ALS mutant SOD1 affects pathological modifications of TDP-43

被引:0
|
作者
Jeon, G. S. [1 ]
Ahn, S. H. [1 ]
Im, S. Y. [1 ]
Sung, J. -J. [1 ]
机构
[1] Seoul Natl Univ Hosp, Neurol, Seoul, South Korea
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
WTH07-21
引用
收藏
页码:220 / 220
页数:1
相关论文
共 50 条
  • [11] Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS
    Jacqueline C Mitchell
    Remy Constable
    Eva So
    Caroline Vance
    Emma Scotter
    Leanne Glover
    Tibor Hortobagyi
    Eveline S. Arnold
    Shuo-Chien Ling
    Melissa McAlonis
    Sandrine Da Cruz
    Magda Polymenidou
    Lino Tessarolo
    Don W Cleveland
    Christopher E Shaw
    Acta Neuropathologica Communications, 3
  • [12] Wild type human TDP-43 potentiates ALS-linked mutant TDP-43 driven progressive motor and cortical neuron degeneration with pathological features of ALS
    Mitchell, Jacqueline C.
    Constable, Remy
    So, Eva
    Vance, Caroline
    Scotter, Emma
    Glover, Leanne
    Hortobagyi, Tibor
    Arnold, Eveline S.
    Ling, Shuo-Chien
    McAlonis, Melissa
    Da Cruz, Sandrine
    Polymenidou, Magda
    Tessarolo, Lino
    Cleveland, Don W.
    Shaw, Christopher E.
    ACTA NEUROPATHOLOGICA COMMUNICATIONS, 2015, 3 : 36
  • [13] TDP-43 Identified from a Genome Wide RNAi Screen for SOD1 Regulators
    Somalinga, Balajee R.
    Day, Cameron E.
    Wei, Shuguang
    Roth, Michael G.
    Thomas, Philip J.
    PLOS ONE, 2012, 7 (04):
  • [14] Pathological TDP-43 distinguishes sporadic amyotrophic lateral sclerosis from amyotrophic lateral sclerosis with SOD1 mutations
    Mackenzie, Ian R. A.
    Bigio, Eileen H.
    Ince, Paul G.
    Geser, Felix
    Neumann, Manuela
    Cairns, Nigel J.
    Kwong, Linda K.
    Forman, Mark S.
    Ravits, John
    Stewart, Heather
    Eisen, Andrew
    Mcclusky, Leo
    Kretzschmar, Hans A.
    Monoranu, Camelia M.
    Highley, J. Robin
    Kirby, Janine
    Siddique, Teepu
    Shaw, Pamela J.
    Lee, Virginia M-Y.
    Trojanowski, John Q.
    ANNALS OF NEUROLOGY, 2007, 61 (05) : 427 - 434
  • [15] Abnormal mitochondrial transport and morphology are common pathological denominators in SOD1 and TDP43 ALS mouse models
    Magrane, Jordi
    Cortez, Czrina
    Gan, Wen-Biao
    Manfredi, Giovanni
    HUMAN MOLECULAR GENETICS, 2014, 23 (06) : 1413 - 1424
  • [16] Structure of pathological TDP-43 filaments from ALS with FTLD
    Arseni, Diana
    Hasegawa, Masato
    Murzin, Alexey G.
    Kametani, Fuyuki
    Arai, Makoto
    Yoshida, Mari
    Ryskeldi-Falcon, Benjamin
    NATURE, 2022, 601 (7891) : 139 - +
  • [17] Structure of pathological TDP-43 filaments from ALS with FTLD
    Diana Arseni
    Masato Hasegawa
    Alexey G. Murzin
    Fuyuki Kametani
    Makoto Arai
    Mari Yoshida
    Benjamin Ryskeldi-Falcon
    Nature, 2022, 601 : 139 - 143
  • [18] Oxidative stress induced by glutathione depletion reproduces pathological modifications of TDP-43 linked to TDP-43 proteinopathies
    Iguchi, Yohei
    Katsuno, Masahisa
    Takagi, Shinnosuke
    Ishigaki, Shinsuke
    Niwa, Jun-ichi
    Hasegawa, Masato
    Tanaka, Fumiaki
    Sobue, Gen
    NEUROBIOLOGY OF DISEASE, 2012, 45 (03) : 862 - 870
  • [19] AN AUTOPSY CASE OF SOD1-RELATED ALS WITH TDP-43 POSITIVE INCLUSIONS
    Okamoto, Y.
    Ihara, M.
    Urushitani, M.
    Yamashita, H.
    Kondo, T.
    Tanigaki, A.
    Oono, M.
    Kawamata, J.
    Ikemoto, A.
    Kawamoto, Y.
    Takahashi, R.
    Ito, H.
    NEUROLOGY, 2011, 77 (22) : 1993 - 1995
  • [20] TDP-43 in FTD and ALS
    Neumann, M.
    BRAIN PATHOLOGY, 2010, 20 : 7 - 7