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Proceedings of the National Academy of Sciences of the United States of America|November 14, 1997
Hereditary hemochromatosis: effects of C282Y and H63D mutations on association with beta2-microglobulin, intracellular processing, and cell surface expression of the HFE protein in COS-7 cellsA Waheed, S Parkkila, X Y Zhou, et al.Proceedings of the National Academy of Sciences of the United States of America|March 21, 1998
The hemochromatosis gene product complexes with the transferrin receptor and lowers its affinity for ligand bindingJ N Feder, D M Penny, A Irrinki, et al.The Journal of Biological Chemistry|May 30, 1997
The hemochromatosis founder mutation in HLA-H disrupts beta2-microglobulin interaction and cell surface expressionJ N Feder, Z Tsuchihashi, A Irrinki, et al.Proceedings of the National Academy of Sciences of the United States of America|April 16, 1998
HFE gene knockout produces mouse model of hereditary hemochromatosisX Y Zhou, S Tomatsu, R E Fleming, et al.Genome Research|May 1, 1997
A 1.1-Mb transcript map of the hereditary hemochromatosis locusD A Ruddy, G S Kronmal, V K Lee, et al.Nature Genetics|August 1, 1996
A novel MHC class I-like gene is mutated in patients with hereditary haemochromatosisJ N Feder, A Gnirke, W Thomas, et al.Pageof 3