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Results: 1-10 |
Results: 10
Properly formed but improperly localized synaptic specializations in the absence of laminin alpha 4
Authors: Patton, BL Cunningham, JM Thyboll, J Kortesmaa, J Westerblad, H Edstrom, L Tryggvason, K Sanes, JR
Citation: Bl. Patton et al., Properly formed but improperly localized synaptic specializations in the absence of laminin alpha 4, NAT NEUROSC, 4(6), 2001, pp. 597-604
Huntington disease phenocopy is a familial prion disease
Authors: Moore, RC Xiang, FQ Monaghan, J Han, D Zhang, ZP Edstrom, L Anvret, M Prusiner, SB
Citation: Rc. Moore et al., Huntington disease phenocopy is a familial prion disease, AM J HU GEN, 69(6), 2001, pp. 1385-1388
Acute quadriplegia and loss of muscle myosin in patients treated with nondepolarizing neuromuscular blocking agents and corticosteroids: Mechanisms at the cellular and molecular levels
Authors: Larsson, L Li, XP Edstrom, L Eriksson, LI Zackrisson, H Argentini, C Schiaffino, S
Citation: L. Larsson et al., Acute quadriplegia and loss of muscle myosin in patients treated with nondepolarizing neuromuscular blocking agents and corticosteroids: Mechanisms at the cellular and molecular levels, CRIT CARE M, 28(1), 2000, pp. 34-45
Independent regulation of the myotonic dystrophy 1 locus genes postnatallyand during adult skeletal muscle regenerator
Authors: Eriksson, M Ansved, T Edstrom, L Wells, DJ Watt, DJ Anvret, M Carey, N
Citation: M. Eriksson et al., Independent regulation of the myotonic dystrophy 1 locus genes postnatallyand during adult skeletal muscle regenerator, J BIOL CHEM, 275(26), 2000, pp. 19964-19969
Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels
Authors: Eriksson, N Ansved, T Edstrom, L Anvret, M Carey, N
Citation: N. Eriksson et al., Simultaneous analysis of expression of the three myotonic dystrophy locus genes in adult skeletal muscle samples: the CTG expansion correlates inversely with DMPK and 59 expression levels, but not DMAHP levels, HUM MOL GEN, 8(6), 1999, pp. 1053-1060
A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21
Authors: Xiang, FQ Nicolao, P Chapon, F Edstrom, L Anvret, M Zhang, ZP
Citation: Fq. Xiang et al., A second locus for autosomal dominant myopathy with proximal muscle weakness and early respiratory muscle involvement: a likely chromosomal locus on 2q21, NEUROMUSC D, 9(5), 1999, pp. 308-312
Levels of transforming growth factor alpha (TGF-alpha) in human cerebrospinal fluid
Authors: Van Setten, GB Edstrom, L Stibler, H Rasmussen, S Schultz, G
Citation: Gb. Van Setten et al., Levels of transforming growth factor alpha (TGF-alpha) in human cerebrospinal fluid, INT J DEV N, 17(2), 1999, pp. 131-134
Genetic linkage of Welander distal myopathy to chromosome 2p13
Authors: Ahlberg, G von Tell, D Borg, K Edstrom, L Anvret, M
Citation: G. Ahlberg et al., Genetic linkage of Welander distal myopathy to chromosome 2p13, ANN NEUROL, 46(3), 1999, pp. 399-404
Dystrophia Myotonica Clinical, pathophysiological and molecular aspects
Authors: Edstrom, L
Citation: L. Edstrom, Dystrophia Myotonica Clinical, pathophysiological and molecular aspects, SC J RE MED, 1999, pp. 47-52
Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q
Authors: Nicolao, P Xiang, FQ Gunnarsson, LG Giometto, B Edstrom, L Anvret, M Zhang, ZP
Citation: P. Nicolao et al., Autosomal dominant myopathy with proximal weakness and early respiratory muscle involvement maps to chromosome 2q, AM J HU GEN, 64(3), 1999, pp. 788-792
Risultati: 1-10 |