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Cystathionine
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1	PDF Document Add to Reading List Source URL: www.pbs.gov.au Language: English - Date: 2015-03-23 21:11:42 Homocysteine Trimethylglycine Cofactors Vitamin B12 Methionine Folic acid Cystathionine beta synthase Chemistry Homocystinuria Quaternary ammonium compounds
2	Microsoft Word - 1 PG CV_Prof Moore.doc Add to Reading List Source URL: www.nus.edu.sg Language: English - Date: 2010-12-01 21:27:05 Pollutants Sulfides H2S Cystathionine Iron(II) sulfide Chemistry Acids Hydrogen sulfide
3	Microsoft PowerPoint - 3 dick Deth Methylation Panel.ppt Add to Reading List Source URL: www.autismeval.com Language: English - Date: 2006-06-25 15:37:03 Proteinogenic amino acids Vitamin B12 Cofactors Methionine Glutathione S-Adenosyl methionine Homocysteine Cysteine Cystathionine beta synthase Chemistry Thiols Glucogenic amino acids
4	Department of Clinical Chemistry / Central Laboratory University Hospital of Saarland Symposium "Turning Science into Caring“, Utrecht NL, June 8, 2010 Add to Reading List Source URL: www.abbottnederland.nl Language: English - Date: 2014-10-13 08:01:25 Vitamin B12 Cofactors Dicarboxylic acids Methionine synthase Methionine Homocysteine Folic acid Cystathionine Hydroxocobalamin Chemistry Nutrition B vitamins
5	Viktor Kožich Henk Blom Stefan Kölker Marike Groenendijk Outline Add to Reading List Source URL: ec.europa.eu Language: English - Date: 2014-12-08 11:13:53 Homocysteine Coenzymes Methylenetetrahydrofolate reductase Cystathionine beta synthase Methionine S-Adenosyl methionine S-Adenosyl-L-homocysteine Chemistry Homocystinuria Vitamin B12
6	The Dominant Role of Sp1 in Regulating the Cystathionine β-Synthase –1a and –1b Promoters Allows Tissue-Specific Regulation of CBS Expression By Kruppel-Like Factors. Kenneth N. Maclean and Jan P. Kraus University o Add to Reading List Source URL: www.colemaninstitute.org Language: English - Date: 2012-04-05 12:56:41 Molecular genetics Proteins Genetics Kruppel-like factors Sp1 transcription factor Ccaat-enhancer-binding proteins Sp3 transcription factor Cellular differentiation Promoter Biology Transcription factors Gene expression
7	Homocystinuria What is homocystinuria? Homocystinuria is an inherited condition that affects the way a person’s body uses a part of food called methionine (a precursor to homocystine). A person with homocystinuria cann Add to Reading List Source URL: health.state.tn.us Language: English - Date: 2007-05-01 14:53:38 Homocystinuria Rare diseases Cystathionine beta synthase Homocysteine Recessive Methionine Cystinuria Phenylketonuria Newborn screening Medicine Health Genetic genealogy
8	Homocystinuria Homocystinuria is an autosomal recessive disorder of methionine metabolism. The most common cause of homocystinuria is a deficiency of the amino acid cystathionine B-synthase. Due to this deficiency, eleva Add to Reading List Source URL: www.maine.gov Language: English - Date: 2011-11-10 05:38:06 Homocystinuria Homocysteine Marfan syndrome Methionine Cystathionine beta synthase Cystinuria Newborn screening Hypermethioninemia Health Chemistry Genetic genealogy
9	Overview of Newborn Screening for Homocystinuria – For Parents What is newborn screening? What are the symptoms of homocystinuria? Before babies go home from the nursery, they Add to Reading List Source URL: www.in.gov Language: English - Date: 2014-10-23 17:39:46 Homocystinuria Cystathionine beta synthase Newborn screening Arachnodactyly Cystinuria Methionine Low-protein diet Health Medicine Chemistry
10	Homocystinuria What is homocystinuria? Homocystinuria is an inherited condition that affects the way a person’s body uses a part of food called methionine (a precursor to homocystine). A person with homocystinuria cann Add to Reading List Source URL: health.tn.gov Language: English - Date: 2007-05-01 14:53:38 Homocystinuria Rare diseases Cystathionine beta synthase Homocysteine Recessive Methionine Cystinuria Phenylketonuria Newborn screening Medicine Health Genetic genealogy

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