Spinocerebellar ataxia type 2 (SCA2) is associated with TDP-43 pathology

被引：36
作者：
Toyoshima, Yasuko [1 ]
Tanaka, Hajime [2 ]
Shimohata, Mitsuteru [2 ]
Kimura, Kakuhei [3 ]
Morita, Takashi [3 ]
Kakita, Akiyoshi [1 ]
Takahashi, Hitoshi [1 ]
机构：
[1] Niigata Univ, Brain Res Inst, Dept Pathol, Chuo Ku, Niigata 9518585, Japan
[2] Shinrakuen Hosp, Dept Neurol, Niigata, Japan
[3] Shinrakuen Hosp, Dept Pathol, Niigata, Japan
来源：
ACTA NEUROPATHOLOGICA | 2011年 / 122卷 / 03期
关键词：
LENGTH POLYGLUTAMINE EXPANSIONS; INCLUSIONS; DISEASE; ALS;
D O I：
10.1007/s00401-011-0862-7
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：375 / 378
页数：4
相关论文
共 50 条
  • [41] Loss of Nuclear TDP-43 Is Associated with Decondensation of LINE Retrotransposons
    Liu, Elaine Y.
    Russ, Jenny
    Cali, Christopher P.
    Phan, Jessica M.
    Amlie-Wolf, Alexandre
    Lee, Edward B.
    CELL REPORTS, 2019, 27 (05): : 1409 - +
  • [42] Spinocerebellar ataxia type 2-neuronopathy or neuropathy?
    Pelosi, Luciana
    Iodice, Rosa
    Antenora, Antonella
    Kilfoyle, Dean
    Mulroy, Eoin
    Rodrigues, Miriam
    Roxburgh, Richard
    Iovino, Aniello
    Filla, Alessandro
    Manganelli, Fiore
    Santoro, Lucio
    MUSCLE & NERVE, 2019, 60 (03) : 271 - 278
  • [43] Antisense oligonucleotide therapy for spinocerebellar ataxia type 2
    Scoles, Daniel R.
    Meera, Pratap
    Schneider, Matthew D.
    Paul, Sharan
    Dansithong, Warunee
    Figueroa, Karla P.
    Hung, Gene
    Rigo, Frank
    Bennett, C. Frank
    Otis, Thomas S.
    Pulst, Stefan M.
    NATURE, 2017, 544 (7650) : 362 - +
  • [44] TDP-43 pathology is present in most post-encephalitic parkinsonism brains
    Ling, H.
    Holton, J. L.
    Lees, A. J.
    Revesz, T.
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2014, 40 (05) : 654 - 657
  • [45] Mechanisms underlying TDP-43 pathology and neurodegeneration: An updated Mini-Review
    Nilaver, Benjamin I.
    Urbanski, Henryk F.
    FRONTIERS IN AGING NEUROSCIENCE, 2023, 15
  • [46] Neuronal Expression of UBQLN2P497H Exacerbates TDP-43 Pathology in TDP-43G348C Mice through Interaction with Ubiquitin
    Picher-Martel, Vincent
    Renaud, Laurence
    Bareil, Christine
    Julien, Jean-Pierre
    MOLECULAR NEUROBIOLOGY, 2019, 56 (07) : 4680 - 4696
  • [47] Spinocerebellar ataxia type 2: progression before diagnosis
    Klockgether, Thomas
    LANCET NEUROLOGY, 2014, 13 (05) : 445 - 446
  • [48] Is there a glucose metabolic signature of spreading TDP-43 pathology in amyotrophic lateral sclerosis?
    van Weehaeghe, Donatienne
    Ceccarini, Jenny
    Willekens, Stefanie M.
    de Vocht, Joke
    van Damme, Philip
    van Laere, Koen
    QUARTERLY JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING, 2020, 64 (01) : 96 - 104
  • [49] TDP-43 mediates SREBF2-regulated gene expression required for oligodendrocyte myelination
    Ho, Wan Yun
    Chang, Jer-Cherng
    Lim, Kenneth
    Cazenave-Gassiot, Amaury
    Nguyen, Aivi T.
    Foo, Juat Chin
    Muralidharan, Sneha
    Viera-Ortiz, Ashley
    Ong, Sarah J. M.
    Hor, Jin Hui
    Agrawal, Ira
    Hoon, Shawn
    Arogundade, Olubankole Aladesuyi
    Rodriguez, Maria J.
    Lim, Su Min
    Kim, Seung Hyun
    Ravits, John
    Ng, Shi-Yan
    Wenk, Markus R.
    Lee, Edward B.
    Tucker-Kellogg, Greg
    Ling, Shuo-Chien
    JOURNAL OF CELL BIOLOGY, 2021, 220 (09)
  • [50] Heart rate variability in type 2 spinocerebellar ataxia
    Montes-Brown, J.
    Sanchez-Cruz, G.
    Garcia, A. M.
    Baez, M. E.
    Velazquez-Perez, L.
    ACTA NEUROLOGICA SCANDINAVICA, 2010, 122 (05): : 329 - 335
12345