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Results: 1-5 |
Results: 5

Authors: Guida, S Trettel, F Pagnutti, S Mantuano, E Tottene, A Veneziano, L Fellin, T Spadaro, M Stauderman, KA Williams, ME Volsen, S Ophoff, RA Frants, RR Jodice, C Frontali, M Pietrobon, D
Citation: S. Guida et al., Complete loss of P/Q calcium channel activity caused by a CACNA1A missensemutation carried by patients with episodic ataxia type 2, AM J HU GEN, 68(3), 2001, pp. 759-764

Authors: Hilditch-Maguire, P Trettel, F Passani, LA Auerbach, A Persichetti, F MacDonald, ME
Citation: P. Hilditch-maguire et al., Huntingtin: an iron-regulated protein essential for normal nuclear and perinuclear organelles, HUM MOL GEN, 9(19), 2000, pp. 2789-2797

Authors: Trettel, F Rigamonti, D Hilditch-Maguire, P Wheeler, VC Sharp, AH Persichetti, F Cattaneo, E MacDonald, ME
Citation: F. Trettel et al., Dominant phenotypes produced by the HD mutation in STHdh(Q111) striatal cells, HUM MOL GEN, 9(19), 2000, pp. 2799-2809

Authors: Trettel, F Mantuano, E Calabresi, V Veneziano, L Olsen, AS Georgescu, A Gordon, L Sabbadini, G Frontali, M Jodice, C
Citation: F. Trettel et al., A fine physical map of the CACNA1A gene region on 19p13.1-p13.2 chromosome, GENE, 241(1), 2000, pp. 45-50

Authors: Persichetti, F Trettel, F Huang, CC Fraefel, C Timmers, HTM Gusella, JF MacDonald, ME
Citation: F. Persichetti et al., Mutant huntingtin forms in vivo complexes with distinct context-dependent conformations of the polyglutamine segment, NEUROBIOL D, 6(5), 1999, pp. 364-375
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