5 results for author:"Cadet E." in Literature citations
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| An unusual case of hemochromatosis due to a new compound heterozygosity in HFE (p.[Gly43Asp;His63Asp]+[Cys282Tyr]): structural implications with respect to binding with transferrin receptor 1. Dupradeau F.-Y., Pissard S., Coulhon M.-P., Cadet E., Foulon K., Fourcade C., Goossens M., Case D.A., Rochette J. Hum. Mutat. 29:206-206(2008) · UniProtKB (1) |
| Juvenile hemochromatosis caused by a novel combination of hemojuvelin G320V/R176C mutations in a 5-year old girl. Aguilar-Martinez P., Lok C.Y., Cunat S., Cadet E., Robson K., Rochette J. Haematologica 92:421-422(2007) · Mapped (3) |
| Recent advances in understanding haemochromatosis: a transition state. Robson K.J.H., Merryweather-Clarke A.T., Cadet E., Viprakasit V., Zaahl M.G., Pointon J.J., Weatherall D.J., Rochette J. J. Med. Genet. 41:721-730(2004) · UniProtKB (1) |
| Digenic inheritance of mutations in HAMP and HFE results in different types of haemochromatosis. Merryweather-Clarke A.T., Cadet E., Bomford A., Capron D., Viprakasit V., Miller A., McHugh P.J., Chapman R.W., Pointon J.J., Wimhurst V.L. et al. Hum. Mol. Genet. 12:2241-2247(2003) · UniProtKB (1) |
| Novel mutation in ferroportin 1 gene is associated with autosomal dominant iron overload. Jouanolle A.-M., Douabin-Gicquel V., Halimi C., Loreal O., Fergelot P., Delacour T., de Lajarte-Thirouard A.-S., Turlin B., Le Gall J.-Y., Cadet E. et al. J. Hepatol. 39:286-289(2003) · UniProtKB (1) |