Results 151 to 160 of about 990 (176)

T.O.1 Sialic acid metabolites preclude the development of myopathic phenotype in the DMRV/hIBM mouse model

Neuromuscular Disorders, 2009
M.C. Malicdan, S. Noguchi, Y.K. Hayashi, I. Nonaka, I. Nishino   +4 more
semanticscholar   +2 more sources

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Nature Genetics, 2001
Hagit Hochner, Tsviya Olender, Mark Barash   +2 more
exaly   +2 more sources

P2.61 Metabolic changes in sialic acid synthesis pathway in DMRV/hIBM model mice with long-term sialic acid treatment

Neuromuscular Disorders, 2011
Satoru Noguchi, M. C. V. Malicdan, F. Funato, I. Nishino   +3 more
semanticscholar   +2 more sources

P4.46 Expression of human GNE through adeno-associated virus mediated therapy delays progression of myopathy in the DMRV/hIBM mouse model

Neuromuscular Disorders, 2011
M. C. V. Malicdan, T. Okada, Ilan Sela, Shin'ichi Takeda, F. Funato, I. Nonaka, Yuichi Hayashi, L. Yakovlev, Z. Argov, I. Nishino, S. Mitrani-Rosaenbaum, Satoru Noguchi   +11 more
semanticscholar   +2 more sources

G.P.13.09 Proteomic analysis of distal myopathy with rimmed vacuoles (DMRV) or hereditary inclusion body myopathy (hIBM)

Neuromuscular Disorders, 2007
M. Malicdan, S. Noguchi, G. Kawahara, Y. Hayashi, I. Nishino   +4 more
semanticscholar   +2 more sources

G.P.5.05 The evaluation of N-acetylmannosamine in model mouse towards the development of therapeutic strategy in DMRV/hIBM

Neuromuscular Disorders, 2009
S. Noguchi, M. Malicdan, Y. Hayashi, I. Nonaka, I. Nishino   +4 more
semanticscholar   +2 more sources

G.P.5.04 Ultrastructural evidence of amyloidogenesis: An upstream event to myofiber degeneration in a mouse model of DMRV/hIBM

Neuromuscular Disorders, 2009
Tomoharu Tokutomi, M. C. V. Malicdan, Satoru Noguchi, I. Nonaka, Yuichi Hayashi, I. Nishino   +5 more
semanticscholar   +2 more sources

P2.07 Dual observation of single myofibers provide clue on dynamics of protein accumulation in distal myopathy with rimmed vacuoles (DMRV)-hereditary inclusion body myopathy (hIBM) mouse model

Neuromuscular Disorders, 2010
S. Noguchi, M. Malicdan, I. Nonaka, I. Nishino   +3 more
semanticscholar   +2 more sources

G.P.17.05 Predictive role of NCAM in the identification of patients with HIBM due to GNE mutations with atypical clinical phenotype

Neuromuscular Disorders, 2007
A. Broccolini, C. Rodolico, T. Gidaro, R. Leo, Gabriella Silvestri, Roberta Morosetti, Carla Gliubizzi, C. Blasi, Lucia Morandi, Marina Mora, A. Toscano, Gianluca Vita, E. Ricci, P. A. Tonali, Massimiliano Mirabella   +14 more
semanticscholar   +2 more sources

G.P.5.14 Treatment of hyposialylation in human and murine DMRV/hIBM culture cells with various kinds of sialic acid derivatives and its precursors

Neuromuscular Disorders, 2008
S. Noguchi, M. Malicdan, I. Nishino
semanticscholar   +2 more sources