-
1
-
-
0001585429
-
Glucose-6-phosphate dehydrogenase deficiency
-
Scriver CR, Beaudet AL, Sly WS, Valle D (eds). London: McGraw-Hill
-
Luzzatto L, Metha A: Glucose-6-phosphate dehydrogenase deficiency. In Scriver CR, Beaudet AL, Sly WS, Valle D (eds): "The Metabolic Basis of Inherited Disease." Ed. 7. London: McGraw-Hill, 1995.
-
(1995)
The Metabolic Basis of Inherited Disease." Ed. 7
-
-
Luzzatto, L.1
Metha, A.2
-
2
-
-
0025366174
-
The genetics of glucose-6-phosphate dehydrogenase deficiency
-
Beutler E: The genetics of glucose-6-phosphate dehydrogenase deficiency. Semin Hematol 27:137, 1990.
-
(1990)
Semin Hematol
, vol.27
, pp. 137
-
-
Beutler, E.1
-
3
-
-
0025965939
-
Glucose-6-phosphate dehydrogenase deficiency
-
Beutler E: Glucose-6-phosphate dehydrogenase deficiency. N Engl J Med 324:169, 1991.
-
(1991)
N Engl J Med
, vol.324
, pp. 169
-
-
Beutler, E.1
-
4
-
-
0006190008
-
Anémie hémolytique constitutionnelle avec déficit en 6-phosphogluconate dehydrogenase
-
Lausecker C, Heidt P, Fischer D, Hartleyb H, Lohr GW: Anémie hémolytique constitutionnelle avec déficit en 6-phosphogluconate dehydrogenase. Arch Fr Pediatr 22:789, 1965.
-
(1965)
Arch Fr Pediatr
, vol.22
, pp. 789
-
-
Lausecker, C.1
Heidt, P.2
Fischer, D.3
Hartleyb, H.4
Lohr, G.W.5
-
5
-
-
10544254402
-
Anémie hémolytique congénitale non-sphérocytaire avec déficit incomplet en 6-phosphogluconate déshydrogénase
-
Scialom C, Najean Y, Bernard J: Anémie hémolytique congénitale non-sphérocytaire avec déficit incomplet en 6-phosphogluconate déshydrogénase. N Rev Fr Hematol 6:452, 1966.
-
(1966)
N Rev Fr Hematol
, vol.6
, pp. 452
-
-
Scialom, C.1
Najean, Y.2
Bernard, J.3
-
6
-
-
0006236102
-
A new inherited enzymatic deficiency of human erythrocytes. 6-phosphogluconate dehydrogenase deficiency
-
Brewer GJ, Dern RJ: A new inherited enzymatic deficiency of human erythrocytes. 6-phosphogluconate dehydrogenase deficiency. Am J Hum Genet 16:472, 1964.
-
(1964)
Am J Hum Genet
, vol.16
, pp. 472
-
-
Brewer, G.J.1
Dern, R.J.2
-
7
-
-
0014031559
-
Erythrocyte 6 phosphogluconate dehydrogenase polymorphism
-
Parr CW: Erythrocyte 6 phosphogluconate dehydrogenase polymorphism. Nature 210:487, 1966.
-
(1966)
Nature
, vol.210
, pp. 487
-
-
Parr, C.W.1
-
8
-
-
0019082670
-
Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the glycolytic enzymes of erythrocytes
-
Aragon JJ, Feliu JE, Frenkel RA, Sols A: Permeabilization of animal cells for kinetic studies of intracellular enzymes: In situ behavior of the glycolytic enzymes of erythrocytes. Proc Natl Acad Sci USA 77:6324, 1980.
-
(1980)
Proc Natl Acad Sci USA
, vol.77
, pp. 6324
-
-
Aragon, J.J.1
Feliu, J.E.2
Frenkel, R.A.3
Sols, A.4
-
9
-
-
0017185162
-
The removal of leukocytes and platelets from whole blood
-
Beutler E, West C, Blume KG: The removal of leukocytes and platelets from whole blood. J Lab Clin Med 88:328, 1976.
-
(1976)
J Lab Clin Med
, vol.88
, pp. 328
-
-
Beutler, E.1
West, C.2
Blume, K.G.3
-
10
-
-
0014974075
-
The autoxidation of human red cell lipids induced by hydrogen peroxide
-
Stocks J, Dormandy TL: The autoxidation of human red cell lipids induced by hydrogen peroxide. Br J Haematol 20:95, 1972.
-
(1972)
Br J Haematol
, vol.20
, pp. 95
-
-
Stocks, J.1
Dormandy, T.L.2
-
11
-
-
0017347447
-
International Committee for Standardization in Hematology Recommended methods for red cell enzyme analysis
-
Beutler E, Blume KG, Kaplan JC, Lohr CW, Ramot B, Valentine WN: International Committee for Standardization in Hematology Recommended methods for red cell enzyme analysis. Br J Haematol 35:331, 1977.
-
(1977)
Br J Haematol
, vol.35
, pp. 331
-
-
Beutler, E.1
Blume, K.G.2
Kaplan, J.C.3
Lohr, C.W.4
Ramot, B.5
Valentine, W.N.6
-
12
-
-
0022607599
-
Blood cell phosphogluconolactonase: Assay and properties
-
Beutler E, Kuhl W, Gelbart T: Blood cell phosphogluconolactonase: Assay and properties. Br J Haemalol 62:577, 1986.
-
(1986)
Br J Haemalol
, vol.62
, pp. 577
-
-
Beutler, E.1
Kuhl, W.2
Gelbart, T.3
-
13
-
-
73649194769
-
Improved method for determination of blood glutathione
-
Beutler E, Duron O, Kelly BM: Improved method for determination of blood glutathione. J Lab Clin Med 61:882, 1963.
-
(1963)
J Lab Clin Med
, vol.61
, pp. 882
-
-
Beutler, E.1
Duron, O.2
Kelly, B.M.3
-
14
-
-
0013828826
-
Studies on erythrocyte glycolysis. Determination of the glycolytic intermediates in human erythrocytes
-
Minakami L, Suzuki C, Saito T, Yoshikawa K: Studies on erythrocyte glycolysis. Determination of the glycolytic intermediates in human erythrocytes. J Biochem 58:543, 1965.
-
(1965)
J Biochem
, vol.58
, pp. 543
-
-
Minakami, L.1
Suzuki, C.2
Saito, T.3
Yoshikawa, K.4
-
15
-
-
0020438908
-
A kinetic study of pyrophosphate: Fructose 6-phosphate phosphotransferase from potato tubers
-
Van Schaftingen E, Lederer B, Bartrons R, Hers HGA: A kinetic study of pyrophosphate: Fructose 6-phosphate phosphotransferase from potato tubers. Eur J Biochem 129:191, 1982.
-
(1982)
Eur J Biochem
, vol.129
, pp. 191
-
-
Van Schaftingen, E.1
Lederer, B.2
Bartrons, R.3
Hers, H.G.A.4
-
16
-
-
0024582613
-
Fructose 2,6-bisphosphate and 6-phosphofructo 2-kinase in density fractionated human red blood cells
-
Colomer D, Gallego C, Vives Corrons JL, Carreras J, Bartrons R: Fructose 2,6-bisphosphate and 6-phosphofructo 2-kinase in density fractionated human red blood cells. Med Sci Res 17:405, 1989.
-
(1989)
Med Sci Res
, vol.17
, pp. 405
-
-
Colomer, D.1
Gallego, C.2
Vives Corrons, J.L.3
Carreras, J.4
Bartrons, R.5
-
17
-
-
0018099626
-
Glyceraldehyde 3-phosphate dehydrogenase activity studied under physiological conditions with a linear assay
-
Aragon JL, Sols A: Glyceraldehyde 3-phosphate dehydrogenase activity studied under physiological conditions with a linear assay. Biochem Biophys Res Commun 82:1098, 1978.
-
(1978)
Biochem Biophys Res Commun
, vol.82
, pp. 1098
-
-
Aragon, J.L.1
Sols, A.2
-
18
-
-
0018171320
-
Purification of 6-phosphogluconate dehydrogenase from human erythrocytes by blue dextran chromatography
-
Ravazzolo R, Bruzzone G, Garré C, Ajnar F, Salvidio E: Purification of 6-phosphogluconate dehydrogenase from human erythrocytes by blue dextran chromatography. Bull Mol Biol Med 3:148, 1978.
-
(1978)
Bull Mol Biol Med
, vol.3
, pp. 148
-
-
Ravazzolo, R.1
Bruzzone, G.2
Garré, C.3
Ajnar, F.4
Salvidio, E.5
-
19
-
-
0000539176
-
Separation of leukocytes from blood and bone marrow
-
Böyum A: Separation of leukocytes from blood and bone marrow. Scand J Clin Invest 21:51, 1968.
-
(1968)
Scand J Clin Invest
, vol.21
, pp. 51
-
-
Böyum, A.1
-
20
-
-
0027520218
-
Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis
-
Calabro V, Mason P, Filosa S, Civitelli D, Cittadella R, Tagarelli A, Martini G, Brancati C, Luzzatto L: Genetic heterogeneity of glucose-6-phosphate dehydrogenase deficiency revealed by single-strand conformation and sequence analysis. Am J Hum Genet 52:527, 1993.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 527
-
-
Calabro, V.1
Mason, P.2
Filosa, S.3
Civitelli, D.4
Cittadella, R.5
Tagarelli, A.6
Martini, G.7
Brancati, C.8
Luzzatto, L.9
-
21
-
-
0004497053
-
Molecular cloning and nucleotide sequence of cDNA from human glucose-6-phosphate dehydrogenase variant A(-)
-
Hirono A, Beutler E: Molecular cloning and nucleotide sequence of cDNA from human glucose-6-phosphate dehydrogenase variant A(-). Proc Natl Acad Sci USA 85:3951, 1988.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 3951
-
-
Hirono, A.1
Beutler, E.2
-
22
-
-
0344985724
-
Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anaemia
-
Vulliamy TJ, D'Urso M, Battistuzzi G, Estrada M, Foulkes NS, Martini G, Calabro V, Poggi V, Giordano R, Town M, Luzzatto L, Persico MG: Diverse point mutations in the human glucose-6-phosphate dehydrogenase gene cause enzyme deficiency and mild or severe hemolytic anaemia. Proc Natl Acad Sci USA 85:5171, 1988.
-
(1988)
Proc Natl Acad Sci USA
, vol.85
, pp. 5171
-
-
Vulliamy, T.J.1
D'Urso, M.2
Battistuzzi, G.3
Estrada, M.4
Foulkes, N.S.5
Martini, G.6
Calabro, V.7
Poggi, V.8
Giordano, R.9
Town, M.10
Luzzatto, L.11
Persico, M.G.12
-
23
-
-
0026756752
-
A new polymorphic site in the G6PD gene
-
Beutler E, Westwood B, Snipe B: A new polymorphic site in the G6PD gene. Hum Genet 89:485, 1993.
-
(1993)
Hum Genet
, vol.89
, pp. 485
-
-
Beutler, E.1
Westwood, B.2
Snipe, B.3
-
24
-
-
0024493798
-
Two point mutations are responsible for G6PD polymorphism in Sardinia
-
De Vita G, Alcalay M, Sampietro M, Cappelini MD, Fiorelli G, Toniolo D: Two point mutations are responsible for G6PD polymorphism in Sardinia. Am J Hum Genet 44:233, 1989.
-
(1989)
Am J Hum Genet
, vol.44
, pp. 233
-
-
De Vita, G.1
Alcalay, M.2
Sampietro, M.3
Cappelini, M.D.4
Fiorelli, G.5
Toniolo, D.6
-
25
-
-
0026002955
-
Two new polymorphic sites in the G6PD gene of people of African origin and the evolution of the variants' G6PD A and A
-
Vulliamy TJ, Othman A, Town M, Nathwani A, Falusi AG, Mason PJ, Luzzatto L: Two new polymorphic sites in the G6PD gene of people of African origin and the evolution of the variants' G6PD A and A-. Proc Natl Acad Sci USA 88:8568, 1991.
-
(1991)
Proc Natl Acad Sci USA
, vol.88
, pp. 8568
-
-
Vulliamy, T.J.1
Othman, A.2
Town, M.3
Nathwani, A.4
Falusi, A.G.5
Mason, P.J.6
Luzzatto, L.7
-
28
-
-
0013881895
-
Hereditary variation of erythrocytic 6-phosphogluconate dehydrogenase
-
Dern RJ, Brewer GJ, Tashian RE: Hereditary variation of erythrocytic 6-phosphogluconate dehydrogenase. J Lab Clin Med 67:255, 1966.
-
(1966)
J Lab Clin Med
, vol.67
, pp. 255
-
-
Dern, R.J.1
Brewer, G.J.2
Tashian, R.E.3
-
29
-
-
0022363712
-
6-phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency possible interaction with glucose 6-phosphate dehydrogenase deficiency
-
Beutler E, Kuhl W, Gelbart T: 6-phosphogluconolactonase deficiency, a hereditary erythrocyte enzyme deficiency possible interaction with glucose 6-phosphate dehydrogenase deficiency. Proc Natl Acad Sci USA 82:3876, 1985.
-
(1985)
Proc Natl Acad Sci USA
, vol.82
, pp. 3876
-
-
Beutler, E.1
Kuhl, W.2
Gelbart, T.3
-
30
-
-
0017755599
-
Combined G-6PD and 6-PGD deficiency in a Hindu boy
-
Dash S, Bhagwat AC: Combined G-6PD and 6-PGD deficiency in a Hindu boy. Acta Haematol 57:351, 1977.
-
(1977)
Acta Haematol
, vol.57
, pp. 351
-
-
Dash, S.1
Bhagwat, A.C.2
-
31
-
-
0023655408
-
Role of fructose 2,6-bisphosphate in the control of glycolysis in mammalian tissues
-
Hue L, Rider MH: Role of fructose 2,6-bisphosphate in the control of glycolysis in mammalian tissues. Biochem J 245:313, 1987.
-
(1987)
Biochem J
, vol.245
, pp. 313
-
-
Hue, L.1
Rider, M.H.2
-
32
-
-
0023918674
-
Hormonal regulation of hepatic gluconeogenesis and glycolysis
-
Pilkis SJ, El-Maghrabi MR: Hormonal regulation of hepatic gluconeogenesis and glycolysis. Ann Rev Biochem 57:755, 1988.
-
(1988)
Ann Rev Biochem
, vol.57
, pp. 755
-
-
Pilkis, S.J.1
El-Maghrabi, M.R.2
-
33
-
-
0026321442
-
Erythrocyte fructose 2,6-bisphosphate content in congenital hemolytic anemias
-
Colomer D, Pujades A, Carballo E, Vives Corrons JL: Erythrocyte fructose 2,6-bisphosphate content in congenital hemolytic anemias. Hemoglobin 15:517, 1991.
-
(1991)
Hemoglobin
, vol.15
, pp. 517
-
-
Colomer, D.1
Pujades, A.2
Carballo, E.3
Vives Corrons, J.L.4
-
34
-
-
0023043494
-
The reduction-oxidation status may influence the degradation of glyceraldehyde-3-phosphate dehydrogenase
-
Knecht E, Roche E: The reduction-oxidation status may influence the degradation of glyceraldehyde-3-phosphate dehydrogenase. FEES Lett 206:339, 1986.
-
(1986)
FEES Lett
, vol.206
, pp. 339
-
-
Knecht, E.1
Roche, E.2
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