Physiologic mechanisms to maintain methionine status during protein malnutrition

Nutrition

Volumn 18, Issue 1, 2002, Pages 96-97

  Ubbink, Johan B ^a  

^a UNIVERSITY OF PRETORIA   (South Africa)

Author keywords

[No Author keywords available]

Indexed keywords

CYANOCOBALAMIN; ESSENTIAL AMINO ACID; FOLIC ACID; HOMOCYSTEINE; METHIONINE; PREALBUMIN; S ADENOSYLMETHIONINE;

AMINO ACID METABOLISM; CONFERENCE PAPER; CORONARY ARTERY DISEASE; DIET RESTRICTION; GOITER; HUMAN; HYPERHOMOCYSTEINEMIA; METHYLATION; PRIORITY JOURNAL; PROTEIN MALNUTRITION; RISK FACTOR; VITAMIN DEFICIENCY;

ADAPTATION, PHYSIOLOGICAL; AMINO ACIDS, ESSENTIAL; DIETARY PROTEINS; HOMEOSTASIS; HOMOCYSTEINE; HUMANS; METHIONINE; NUTRITION DISORDERS;

EID: 0036150445     PISSN: 08999007     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0899-9007(01)00764-X     Document Type: Conference Paper

References (8)

1. Metabolism of sulfur-containing amino acids
2. The pathogenesis of homocysteinemia; interruption of the coordinate regulation by S-adenosylmethionine of the remethylation and transsulfuration of homocysteine
3. Plasma homocysteine and methionine tolerance in early-onset vascular disease
4. Diagnosis of cobalamin deficiency; II. Relative sensitivities of serum cobalamin, methylmalonic acid, and total homocysteine concentrations
5. Homocysteinemia due to folate deficiency
6. Homocysteine and vascular disease
7. Cardiovascular disease in developing countries; myths, realities and opportunities