Incomplete glycosylation of α-dystroglycan in hereditary inclusion body myopathy

被引:0
|
作者
Huizing, M
Rakocevic, G
Sparks, S
Gahl, W
Dalakas, M
Krasnewich, D
机构
[1] NIH, NHGRI, Med Genet Branch, Bethesda, MD 20892 USA
[2] NIH, Nat Inst Neurol & Stroke, Neuromuscular Dis Section, Bethesda, MD 20892 USA
关键词
D O I
暂无
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
293
引用
收藏
页码:903 / 903
页数:1
相关论文
共 50 条
  • [11] The Proteomic Profile of Hereditary Inclusion Body Myopathy
    Sela, Ilan
    Krentsis, Irit Milman
    Shlomai, Zipora
    Sadeh, Menachem
    Dabby, Ron
    Argov, Zohar
    Ben-Bassat, Hannah
    Mitrani-Rosenbaum, Stella
    PLOS ONE, 2011, 6 (01):
  • [12] Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy
    Hinderlich, S
    Salama, I
    Eisenberg, I
    Mitrani-Rosenbaum, S
    NEUROLOGY, 2003, 61 (01) : 145 - 145
  • [13] Distal myopathy with rimmed vacuoles is allelic to hereditary inclusion body myopathy
    Nishino, I
    Noguchi, S
    Murayama, K
    Driss, A
    Sugie, K
    Oya, Y
    Nagata, T
    Chida, K
    Takahashi, T
    Takusa, Y
    Ohi, T
    Nishimiya, J
    Sunohara, N
    Ciafaloni, E
    Kawai, M
    Aoki, M
    Nonaka, I
    NEUROLOGY, 2002, 59 (11) : 1689 - 1693
  • [14] Identification of novel pathways in hereditary inclusion body myopathy
    Mitrani-Rosenbaum, S
    Eisenberg, I
    Amsili, S
    Shefi, N
    Itshaki, Z
    Shlomai, Z
    Levitski, R
    Ben-Bassat, H
    GLYCOBIOLOGY, 2005, 15 (11) : 1248 - 1249
  • [15] GNE Gene Replacement in Hereditary Inclusion Body Myopathy
    Maples, Phillip B.
    Darvish, Daniel
    Nemunaitis, Gregory
    Chang, Esther
    Ogden, Julie
    Nemunaitis, John
    MOLECULAR THERAPY, 2006, 13 : S215 - S216
  • [16] Muscle imaging in hereditary inclusion-body myopathy
    Tasca, G.
    Broccolini, A.
    Rodolico, C.
    Gidaro, T.
    Morosetti, R.
    Monforte, M.
    Barca, E.
    Ricci, E.
    Mirabella, M.
    NEUROMUSCULAR DISORDERS, 2011, 21 (9-10) : 679 - 679
  • [17] Analysis of the muscular transcriptome in hereditary inclusion body myopathy
    Eisenberg, I
    Shefi, N
    Itshaki, Z
    Kho, A
    Kang, P
    Argov, Z
    Sadeh, M
    Dabby, R
    Kunkel, L
    Friedman, N
    Mitrani-Rosenbaum, S
    NEUROMUSCULAR DISORDERS, 2005, 15 (9-10) : 695 - 696
  • [18] Is hereditary inclusion body myopathy a ''familial prion disease''?
    Cervenakova, L
    Sivakumar, K
    Nagle, J
    Dalakas, MC
    Goldfarb, LG
    ANNALS OF NEUROLOGY, 1996, 40 (01) : 128 - 128
  • [19] Hereditary Inclusion Body Myopathy (HIBM2)
    Jay, Chris M.
    Levonyak, Nick
    Nemunaitis, Gregory
    Maples, Phillip B.
    Nemunaitis, John
    GENE REGULATION AND SYSTEMS BIOLOGY, 2009, 3 : 181 - 190
  • [20] Novel clues in the pathophysiology of Hereditary Inclusion Body Myopathy
    Eisenberg, Iris
    Shefi, Noa
    Itshaki, Zohar
    Dabby, Ron
    Koopman, W. J. H.
    Sadeh, Menachem
    Mitrani-Rosenbaum, Stella
    NEUROMUSCULAR DISORDERS, 2006, 16 : S114 - S114