Molecular mechanisms of pediatric nutrition

Nestle Nutrition Workshop Series: Pediatric Program

Volumn 66, Issue , 2010, Pages 55-64

  Ruemmele, Frank ^a  

^a HÔPITAL NECKER ENFANTS MALADES   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ANIMAL; CHILD; CONFERENCE PAPER; GENETIC EPIGENESIS; GENETIC VARIABILITY; HUMAN; INFANT; MASS COMMUNICATION; METHODOLOGY; NEWBORN; NUTRIGENOMICS; NUTRITIONAL SCIENCE; PRESCHOOL CHILD;

ANIMALS; CHILD; CHILD NUTRITION SCIENCES; CHILD, PRESCHOOL; DIFFUSION OF INNOVATION; EPIGENESIS, GENETIC; GENETIC VARIATION; HUMANS; INFANT; INFANT, NEWBORN; NUTRIGENOMICS;

EID: 77955889523     PISSN: 16616677     EISSN: 16623878     Source Type: Book Series    
DOI: 10.1159/000318948     Document Type: Conference Paper

References (4)

1. Schaeffer L, Gohlke H, Müller M, et al: Common genetic variants of the FADS1 FADS2 gene cluster and their reconstructed haplotypes are associated with the fatty acid composition in phospholipids. Hum Mol Genet 2006;15:1745-1756.
2. Lattka E, Illig T, Heinrich J, Koletzko B: Do FADS genotypes enhance our knowledge about fatty acid related phenotypes? Clin Nutr 2009, Nov 28, Epub ahead of print.
3. Lattka E, Illig T, Heinrich J, Koletzko B: FADS gene cluster polymorphisms: important modulators of fatty acid levels and their impact on atopic diseases. J Nutrigenet Nutrigenomics 2009;2:119-128.
4. Lattka E, Illig T, Koletzko B, Heinrich J: Genetic variants of the FADS1 FADS2 gene cluster as related to essential fatty acid metabolism. Curr Opin Lipidol 2010;21:64-69.