Increased plasma homocysteine and S-adenosylhomocysteine and decreased methionine is associated with altered phosphatidylcholine and phosphatidylethanolamine in cystic fibrosis-Reference-Cited by-同舟云学术

Increased plasma homocysteine and S-adenosylhomocysteine and decreased methionine is associated with altered phosphatidylcholine and phosphatidylethanolamine in cystic fibrosis

Published:2003-09 Issue:3 Volume:143 Page:351-356
ISSN:0022-3476
Container-title:The Journal of Pediatrics
language:en
Short-container-title:The Journal of Pediatrics

Author:

Innis Sheila M,Davidson A.George F,Chen Alice,Dyer Roger,Melnyk Stepan,James S.Jill

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology, and Child Health

Reference33 articles.

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4. CFTR regulates outwardly rectifying chloride channels through an autocrine mechanism involving ATP;Schwiebert;Cell,1995

5. Liver and biliary problems in cystic fibrosis;Colombo;Semin Liver Dis,1998

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