An ELISA assay for measuring the survival of motor neurons (SMN) protein and the search for a drug treatment for spinal muscular atrophy

被引:0
|
作者
Man, NT
Lam, LT
Lynch, T
Sewry, C
MacKenzie, A
Morris, GE
机构
[1] Robert Jones & Agnes Hunt Orthopaed Hosp, CIND, Oswestry SY10 7AG, Shrops, England
[2] Childrens Hosp Eastern Ontario, Ottawa, ON K1H 8L1, Canada
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:726 / 726
页数:1
相关论文
共 50 条
  • [31] Impact of missense mutations in survival motor neuron protein (SMN1) leading to Spinal Muscular Atrophy (SMA): A computational approach
    Sneha, P.
    Zenith, Tanzila U.
    Abu Habib, Ummay Salma
    Evangeline, Judith
    Kumar, D. Thirumal
    Doss, C. George Priya
    Siva, R.
    Zayed, Hatem
    METABOLIC BRAIN DISEASE, 2018, 33 (06) : 1823 - 1834
  • [32] THE MOTOR NEURON RESPONSE TO SMN1 DEFICIENCY IN SPINAL MUSCULAR ATROPHY
    Arnold, W. David
    Mo, Xiaokui
    Kolb, Stephen J.
    Burghes, Arthur H.
    Kissel, John T.
    MUSCLE & NERVE, 2014, 50 (03) : 457 - 458
  • [33] THE MOTOR NEURON RESPONSE TO SMN1 DEFICIENCY IN SPINAL MUSCULAR ATROPHY
    Kang, Peter B.
    Gooch, Clifton L.
    McDermott, Michael P.
    Darras, Basil T.
    Finkel, Richard S.
    Yang, Michele L.
    Sproule, Douglas M.
    Chung, Wendy K.
    Kaufmann, Petra
    de Vivo, Darryl C.
    MUSCLE & NERVE, 2014, 49 (05) : 636 - 644
  • [34] Correlation between severity and SMN protein level in spinal muscular atrophy
    Suzie Lefebvre
    Philippe Burlet
    Qing Liu
    Solange Bertrandy
    Olivier Clermont
    Arnold Munnich
    Gideon Dreyfuss
    Judith Melki
    Nature Genetics, 1997, 16 : 265 - 269
  • [35] Correlation between severity and SMN protein level in spinal muscular atrophy
    Lefebvre, S
    Burlet, P
    Liu, Q
    Bertrandy, S
    Clermont, O
    Munnich, A
    Dreyfuss, G
    Melki, J
    NATURE GENETICS, 1997, 16 (03) : 265 - 269
  • [36] Impact of missense mutations in survival motor neuron protein (SMN1) leading to Spinal Muscular Atrophy (SMA): A computational approach
    P. Sneha
    Tanzila U. Zenith
    Ummay Salma Abu Habib
    Judith Evangeline
    D. Thirumal Kumar
    C. George Priya Doss
    R. Siva
    Hatem Zayed
    Metabolic Brain Disease, 2018, 33 : 1823 - 1834
  • [37] Molecular analysis of survival motor neuron (SMN) and neuronal apoptosis inhibitory protein (NAIP) genes of spinal muscular atrophy patients and their parents
    J.-G. Chang
    Yuh-Jyh Jong
    Shuan-Pei Lin
    Bing-Wen Soong
    Chang-Hai Tsai
    T.-Y. Yang
    Chih-Peng Chang
    Wen-Shin Wang
    Human Genetics, 1997, 100 : 577 - 581
  • [38] Abnormal motor phenotype in the SMNΔ7 mouse model of spinal muscular atrophy
    Butchbach, Matthew E. R.
    Edwards, Jonathan D.
    Burghes, Arthur H. M.
    NEUROBIOLOGY OF DISEASE, 2007, 27 (02) : 207 - 219
  • [39] The Spinal Muscular Atrophy Disease Protein SMN Is Linked to the Golgi Network
    Ting, Chen-Hung
    Wen, Hsin-Lan
    Liu, Hui-Chun
    Hsieh-Li, Hsiu-Mei
    Li, Hung
    Lin-Chao, Sue
    PLOS ONE, 2012, 7 (12):
  • [40] Other forms of survival motor neuron protein and spinal muscular atrophy: An opinion
    Burghes, H. M.
    NEUROMUSCULAR DISORDERS, 2008, 18 (01) : 82 - 83