S-adenosylhomocysteine hydrolase deficiency in a human: A genetic disorder of methionine metabolism-Reference-Cited by-同舟云学术

S-adenosylhomocysteine hydrolase deficiency in a human: A genetic disorder of methionine metabolism

Published:2004-03-15 Issue:12 Volume:101 Page:4234-4239
ISSN:0027-8424
Container-title:Proceedings of the National Academy of Sciences
language:en
Short-container-title:Proceedings of the National Academy of Sciences

Author:

Baric I.,Fumic K.,Glenn B.,Cuk M.,Schulze A.,Finkelstein J. D.,James S. J.,Mejaski-Bosnjak V.,Pazanin L.,Pogribny I. P.,Rados M.,Sarnavka V.,Scukanec-Spoljar M.,Allen R. H.,Stabler S.,Uzelac L.,Vugrek O.,Wagner C.,Zeisel S.,Mudd S. H.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference47 articles.

1. The Enzymatic Synthesis of S-Adenosyl-l-homocysteine from Adenosine and Homocysteine

2. Relationship between tissue levels of S-adenosylmethionine, S-adenosylhomocysteine, and transmethylation reactions

3. Serum betaine, N,N-dimethylglycine and N-methylglycine levels in patients with cobalamin and folate deficiency and related inborn errors of metabolism

4. Quantitation of total homocysteine, total cysteine, and methionine in normal serum and urine using capillary gas chromatography-mass spectrometry

5. Elevation of serum cystathionine levels in patients with cobalamin and folate deficiency

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