Got some amino acids to spare?

American Journal of Clinical Nutrition

Volumn 74, Issue 6, 2001, Pages 709-711

  Young, V R ^a  

^a MASSACHUSETTS INSTITUTE OF TECHNOLOGY   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINO ACID; CYSTEINE; CYSTINE; METHIONINE; PHENYLALANINE; PROTEIN; TRACER; TYROSINE;

ABSORPTION; AGE; AMINO ACID METABOLISM; HUMAN; MEDICAL RESEARCH; METHODOLOGY; NUTRITION; NUTRITIONAL REQUIREMENT; OXIDATION; PROTEIN DIET; PROTEIN INTAKE; QUANTITATIVE ASSAY; SHORT SURVEY;

EID: 0035190679     PISSN: 00029165     EISSN: None     Source Type: Journal    
DOI: 10.1093/ajcn/74.6.709     Document Type: Short Survey

References (14)

1. A theoretical basis for increasing current estimates of the amino acid requirements in adult man, with experimental support
2. Energy and protein requirements. Report of a joint FAO/WHO/UNU Expert Consultation
3. 13C]phenylalanine
4. Lysine requirements of healthy adult Indian subjects, measured by an indicator amino acid balance technique
5. Dietary cysteine reduces the methionine requirement in men
6. Tyrosine requirement of healthy men receiving a fixed phenylalanine intake determined by using indicator amino acid oxidation
7. Cysteine kinetics and oxidation at different intakes of methionine and cystine in young adults
8. Methionine and cysteine kinetics at different intakes of cystine in healthy adult men
9. Methionine metabolism in mammals. The methionine sparing effect of cystine
10. 13C]phenylalanine
11. 2]phenylalanine oral tracer studies at generous, intermediate, and low phenylalanine intakes to estimate aromatic amino acid requirements in adults
12. The need of essential amino acids in children. An evaluation based on the intake of phenylalanine, tyrosine, leucine, isoleucine, and valine in children with phenylketonuria, tyrosine amino transferase defect and maple syrup urine disease
13. Tyrosine requirements in children with classical PKU determined by indicator amino acid oxidation
14. Phenylalanine (PHE) requirement in children with classical phenylketonuria (PKU)