Authors:
Fletcher, CF
Tottene, A
Lennon, VA
Wilson, SM
Dubel, SJ
Paylor, R
Hosford, DA
Tessarollo, L
Tessarollo, L
McEnery, MW
Pietrobon, D
Copeland, NG
Jenkins, NA
Citation: Cf. Fletcher et al., Dystonia and cerebellar atrophy in Cacna1a null mice lacking P/Q calcium channel activity, FASEB J, 15(7), 2001, pp. 1288-1290
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
Citation: A. Tottene et al., alpha(1E) subunits form the pore of three cerebellar R-type calcium channels with different pharmacological and permeation properties, J NEUROSC, 20(1), 2000, pp. 171-178
Authors:
Schramm, M
Vajna, R
Pereverzev, A
Tottene, A
Klockner, U
Pietrobon, D
Hescheler, J
Schneider, T
Citation: M. Schramm et al., Isoforms of alpha 1E voltage-gated calcium channels in rat cerebellar granule cells - Detection of major calcium channel alpha 1-transcripts by reverse transcription-polymerase chain reaction, NEUROSCIENC, 92(2), 1999, pp. 565-575
Authors:
Hans, M
Luvisetto, S
Williams, ME
Spagnolo, M
Urrutia, A
Tottene, A
Brust, PF
Johnson, EC
Harpold, MM
Stauderman, KA
Pietrobon, D
Citation: M. Hans et al., Functional consequences of mutations in the human alpha(1A) calcium channel subunit linked to familial hemiplegic migraine, J NEUROSC, 19(5), 1999, pp. 1610-1619