Page last updated: 2024-08-17

nadp and Deficiency, Glucosephosphatase

nadp has been researched along with Deficiency, Glucosephosphatase in 5 studies

Research

Studies (5)

TimeframeStudies, this research(%)All Research%
pre-19902 (40.00)18.7374
1990's1 (20.00)18.2507
2000's1 (20.00)29.6817
2010's1 (20.00)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Chou, JY; Jun, HS; Lee, YM; Mansfield, BC; Weinstein, DA1
Chen, L; Du, C; Duan, S; Geng, Q; Guo, Y; He, Y; Jiang, C; Jiang, W; Li, H; Lin, Q; Liu, C; Liu, P; Qi, Y; Ren, X; Si, E; Tian, Q; Wen, J; Ye, W; Yu, G; Zhang, Q; Zheng, Y1
Gitzelmann, R; Matsunaga, T; Seger, R; Steinmann, B; Tiefenauer, L1
Bari, M; Micheli, V; Pompucci, G; Simmonds, HA1
Möller, NP; Steensgaard, J1

Other Studies

5 other study(ies) available for nadp and Deficiency, Glucosephosphatase

ArticleYear
Molecular mechanisms of neutrophil dysfunction in glycogen storage disease type Ib.
    Blood, 2014, May-01, Volume: 123, Issue:18

    Topics: Adenosine Triphosphate; Adolescent; Adult; Antiporters; Child; Child, Preschool; Enzyme Activation; Glucose; Glucose-6-Phosphatase; Glycogen Storage Disease Type I; Humans; Hypoxia-Inducible Factor 1, alpha Subunit; Immunophenotyping; Intracellular Space; Lactic Acid; Monosaccharide Transport Proteins; NADP; NADPH Oxidases; Neutrophils; Phenotype; PPAR gamma; Signal Transduction; Young Adult

2014
Structure and function of glucose-6-phosphate dehydrogenase-deficient variants in Chinese population.
    Human genetics, 2006, Volume: 119, Issue:5

    Topics: Amino Acid Substitution; Arginine; China; Female; Genetic Testing; Genetic Variation; Glucosephosphate Dehydrogenase; Glucosephosphate Dehydrogenase Deficiency; Glycogen Storage Disease Type I; Humans; Male; NADP; Protein Structure, Secondary; Structure-Activity Relationship

2006
Short communication. Glycogenosis Ib: neutrophil microbicidal defects due to impaired hexose monophosphate shunt.
    Pediatric research, 1984, Volume: 18, Issue:3

    Topics: Adolescent; Adult; Blood Bactericidal Activity; Glycogen Storage Disease Type I; Hexosephosphates; Humans; Male; NADP; Neutrophils; Superoxides

1984
HPLC determination of oxidized and reduced pyridine coenzymes in human erythrocytes.
    Clinica chimica acta; international journal of clinical chemistry, 1993, Oct-29, Volume: 220, Issue:1

    Topics: Chromatography, High Pressure Liquid; Erythrocytes; Glycogen Storage Disease Type I; Humans; Lesch-Nyhan Syndrome; NAD; NADP; Oxidation-Reduction; Purine-Nucleoside Phosphorylase; Ribose-Phosphate Pyrophosphokinase

1993
Studies on the glutathione stability of normal and glucose-6-phospate-dehydrogenase-deficient human erythrocytes.
    Scandinavian journal of clinical and laboratory investigation, 1971, Volume: 28, Issue:3

    Topics: Adult; Citrates; Edetic Acid; Enzyme Activation; Erythrocytes; Erythrocytes, Abnormal; Glucose; Glucosephosphate Dehydrogenase; Glutathione; Glycogen Storage Disease Type I; Heparin; Humans; Male; Middle Aged; NADP; Oxidation-Reduction; Oxidoreductases; Phosphogluconate Dehydrogenase

1971