CMT-ASSOCIATED HSPB1 MUTATIONS AFFECT MICROTUBULE DYNAMICS AND REVEAL A NOVEL FUNCTION OF WILD-TYPE HSPB1 IN MICROTUBULE NUCLEATION

被引:0
|
作者
Almeida-Souza, L. [1 ]
Asselbergh, B. [1 ]
d'Ydewalle, C. [2 ]
Goethals, S. [1 ]
de Winter, V [1 ]
Irobi, J. [1 ]
Van den Bosch, L. [2 ]
Timmerman, V [1 ]
Janssens, S. [1 ]
机构
[1] Univ Antwerp, Antwerp, Belgium
[2] Univ Leuven, Louvain, 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:S3 / S3
页数:1
相关论文
共 26 条
  • [1] 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
  • [2] 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, 2017, 22 (03) : 295 - 296
  • [3] 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
  • [4] FUNCTIONAL STUDIES ON NOVEL HSPB1 MUTATIONS: PRELIMINARY RESULTS
    Capponi, S.
    Geroldi, A.
    De Almeida-Souza, L.
    Holmgren, A.
    De Winter, V
    Ciotti, P.
    Gulli, R.
    Grandis, M.
    Schenone, A.
    Mandich, P.
    Timmerman, V
    Irobi, J.
    Bellone, E.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2012, 17 : S12 - S13
  • [5] 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
  • [6] 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
  • [7] A novel HSPB1 mutation in an Italian patient with CMT2/dHMN phenotype
    Luigetti, M.
    Fabrizi, G. M.
    Madia, F.
    Ferrarini, M.
    Conte, A.
    Del Grande, A.
    Tasca, G.
    Tonali, P. A.
    Sabatelli, M.
    JOURNAL OF THE NEUROLOGICAL SCIENCES, 2010, 298 (1-2) : 114 - 117
  • [8] Neuropathology of a human autopsy of HSPB1 distal hereditary motor neuropathy-dHMN (p.Ser135Phe) and transgenic mice with mutant/wild-type HSPB1 overexpression
    Phadke, R.
    Rossor, A. M.
    Benoy, V.
    Kalmar, B.
    King, R. M. H.
    Greensmith, L.
    Bosch, L. V. D.
    Reilly, M. M.
    Houlden, H.
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 2016, 42 : 25 - 26
  • [9] Two causative mutations in HSPB1 (HSP27) in the Korean autosomal dominant axonal CMT families
    Kim, H.
    Kim, H.
    Hong, G-R.
    Cho, E.
    Choi, B. O.
    Chung, K. W.
    MOLECULAR BIOLOGY OF THE CELL, 2013, 24
  • [10] Mutations in the HSP27 (HSPB1) gene cause dominant, recessive, and sporadic distal HMN/CMT type 2
    Houlden, H.
    Laura, M.
    Wavrant-De Vrieze, F.
    Blake, J.
    Wood, N.
    Reilly, M. M.
    NEUROLOGY, 2008, 71 (21) : 1660 - 1668