A β subunit-dependent mutant P/Q channel phenotype for a widely expressed α1A subunit splice form in spinocerebellar ataxia type 6 (SCA6)

被引：0
|
作者：
Gomez, CM
Riedl, MS
Thompson, RM
Raike, RS
Restituito, S
Charnet, P
机构：
来源：
NEUROLOGY | 2000年 / 54卷 / 07期
关键词：
D O I：
暂无
中图分类号：
R74 [神经病学与精神病学];
学科分类号：
摘要：
引用
收藏
页码：A465 / A465
页数：1
相关论文
共 50 条
  • [41] Transmitter release deficits at the neuromuscular synapse of mice with mutations in the Cav2.1 (α1A) subunit of the P/Q-type Ca2+ channel
    Plomp, JJ
    Van Den Maagdenberg, AM
    Ferrari, MD
    Frants, RR
    Molenaar, PC
    MYASTHENIA GRAVIS AND RELATED DISORDERS: BIOMCHEMICAL BASIS FOR DISEASE OF THE NEUROMUSCULAR JUNCTION, 2003, 998 : 29 - 32
  • [42] Vascular smooth muscle cells express the α1A subunit of a P-/Q-type voltage-dependent Ca2+ channel, and it is functionally important in renal afferent arterioles
    Hansen, PB
    Jensen, BL
    Andreasen, D
    Friis, UG
    Skott, O
    CIRCULATION RESEARCH, 2000, 87 (10) : 896 - 902
  • [43] Involvement of the P/Q-type Ca2+ channel α1A subunit (CACNA1A) gene region on 19p13 in migraine with and without aura.
    Ophoff, RA
    Terwindt, GM
    Ferrari, MD
    Sandkuijl, LA
    Frants, RR
    AMERICAN JOURNAL OF HUMAN GENETICS, 1997, 61 (04) : A317 - A317
  • [44] ALS-CSF induced increase of P/Q-type Ca2+channel α1A subunit expression in presynaptic terminals on the rat spinal motor neurons
    Ramanathan, Gunasekaran
    NEUROSCIENCE RESEARCH, 2006, 55 : S138 - S138
  • [45] A novel R1347Q mutation in the predicted voltage sensor segment of the P/Q-type calcium-channel α1A-subunit in a family with progressive cerebellar ataxia and hemiplegic migraine
    Alonso, I
    Barros, J
    Tuna, A
    Seixas, A
    Coutinho, P
    Sequeiros, J
    Silveira, I
    CLINICAL GENETICS, 2004, 65 (01) : 70 - 72
  • [46] The ataxic groggy rat has a missense mutation in the P/Q-type voltage-gated Ca2+ channel α1A subunit gene and exhibits absence seizures
    Tokuda, Satoko
    Kuramoto, Takashi
    Tanaka, Kenta
    Kaneko, Shuji
    Takeuchi, Ikuo K.
    Sasa, Masashi
    Serikawa, Tadao
    BRAIN RESEARCH, 2007, 1133 (01) : 168 - 177
  • [47] Lambert-Eaton myasthenic syndrome -: Antigenicity of recombinant human P/Q-type calcium channel α1 subunit putative ion pore region (domain IV, S5-S6)
    Black, JL
    Griesmann, GE
    Erickson, J
    Kryzer, TJ
    Lamke, GT
    Lennon, VA
    MYASTHENIA GRAVIS AND RELATED DISEASES: DISORDERS OF THE NEUROMUSCULAR JUNCTION, 1998, 841 : 691 - 695
  • [48] Assignment of the calcium channel, voltage-dependent, P/Q type, alpha 1A subunit gene (CACNA1A) and the ataxin 7 gene (ATXN7) to canine chromosome 20 by fluorescence in situ hybridization and confirmation by radiation hybrid mapping
    Kuiper, H
    Drögemüller, C
    Evanno, G
    Guyon, R
    André, C
    Distl, O
    CYTOGENETIC AND GENOME RESEARCH, 2005, 111 (01) : 96C - U9
  • [49] Analysis of the 5′-upstream region of mouse P/Q-type Ca2+ channel α1A subunit gene for expression in pancreatic islet β cells using transgenic mice and HIT-T15 cells
    Takahashi, E
    Miyamoto, N
    Nagasu, T
    JOURNAL OF MOLECULAR ENDOCRINOLOGY, 2000, 24 (02) : 225 - 232
  • [50] Neuron-specific expression of reporter gene in transgenic mice carrying the 5'-upstream region of mouse P/Q-type Ca2+ channel α1A subunit gene fused to E-coli laZ reporter gene
    Takahashi, E
    Miyamoto, N
    Oki, T
    Kajiwara, N
    Furuya, K
    Yanai-Taniguchi, K
    Yagami, K
    Niidome, T
    Tanaka, I
    Katayama, K
    BRAIN RESEARCH, 1999, 850 (1-2) : 47 - 54
12345