Search Results - "GANDON, G"

  • Showing 1 - 16 results of 16
Refine Results
  1. 1
  2. 2
  3. 3
  4. 4
  5. 5

    Évaluation du nouveau test Access ®OV Monitor pour le dosage du CA 125 by Gandon, G., Quillien, V., Godey, F.

    Published in Immuno-analyse & biologie spécialisée (01-08-2004)
    “…Le test Access OV Monitor (Beckman-Coulter) est une technique immunoenzymatique chimiluminescente, utilisée pour le dosage du CA 125. L'évaluation analytique a…”
    Get full text
    Journal Article
  6. 6
  7. 7
  8. 8

    Evidence of specific T-cell priming from the first-in-man single ascending dose study of peptide copolymer PI-2301 for the treatment of multiple sclerosis by Kovalchin, J, Krieger, J, Collins, K, Rafuse, K, Avril, T, Gandon, G, Patat, A, Fauchoux, N, Patel, U, Mascioli, E, Zanelli, E

    Published in Multiple sclerosis (01-09-2008)
    “…Background: PI-2301 is a second-generation compound in a class of immunomodulators called peptide copolymers which has shown efficacy in various preclinical…”
    Get full text
    Journal Article
  9. 9

    Prevalence of the C282Y mutation in Brittany: penetrance of genetic hemochromatosis? by Jouanolle, A M, Fergelot, P, Raoul, M L, Gandon, G, Roussey, M, Deugnier, Y, Feingold, J, Le Gall, J Y, David, V

    Published in Annales de génétique (1998)
    “…Hemochromatosis (GH) is an inborn error of iron metabolism, characterized by progressive iron loading that, if untreated, causes high morbidity and death. The…”
    Get more information
    Journal Article
  10. 10

    A candidate gene for hemochromatosis : frequency of the C282Y and H63D mutations by JOUANOLLE, A. M, FERGELOT, P, GANDON, G, YAOUANQ, J, LE GALL, J. Y, DAVID, V

    Published in Human genetics (01-10-1997)
    “…The gene whose alteration causes hereditary hemochromatosis (HFE according to the international nomenclature) was, more than 20 years ago, shown to map to…”
    Get full text
    Journal Article
  11. 11

    Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families by Adams, PC, Campion, ML, Gandon, G, LeGall, J, David, V, Jouanolle, AM

    Published in Hepatology (Baltimore, Md.) (01-10-1997)
    “…A candidate gene (HFE) has been described for hereditary hemochromatosis on chromosome 6. The study of well-defined atypical hemochromatosis families using…”
    Get full text
    Journal Article
  12. 12

    Clinical and family studies in genetic hemochromatosis: Microsatellite and HFE studies in five atypical families by Adams, P C, Campion, M L, Gandon, G, LeGall, J, David, V, Jouanolle, A M

    Published in Hepatology (Baltimore, Md.) (01-10-1997)
    “…A candidate gene (HFE) has been described for hereditary hemochromatosis on chromosome 6. The study of well‐defined atypical hemochromatosis families using…”
    Get full text
    Journal Article
  13. 13

    Linkage disequilibrium and extended haplotypes in the HLA-A to D6S105 region : implications for mapping the hemochromatosis gene (HFE) by GANDON, G, JOUANOLLE, A. M, CHAUVEL, B, MAUVIEUX, V, LE TREUT, A, FEINGOLD, J, LE GALL, J. Y, DAVID, V, YAOUANQ, J

    Published in Human genetics (1996)
    “…The hemochromatosis gene (HFE) maps to 6p21.3, in close linkage with the HLA Class I genes. Linkage disequilibrium (LD) studies were designed to narrow down…”
    Get full text
    Journal Article
  14. 14
  15. 15

    A highly informative dinucleotide repeat polymorphism telomeric to HLA-F by Andrieux, N, Jouanolle, A M, Gandon, G, Mosser, J

    Published in Immunogenetics (New York) (1997)
    “…In a positional cloning approach to the hemochromatosis gene (HFE), we constructed a YAC contig and an STS map spanning at least 3.9 megabases (Mb) of the…”
    Get full text
    Journal Article
  16. 16