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Bioorganic and Medicinal Chemistry Letters, ISSN 0960-894X, 01/2014, Volume 24, Issue 1, pp. 113 - 116
A novel strategy to prepare bisubstrate based inhibitors for histone acetyltransferases is presented. To obtain these, azido peptides derived from histone H3... 
Coenzyme A
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2013, Volume 8, Issue 7, p. e60581
Most conditions detected by expanded newborn screening result from deficiency of one of the enzymes that degrade acyl-coenzyme A (CoA) esters in mitochondria.... 
RAT-LIVER | 3-HYDROXY-3-METHYLGLUTARYL-COA LYASE | INHIBITION | METABOLISM | COENZYME-A PROFILES | PYRUVATE-CARBOXYLASE | QUANTIFICATION | MULTIDISCIPLINARY SCIENCES | DEFICIENT MICE | LYASE HL | SPECTROMETRY | Hyperammonemia - metabolism | Humans | Hypoglycemia - mortality | Acetyl Coenzyme A - genetics | Acyl Coenzyme A - genetics | Hepatocytes - metabolism | Mitochondria - ultrastructure | Genes, Lethal | Mitochondria - genetics | Pyruvic Acid - metabolism | Hyperammonemia - mortality | Gene Order | Hypoglycemia - genetics | Gene Targeting | Hyperammonemia - genetics | Leucine - metabolism | Carbon Dioxide - metabolism | Liver - metabolism | Acyl Coenzyme A - deficiency | Metabolome | Mitochondria - metabolism | Gene Knockout Techniques | Hypoglycemia - metabolism | Acetyl Coenzyme A - metabolism | Mice, Knockout | Peroxisomes | Phenotype | Animals | Gluconeogenesis - genetics | Metabolic Networks and Pathways | Models, Biological | Lethargy | Mice | Enzymes | Esters | Metabolites | Glutamate | Analysis | Organic acids | Glutamic acid | Inborn errors of metabolism | Ketogenesis | Laboratories | Liver | Pyruvic acid | Leucine | Defects | Degradation | Proteins | Mitochondria | Rodents | Coenzyme A | Chemical synthesis | Gluconeogenesis | Urine | Medical research | Incubation | Hyperammonemia | Hypoglycemia | Metabolism | Fatty acids | Studies | Urea | Hepatocytes | Carboxylation | Scientific imaging | Mass spectrometry | Acetyl Coenzyme A | Life Sciences | Hépatology and Gastroenterology | Carbon Dioxide | Human health and pathology | Pyruvic Acid | Acyl Coenzyme A
Journal Article
Proceedings of the National Academy of Sciences of the United States of America, ISSN 0027-8424, 4/2012, Volume 109, Issue 16, pp. 6018 - 6023
Journal Article
International Journal of Pharmaceutics, ISSN 0378-5173, 01/2010, Volume 383, Issue 1-2, p. 147
This study aimed to develop a stable solid dispersion of Coenzyme Q.sub.10 (CoQ.sub.10) with high aqueous solubility and dissolution rate. Among various... 
Coenzymes
Journal Article
Journal Article
Journal Article
Muscle & Nerve, ISSN 0148-639X, 09/2017, Volume 56, Issue 3, pp. 479 - 485
ABSTRACT Introduction c.250G>A (p.Ala84Thr) in ETFDH is the most common mutation that causes later‐onset multiple acyl‐coenzyme A dehydrogenase deficiency... 
coenzyme Q10 | ETFDH | multiple acyl‐coenzyme A dehydrogenase deficiency | neurite shortening | carnitine | lipid storage myopathy | riboflavin | multiple acyl-coenzyme A dehydrogenase deficiency | SUPEROXIDE | COENZYME | ALPHA-SUBUNIT | UBIQUINONE OXIDOREDUCTASE | ACIDEMIA TYPE-II | COA DEHYDROGENASE-DEFICIENCY | OXIDATION DEFECTS | MYOPATHY | NEUROSCIENCES | CLINICAL NEUROLOGY | ELECTRON-TRANSFER FLAVOPROTEIN | DYSFUNCTION | Neuronal Outgrowth - physiology | Cell Line | Electron-Transferring Flavoproteins - genetics | Reactive Oxygen Species - metabolism | Humans | Ubiquinone - analogs & derivatives | Iron-Sulfur Proteins - genetics | Oxidoreductases Acting on CH-NH Group Donors - genetics | Mitochondria - metabolism | Neurites - metabolism | Neuronal Outgrowth - drug effects | Electron-Transferring Flavoproteins - biosynthesis | Ubiquinone - pharmacology | Mutation - physiology | Multiple Acyl Coenzyme A Dehydrogenase Deficiency - genetics | Mitochondria - genetics | Oxidoreductases Acting on CH-NH Group Donors - biosynthesis | Iron-Sulfur Proteins - biosynthesis | Multiple Acyl Coenzyme A Dehydrogenase Deficiency - metabolism | Enzymes | Yuan (China) | Genetic aspects | Thiols | Metabolites | Analysis | Axonogenesis | Riboflavin | Exploration | Population studies | Drug screening | Cofactors | Carnitine | Defects | Mitochondria | Coenzyme Q10 | Coenzyme A | Mutation | Supplementation
Journal Article
Journal Article
1971, Methods in enzymology, ISBN 0121818802, Volume 18B., 857
Book
1970, Methods in enzymology, ISBN 0121818799, Volume 18A., 688
Book
Journal Article