Role of the ATP13A2 gene in the etiology of Parkinson's disease

被引：0
|
作者：
Rakovic, Aleksandar
Djarmati, Ana
Winkler, Susen
Pawlack, Heike
Lohmann, Katja
Kostic, Vladimir
Ramirez, Alfredo
Klein, Christine
机构：
来源：
NEUROLOGY | 2008年 / 70卷 / 11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：A321 / A321
页数：1
相关论文
共 50 条
  • [21] ATP13A2 protects dopaminergic neurons in Parkinson's disease: from biology to pathology
    Tao Dang
    Wen-Jing Cao
    Rong Zhao
    Ming Lu
    Gang Hu
    Chen Qiao
    The Journal of Biomedical Research, 2022, 36 (02) : 98 - 108
  • [22] Phenotypic Characterization of an ATP13A2 Knockout Rat Model of Parkinson's disease (PD)
    Kinet, R.
    Sikora, J.
    Arotcarena, M. L.
    Decourt, M.
    Balado, E.
    Doudnikoff, E.
    Bezard, E.
    Fernagut, P. O.
    Dehay, B.
    MOVEMENT DISORDERS, 2024, 39 : S826 - S826
  • [23] Parkinson disease related ATP13A2 evolved early in animal evolution
    Sorensen, Danny Mollerup
    Holemans, Tine
    van Veen, Sarah
    Martin, Shaun
    Arslan, Tugce
    Haagendahl, Ida Winther
    Holen, Henrik Weida
    Hamouda, Norin Nabil
    Eggermont, Jan
    Palmgren, Michael
    Vangheluwe, Peter
    PLOS ONE, 2018, 13 (03):
  • [24] Novel ATP13A2 variant associated with Parkinson disease in Taiwan and Singapore
    Lin, C. H.
    Tan, E. K.
    Chen, M. L.
    Tan, L. C.
    Lim, H. Q.
    Chen, G. S.
    Wu, R. M.
    NEUROLOGY, 2008, 71 (21) : 1727 - 1732
  • [25] Single Heterozygous ATP13A2 Mutations Cause Cellular Dysfunction Associated with Parkinson's Disease
    Park, Jin-Sung
    Koentjoro, Brianada
    Klein, Christine
    Sue, Carolyn M.
    MOVEMENT DISORDERS, 2018, 33 (05) : 852 - 854
  • [26] ATP13A2 Declines Zinc-Induced Accumulation of α-Synuclein in a Parkinson's Disease Model
    Gao, Huiling
    Sun, Hehong
    Yan, Nan
    Zhao, Pu
    Xu, He
    Zheng, Wei
    Zhang, Xiaoyu
    Wang, Tao
    Guo, Chuang
    Zhong, Manli
    INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES, 2022, 23 (14)
  • [27] ATP13A2 missense mutations in juvenile parkinsonism and young onset Parkinson disease
    Di Fonzo, A.
    Chien, H. F.
    Socal, M.
    Giraudo, S.
    Tassorelli, C.
    Iliceto, G.
    Fabbrini, G.
    Marconi, R.
    Fincati, E.
    Abbruzzese, G.
    Marini, P.
    Squitieri, F.
    Horstink, M. W.
    Montagna, P.
    Dalla Libera, A.
    Stocchi, F.
    Goldwurm, S.
    Ferreira, J. J.
    Meco, G.
    Martignoni, E.
    Lopiano, L.
    Jardim, L. B.
    Oostra, B. A.
    Barbosa, E. R.
    Bonifati, V.
    NEUROLOGY, 2007, 68 (19) : 1557 - 1562
  • [28] Mutation screening of ATP13A2 in patients with early-onset Parkinson's disease and familial Parkinson's disease from mainland China
    Mao, X. Y.
    Peng, R.
    Zhang, Z. J.
    MOVEMENT DISORDERS, 2009, 24 : S149 - S149
  • [29] A Rare Case of Parkinson's disease (PD) Associated with Heterozygous ATP13A2 Gene Mutation: What If There Are No Atypical Features with a Later Onset?
    Degirmenci, Y.
    MOVEMENT DISORDERS, 2024, 39 : S791 - S791
  • [30] Knockdown of Parkinson's disease-related gene ATP13A2 reduces tumorigenesis via blocking autophagic flux in colon cancer
    Chen, Qian
    Zhong, Li
    Zhou, Chao
    Feng, Yan
    Liu, Quan-xing
    Zhou, Dong
    Lu, Xiao
    Du, Guang-Sheng
    Jian, Dan
    Luo, Hao
    Wang, Dong
    Zheng, Hong
    Qiu, Yuan
    CELL AND BIOSCIENCE, 2020, 10 (01):
12345