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Results:
1-25
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Results: 25
Authors:
Burgess, DL
Gefrides, LA
Foreman, PJ
Noebels, JL
Citation: Dl. Burgess et al., A cluster of three novel Ca2+ channel gamma subunit genes on chromosome 19q13.43: Evolution and expression profile of the gamma subunit gene family, GENOMICS, 71(3), 2001, pp. 339-350
Authors:
Qiao, XX
Suri, C
Knusel, B
Noebels, JL
Citation: Xx. Qiao et al., Absence of hippocampal mossy fiber sprouting in transgenic mice overexpressing brain-derived neurotrophic factor, J NEUROSC R, 64(3), 2001, pp. 268-276
Authors:
Zwingman, TA
Neumann, PE
Noebels, JL
Herrup, K
Citation: Ta. Zwingman et al., Rocker is a new variant of the voltage-dependent calcium channel gene Cacna1a, J NEUROSC, 21(4), 2001, pp. 1169-1178
Authors:
Qian, J
Noebels, JL
Citation: J. Qian et Jl. Noebels, Presynaptic Ca2+ channels and neurotransmitter release at the terminal of a mouse cortical neuron, J NEUROSC, 21(11), 2001, pp. 3721-3728
Authors:
Jacobs, MP
Fischbach, GD
Davis, MR
Dichter, MA
Dingledine, R
Lowenstein, DH
Morrell, MJ
Noebels, JL
Rogawski, MA
Spencer, SS
Theodore, WH
Citation: Mp. Jacobs et al., Future directions for epilepsy research, NEUROLOGY, 57(9), 2001, pp. 1536-1542
Authors:
Heilstedt, HA
Burgess, DL
Anderson, AE
Chedrawi, A
Tharp, B
Lee, O
Kashork, CD
Starkey, DE
Wu, YQ
Noebels, JL
Shaffer, LG
Shapira, SK
Citation: Ha. Heilstedt et al., Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome, EPILEPSIA, 42(9), 2001, pp. 1103-1111
Authors:
Noebels, JL
Citation: Jl. Noebels, Modeling human epilepsies in mice, EPILEPSIA, 42, 2001, pp. 11-15
Authors:
Matsuura, T
Yamagata, T
Burgess', DL
Rasmussen, A
Grewal, RP
Watase, K
Khajavi, M
McCall, AE
Davis, CF
Zu, L
Achari, M
Pulst, SM
Alonso, E
Noebels, JL
Nelson, DL
Zoghbi, HY
Ashizawa, T
Citation: T. Matsuura et al., Large expansion of the ATTCT pentanucleotide repeat in spinocerebellar ataxia type 10, NAT GENET, 26(2), 2000, pp. 191-194
Authors:
Steinlein, OK
Noebels, JL
Citation: Ok. Steinlein et Jl. Noebels, Ion channels and epilepsy in man and mouse, CUR OP GEN, 10(3), 2000, pp. 286-291
Authors:
Ayata, C
Shimizu-Sasamata, M
Lo, EH
Noebels, JL
Moskowitz, MA
Citation: C. Ayata et al., Impaired neurotransmitter release and elevated threshold for cortical spreading depression in mice with mutations in the alpha 1A subunit of P/Q typecalcium channels, NEUROSCIENC, 95(3), 2000, pp. 639-645
Authors:
Lau, D
de Miera, EVS
Contreras, D
Ozaita, A
Harvey, M
Chow, A
Noebels, JL
Paylor, R
Morgan, JI
Leonard, CS
Rudy, B
Citation: D. Lau et al., Impaired fast-spiking, suppressed cortical inhibition, and increased susceptibility to seizures in mice lacking Kv3.2 K+ channel proteins, J NEUROSC, 20(24), 2000, pp. 9071-9085
Authors:
Qian, J
Noebels, JL
Citation: J. Qian et Jl. Noebels, Presynaptic Ca2+ influx at a mouse central synapse with Ca2+ channel subunit mutations, J NEUROSC, 20(1), 2000, pp. 163-170
Authors:
Liu, M
Pleasure, SJ
Collins, AE
Noebels, JL
Naya, FJ
Tsai, MJ
Lowenstein, DH
Citation: M. Liu et al., Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy, P NAS US, 97(2), 2000, pp. 865-870
Authors:
Liu, M
Pleasure, SJ
Collins, AE
Noebels, JL
Naya, FJ
Tsai, MJ
Lowenstein, DH
Citation: M. Liu et al., Loss of BETA2/NeuroD leads to malformation of the dentate gyrus and epilepsy (vol 97, pg 865, 2000), P NAS US, 97(10), 2000, pp. 5679-5680
Authors:
Kellaway, P
Mizrahi, EM
Noebels, JL
Citation: P. Kellaway et al., Benign focal epilepsies of childhood: Genetically determined pathophysiology, EPILEPSIA, 41(8), 2000, pp. 1049-1050
Authors:
Burgess, DL
Noebels, JL
Citation: Dl. Burgess et Jl. Noebels, Calcium channel defects in models of inherited generalized epilepsy, EPILEPSIA, 41(8), 2000, pp. 1074-1075
Authors:
Burgess, DL
Matsuura, T
Ashizawa, T
Noebels, JL
Citation: Dl. Burgess et al., Genetic localization of the Ca2+ channel gene CACNG2 near SCA10 on chromosome 22q13, EPILEPSIA, 41(1), 2000, pp. 24-27
Authors:
Noebels, JL
Burgess, DL
Qian, J
Citation: Jl. Noebels et al., Nature in the development of epilepsy, ACT NEUR SC, 102, 2000, pp. 11-13
Authors:
Hartmann, HA
Colom, LV
Sutherland, ML
Noebels, JL
Citation: Ha. Hartmann et al., Selective localization of cardiac SCN5A sodium channels in limbic regions of rat brain, NAT NEUROSC, 2(7), 1999, pp. 593-595
Authors:
Burgess, DL
Davis, CF
Gefrides, LA
Noebels, JL
Citation: Dl. Burgess et al., Identification of three novel Ca2+ channel gamma subunit genes reveals molecular diversification by tandem and chromosome duplication, GENOME RES, 9(12), 1999, pp. 1204-1213
Authors:
Burgess, DL
Biddlecome, GH
McDonough, SI
Diaz, ME
Zilinski, CA
Bean, BP
Campbell, KP
Noebels, JL
Citation: Dl. Burgess et al., beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain, MOL CELL NE, 13(4), 1999, pp. 293-311
Authors:
Burgess, DL
Noebels, JL
Citation: Dl. Burgess et Jl. Noebels, Single gene defects in mice: the role of voltage-dependent calcium channels in absence models, EPILEPSY R, 36(2-3), 1999, pp. 111-122
Authors:
Clark, GD
Noebels, JL
Citation: Gd. Clark et Jl. Noebels, Cortin disaster: Lissencephaly genes spell double trouble for the developing brain, ANN NEUROL, 45(2), 1999, pp. 141-143
Authors:
Westenbroek, RE
Bausch, SB
Lin, RCS
Franck, JE
Noebels, JL
Catterall, WA
Citation: Re. Westenbroek et al., Upregulation of L-type Ca2+ channels in reactive astrocytes after brain injury, hypomyelination, and ischemia (vol 18, pg 2321, 1998), J NEUROSC, 19(2), 1999, pp. 868-868
Authors:
Sutherland, ML
Williams, SH
Abedi, R
Overbeek, PA
Pfaffinger, PJ
Noebels, JL
Citation: Ml. Sutherland et al., Overexpression of a Shaker-type potassium channel in mammalian central nervous system dysregulates native potassium channel gene expression, P NAS US, 96(5), 1999, pp. 2451-2455
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