-
1
-
-
0027940492
-
G6PD deficiency
-
Beutler E. G6PD deficiency. Blood 84 (1994) 3613-3636
-
(1994)
Blood
, vol.84
, pp. 3613-3636
-
-
Beutler, E.1
-
2
-
-
0742299380
-
Glucose-6-phosphate dehydrogenase deficiency and related disorders
-
Handin R.I., Lux IV S.E., and Stossel T.P. (Eds), Lippincott Williams and Wilkins, Philadelphia
-
Vulliamy T.J., and Luzzatto L. Glucose-6-phosphate dehydrogenase deficiency and related disorders. In: Handin R.I., Lux IV S.E., and Stossel T.P. (Eds). Blood, Principles and Practice of Hematology (2003), Lippincott Williams and Wilkins, Philadelphia 1921-1950
-
(2003)
Blood, Principles and Practice of Hematology
, pp. 1921-1950
-
-
Vulliamy, T.J.1
Luzzatto, L.2
-
3
-
-
34547702206
-
G6PD deficiency: the genotype-phenotype association
-
Mason P.J., Bautista J.M., and Gilsanz F. G6PD deficiency: the genotype-phenotype association. Blood Rev. 21 (2007) 267-283
-
(2007)
Blood Rev.
, vol.21
, pp. 267-283
-
-
Mason, P.J.1
Bautista, J.M.2
Gilsanz, F.3
-
4
-
-
0033119971
-
Solution of the structure of tetrameric human glucose 6-phosphate dehydrogenase by molecular replacement
-
Au S.W.N., Naylor C.E., Gover S., Vandeputte-Rutten L., Scopes D.A., Mason P.J., Luzzatto L., Lam V.M.S., and Adams M.J. Solution of the structure of tetrameric human glucose 6-phosphate dehydrogenase by molecular replacement. Acta Crystallogr. D: Biol. Crystallogr. 55 (1999) 826-834
-
(1999)
Acta Crystallogr. D: Biol. Crystallogr.
, vol.55
, pp. 826-834
-
-
Au, S.W.N.1
Naylor, C.E.2
Gover, S.3
Vandeputte-Rutten, L.4
Scopes, D.A.5
Mason, P.J.6
Luzzatto, L.7
Lam, V.M.S.8
Adams, M.J.9
-
9
-
-
33747880180
-
Functional properties of two mutants of human glucose 6-phosphate dehydrogenase, R393G and R393H, corresponding to the clinical variants G6PD Wisconsin and Nashville
-
Wang X.T., Lam V.M.S., and Engel P.C. Functional properties of two mutants of human glucose 6-phosphate dehydrogenase, R393G and R393H, corresponding to the clinical variants G6PD Wisconsin and Nashville. Biochim. Biophys. Acta 1762 (2006) 767-774
-
(2006)
Biochim. Biophys. Acta
, vol.1762
, pp. 767-774
-
-
Wang, X.T.1
Lam, V.M.S.2
Engel, P.C.3
-
11
-
-
0039003910
-
Structural defects underlying protein dysfunction in human glucose-6-phosphate dehydrogenase A(-) deficiency
-
Gomez-Gallego F., Garrido-Pertierra A., and Bautista J.M. Structural defects underlying protein dysfunction in human glucose-6-phosphate dehydrogenase A(-) deficiency. J. Biol. Chem. 275 (2000) 9256-9262
-
(2000)
J. Biol. Chem.
, vol.275
, pp. 9256-9262
-
-
Gomez-Gallego, F.1
Garrido-Pertierra, A.2
Bautista, J.M.3
-
14
-
-
63049110913
-
An optimised system for refolding of human glucose 6-phosphate dehydrogenase
-
Wang X.T., and Engel P.C. An optimised system for refolding of human glucose 6-phosphate dehydrogenase. BMC Biotechnol. 9 (2009) 19
-
(2009)
BMC Biotechnol.
, vol.9
, pp. 19
-
-
Wang, X.T.1
Engel, P.C.2
-
15
-
-
37049252628
-
Hybridization of glucose-6-phosphate dehydrogenase from rat and human erythrocytes
-
Beutler E., and Collins Z. Hybridization of glucose-6-phosphate dehydrogenase from rat and human erythrocytes. Science 150 (1965) 1306-1307
-
(1965)
Science
, vol.150
, pp. 1306-1307
-
-
Beutler, E.1
Collins, Z.2
-
16
-
-
0014213365
-
In vitro hybridization of normal and variant human glucose-6-phosphate dehydrogenase
-
Yoshida A., Steinmann L., and Harbert P. In vitro hybridization of normal and variant human glucose-6-phosphate dehydrogenase. Nature 216 (1967) 275-276
-
(1967)
Nature
, vol.216
, pp. 275-276
-
-
Yoshida, A.1
Steinmann, L.2
Harbert, P.3
-
17
-
-
0036375584
-
Recombinant human glucose-6-phosphate dehydrogenase. Evidence for a rapid-equilibrium random-order mechanism
-
Wang X.T., Au S.W.N., Lam V.M.S., and Engel P.C. Recombinant human glucose-6-phosphate dehydrogenase. Evidence for a rapid-equilibrium random-order mechanism. Eur. J. Biochem. 269 (2002) 3417-3424
-
(2002)
Eur. J. Biochem.
, vol.269
, pp. 3417-3424
-
-
Wang, X.T.1
Au, S.W.N.2
Lam, V.M.S.3
Engel, P.C.4
-
18
-
-
73849179051
-
Glucose 6-phosphate dehydrogenase from human erythrocytes. II. Subactive states of the enzyme from normal persons
-
Kirkman H.N., and Hendrickson E.M. Glucose 6-phosphate dehydrogenase from human erythrocytes. II. Subactive states of the enzyme from normal persons. J. Biol. Chem. 237 (1962) 2371-2376
-
(1962)
J. Biol. Chem.
, vol.237
, pp. 2371-2376
-
-
Kirkman, H.N.1
Hendrickson, E.M.2
-
19
-
-
0001491568
-
Human erythrocyte glucose 6-phosphate dehydrogenase. II. Enzyme-coenzyme interrelationship
-
Chung A.E., and Langdon R.G. Human erythrocyte glucose 6-phosphate dehydrogenase. II. Enzyme-coenzyme interrelationship. J. Biol. Chem. 238 (1963) 2317-2324
-
(1963)
J. Biol. Chem.
, vol.238
, pp. 2317-2324
-
-
Chung, A.E.1
Langdon, R.G.2
-
20
-
-
0013852431
-
Different properties of glucose 6-phosphate dehydrogenase from human erythrocytes with normal and abnormal enzyme levels
-
Luzzatto L., and Allan N.C. Different properties of glucose 6-phosphate dehydrogenase from human erythrocytes with normal and abnormal enzyme levels. Biochem. Biophys. Res. Commun. 21 (1965) 547-554
-
(1965)
Biochem. Biophys. Res. Commun.
, vol.21
, pp. 547-554
-
-
Luzzatto, L.1
Allan, N.C.2
-
21
-
-
0014936665
-
Distinctive patterns of NADP binding to dimeric and tetrameric glucose 6-phosphate dehydrogenase from human red cells
-
Bonsignore A., Lorenzoni I., Cancedda R., and De Flora A. Distinctive patterns of NADP binding to dimeric and tetrameric glucose 6-phosphate dehydrogenase from human red cells. Biochem. Biophys. Res. Commun. 39 (1970) 142-148
-
(1970)
Biochem. Biophys. Res. Commun.
, vol.39
, pp. 142-148
-
-
Bonsignore, A.1
Lorenzoni, I.2
Cancedda, R.3
De Flora, A.4
-
22
-
-
0015918157
-
Hemolytic anemia and G6PD deficiency
-
Yoshida A. Hemolytic anemia and G6PD deficiency. Science 179 (1973) 532-537
-
(1973)
Science
, vol.179
, pp. 532-537
-
-
Yoshida, A.1
-
23
-
-
0027512086
-
G6PD "Campinas:" a deficient enzyme with a mutation at the far 3′ end of the gene
-
Baronciani L., Tricta F., and Beutler E. G6PD "Campinas:" a deficient enzyme with a mutation at the far 3′ end of the gene. Hum. Mutat. 2 (1993) 77-78
-
(1993)
Hum. Mutat.
, vol.2
, pp. 77-78
-
-
Baronciani, L.1
Tricta, F.2
Beutler, E.3
-
24
-
-
0031213525
-
-
A. Hirono (1994) Unpublished. Cited in: T. Vulliamy, L. Luzzatto, A. Hirono, E. Beutler, Hematologically important mutations: glucose-6-phosphate dehydrogenase, Blood Cells Mol. Dis. 23 (1997) 302-313.
-
A. Hirono (1994) Unpublished. Cited in: T. Vulliamy, L. Luzzatto, A. Hirono, E. Beutler, Hematologically important mutations: glucose-6-phosphate dehydrogenase, Blood Cells Mol. Dis. 23 (1997) 302-313.
-
-
-
-
25
-
-
0029003588
-
Three new exon 10 glucose-6-phosphate dehydrogenase mutations
-
Beutler E., Westwood B., Melemed A., Dal Borgo P., and Margolis D. Three new exon 10 glucose-6-phosphate dehydrogenase mutations. Blood Cells Mol. Diseases 21 (1995) 64-72
-
(1995)
Blood Cells Mol. Diseases
, vol.21
, pp. 64-72
-
-
Beutler, E.1
Westwood, B.2
Melemed, A.3
Dal Borgo, P.4
Margolis, D.5
-
26
-
-
0025763140
-
DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants
-
Beutler E., Kuhl W., Gelbart T., and Forman L. DNA sequence abnormalities of human glucose-6-phosphate dehydrogenase variants. J. Biol. Chem. 266 (1991) 4145-4150
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 4145-4150
-
-
Beutler, E.1
Kuhl, W.2
Gelbart, T.3
Forman, L.4
-
27
-
-
67651110423
-
-
A. Hirono, H. Fujii, S. Miwa, (1997) Unpublished. Cited in T. Vulliamy, L. Luzzatto, A. Hirono, E. Beutler, Hematologically important mutations: glucose-6-phosphate dehydrogenase, Blood Cells Mol. Diseases 23 (1997) 302-313.
-
A. Hirono, H. Fujii, S. Miwa, (1997) Unpublished. Cited in T. Vulliamy, L. Luzzatto, A. Hirono, E. Beutler, Hematologically important mutations: glucose-6-phosphate dehydrogenase, Blood Cells Mol. Diseases 23 (1997) 302-313.
-
-
-
-
28
-
-
43449133253
-
Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency
-
Minucci A., Concolino P., Vendittelli F., Giardina B., Zuppi C., and Capoluongo E. Glucose-6-phosphate dehydrogenase Buenos Aires: a novel de novo missense mutation associated with severe enzyme deficiency. Clin. Biochem. 41 (2008) 742-745
-
(2008)
Clin. Biochem.
, vol.41
, pp. 742-745
-
-
Minucci, A.1
Concolino, P.2
Vendittelli, F.3
Giardina, B.4
Zuppi, C.5
Capoluongo, E.6
-
29
-
-
0032518592
-
Amino acid substitutions at the dimer interface of human glucose-6-phosphate dehydrogenase that increase thermostability and reduce the stabilising effect of NADP
-
Scopes D.A., Bautista J.M., Naylor C.E., Adams M.J., and Mason P.J. Amino acid substitutions at the dimer interface of human glucose-6-phosphate dehydrogenase that increase thermostability and reduce the stabilising effect of NADP. Eur. J. Biochem. 251 (1998) 382-388
-
(1998)
Eur. J. Biochem.
, vol.251
, pp. 382-388
-
-
Scopes, D.A.1
Bautista, J.M.2
Naylor, C.E.3
Adams, M.J.4
Mason, P.J.5
-
30
-
-
0001594119
-
Initial steady state velocities in the evaluation of enzyme-coenzyme-substrate reaction mechanisms
-
Dalziel K. Initial steady state velocities in the evaluation of enzyme-coenzyme-substrate reaction mechanisms. Acta Chem. Scand. 11 (1957) 1706-1723
-
(1957)
Acta Chem. Scand.
, vol.11
, pp. 1706-1723
-
-
Dalziel, K.1
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