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American Journal of Medical Genetics Part C: Seminars in Medical Genetics, ISSN 1552-4868, 02/2011, Volume 157, Issue 1, pp. 3 - 32
This review covers briefly the major conditions, genetic and non‐genetic, sometimes leading to abnormally elevated methionine, with emphasis on recent... 
adenosyltransferase | homocysteine | hypermethioninemia | methyltransferase | disease | prematurity | citrin | liver | tyrosinemia type I | low‐birth‐weight | fumarylacetoacetate | S‐adenosylmethionine | deficiency | methionine | glycine | S‐adenosylhomocysteine | hydrolase | homocystinuria | cystathionine beta‐synthase | Tyrosinemia type I | Disease | Hydrolase | Low-birth-weight | Cystathionine beta-synthase | Deficiency | Liver | Methionine | Methyltransferase | S-adenosylhomocysteine | Glycine | S-adenosylmethionine | Hypermethioninemia | Homocystinuria | Prematurity | Fumarylacetoacetate | Citrin | Adenosyltransferase | Homocysteine | low-birth-weight | PYRIDOXINE-NONRESPONSIVE HOMOCYSTINURIA | ADENOSYLHOMOCYSTEINE HYDROLASE DEFICIENCY | GENETICS & HEREDITY | cystathionine beta-synthase | GLYCINE N-METHYLTRANSFERASE | S-ADENOSYLMETHIONINE SYNTHETASE | ADENOSYL-L-METHIONINE | TYROSINEMIA TYPE-I | NEONATAL INTRAHEPATIC CHOLESTASIS | METHIONINE ADENOSYLTRANSFERASE-I/III | ASPARTATE GLUTAMATE CARRIER | Methionine - blood | Glycine N-Methyltransferase - genetics | Humans | Glycine N-Methyltransferase - deficiency | Neonatal Screening | Amino Acid Metabolism, Inborn Errors - diagnosis | Methionine Adenosyltransferase - genetics | Tyrosinemias - diagnosis | Cystathionine beta-Synthase - deficiency | Mitochondrial Diseases - complications | Organic Anion Transporters - deficiency | Adenosylhomocysteinase - deficiency | Organic Anion Transporters - genetics | Amino Acid Metabolism, Inborn Errors - genetics | Adenosylhomocysteinase - genetics | Methionine Adenosyltransferase - deficiency | Liver Diseases - complications | Female | Cystathionine beta-Synthase - genetics | Infant, Newborn | Liver Diseases - blood | Mitochondrial Diseases - genetics | Diagnosis, Differential | Tyrosinemias - therapy | cis-trans-Isomerases - deficiency | Calcium-Binding Proteins - deficiency | Tyrosinemias - genetics | Amino Acid Metabolism, Inborn Errors - therapy | cis-trans-Isomerases - genetics | Liver Diseases - metabolism | Mitochondrial Diseases - diagnosis | Calcium-Binding Proteins - genetics | Liver diseases | Isoenzymes | cbs gene | Methionine adenosyltransferase | S-Adenosylmethionine | Mitochondria | Reviews | Differential diagnosis | Mutation | Catalytic subunits
Journal Article
Journal Article
American Journal of Physiology - Endocrinology And Metabolism, ISSN 0193-1849, 12/2007, Volume 293, Issue 6, pp. 1492 - 1502
Deficiency in nutritional determinants of homocysteine (HCY) metabolism, such as vitamin B12 and folate, during pregnancy is known to influence HCY levels in... 
Oxidative stress | Homocysteine | B vitamins | Steatosis | homocysteine | PATHWAYS | PHYSIOLOGY | NITRIC-OXIDE SYNTHASE | METHIONINE ADENOSYLTRANSFERASE ACTIVITY | METHYLENETETRAHYDROFOLATE REDUCTASE | S-ADENOSYLMETHIONINE | ENDOCRINOLOGY & METABOLISM | GENE-EXPRESSION | ISCHEMIA-REPERFUSION | steatosis | oxidative stress | BRAIN | S-Adenosylhomocysteine - metabolism | Folic Acid Deficiency - metabolism | Liver - pathology | Cell Proliferation | Liver - enzymology | Rats, Wistar | Glutathione - metabolism | Choline Deficiency - complications | Homocysteine - metabolism | Vitamin B 12 Deficiency - pathology | Hypoxia - metabolism | Riboflavin Deficiency - pathology | Choline Deficiency - metabolism | Vitamin B Deficiency - metabolism | Vitamin B 12 Deficiency - complications | Female | Vitamin B 12 Deficiency - metabolism | Animals, Newborn | Vitamin B Deficiency - pathology | Liver - metabolism | Homocysteine - blood | Rats | Hypoxia - complications | Choline Deficiency - pathology | Cystathionine beta-Synthase - metabolism | Vitamin B 12 - blood | Food, Formulated | Riboflavin Deficiency - metabolism | Pregnancy | Animals | Folic Acid Deficiency - complications | Folic Acid Deficiency - pathology | Hypoxia - pathology | Folic Acid - blood | Riboflavin Deficiency - complications | Vitamin B Deficiency - complications | Riboflavin - blood | S-Adenosylmethionine - metabolism | Apoptosis | Nitric Oxide Synthase Type II - metabolism
Journal Article
FASEB Journal, ISSN 0892-6638, 03/2009, Volume 23, Issue 3, pp. 883 - 893
Journal Article