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Trends in Endocrinology and Metabolism: TEM|March 12, 2013
Folate and fetal programming: a play in epigenomics?Jean-Louis Guéant, Fares Namour, Rosa-Maria Guéant-Rodriguez, et al.
The American Journal of Clinical Nutrition|August 18, 2017
Association of TCN2 rs1801198 c.776G>C polymorphism with markers of one-carbon metabolism and related diseases: a systematic review and meta-analysis of genetic association studiesAbderrahim Oussalah, Julien Levy, Pierre Filhine-Trésarrieu, et al.
Haematologica|July 14, 2011
Luminal expression of cubilin is impaired in Imerslund-Grasbeck syndrome with compound AMN mutations in intron 3 and exon 7Fares Namour, Gabriele Dobrovoljski, Celine Chery, et al.
Early Human Development|March 7, 2008
Evaluation of neonatal BH4 loading test in neonates screened for hyperphenylalaninemiaFrançois Feillet, Céline Chery, Fares Namour, et al.
World Journal of Surgery|May 23, 2006
Lack of association between microsatellite instability and benign adrenal tumorsFares Namour, Ahmet Ayav, Xiaohong Lu, et al.
Clinical Chemistry and Laboratory Medicine|September 11, 2003
Low frequency of mutated methylenetetrahydrofolate reductase 677C-->T and 1298A-->C genetics single nucleotide polymorphisms (SNPs) in Sub-Saharan populationsCharles E Adjalla, Emile K Amouzou, Ambaliou Sanni, et al.
Genes & Development|April 22, 2003
Targeted recruitment of a histone H4-specific methyltransferase by the transcription factor YY1Natalie Rezai-Zadeh, Xiaohong Zhang, Fares Namour, et al.
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