Search Results - "Graison, E."

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  1. 1

    Classification of Human Chromosome 21 Gene-Expression Variations in Down Syndrome: Impact on Disease Phenotypes by Aït Yahya-Graison, E., Aubert, J., Dauphinot, L., Rivals, I., Prieur, M., Golfier, G., Rossier, J., Personnaz, L., Créau, N., Bléhaut, H., Robin, S., Delabar, J.M., Potier, M.-C.

    Published in American journal of human genetics (01-09-2007)
    “…Down syndrome caused by chromosome 21 trisomy is the most common genetic cause of mental retardation in humans. Disruption of the phenotype is thought to be…”
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    Journal Article
  2. 2

    Homocysteine threshold value based on cystathionine beta synthase and paraoxonase 1 activities in mice by Hamelet, J., Aït-Yahya-Graison, E., Matulewicz, E., Noll, C., Badel-Chagnon, A., Camproux, A-C., Demuth, K., Paul, J-L., Delabar, J. M., Janel, N.

    Published in European journal of clinical investigation (01-12-2007)
    “…Background  Hyperhomocysteinaemia is a metabolic disorder associated with the development of premature atherosclerosis. Among the determinants which predispose…”
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  3. 3

    VARAN: a web server for Variability Analysis of DNA microarray experiments by Golfier, G., Dang, M. Tran, Dauphinot, L., Graison, E., Rossier, J., Potier, M.-C.

    Published in Bioinformatics (01-07-2004)
    “…Here, we describe a tool for VARiability Analysis of DNA microarrays experiments (VARAN), a freely available Web server that performs a signal intensity based…”
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    Paraoxonase-1 expression is up-regulated in Down syndrome fetal liver by Janel, Nathalie, Christophe, Olivier, Yahya-Graison, Emilie Aït, Hamelet, Julien, Paly, Evelyne, Prieur, Marguerite, Delezoïde, Anne-Lise, Delabar, Jean Maurice

    “…Patients with Down syndrome appear to be protected from the development of atherosclerosis. On the contrary, hyperhomocysteinemia is associated with an…”
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    Journal Article