IMPAIRMENT OF AUTOPHAGY AS A POSSIBLE PATHOMECHANISM FOR CMT CAUSING MUTATIONS IN HSPB1

被引:0
|
作者
Haidar, M. [1 ]
De Winter, V [1 ]
Asselbergh, B. [1 ]
Bouhy, D. [1 ]
Timmerman, V [1 ]
机构
[1] Univ Antwerp VIB, Peripheral Neuropathy Res Grp, Antwerp, Belgium
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:295 / 296
页数:2
相关论文
共 50 条
  • [1] IMPAIRMENT OF AUTOPHAGY AS A POSSIBLE PATHOMECHANISM FOR CMT CAUSING MUTATIONS IN HSPB1
    Haidar, M.
    De Winter, V
    Asselbergh, B.
    Bouhy, D.
    Timmerman, V
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2016, 21 (03) : 263 - 263
  • [2] TWO NOVEL MUTATIONS IN HSPB1 IN CMT AND DHMN PHENOTYPES
    Beaudonnet, G.
    Not, A.
    Malinge, M-C
    Deviere, F.
    Iliescu, I.
    Labeyrie, C.
    Theaudin, M.
    Cauquil, C.
    Adams, D.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2015, 20 (02) : 102 - 103
  • [3] MUTATIONS IN HSPB1 CAUSING PERIPHERAL NEUROPATHY STABILIZE MICROTUBULES
    Almeida-Souza, L.
    Asselbergh, B.
    De Winter, V
    Goethals, S.
    Timmerman, V
    Janssens, S.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2013, 18 : 5 - 6
  • [4] A NATURAL HISTORY STUDY OF CMT2 AND DHMN DUE TO MUTATIONS IN HSPB1
    Rossor, A. M.
    Horga, A.
    Laura, M.
    Morrow, J.
    Reilly, M. M.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2015, 20 (02) : 220 - 221
  • [5] CMT-ASSOCIATED HSPB1 MUTATIONS AFFECT MICROTUBULE DYNAMICS AND REVEAL A NOVEL FUNCTION OF WILD-TYPE HSPB1 IN MICROTUBULE NUCLEATION
    Almeida-Souza, L.
    Asselbergh, B.
    d'Ydewalle, C.
    Goethals, S.
    de Winter, V
    Irobi, J.
    Van den Bosch, L.
    Timmerman, V
    Janssens, S.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2011, 16 : S3 - S3
  • [6] Mutations in HspB1 and hereditary neuropathies
    Lydia K. Muranova
    Maria V. Sudnitsyna
    Sergei V. Strelkov
    Nikolai B. Gusev
    Cell Stress and Chaperones, 2020, 25 : 655 - 665
  • [7] Mutations in HspB1 and hereditary neuropathies
    Muranova, Lydia K.
    Sudnitsyna, Maria, V
    Strelkov, Sergei, V
    Gusev, Nikolai B.
    CELL STRESS & CHAPERONES, 2020, 25 (04): : 655 - 665
  • [8] HSPB1 GENE AND PERIPHERAL HEREDITARY NEUROPATHIES: NOVEL MUTATIONS IN DHMN AND CMT2
    Capponi, S.
    Geroldi, A.
    Gulli, R.
    Ciotti, P.
    Schenone, A.
    Grandis, M.
    Doria-Lamba, L.
    Bellone, E.
    Mandich, P.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2009, 14 : 6 - 6
  • [9] Neuropathy-causing mutations in HSPB1 impair autophagy by disturbing the formation of SQSTM1/p62 bodies
    Haidar, Mansour
    Asselbergh, Bob
    Adriaenssens, Elias
    De Winter, Vicky
    Timmermans, Jean-Pierre
    Auer-Grumbach, Michaela
    Juneja, Manisha
    Timmerman, Vincent
    AUTOPHAGY, 2019, 15 (06) : 1051 - 1068
  • [10] In vitro expression of small heat shock protein HSPB8 and HSPB1 mutations causing axonal neuropathy
    Irobi, J.
    Dierick, I.
    de Corte, V.
    Gettemans, J.
    Robberecht, W.
    Van Den Bosch, L.
    Timmermans, J. -P.
    De Jonghe, P.
    Timmerman, V.
    NEUROMUSCULAR DISORDERS, 2006, 16 (9-10) : 645 - 646