency: heterogeneity in phenotype and biochemical findings.
[electronic resource]
by
Pitkänen, S
Feigenbaum, A
Laframboise, R
Robinson, B H
Producer:
19970303
In:
Journal of inherited metabolic disease
vol. 19
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108.
Maternally inherited hypertrophic cardiomyopathy due to a novel T-to-C transition at nucleotide 9997 in the mitochondrial tRNA(glycine) gene.
[electronic resource]
by
Merante, F
Tein, I
Benson, L
Robinson, B H
Producer:
19941006
In:
American journal of human genetics
vol. 55
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109.
The role of London forces in defining noncentrosymmetric order of high dipole moment-high hyperpolarizability chromophores in electrically poled polymeric thin films.
[electronic resource]
by
Dalton, L R
Harper, A W
Robinson, B H
Producer:
20080417
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 94
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110.
Ventricular tachycardia and fibrillation following quinidine.
[electronic resource]
by
BAKER, C G
ROBINSON, B H
TROUNCE, J R
Producer:
20020501
In:
Guy's Hospital reports
vol. 105
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111.
The effect of adenosine triphosphate on the tricarboxylate transporting system of rat liver mitochondria.
[electronic resource]
by
Robinson, B H
Cheema-Dhadli, S
Halperin, M L
Producer:
19750724
In:
The Journal of biological chemistry
vol. 250
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112.
Defective intramitochondrial NADH oxidation in skin fibroblasts from an infant with fatal neonatal lacticacidemia.
[electronic resource]
by
Robinson, B H
McKay, N
Goodyer, P
Lancaster, G
Producer:
19851031
In:
American journal of human genetics
vol. 37
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113.
Disorders of pyruvate carboxylase and the pyruvate dehydrogenase complex.
[electronic resource]
by
Robinson, B H
MacKay, N
Chun, K
Ling, M
Producer:
19970130
In:
Journal of inherited metabolic disease
vol. 19
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114.
Saguenay Lac Saint Jean cytochrome oxidase deficiency: sequence analysis of nuclear encoded COX subunits, chromosomal localization and a sequence anomaly in subunit VIc.
[electronic resource]
by
Lee, N
Morin, C
Mitchell, G
Robinson, B H
Producer:
19980512
In:
Biochimica et biophysica acta
vol. 1406
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115.
Simultaneous detection of mitochondrial respiratory chain activity and reactive oxygen in digitonin-permeabilized cells using flow cytometry.
[electronic resource]
by
Pham, N A
Robinson, B H
Hedley, D W
Producer:
20010108
In:
Cytometry
vol. 41
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116.
Insulin-resistant diabetes with circulating insulin antibodies.
[electronic resource]
by
ROBINSON, B H
LANGMAN, M J
BANFIELD, P J
Producer:
19981101
In:
Guy's Hospital reports
vol. 110
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117.
Properties of the citrate transporter in rat heart: implications for regulation of glycolysis by cytosolic citrate.
[electronic resource]
by
Cheema-Dhadli, S
Robinson, B H
Halperin, M L
Producer:
19760902
In:
Canadian journal of biochemistry
vol. 54
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118.
Immunoextraction of lipoamide dehydrogenase from cultured skin fibroblasts in patients with combined alpha-ketoacid dehydrogenase deficiency.
[electronic resource]
by
Otulakowski, G
Nyhan, W
Sweetman, L
Robinson, B H
Producer:
19851218
In:
Clinica chimica acta; international journal of clinical chemistry
vol. 152
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119.
Effects of palmitoyl CoA on citrate and malate transport by rat liver mitochondria.
[electronic resource]
by
Halperin, M L
Robinson, B H
Fritz, I B
Producer:
19720720
In:
Proceedings of the National Academy of Sciences of the United States of America
vol. 69
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120.
The functional role of conserved acidic residues of the Qcr7 protein of the cytochrome bc(1) complex in Saccharomyces cerevisiae.
[electronic resource]
by
Lee, S Y
Raha, S
Nagar, B
Robinson, B H
Producer:
20011018
In:
Archives of biochemistry and biophysics
vol. 393
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