Maternal Phenylketonuria International Collaborative Study revisited: evaluation of maternal nutritional risk factors besides phenylalanine for fetal congenital heart defects-Reference-Cited by-同舟云学术

Maternal Phenylketonuria International Collaborative Study revisited: evaluation of maternal nutritional risk factors besides phenylalanine for fetal congenital heart defects

Published:2013-06-20 Issue:1 Volume:37 Page:39-42
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Yano Shoji,Moseley Kathryn,Bottiglieri Teodoro,Arning Erland,Azen Colleen

Publisher

Wiley

Subject

Genetics(clinical),Genetics

Link

http://link.springer.com/content/pdf/10.1007/s10545-013-9627-x

Reference16 articles.

1. Blau N, van Spronsen FJV, Levy HL (2010) Phenylketonuria. Lancet 376:1417–1427

2. Campbell WA, Sah DE, Medina MM, Albina JE, Coleman WB, Thompson NL (2000) TA1/LAT-1/CD98 light chain and system L activity, but not 4F2/CD98 heavy chain, respond to arginine availability in rat hepatic cells. Loss of response in tumor cells. J Biol Chem 275(8):5347–5354

3. Chowdhury S, Cleves MA, MacLeod SL, James SJ, Zhao W, Hobbs CA (2011) Maternal DNA hypomethylation and congenital heart defects. Birth Defects Res A 91:69–76

4. Chrostowski MK, McGonnigal BG, Stabila JP, Padbury JF (2009) LAT-1 expression in pre- and post-implantation embryos and placenta. Placenta 30:270–276

5. Cooney CA, Dave AA, Wolff GL (2001) Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring. J Nutr 132:2393S–2400S

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