Page last updated: 2024-08-17

nadp and Nervous System Disorders

nadp has been researched along with Nervous System Disorders in 8 studies

Research

Studies (8)

TimeframeStudies, this research(%)All Research%
pre-19901 (12.50)18.7374
1990's2 (25.00)18.2507
2000's0 (0.00)29.6817
2010's5 (62.50)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Amaral, AU; Busanello, EN; Gasparotto, J; Gelain, DP; Gregersen, N; Tonin, AM; Wajner, M1
Li, F; Meng, R; Sun, X; Wang, J; Yang, Z; Zhang, A1
Barres, BA; Medress, ZA; Vargas, ME; Wang, JT1
Amaral, AU; Cecatto, C; Hickmann, FH; Rodrigues, MD; Wajner, M1
Amaral, AU; Cecatto, C; da Silva, JC; Godoy, KDS; Wajner, M1
Boyd, S; Brock, G; Lue, TF; Nunes, L; Padma-Nathan, H1
Beninger, RJ; Boegman, RJ; Jhamandas, K1
Datta, NS; Hajra, AK; Webber, KO1

Other Studies

8 other study(ies) available for nadp and Nervous System Disorders

ArticleYear
Mitochondrial bioenergetics deregulation caused by long-chain 3-hydroxy fatty acids accumulating in LCHAD and MTP deficiencies in rat brain: a possible role of mPTP opening as a pathomechanism in these disorders?
    Biochimica et biophysica acta, 2014, Volume: 1842, Issue:9

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Acyl-CoA Dehydrogenase, Long-Chain; Adenosine Triphosphate; Animals; Calcium; Cardiomyopathies; Cerebral Cortex; Cytochromes c; Energy Metabolism; Homeostasis; Hydrogen Peroxide; Lauric Acids; Lipid Metabolism, Inborn Errors; Membrane Potential, Mitochondrial; Mitochondria; Mitochondrial Membrane Transport Proteins; Mitochondrial Myopathies; Mitochondrial Permeability Transition Pore; Mitochondrial Swelling; Mitochondrial Trifunctional Protein; Myristic Acids; NADP; Nervous System Diseases; Oxidants; Palmitic Acids; Rats; Rats, Wistar; Rhabdomyolysis

2014
[The changes of LCHAD in preeclampsia with different clinical features and the correlation with NADPH P47-phox, p38MAPK-α, COX-2 and serum FFA and TG].
    Zhonghua fu chan ke za zhi, 2015, Volume: 50, Issue:2

    Topics: 3-Hydroxyacyl CoA Dehydrogenases; Cardiomyopathies; Cohort Studies; Cyclooxygenase 2; Fatty Acids; Female; Humans; Hypertension; Lipid Metabolism, Inborn Errors; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; NADP; NADPH Oxidases; Nervous System Diseases; Oxidation-Reduction; Oxidative Stress; p38 Mitogen-Activated Protein Kinases; Placenta; Pre-Eclampsia; Pregnancy; Pregnancy Trimester, Third; Prospective Studies; Rhabdomyolysis; RNA, Messenger; Triglycerides

2015
Local axonal protection by WldS as revealed by conditional regulation of protein stability.
    Proceedings of the National Academy of Sciences of the United States of America, 2015, Aug-18, Volume: 112, Issue:33

    Topics: Animals; Axons; Cytoplasm; Disease Progression; Gene Expression Profiling; Gene Expression Regulation; HEK293 Cells; Humans; Ligands; Mice; Mice, Inbred C57BL; Microscopy, Fluorescence; Models, Neurological; NADP; Nerve Tissue Proteins; Nervous System Diseases; Protein Stability; Rats; Rats, Sprague-Dawley; Rats, Transgenic; Time Factors; Transfection; Wallerian Degeneration

2015
Deregulation of mitochondrial functions provoked by long-chain fatty acid accumulating in long-chain 3-hydroxyacyl-CoA dehydrogenase and mitochondrial permeability transition deficiencies in rat heart--mitochondrial permeability transition pore opening as
    The FEBS journal, 2015, Volume: 282, Issue:24

    Topics: Adenosine Triphosphate; Animals; Calcium Channel Blockers; Calcium Signaling; Cardiomyopathies; Cell Membrane Permeability; Enzyme Inhibitors; Humans; Lipid Metabolism, Inborn Errors; Long-Chain-3-Hydroxyacyl-CoA Dehydrogenase; Membrane Potential, Mitochondrial; Mitochondria, Heart; Mitochondrial Membrane Transport Proteins; Mitochondrial Membranes; Mitochondrial Myopathies; Mitochondrial Permeability Transition Pore; Mitochondrial Swelling; Mitochondrial Trifunctional Protein; Myristic Acids; NADP; Nervous System Diseases; Organ Specificity; Oxidative Phosphorylation; Palmitic Acids; Rats, Wistar; Rhabdomyolysis

2015
Disturbance of mitochondrial functions provoked by the major long-chain 3-hydroxylated fatty acids accumulating in MTP and LCHAD deficiencies in skeletal muscle.
    Toxicology in vitro : an international journal published in association with BIBRA, 2016, Volume: 36

    Topics: Animals; Calcium; Cardiomyopathies; Lipid Metabolism, Inborn Errors; Membrane Potential, Mitochondrial; Mitochondria, Muscle; Mitochondrial Myopathies; Mitochondrial Trifunctional Protein; Muscle, Skeletal; Myristic Acids; NADP; Nervous System Diseases; Oxygen Consumption; Palmitic Acids; Rats, Wistar; Rhabdomyolysis

2016
Nitric oxide synthase: a new diagnostic tool for neurogenic impotence.
    Urology, 1993, Volume: 42, Issue:4

    Topics: Amino Acid Oxidoreductases; Biopsy; Erectile Dysfunction; Humans; Male; NADP; Nerve Fibers; Nervous System Diseases; Nitric Oxide Synthase; Penis; Staining and Labeling

1993
Neurotoxicity of tryptophan metabolites.
    Annals of the New York Academy of Sciences, 1990, Volume: 585

    Topics: Animals; Cerebral Cortex; Choline O-Acetyltransferase; Kynurenic Acid; Male; NADP; Nervous System Diseases; Neurons; Picolinic Acids; Pyridines; Quinolinic Acid; Quinolinic Acids; Rats; Rats, Inbred Strains; Tryptophan

1990
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