Compounds > nadp
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nadp and Lipid Metabolism, Inborn Error

nadp has been researched along with Lipid Metabolism, Inborn Error in 7 studies

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19901 (14.29)18.7374
1990's0 (0.00)18.2507
2000's1 (14.29)29.6817
2010's5 (71.43)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
Amaral, AU; Cecatto, C; Hickmann, FH; Rodrigues, MD; Wajner, M1
Amaral, AU; Cecatto, C; da Silva, JC; Godoy, KDS; Ribeiro, RT; Wajner, A; Wajner, M1
Amaral, AU; Cecatto, C; da Silva, JC; Godoy, KDS; Wajner, M1
Andersson, HC; FitzPatrick, DR; Hennekam, RC; Kelley, RI; Koster, J; Romeijn, GJ; Vreken, P; Wanders, RJ; Waterham, HR1
Baymann, NA; Bourre, JM; Daudu, OL1

Other Studies

7 other study(ies) available for nadp and Lipid Metabolism, Inborn Error

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
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
cis-4-Decenoic and decanoic acids impair mitochondrial energy, redox and Ca(2+) homeostasis and induce mitochondrial permeability transition pore opening in rat brain and liver: Possible implications for the pathogenesis of MCAD deficiency.
    Biochimica et biophysica acta, 2016, Volume: 1857, Issue:9

    Topics: Acyl-CoA Dehydrogenase; Animals; Brain; Calcium; Decanoic Acids; Energy Metabolism; Fatty Acids, Monounsaturated; Lipid Metabolism, Inborn Errors; Liver; Mitochondria; Mitochondrial Membrane Transport Proteins; Mitochondrial Permeability Transition Pore; NADP; Rats; Rats, Wistar

2016
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
Mutations in the 3beta-hydroxysterol Delta24-reductase gene cause desmosterolosis, an autosomal recessive disorder of cholesterol biosynthesis.
    American journal of human genetics, 2001, Volume: 69, Issue:4

    Topics: Amino Acid Sequence; Animals; Child, Preschool; Cholesterol; Cloning, Molecular; Desmosterol; DNA Mutational Analysis; Female; Flavin-Adenine Dinucleotide; Genes, Recessive; Humans; Infant, Newborn; Lipid Metabolism, Inborn Errors; Male; Molecular Sequence Data; Mutation; NADP; Nerve Tissue Proteins; Oxidoreductases; Oxidoreductases Acting on CH-CH Group Donors; Phenotype; Plants; Saccharomyces cerevisiae; Sequence Alignment

2001
Biosynthesis of lignoceric acid from behenyl0COA in mouse brain microsomes. Comparison between normal and Quaking mutant.
    Biochemical and biophysical research communications, 1975, Apr-21, Volume: 63, Issue:4

    Topics: Animals; Brain; Chromatography, Gas; Chromatography, Thin Layer; Coenzyme A; Fatty Acids; Kinetics; Lipid Metabolism, Inborn Errors; Malonates; Mice; Microsomes; Mutation; Myelin Sheath; NADP; Oxidation-Reduction; Phospholipids; Time Factors

1975