SQSTM1 AND VCP MUTATIONS IN A SERIES OF 205 INCLUSION BODY MYOSITIS CASES

被引:0
|
作者
Gang, Q.
Bettencourt, C.
Brady, S.
Holton, J. L.
Pittman, A. M.
Hughes, D.
Healy, E.
Parton, M.
Hilton-Jones, D.
Shieh, P. B.
Needham, M.
Liang, C.
Zanoteli, E.
Valente de Camargo, L.
De Paepe, B.
De Bleecker, J.
Shaibani, A.
Ripolone, M.
Violano, R.
Moggio, M.
Barohn, R. J.
Dimachkie, M. M.
Mora, M.
Mantegazza, R.
Zanotti, S.
Singleton, A. B.
Hanna, M. G.
Houlden, H.
Machado, P. M.
机构
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:S2 / S2
页数:1
相关论文
共 50 条
  • [21] Wildtype SQSTM1 protein co-localizes and aggregates in vivo with SQSTM1 proteins carrying mutations in the UBA domain.
    Johnson-Pais, TL
    Ench, YM
    Wisdom, JH
    Singer, FR
    Leach, RJ
    JOURNAL OF BONE AND MINERAL RESEARCH, 2004, 19 : S102 - S102
  • [22] VALOSIN CONTAINING PROTEIN (VCP) AND MYOFIBRILLAR MYOPATHIES (MFM) GENES' MUTATIONS ARE NOT ASSOCIATED WITH SPORADIC INCLUSION BODY MYOSITIS (sIBM)
    Machado, P.
    Hudson, J.
    Miller, A.
    Morrow, J.
    Parton, M.
    Bushby, K.
    Hanna, M.
    JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 2012, 83 (03):
  • [23] Inclusion body myositis and anesthesia: a case series
    Mortenson, Andrew R.
    Sprung, Juraj
    Cavalcante, Alexandre N.
    Watson, James C.
    Weingarten, Toby N.
    JOURNAL OF CLINICAL ANESTHESIA, 2016, 31 : 282 - 287
  • [24] INCLUSION BODY MYOSITIS - ANALYSIS OF 32 CASES
    SAYERS, ME
    CHOU, SM
    CALABRESE, LH
    JOURNAL OF RHEUMATOLOGY, 1992, 19 (09) : 1385 - 1389
  • [25] Filamin and Valosin Containing Protein (VCP) interaction in Inclusion Body Myositis.
    Britson, K.
    Michelle, E. H.
    Castro, C.
    Aksentijevich, I.
    Schiffenbauer, A.
    Mankodi, A.
    Kastner, D.
    Mammen, A.
    Weihl, C. C.
    Siegel, R.
    Lloyd, T. E.
    MOLECULAR BIOLOGY OF THE CELL, 2017, 28
  • [26] SQSTM1 mutations - Bridging Paget disease of bone and ALS/FTLD
    Rea, Sarah L.
    Majcher, Veronika
    Searle, Mark S.
    Layfield, Rob
    EXPERIMENTAL CELL RESEARCH, 2014, 325 (01) : 27 - 37
  • [27] Absence of Somatic SQSTM1 Mutations in Paget's Disease of Bone
    Matthews, Brya G.
    Naot, Dorit
    Bava, Usha
    Callon, Karen E.
    Pitto, Rocco P.
    McCowan, Stuart A.
    Wattie, Diana
    Cundy, Tim
    Cornish, Jill
    Reid, Ian R.
    JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2009, 94 (02): : 691 - 694
  • [29] SQSTM1/p62 Mutations in Amyotrophic Lateral Sclerosis
    Fecto, Faisal
    Yan, Jianhua
    Vemula, Pavan
    Liu, Erdong
    Yang, Yi
    Chen, Wenjie
    Zheng, Jian Guo
    Shi, Yong
    Siddique, Nailah
    Donkervoort, Sandra
    Ajroud-Driss, Senda
    Sufit, Robert
    Heller, Scott
    Deng, Han-Xiang
    Siddique, Teepu
    NEUROLOGY, 2011, 76 (09) : A554 - A554
  • [30] SQSTM1 mutations in frontotemporal lobar degeneration and amyotrophic lateral sclerosis
    Rubino, Elisa
    Rainero, Innocenzo
    Chio, Adriano
    Rogaeva, Ekaterina
    Galimberti, Daniela
    Fenoglio, Pierpaola
    Grinberg, Yakov
    Isaia, Giancarlo
    Calvo, Andrea
    Gentile, Salvatore
    Bruni, Amalia Cecilia
    St George-Hyslop, Peter Henry
    Scarpini, Elio
    Gallone, Salvatore
    Pinessi, Lorenzo
    NEUROLOGY, 2012, 79 (15) : 1556 - 1562