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Molecular Genetics and Metabolism, ISSN 1096-7192, 07/2017, Volume 121, Issue 3, p. 199
Cystathionine [beta]-synthase (CBS) deficiency (Online Mendelian Inheritance in Man [OMIM] 236,200) is an autosomal recessive disorder that is caused by... 
Infants (Newborn) | Sulfur compounds | Enzymes | Liver diseases | Analysis | Liver | Television programs | Physiological aspects | Genetics | Homocysteine
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 07/2017, Volume 38, Issue 7, pp. 863 - 869
Journal Article
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 4785 - 4785
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 01/2016, Volume 1363, Issue 1, p. 80
  Cystathionine [beta] synthase (CBS) is a key enzyme in the methionine and cysteine metabolic pathway, acting as a metabolic gatekeeper to regulate the flow... 
Physiological aspects | Cysteine | Analysis | Metabolites | Metabolism | Amino acids
Journal Article
Human Mutation, ISSN 1059-7794, 07/2017, Volume 38, Issue 7, pp. 863 - 869
Journal Article
Journal of Biological Chemistry, ISSN 0021-9258, 2018, Volume 293, Issue 36, pp. 13921 - 13931
Mutations in the cystathionine -synthase (CBS) gene are the cause of classical homocystinuria, the most common inborn error in sulfur metabolism. The p.G307S... 
G307S | ACTIVATION | PROTEIN | pyridoxal phosphate | BIOCHEMISTRY & MOLECULAR BIOLOGY | mouse genetics | transsulfuration pathway | inborn error of metabolism | missense mutation | DEFICIENCY | p | RESCUE | pyridoxine | HEME | methionine | cystathionine -synthase | GENE-EXPRESSION | homocystinuria | bortezomib | BETA-SYNTHASE | CHARMM | MOLECULAR-BASIS | structural model | sulfur metabolism
Journal Article
Annals of the New York Academy of Sciences, ISSN 0077-8923, 01/2016, Volume 1363, Issue 1, pp. 80 - 90
Journal Article
Cancer Research, ISSN 0008-5472, 08/2015, Volume 75, Issue 15 Supplement, pp. 5315 - 5315
Journal Article
Analytical Chemistry, ISSN 0003-2700, 02/2014, Volume 86, Issue 3, p. 1583
  Methionine is an essential proteogenic amino acid. In addition, it is a methyl donor for DNA and protein methylation and a propylamine donor for polyamine... 
Proteins | DNA methylation | Amino acids | Biochemistry | Biosynthesis | Mass spectrometry | Chromatography
Journal Article
Analytical Chemistry (Washington), ISSN 0003-2700, 02/2014, Volume 86, Issue 3, pp. 1583 - 1583
Methionine is an essential proteogenic amino acid. In addition, it is a methyl donor for DNA and protein methylation and a propylamine donor for polyamine... 
Enzymes | Pathways | Mathematical analysis | Methionine | Deletion | Fluxes | Pools | Metabolism
Journal Article
Human Mutation, ISSN 1059-7794, 07/2017, Volume 38, Issue 7, pp. 863 - 869
Mutations in the cystathionine beta‐synthase ( CBS ) gene are the cause of classical homocystinuria, the most common inborn error in sulfur metabolism. The... 
homocysteine | pyridoxine | bortezomib | CBS | methionine | Pyridoxine - chemistry | Humans | Mice, Inbred C57BL | Homocysteine - blood | Proteasome Inhibitors - chemistry | Male | Mice, Transgenic | Bortezomib - pharmacology | Mice, Inbred C3H | Animals | DNA Mutational Analysis | Alleles | Female | Mice | Mutation | Cystathionine beta-Synthase - genetics | Homocystinuria - genetics
Journal Article
Heart, ISSN 1355-6037, 08/2013, Volume 99, Issue Suppl 3, pp. A43 - A44
Objectives We recently reported that elevation of plasma homocysteine level—hyperhomocysteinemia (HHcy) accelerates atherosclerosis and vascular inflammation... 
Journal Article
Value in Health, ISSN 1098-3015, 2015, Volume 18, Issue 7, pp. A562 - A562
Journal Article
Cancer Research, ISSN 0008-5472, 04/2012, Volume 72, Issue 8 Supplement, pp. 2173 - 2173
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