Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease-Reference-Cited by-同舟云学术

Mutations disrupting the Kennedy phosphatidylcholine pathway in humans with congenital lipodystrophy and fatty liver disease

Published:2014-06-02 Issue:24 Volume:111 Page:8901-8906
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:

Payne F.,Lim K.,Girousse A.,Brown R. J.,Kory N.,Robbins A.,Xue Y.,Sleigh A.,Cochran E.,Adams C.,Dev Borman A.,Russel-Jones D.,Gorden P.,Semple R. K.,Saudek V.,O'Rahilly S.,Walther T. C.,Barroso I.,Savage D. B.

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

Reference26 articles.

1. The Kennedy pathway-De novo synthesis of phosphatidylethanolamine and phosphatidylcholine

2. Phosphatidylcholine metabolism: masochistic enzymology, metabolic regulation, and lipoprotein assembly

3. Dual-energy x-ray absorptiometry for total-body and regional bone-mineral and soft-tissue composition

4. Nonalcoholic Fatty Liver Disease: Pathologic Patterns and Biopsy Evaluation in Clinical Research

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