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
来源：
JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM | 2017年 / 22卷 / 03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：295 / 296
页数：2
相关论文
共 50 条
  • [21] 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
  • [22] Charcot-Marie-Tooth causing HSPB1 mutations increase Cdk5-mediated phosphorylation of neurofilaments
    Holmgren, Anne
    Bouhy, Delphine
    De Winter, Vicky
    Asselbergh, Bob
    Timmermans, Jean-Pierre
    Irobi, Joy
    Timmerman, Vincent
    ACTA NEUROPATHOLOGICA, 2013, 126 (01) : 93 - 108
  • [23] Effects of N-terminal disease mutations on HspB1 polydispersity
    Klevit, Rachel
    Clouser, Amanda
    Chu, Thanh
    ABSTRACTS OF PAPERS OF THE AMERICAN CHEMICAL SOCIETY, 2017, 253
  • [24] CHARCOT-MARIE-TOOTH CAUSING HSPB1 MUTATIONS INCREASE CDK5-MEDIATED PHOSPHORYLATION OF NEUROFILAMENTS
    Holmgren, A.
    Bouhy, D.
    De Winter, V
    Asselbergh, B.
    Irobi, J.
    Timmerman, V
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2013, 18 : 47 - 47
  • [25] HSPB1 mutations causing hereditary neuropathy in humans disrupt non-cell autonomous protection of motor neurons
    Heilman, Patrick L.
    Song, SungWon
    Miranda, Carlos J.
    Meyer, Kathrin
    Srivastava, Amit K.
    Knapp, Amy
    Wier, Christopher G.
    Kaspar, Brian K.
    Kolb, Stephen J.
    EXPERIMENTAL NEUROLOGY, 2017, 297 : 101 - 109
  • [26] HOMOZYGOUS MUTATION IN HSPB1 CAUSING DISTAL VACUOLAR MYOPATHY AND MOTOR NEUROPATHY
    Bugiardini, Enrico
    Rossor, Alexander M.
    Lynch, David S.
    Swash, Michael
    Pittman, Alan M.
    Blake, Julian C.
    Hanna, Michael G.
    Houlden, Henry
    Holton, Janice L.
    Reilly, Mary M.
    Matthews, Emma
    NEUROLOGY-GENETICS, 2017, 3 (04)
  • [27] Mutation of the small HSP27/HSPB1 causes CMT neuropathy with abnormal neurofilament assembly
    Cerri, F.
    Coviello, S.
    Previtali, S. C.
    Benedetti, S.
    Scarlato, M.
    Dacci, P.
    Fazio, R.
    Comi, G.
    Quattrini, A.
    Bolino, A.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2007, 12 : 17 - 17
  • [28] HSPB1 Regulates Autophagy and Apoptosis in Vascular Smooth Muscle Cells in Arteriosclerosis Obliterans
    Chen, Keqin
    Hou, Changmiao
    Xu, Lei
    Peng, Hanwu
    He, Chaogui
    Liu, Jing
    Wang, Guoqing
    Huang, Shaoshuai
    Liu, Xiehong
    CARDIOVASCULAR THERAPEUTICS, 2022, 2022
  • [29] PHENOTYPIC SPECTRUM AND INCIDENCE OF HSPB1, HSPB3 AND HSPB8 MUTATIONS IN PATIENTS WITH DISTAL HEREDITARY MOTOR NEUROPATHY
    Echaniz-Laguna, A.
    Petiot, P.
    Pereon, Y.
    Salachas, F.
    Delmont, E.
    Pouget, J.
    Morales, R.
    Goizet, C.
    Latour, P.
    Stojkovic, T.
    JOURNAL OF THE PERIPHERAL NERVOUS SYSTEM, 2015, 20 (02) : 135 - 135
  • [30] Pilot phenotype and natural history study of hereditary neuropathies caused by mutations in the HSPB1 gene
    Rossor, Alexander M.
    Morrow, Jasper M.
    Polke, James M.
    Murphy, Sinead M.
    Houlden, Henry
    Laura, Matilde
    Manji, Hadi
    Blake, Julian
    Reilly, Mary M.
    NEUROMUSCULAR DISORDERS, 2017, 27 (01) : 50 - 56
12345