nadp has been researched along with Syndrome in 7 studies
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 | 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 |
2 review(s) available for nadp and Syndrome
Article | Year |
---|---|
Enasidenib and ivosidenib in AML.
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.
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 |
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.
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.
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.
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.
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.
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 |