Page last updated: 2024-08-17

nadp and Syndrome

nadp has been researched along with Syndrome in 7 studies

Research

Studies (7)

Timeframe	Studies, this research(%)	All Research%
pre-1990	2 (28.57)	18.7374
1990's	1 (14.29)	18.2507
2000's	2 (28.57)	29.6817
2010's	1 (14.29)	24.3611
2020's	1 (14.29)	2.80

Authors

Authors	Studies
Cardinali, V; Cerchione, C; Falini, B; Martelli, MP; Martinelli, G; Martino, G	1
Andrew, M; Begtrup, A; Boyle, L; Cho, MT; Chung, WK; Dauber, A; Douglas, J; Feingold, M; Hwa, V; Kramer, N; Monaghan, KG; Pop, A; Retterer, K; Roos, B; Saitta, S; Salomons, GS; Wamelink, MMC; Wynn, J	1
Agrawal, V; Crock, P; Huang, N; Migeon, CJ; Miller, WL; Murphy, N; Russell, WE; Sahakitrungruang, T; Tee, MK	1
Greenberg, ML; Gu, Z; Ma, L; Vaz, FM; Wanders, RJ	1
Nicklas, WJ	1
Arévalo, JC; Llanillo, M; Pérez-González, MN; Sánchez-Bernal, C	1
Datta, NS; Hajra, AK; Webber, KO	1

Reviews

2 review(s) available for nadp and Syndrome

Article	Year
Enasidenib and ivosidenib in AML. Minerva medica, 2020, Volume: 111, Issue:5 Topics: Aminopyridines; Antineoplastic Agents; Cell Differentiation; Clinical Trials as Topic; Glutarates; Glycine; Humans; Isocitrate Dehydrogenase; Isocitrates; Ketoglutaric Acids; Leukemia, Myeloid, Acute; Multicenter Studies as Topic; Mutation, Missense; NADP; Pyridines; Syndrome; Triazines	2020
Amino acid metabolism in the central nervous system: role of glutamate dehydrogenase. Advances in neurology, 1984, Volume: 41 Topics: Amino Acid Metabolism, Inborn Errors; Animals; Central Nervous System; Cerebellar Ataxia; Enzyme Activation; gamma-Aminobutyric Acid; Glutamate Dehydrogenase; Glutamate Synthase; Glutamates; Glutamic Acid; Glutamine; Humans; Leucine; Mitochondria; NADP; Nerve Endings; Neuroglia; Rats; Syndrome	1984

Article

Year

Enasidenib and ivosidenib in AML.

Minerva medica, 2020, Volume: 111, Issue:5

Topics: Aminopyridines; Antineoplastic Agents; Cell Differentiation; Clinical Trials as Topic; Glutarates; Glycine; Humans; Isocitrate Dehydrogenase; Isocitrates; Ketoglutaric Acids; Leukemia, Myeloid, Acute; Multicenter Studies as Topic; Mutation, Missense; NADP; Pyridines; Syndrome; Triazines

2020

Amino acid metabolism in the central nervous system: role of glutamate dehydrogenase.

Advances in neurology, 1984, Volume: 41

Topics: Amino Acid Metabolism, Inborn Errors; Animals; Central Nervous System; Cerebellar Ataxia; Enzyme Activation; gamma-Aminobutyric Acid; Glutamate Dehydrogenase; Glutamate Synthase; Glutamates; Glutamic Acid; Glutamine; Humans; Leucine; Mitochondria; NADP; Nerve Endings; Neuroglia; Rats; Syndrome

1984

Other Studies

5 other study(ies) available for nadp and Syndrome

Article	Year
Mutations in TKT Are the Cause of a Syndrome Including Short Stature, Developmental Delay, and Congenital Heart Defects. American journal of human genetics, 2016, 06-02, Volume: 98, Issue:6 Topics: Adult; Child; Child, Preschool; Developmental Disabilities; Dwarfism; Female; Glutathione; Heart Defects, Congenital; Humans; Male; Mutation; NADP; Pedigree; Syndrome; Transketolase; Young Adult	2016
Clinical, genetic, and enzymatic characterization of P450 oxidoreductase deficiency in four patients. The Journal of clinical endocrinology and metabolism, 2009, Volume: 94, Issue:12 Topics: Adolescent; Adult; Bone and Bones; Catalysis; Cytochromes c; Disorders of Sex Development; DNA; Escherichia coli; Female; Genetic Vectors; Genitalia; Hormones; Humans; Infant, Newborn; Infertility; Male; Mutation; NADP; NADPH-Ferrihemoprotein Reductase; Pregnancy; Steroid 17-alpha-Hydroxylase; Syndrome	2009
The human TAZ gene complements mitochondrial dysfunction in the yeast taz1Delta mutant. Implications for Barth syndrome. The Journal of biological chemistry, 2004, Oct-22, Volume: 279, Issue:43 Topics: Acyltransferases; Adenosine Triphosphate; Alamethicin; Alternative Splicing; Cardiolipins; Cardiomyopathies; Cell Membrane; Cloning, Molecular; Cytosol; DNA; Ethanol; Exons; Genetic Complementation Test; Humans; Immunoblotting; Mitochondria; Mutation; NAD; NADP; Open Reading Frames; Oxygen; Oxygen Consumption; Phosphorylation; Proteins; Saccharomyces cerevisiae; Subcellular Fractions; Substrate Specificity; Syndrome; Temperature; Transcription Factors	2004
Phospholipid fatty acid and lipid peroxidation in liver microsomes from guinea pigs fed oil related to the toxic oil syndrome. Comparative biochemistry and physiology. Part C, Pharmacology, toxicology & endocrinology, 1998, Volume: 120, Issue:1 Topics: Aniline Compounds; Animals; Antioxidants; Cricetinae; Fatty Acids; Glucosephosphate Dehydrogenase; Glutathione Peroxidase; Lipid Peroxidation; Male; Malondialdehyde; Microsomes, Liver; NADP; Phospholipids; Plant Oils; Poisoning; Superoxide Dismutase; Syndrome	1998
Properties of the enzymes catalyzing the biosynthesis of lysophosphatidate and its ether analog in cultured fibroblasts from Zellweger syndrome patients and normal controls. Archives of biochemistry and biophysics, 1987, May-01, Volume: 254, Issue:2 Topics: Acyltransferases; Aldehyde Oxidoreductases; Alkyl and Aryl Transferases; Cells, Cultured; Dihydroxyacetone Phosphate; Fibroblasts; Glycerol-3-Phosphate O-Acyltransferase; Glycerophosphates; Humans; Hydrogen-Ion Concentration; Kinetics; Lysophospholipids; NADP; Nervous System Diseases; Phosphatidic Acids; Sugar Alcohol Dehydrogenases; Syndrome; Transferases	1987