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Results: 1-25 |
Results: 25
The 2,3-bisphosphoglycerate-independent phosphoglycerate mutase from Trypanosoma brucei: metal-ion dependency and phosphoenzyme formation
Authors: Collet, JF Stroobant, V Van Schaftingen, E
Citation: Jf. Collet et al., The 2,3-bisphosphoglycerate-independent phosphoglycerate mutase from Trypanosoma brucei: metal-ion dependency and phosphoenzyme formation, FEMS MICROB, 204(1), 2001, pp. 39-44
Analysis of the cooperativity of human beta-cell glucokinase through the stimulatory effect of glucose on fructose phosphorylation
Authors: Moukil, MA Van Schaftingen, E
Citation: Ma. Moukil et E. Van Schaftingen, Analysis of the cooperativity of human beta-cell glucokinase through the stimulatory effect of glucose on fructose phosphorylation, J BIOL CHEM, 276(6), 2001, pp. 3872-3878
Novel arguments in favor of the substrate-transport model of glucose-6-phosphatase
Authors: Gerin, I Noel, G Van Schaftingen, E
Citation: I. Gerin et al., Novel arguments in favor of the substrate-transport model of glucose-6-phosphatase, DIABETES, 50(7), 2001, pp. 1531-1538
High frequency of cytolytic T lymphocytes directed against a tumor-specific mutated antigen detectable with HLA tetramers in the blood of a lung carcinoma patient with long survival
Authors: Karanikas, V Colau, D Baurain, JF Chiari, R Thonnard, J Gutierrez-Roelens, I Goffinet, C Van Schaftingen, E Weynants, P Boon, T Coulie, PG
Citation: V. Karanikas et al., High frequency of cytolytic T lymphocytes directed against a tumor-specific mutated antigen detectable with HLA tetramers in the blood of a lung carcinoma patient with long survival, CANCER RES, 61(9), 2001, pp. 3718-3724
High residual activity of PMM2 in patients' fibroblasts: Possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency)
Authors: Grunewald, S Schollen, E Van Schaftingen, E Jaeken, J Matthijs, G
Citation: S. Grunewald et al., High residual activity of PMM2 in patients' fibroblasts: Possible pitfall in the diagnosis of CDG-Ia (phosphomannomutase deficiency), AM J HU GEN, 68(2), 2001, pp. 347-354
"Overexpression and purification of fructose-1-phosphate kinase from Escherichia coli: Application to the assay of fructose 1-phosphate," (vol 19, pg48, 2000)
Authors: Veiga-da-Cunha, M Hoyoux, A Van Schaftingen, E
Citation: M. Veiga-da-cunha et al., "Overexpression and purification of fructose-1-phosphate kinase from Escherichia coli: Application to the assay of fructose 1-phosphate," (vol 19, pg48, 2000), PROT EX PUR, 20(1), 2000, pp. 132-132
Overexpression and purification of fructose-1-phosphate kinase from Escherichia coli: Application to the assay of fructose 1-phosphate
Authors: Veiga-da-Cunha, M Houyoux, A Van Schaftingen, E
Citation: M. Veiga-da-cunha et al., Overexpression and purification of fructose-1-phosphate kinase from Escherichia coli: Application to the assay of fructose 1-phosphate, PROT EX PUR, 19(1), 2000, pp. 48-52
Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG
Authors: Aebi, M Helenius, A Schenk, B Barone, R Fiumara, A Berger, EG Hennet, T Imbach, T Stutz, A Bjursell, C Uller, A Wahlstrom, JG Briones, P Cardo, E Clayton, P Winchester, B Cormier-Daire, V de Lonlay, P Cuer, M Dupre, T Seta, N de Koning, T Dorland, L de Loos, F Kupers, L Fabritz, L Hasilik, M Marquardt, T Niehues, R Freeze, H Grunewald, S Heykants, L Jaeken, J Matthijs, G Schollen, E Keir, G Kjaergaard, S Schwartz, M Skovby, F Klein, A Roussel, P Korner, C Lubke, T Thiel, C von Figura, K Koscielak, J Krasnewich, D Lehle, L Peters, V Raab, M Saether, O Schachter, H Van Schaftingen, E Verbert, A Vilaseca, A Wevers, R Yamashita, K
Citation: M. Aebi et al., Carbohydrate-deficient glycoprotein syndromes become congenital disorders of glycosylation: an updated nomenclature for CDG, GLYCOBIOLOG, 10(6), 2000, pp. III-V
The gene encoding rat 3-phosphoglycerate dehydrogenase
Authors: Robbi, M Achouri, Y Szpirer, C Van Schaftingen, E
Citation: M. Robbi et al., The gene encoding rat 3-phosphoglycerate dehydrogenase, MAMM GENOME, 11(11), 2000, pp. 1034-1036
How many forms of glycogen storage disease type I?
Authors: Veiga-da-Cunha, M Gerin, I Van Schaftingen, E
Citation: M. Veiga-da-cunha et al., How many forms of glycogen storage disease type I?, EUR J PED, 159(5), 2000, pp. 314-318
Conversion of a synthetic fructosamine into its 3-phospho derivative in human erythrocytes
Authors: Delpierre, G Vanstapel, F Stroobant, V Van Schaftingen, E
Citation: G. Delpierre et al., Conversion of a synthetic fructosamine into its 3-phospho derivative in human erythrocytes, BIOCHEM J, 352, 2000, pp. 835-839
Carbohydrate-deficient glycoprotein syndrome: Beyond the screen
Authors: Fletcher, JM Matthijs, G Jaeken, J Van Schaftingen, E Nelson, PV
Citation: Jm. Fletcher et al., Carbohydrate-deficient glycoprotein syndrome: Beyond the screen, J INH MET D, 23(4), 2000, pp. 396-398
Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicism
Authors: Knopf, C Rod, R Jaeken, J Berant, M Van Schaftingen, E Fryns, JP Brill-Zamir, R Gershoni-Baruch, R Lischinsky, S Mandel, H
Citation: C. Knopf et al., Transferrin protein variant mimicking carbohydrate-deficient glycoprotein syndrome in trisomy 7 mosaicism, J INH MET D, 23(4), 2000, pp. 399-403
Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype
Authors: Weston, BW Lin, JL Muenzer, J Cameron, HS Arnold, RR Seydewitz, HH Mayatepek, E Van Schaftingen, E Veiga-Da-Cunha, M Matern, D Chen, YT
Citation: Bw. Weston et al., Glucose-6-phosphatase mutation G188R confers an atypical glycogen storage disease type 1b phenotype, PEDIAT RES, 48(3), 2000, pp. 329-334
Study of the regulatory properties of glucokinase by site-directed mutagenesis - Conversion of glucokinase to an enzyme with high affinity for glucose
Authors: Moukil, MA Veiga-da-Cunha, M Van Schaftingen, E
Citation: Ma. Moukil et al., Study of the regulatory properties of glucokinase by site-directed mutagenesis - Conversion of glucokinase to an enzyme with high affinity for glucose, DIABETES, 49(2), 2000, pp. 195-201
Identification, cloning, and heterologous expression of a mammalian fructosamine-3-kinase
Authors: Delpierre, G Rider, MH Collard, F Stroobant, V Vanstapel, F Santos, H Van Schaftingen, E
Citation: G. Delpierre et al., Identification, cloning, and heterologous expression of a mammalian fructosamine-3-kinase, DIABETES, 49(10), 2000, pp. 1627-1634
3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome
Authors: Pineda, M Vilaseca, MA Artuch, R Santos, S Gonzalez, MMG Sau, I Aracil, A Van Schaftingen, E Jaeken, J
Citation: M. Pineda et al., 3-phosphoglycerate dehydrogenase deficiency in a patient with West syndrome, DEVELOP MED, 42(9), 2000, pp. 629-633
The Putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a
Authors: Veiga-Da-Cunha, M Gerin, I Chen, YT Lee, PJ Leonard, JV Maire, I Wendel, U Vikkula, M Van Schaftingen, E
Citation: M. Veiga-da-cunha et al., The Putative glucose 6-phosphate translocase gene is mutated in essentially all cases of glycogen storage disease type I non-a, EUR J HUM G, 7(6), 1999, pp. 717-723
Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency)
Authors: Carchon, H Van Schaftingen, E Matthijs, G Jaeken, J
Citation: H. Carchon et al., Carbohydrate-deficient glycoprotein syndrome type IA (phosphomannomutase-deficiency), BBA-MOL BAS, 1455(2-3), 1999, pp. 155-165
Structure of the gene mutated in glycogen storage disease type Ib
Authors: Gerin, I Veiga-da-Cunha, M Noel, C Van Schaftingen, E
Citation: I. Gerin et al., Structure of the gene mutated in glycogen storage disease type Ib, GENE, 227(2), 1999, pp. 189-195
Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes
Authors: Pirard, M Achouri, Y Collet, JF Schollen, E Matthijs, G Van Schaftingen, E
Citation: M. Pirard et al., Kinetic properties and tissular distribution of mammalian phosphomannomutase isozymes, BIOCHEM J, 339, 1999, pp. 201-207
Mechanistic studies of phosphoserine phosphatase, an enzyme related to P-type ATPases
Authors: Collet, JF Stroobant, V Van Schaftingen, E
Citation: Jf. Collet et al., Mechanistic studies of phosphoserine phosphatase, an enzyme related to P-type ATPases, J BIOL CHEM, 274(48), 1999, pp. 33985-33990
acs1 of Haemophilus influenzae type a capsulation locus region II encodes a bifunctional ribulose 5-phosphate reductase-CDP-ribitol pyrophosphorylase
Authors: Follens, A Veiga-Da-Cunha, M Merckx, R Van Schaftingen, E Van Eldere, J
Citation: A. Follens et al., acs1 of Haemophilus influenzae type a capsulation locus region II encodes a bifunctional ribulose 5-phosphate reductase-CDP-ribitol pyrophosphorylase, J BACT, 181(7), 1999, pp. 2001-2007
Identification of the cDNA en coding human 6-phosphogluconolactonase, the enzyme catalyzing the second step of the pentose phosphate pathway
Authors: Collard, F Collet, JF Gerin, I Veiga-da-Cunha, M Van Schaftingen, E
Citation: F. Collard et al., Identification of the cDNA en coding human 6-phosphogluconolactonase, the enzyme catalyzing the second step of the pentose phosphate pathway, FEBS LETTER, 459(2), 1999, pp. 223-226
Glucokinase regulatory protein is essential for the proper subcellular localisation of liver glucokinase
Authors: de la Iglesia, N Veiga-da-Cunha, M Van Schaftingen, E Guinovart, JJ Ferrer, JC
Citation: N. De La Iglesia et al., Glucokinase regulatory protein is essential for the proper subcellular localisation of liver glucokinase, FEBS LETTER, 456(2), 1999, pp. 332-338
Risultati: 1-25 |