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Results: 1-5 |
Results: 5

Authors: Rosenberg, RN Aminoff, M Boller, F Griggs, RC Hachinski, V Hallett, M Johnson, RT Kennard, C Lang, AE Lisak, R Newsom-Davis, J Pedley, TA Selzer, ME Zochodne, D
Citation: Rn. Rosenberg et al., Reporting clinical trials - Full access to all the data, STROKE, 32(12), 2001, pp. 2734-2734

Authors: Nykjaer, A Fyfe, JC Kozyraki, R Leheste, JR Jacobsen, C Nielsen, MS Verroust, PJ Aminoff, M de la Chapelle, A Moestrup, SK Ray, R Gliemann, J Willnow, TE Christensen, EI
Citation: A. Nykjaer et al., Cubilin dysfunction causes abnormal metabolism of the steroid hormone 25(OH) vitamin D-3, P NAS US, 98(24), 2001, pp. 13895-13900

Authors: Kristiansen, M Aminoff, M Jacobsen, C de la Chapelle, A Krahe, R Verroust, PJ Moestrup, SK
Citation: M. Kristiansen et al., Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor-vitamin B-12 by cubilin, BLOOD, 96(2), 2000, pp. 405-409

Authors: Kozyraki, R Fyfe, J Kristiansen, M Gerdes, C Jacobsen, C Cui, SY Christensen, EI Aminoff, M de la Chapelle, A Krahe, R Verroust, PJ Moestrup, SK
Citation: R. Kozyraki et al., The intrinsic factor-vitamin B-12 receptor, cubilin, is a high-affinity apolipoprotein A-I receptor facilitating endocytosis of high-density lipoprotein, NAT MED, 5(6), 1999, pp. 656-661

Authors: Aminoff, M Carter, JE Chadwick, RB Johnson, C Grasbeck, R Abdelaal, MA Broch, H Jenner, LB Verroust, PJ Moestrup, SK de la Chapelle, A Krahe, R
Citation: M. Aminoff et al., Mutations in CUBN, encoding the intrinsic factor-vitamin B-12 receptor, cubilin, cause hereditary megaloblastic anaemia 1, NAT GENET, 21(3), 1999, pp. 309-313
Risultati: 1-5 |