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Lyase
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#	Item
51	Pectic Enzyme: An Elicitor of Necrosis in Cotton Inoculated with Bacteria Add to Reading List Source URL: digital.library.okstate.edu Language: English - Date: 2009-01-09 17:06:02 Xanthomonadales Xanthomonas campestris Pectin Bacterial blight Pectate lyase Pseudomonas syringae Necrosis Enzyme Polygalacturonase Biology Chemistry Microbiology
52	Medium Chain Acyl-CoA Dehydrogenase Deficiency (MCAD) Add to Reading List Source URL: health.mo.gov Language: English - Date: 2009-02-03 16:51:23 Medical genetics Argininosuccinic aciduria Urea cycle disorder Newborn screening Argininosuccinate lyase Carbamoyl phosphate synthetase I deficiency Glutaric acidemia type 2 Health Rare diseases Genetic genealogy
53	PARENT FACT SHEET DISORDER Argininosuccinic Acidemia (ASA) CAUSE ASA occurs when an enzyme called argininosuccinic acid lyase is either missing or not working Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 11:26:15 Biology Argininosuccinic aciduria Arginine Urea Ammonia Argininosuccinic acid Protein Urea cycle disorder Ornithine transcarbamylase deficiency Chemistry Urea cycle Metabolism
54	Disease Name Argininosuccinic Acidemia Alternate name(s) Acronym Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 08:46:16 Health Urea cycle disorder Argininosuccinate synthase Argininosuccinate lyase Argininosuccinic aciduria Argininosuccinic acid Citrullinemia Trichorrhexis nodosa Hyperammonemia Urea cycle Metabolism Biology
55	Disease Name Hydroxymethylglutaric aciduria (3-OH 3-CH3 glutaric aciduria) Alternate name(s) Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-08 19:53:26 3-hydroxy-3-methylglutaryl-CoA lyase Rare diseases Hypoglycemia Pediatrics Glutaric aciduria type 1 Glycogen storage disease type I Health Medicine 3-hydroxy-3-methylglutaryl-CoA lyase deficiency
56	Parent Fact Sheet DISORDER Hydroxymethylglutaric Aciduria (3-OH 3 CH3 glutaric aciduria) (HMG) CAUSE Add to Reading List Source URL: chfs.ky.gov Language: English - Date: 2014-08-09 02:11:05 Medical genetics Coenzymes Thioesters HMG-CoA Organic acidemia 3-hydroxy-3-methylglutaryl-CoA lyase Fatty-acid metabolism disorder 3-hydroxy-3-methylglutaryl-CoA lyase deficiency Health Genetic genealogy
57	2 Lyases JASSEM G. MAHDI DAVID R. KELLY Cardiff, Wales, UK Add to Reading List Source URL: www.wiley-vch.de Language: English - Date: 2004-04-15 03:16:41 Lyases Carboxy-lyases Phenylalanine ammonia-lyase Aspartate 4-decarboxylase Diaminopimelate decarboxylase Tyrosine decarboxylase Valine decarboxylase Threonine ammonia-lyase Acetolactate decarboxylase Chemical kinetics Physical chemistry Chemistry
58	Microsoft Word - ~[removed]doc Add to Reading List Source URL: www.wiley-vch.de Language: English - Date: 2007-12-12 02:33:14 Metabolism Metabolic pathways Cellular respiration Exercise physiology Citric acid cycle Isocitrate lyase Gluconeogenesis Glyoxylate cycle Pyruvic acid Biology Chemistry Biochemistry
59	Vol[removed]SHORT COMMUNICATIONS establish that the exchange of hydrogen atoms between water and deoxyadenosylcobalamin is an Add to Reading List Source URL: rdbiotech.drivehq.com Language: English - Date: 2007-08-19 19:31:22 Metabolism Dicarboxylic acid Otologicals Isocitrate lyase Succinyl-CoA Coenzyme A Lipid Carboxylic acid Chloramphenicol Chemistry Organic chemistry Coenzymes
60	Disclaimer : The Competition DG makes the information provided by the notifying parties in section 1.2 of Form CO available to the public in order to increase transparency. This information has been prepared by the notif Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2008-12-04 08:42:02 American Sign Language Argininosuccinate lyase

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