-
1
-
-
0022484795
-
Human myotube differentiation in vitro in different culture conditions
-
Delaporte, C., Dautreaux, B., & Fardeau, M. Human myotube differentiation in vitro in different culture conditions. Biol. Cell. 57, 17-22 (1986).
-
(1986)
Biol. Cell.
, vol.57
, pp. 17-22
-
-
Delaporte, C.1
Dautreaux, B.2
Fardeau, M.3
-
2
-
-
0023424999
-
Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: Importance of dorsal root ganglia for achieving successful functional innervation
-
Kobayashi, T., Askanas, V., & Engel, W.K. Human muscle cultured in monolayer and cocultured with fetal rat spinal cord: importance of dorsal root ganglia for achieving successful functional innervation. J. Neurosci. 7, 3131-3141 (1987).
-
(1987)
J. Neurosci.
, vol.7
, pp. 3131-3141
-
-
Kobayashi, T.1
Askanas, V.2
Engel, W.K.3
-
3
-
-
0028947081
-
Constitutive muscular abnormalities in culture in spinal muscular atrophy
-
Braun, S., Croizat, B., Lagrange, M.C., Warter, J.M., & Poindron, P. Constitutive muscular abnormalities in culture in spinal muscular atrophy. Lancet. 345, 694-695 (1995).
-
(1995)
Lancet.
, vol.345
, pp. 694-695
-
-
Braun, S.1
Croizat, B.2
Lagrange, M.C.3
Warter, J.M.4
Poindron, P.5
-
4
-
-
0016435481
-
A new program for investigating adult human skeletal muscle grown aneurally in tissue culture
-
Askanas, V. & Engel, W.K. A new program for investigating adult human skeletal muscle grown aneurally in tissue culture. Neurology. 25, 58-67 (1975).
-
(1975)
Neurology.
, vol.25
, pp. 58-67
-
-
Askanas, V.1
Engel, W.K.2
-
5
-
-
0034714497
-
Cell types required to efficiently innervate human muscle cells in vitro
-
doi:10.1006/excr.2000.4968
-
Guettier-Sigrist, S., Coupin, G., Warter, J.M., & Poindron, P. Cell types required to efficiently innervate human muscle cells in vitro. Exp. Cell Res. 259, 204-212, doi:10.1006/excr.2000.4968 (2000).
-
(2000)
Exp. Cell Res.
, vol.259
, pp. 204-212
-
-
Guettier-Sigrist, S.1
Coupin, G.2
Warter, J.M.3
Poindron, P.4
-
6
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre, S., et al. Identification and characterization of a spinal muscular atrophy-determining gene. Cell. 80, 155-165 (1995).
-
(1995)
Cell.
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
-
7
-
-
0030931720
-
Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos
-
Schrank, B., et al. Inactivation of the survival motor neuron gene, a candidate gene for human spinal muscular atrophy, leads to massive cell death in early mouse embryos. Proc. Natl. Acad. Sci. U.S.A. 94, 9920-9925 (1997).
-
(1997)
Proc. Natl. Acad. Sci. U.S.A.
, vol.94
, pp. 9920-9925
-
-
Schrank, B.1
-
8
-
-
0033987669
-
A mouse model for spinal muscular atrophy
-
doi:10.1038/71709
-
Hsieh-Li, H.M., et al. A mouse model for spinal muscular atrophy. Nat. Genet. 24, 66-70, doi:10.1038/71709 (2000).
-
(2000)
Nat. Genet.
, vol.24
, pp. 66-70
-
-
Hsieh-Li, H.M.1
-
9
-
-
0034639645
-
The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy
-
Monani, U.R., et al. The human centromeric survival motor neuron gene (SMN2) rescues embryonic lethality in Smn(-/-) mice and results in a mouse with spinal muscular atrophy. Hum. Mol. Genet. 9, 333-339 (2000).
-
(2000)
Hum. Mol. Genet.
, vol.9
, pp. 333-339
-
-
Monani, U.R.1
-
10
-
-
79959658484
-
The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy
-
doi:10.1242/dmm.007245
-
Sleigh, J.N., Gillingwater, T.H., & Talbot, K. The contribution of mouse models to understanding the pathogenesis of spinal muscular atrophy. Dis. Model. Mech. 4, 457-467, doi:10.1242/dmm.007245 (2011).
-
(2011)
Dis. Model. Mech.
, vol.4
, pp. 457-467
-
-
Sleigh, J.N.1
Gillingwater, T.H.2
Talbot, K.3
-
11
-
-
0036591684
-
Muscular dystrophies involving the dystrophin-glycoprotein complex: An overview of current mouse models
-
Durbeej, M. & Campbell, K.P. Muscular dystrophies involving the dystrophin-glycoprotein complex: an overview of current mouse models. Curr. Opin. Genet. Dev. 12, 349-361 (2002).
-
(2002)
Curr. Opin. Genet. Dev.
, vol.12
, pp. 349-361
-
-
Durbeej, M.1
Campbell, K.P.2
-
12
-
-
49649095887
-
Neuroscience: Standard model
-
doi:10.1038/454682a
-
Schnabel, J. Neuroscience: Standard model. Nature. 454, 682-685, doi:10.1038/454682a (2008).
-
(2008)
Nature.
, vol.454
, pp. 682-685
-
-
Schnabel, J.1
-
13
-
-
33947323759
-
Lost in translation: Treatment trials in the SOD1 mouse and in human ALS
-
doi:10.1016/j.nbd.2006.12.015
-
Benatar, M. Lost in translation: treatment trials in the SOD1 mouse and in human ALS. Neurobiol. Dis. 26, 1-13, doi:10.1016/j.nbd.2006.12.015 (2007).
-
(2007)
Neurobiol. Dis.
, vol.26
, pp. 1-13
-
-
Benatar, M.1
-
14
-
-
0034804933
-
Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system
-
Dorchies, O.M., et al. Normal innervation and differentiation of X-linked myotubular myopathy muscle cells in a nerve-muscle coculture system. Neuromuscul. Disord. 11, 736-746 (2001).
-
(2001)
Neuromuscul. Disord.
, vol.11
, pp. 736-746
-
-
Dorchies, O.M.1
-
15
-
-
0032487428
-
Impaired innervation of cultured human muscle overexpressing betaAPP experimentally and genetically: Relevance to inclusion-body myopathies
-
McFerrin, J., Engel, W.K., & Askanas, V. Impaired innervation of cultured human muscle overexpressing betaAPP experimentally and genetically: relevance to inclusion-body myopathies. Neuroreport. 9, 3201-3205 (1998).
-
(1998)
Neuroreport.
, vol.9
, pp. 3201-3205
-
-
McFerrin, J.1
Engel, W.K.2
Askanas, V.3
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