Different Ways of Calcium Signaling Disruption in Huntington's Disease and Spinocerebellar Ataxia Type 1

被引：0
|
作者：
Grekhnyov, Dmitry [1 ]
Vigont, Vladimir [1 ]
Kaznacheyeva, Elena [1 ]
机构：
[1] Russian Acad Sci, Inst Cytol, Dept Ion Channels Cell Membranes, St Petersburg, Russia
来源：
BIOPHYSICAL JOURNAL | 2020年 / 118卷 / 03期
基金：
俄罗斯科学基金会;
关键词：
D O I：
暂无
中图分类号：
Q6 [生物物理学];
学科分类号：
071011 ;
摘要：
1985-Pos
引用
收藏
页码：404A / 404A
页数：1
相关论文
共 50 条
  • [21] Spinocerebellar ataxia type 7 presenting as Stargardt's disease
    Tsivgoulis, G.
    Spergos, K.
    Vassilopoulou, S.
    Rallis, K.
    Christodoulou, K.
    Markomichelakis, N.
    Vassilopoulos, D.
    EUROPEAN JOURNAL OF NEUROLOGY, 2006, 13 : 285 - 285
  • [22] Genetic fitness in Huntington's Disease and Spinocerebellar Ataxia 1: A population genetics model for CAG repeat expansions
    Frontali, M
    Sabbadini, G
    Novelletto, A
    Jodice, C
    Naso, F
    Spadaro, M
    Giunti, P
    Jacopini, AG
    Veneziano, L
    Mantuano, E
    Malaspina, P
    Ulizzi, L
    Brice, A
    Durr, A
    Terrenato, L
    ANNALS OF HUMAN GENETICS, 1996, 60 : 423 - 435
  • [23] Modulation of age at onset in Huntington's disease and spinocerebellar ataxia type 2 patients originated from eastern India
    Chattopadhyay, B
    Ghosh, S
    Gangopadhyay, PK
    Das, SK
    Roy, T
    Sinha, KK
    Jha, DK
    Mukherjee, SC
    Chakraborty, A
    Singhal, BS
    Bhattacharya, AK
    Bhattacharyya, NP
    NEUROSCIENCE LETTERS, 2003, 345 (02) : 93 - 96
  • [24] Disruption of Visual and Motor Connectivity in Spinocerebellar Ataxia Type 7
    Hernandez-Castillo, Carlos R.
    Alcauter, Sarael
    Galvez, Victor
    Barrios, Fernando A.
    Yescas, Petra
    Ochoa, Adriana
    Garcia, Lizbeth
    Diaz, Rosalinda
    Gao, Wei
    Fernandez-Ruiz, Juan
    MOVEMENT DISORDERS, 2013, 28 (12) : 1708 - 1716
  • [25] From Mild Ataxia to Huntington Disease Phenocopy: The Multiple Faces of Spinocerebellar Ataxia 17
    Koutsis, Georgios
    Panas, Marios
    Paraskevas, George P.
    Bougea, AnastasiaM.
    Kladi, Athina
    Karadima, Georgia
    Kapaki, Elisabeth
    CASE REPORTS IN NEUROLOGICAL MEDICINE, 2014, 2014
  • [26] Single cell analysis of trinucleotide repeat expansion mutations in Huntington disease, spinocerebellar ataxia type 1, and myotonic dystrophy
    Chong, SS
    Liu, L
    Hughes, MR
    IN VITRO FERTILIZATION AND ASSISTED REPRODUCTION, 1997, : 751 - 757
  • [27] Spinocerebellar ataxia type 1 in Russia
    Illarioshkin, SN
    Slominsky, PA
    Ovchinnikov, IV
    Markova, ED
    Miklina, NI
    Klyushnikov, SA
    Shadrina, M
    Vereshchagin, NV
    Limborskaya, SA
    IvanovaSmolenskaya, IA
    JOURNAL OF NEUROLOGY, 1996, 243 (07) : 506 - 510
  • [28] SPINOCEREBELLAR ATAXIA TYPE-1
    ZOGHBI, HY
    ORR, HT
    SEMINARS IN CELL BIOLOGY, 1995, 6 (01): : 29 - 35
  • [29] Spinocerebellar ataxia type 1 in Serbia
    Dragasevic, N. T.
    Ristic, A. J.
    Culjkovic, B.
    Keckarevic, M.
    Svetel, M.
    Romac, S.
    Kostic, V. S.
    EUROPEAN JOURNAL OF NEUROLOGY, 2004, 11 : 297 - 297
  • [30] SPINOCEREBELLAR ATAXIA TYPE-1
    ZOGHBI, HY
    CLINICAL NEUROSCIENCE, 1995, 3 (01) : 5 - 11
12345