-
1
-
-
4944242332
-
Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients
-
Arnold, A. S., Gueye, M., Guettier-Sigrist, S., Courdier-Fruh, I., Coupin, G., Poindron, P., et al. (2004). Reduced expression of nicotinic AChRs in myotubes from spinal muscular atrophy I patients. Lab. Invest. 84, 1271–1278. doi: 10.1038/labinvest.3700163.
-
(2004)
Lab. Invest.
, vol.84
, pp. 1271-1278
-
-
Arnold, A.S.1
Gueye, M.2
Guettier-Sigrist, S.3
Courdier-Fruh, I.4
Coupin, G.5
Poindron, P.6
-
2
-
-
0001978682
-
Overwork weakness in partially denervated skeletal muscle
-
Bennett, R. L., and Knowlton, G. C. (1958). Overwork weakness in partially denervated skeletal muscle. Clin. Orthop. 12, 22–29.
-
(1958)
Clin. Orthop
, vol.12
, pp. 22-29
-
-
Bennett, R.L.1
Knowlton, G.C.2
-
3
-
-
84923603007
-
Mechanisms controlling neuromuscular junction stability
-
Bloch-Gallego, E. (2015). Mechanisms controlling neuromuscular junction stability. Cell. Mol. Life Sci. 72, 1029–1043. doi: 10.1007/s00018-014-1768-z.
-
(2015)
Cell. Mol. Life Sci
, vol.72
, pp. 1029-1043
-
-
Bloch-Gallego, E.1
-
4
-
-
84945941526
-
Systemic, postsymptomatic antisense oligonucleotide rescues motor unit maturation delay in a new mouse model for type II/III spinal muscular atrophy
-
Bogdanik, L. P., Osborne, M. A., Davis, C., Martin, W. P., Austin, A., Rigo, F., et al. (2015). Systemic, postsymptomatic antisense oligonucleotide rescues motor unit maturation delay in a new mouse model for type II/III spinal muscular atrophy. Proc. Natl. Acad. Sci. U S A 112, E5863–E5872. doi: 10.1073/pnas.1509758112.
-
(2015)
Proc. Natl. Acad. Sci. U S A
, vol.112
, pp. E5863-E5872
-
-
Bogdanik, L.P.1
Osborne, M.A.2
Davis, C.3
Martin, W.P.4
Austin, A.5
Rigo, F.6
-
5
-
-
84885622197
-
Spinal muscular atrophy: New findings for an old pathology
-
Bottai, D., and Adami, R. (2013). Spinal muscular atrophy: new findings for an old pathology. Brain Pathol. 23, 613–622. doi: 10.1111/bpa.12071.
-
(2013)
Brain Pathol
, vol.23
, pp. 613-622
-
-
Bottai, D.1
Adami, R.2
-
6
-
-
67651004474
-
SMN, profilin IIa and plastin 3: A link between the deregulation of actin dynamics and SMA pathogenesis
-
Bowerman, M., Anderson, C. L., Beauvais, A., Boyl, P. P., Witke, W., and Kothary, R. (2009). SMN, profilin IIa and plastin 3: a link between the deregulation of actin dynamics and SMA pathogenesis. Mol. Cell. Neurosci. 42, 66–74. doi: 10.1016/j.mcn.2009.05.009.
-
(2009)
Mol. Cell. Neurosci
, vol.42
, pp. 66-74
-
-
Bowerman, M.1
Erson, C.L.2
Beauvais, A.3
Boyl, P.P.4
Witke, W.5
Kothary, R.6
-
7
-
-
34648847089
-
Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity
-
Bowerman, M., Shafey, D., and Kothary, R. (2007). Smn depletion alters profilin II expression and leads to upregulation of the RhoA/ROCK pathway and defects in neuronal integrity. J. Mol. Neurosci. 32, 120–131. doi: 10.1007/s12031-007-0024-5.
-
(2007)
J. Mol. Neurosci
, vol.32
, pp. 120-131
-
-
Bowerman, M.1
Shafey, D.2
Kothary, R.3
-
8
-
-
84880960483
-
Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: Potential role in reinnervation ability and disease progression
-
Bruneteau, G., Simonet, T., Bauché, S., Mandjee, N., Malfatti, E., Girard, E., et al. (2013). Muscle histone deacetylase 4 upregulation in amyotrophic lateral sclerosis: potential role in reinnervation ability and disease progression. Brain 136, 2359–2368. doi: 10.1093/brain/awt164.
-
(2013)
Brain
, vol.136
, pp. 2359-2368
-
-
Bruneteau, G.1
Simonet, T.2
Bauché, S.3
Mandjee, N.4
Malfatti, E.5
Girard, E.6
-
9
-
-
3042841954
-
Activity-dependent synaptic competition at mammalian neuromuscular junctions
-
Buffelli, M., Busetto, G., Bidoia, C., Favero, M., and Cangiano, A. (2004). Activity-dependent synaptic competition at mammalian neuromuscular junctions. News Physiol. Sci. 19, 85–91. doi: 10.1152/nips.01464.2003.
-
(2004)
News Physiol. Sci
, vol.19
, pp. 85-91
-
-
Buffelli, M.1
Busetto, G.2
Bidoia, C.3
Favero, M.4
Cangiano, A.5
-
10
-
-
67651083390
-
Spinal muscular atrophy: Why do low levels of survival motor neuron protein make motor neurons sick?
-
Burghes, A. H., and Beattie, C. E. (2009). Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? Nat. Rev. Neurosci. 10, 597–609. doi: 10.1038/nrn2670.
-
(2009)
Nat. Rev. Neurosci
, vol.10
, pp. 597-609
-
-
Burghes, A.H.1
Beattie, C.E.2
-
11
-
-
45849084987
-
Temporal regulation of metamorphic processes in Drosophila by the let-7 and miR-125 heterochronic microRNAs
-
Caygill, E. E., and Johnston, L. A. (2008). Temporal regulation of metamorphic processes in Drosophila by the let-7 and miR-125 heterochronic microRNAs. Curr. Biol. 18, 943–950. doi: 10.1016/j.cub.2008.06.020.
-
(2008)
Curr. Biol
, vol.18
, pp. 943-950
-
-
Caygill, E.E.1
Johnston, L.A.2
-
12
-
-
71749091926
-
Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model
-
Cifuentes-Diaz, C., Nicole, S., Velasco, M. E., Borra-Cebrian, C., Panozzo, C., Frugier, T., et al. (2002). Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model. Hum. Mol. Genet. 11, 1439–1447. doi: 10.1093/hmg/11.12.1439.
-
(2002)
Hum. Mol. Genet
, vol.11
, pp. 1439-1447
-
-
Cifuentes-Diaz, C.1
Nicole, S.2
Velasco, M.E.3
Borra-Cebrian, C.4
Panozzo, C.5
Frugier, T.6
-
13
-
-
84959522446
-
Cross disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology
-
[Epub ahead of print]
-
Comley, L. H., Nijssen, J., Frost-Nylen, J., and Hedlund, E. (2015). Cross disease comparison of amyotrophic lateral sclerosis and spinal muscular atrophy reveals conservation of selective vulnerability but differential neuromuscular junction pathology. J. Comp. Neurol. doi: 10.1002/cne.23917 [Epub ahead of print].
-
(2015)
J. Comp. Neurol
-
-
Comley, L.H.1
Nijssen, J.2
Frost-Nylen, J.3
Hedlund, E.4
-
14
-
-
70349485394
-
Motoneuron transplantation rescues the phenotype of SMARD1 (Spinal muscular atrophy with respiratory distress type 1)
-
Corti, S., Nizzardo, M., Nardini, M., Donadoni, C., Salani, S., Del Bo, R., et al. (2009). Motoneuron transplantation rescues the phenotype of SMARD1 (spinal muscular atrophy with respiratory distress type 1). J. Neurosci. 29, 11761–11771. doi: 10.1523/JNEUROSCI.2734-09.2009.
-
(2009)
J. Neurosci
, vol.29
, pp. 11761-11771
-
-
Corti, S.1
Nizzardo, M.2
Nardini, M.3
Donadoni, C.4
Salani, S.5
Del Bo, R.6
-
15
-
-
80054712173
-
The spinal muscular atrophy mouse model, SMAΔ7, displays altered axonal transport without global neurofilament alterations
-
Dale, J. M., Shen, H., Barry, D. M., Garcia, V. B., Rose, F. F., Jr., Lorson, C. L., et al. (2011). The spinal muscular atrophy mouse model, SMAΔ7, displays altered axonal transport without global neurofilament alterations. Acta Neuropathol. 122, 331–341. doi: 10.1007/s00401-011-0848-5.
-
(2011)
Acta Neuropathol
, vol.122
, pp. 331-341
-
-
Dale, J.M.1
Shen, H.2
Barry, D.M.3
Garcia, V.B.4
Rose, F.F.5
Lorson, C.L.6
-
16
-
-
80055114781
-
Spinal muscular atrophy. Orphanet
-
D’Amico, A., Mercuri, E., Tiziano, F. D., and Bertini, E. (2011). Spinal muscular atrophy. Orphanet J. Rare Dis. 6:71. doi: 10.1186/1750-1172-6-71.
-
(2011)
J. Rare Dis
, vol.6
-
-
D’Amico, A.1
Mercuri, E.2
Tiziano, F.D.3
Bertini, E.4
-
17
-
-
15844417385
-
The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo
-
DeChiara, T. M., Bowen, D. C., Valenzuela, D. M., Simmons, M. V., Poueymirou, W. T., Thomas, S., et al. (1996). The receptor tyrosine kinase MuSK is required for neuromuscular junction formation in vivo. Cell 85, 501–512. doi: 10.1016/s0092-8674(00)81251-9.
-
(1996)
Cell
, vol.85
, pp. 501-512
-
-
Dechiara, T.M.1
Bowen, D.C.2
Valenzuela, D.M.3
Simmons, M.V.4
Poueymirou, W.T.5
Thomas, S.6
-
18
-
-
84891931388
-
Selective vulnerability of spinal and cortical motor neuron subpopulations in delta7 SMA mice
-
d’Errico, P., Boido, M., Piras, A., Valsecchi, V., De Amicis, E., Locatelli, D., et al. (2013). Selective vulnerability of spinal and cortical motor neuron subpopulations in delta7 SMA mice. PLoS One 8:e82654. doi: 10.1371/journal.pone.0082654.
-
(2013)
Plos One
, vol.8
-
-
D’Errico, P.1
Boido, M.2
Piras, A.3
Valsecchi, V.4
De Amicis, E.5
Locatelli, D.6
-
19
-
-
84908395084
-
Presynaptic localization of SMN and hnRNP R in axon terminals of embryonic and postnatal mouse motoneurons
-
Dombert, B., Sivadasan, R., Simon, C. M., Jablonka, S., and Sendtner, M. (2014). Presynaptic localization of SMN and hnRNP R in axon terminals of embryonic and postnatal mouse motoneurons. PLoS One 9:e110846. doi: 10.1371/journal.pone.0110846.
-
(2014)
Plos One
, vol.9
-
-
Dombert, B.1
Sivadasan, R.2
Simon, C.M.3
Jablonka, S.4
Sendtner, M.5
-
20
-
-
84862145991
-
Spinal muscular atrophy: The role of SMN in axonal mRNA regulation
-
Fallini, C., Bassell, G. J., and Rossoll, W. (2012). Spinal muscular atrophy: the role of SMN in axonal mRNA regulation. Brain Res. 1462, 81–92. doi: 10.1016/j.brainres.2012.01.044.
-
(2012)
Brain Res
, vol.1462
, pp. 81-92
-
-
Fallini, C.1
Bassell, G.J.2
Rossoll, W.3
-
21
-
-
0036154959
-
Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: Fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy
-
Feldkötter, M., Schwarzer, V., Wirth, R., Wienker, T. F., and Wirth, B. (2002). Quantitative analyses of SMN1 and SMN2 based on real-time lightCycler PCR: fast and highly reliable carrier testing and prediction of severity of spinal muscular atrophy. Am. J. Hum. Genet. 70, 358–368. doi: 10.1086/338627.
-
(2002)
Am. J. Hum. Genet
, vol.70
, pp. 358-368
-
-
Feldkötter, M.1
Schwarzer, V.2
Wirth, R.3
Wienker, T.F.4
Wirth, B.5
-
22
-
-
65949090754
-
Transcriptional response of the neuromuscular system to exercise training and potential implications for ALS
-
Ferraiuolo, L., De Bono, J. P., Heath, P. R., Holden, H., Kasher, P., Channon, K. M., et al. (2009). Transcriptional response of the neuromuscular system to exercise training and potential implications for ALS. J. Neurochem. 109, 1714–1724. doi: 10.1111/j.1471-4159.2009.06080.x.
-
(2009)
J. Neurochem
, vol.109
, pp. 1714-1724
-
-
Ferraiuolo, L.1
De Bono, J.P.2
Heath, P.R.3
Holden, H.4
Kasher, P.5
Channon, K.M.6
-
23
-
-
0029893117
-
Defective neuromuscular synaptogenesis in agrin-deficient mutant mice
-
Gautam, M., Noakes, P. G., Moscoso, L., Rupp, F., Scheller, R. H., Merlie, J. P., et al. (1996). Defective neuromuscular synaptogenesis in agrin-deficient mutant mice. Cell 85, 525–535. doi: 10.1016/s0092-8674(00)81253-2.
-
(1996)
Cell
, vol.85
, pp. 525-535
-
-
Gautam, M.1
Noakes, P.G.2
Moscoso, L.3
Rupp, F.4
Scheller, R.H.5
Merlie, J.P.6
-
24
-
-
23844454498
-
Regular exercise prolongs survival in a type 2 spinal muscular atrophy model mouse
-
Grondard, C., Biondi, O., Armand, A. S., Lécolle, S., Della Gaspera, B., Pariset, C., et al. (2005). Regular exercise prolongs survival in a type 2 spinal muscular atrophy model mouse. J. Neurosci. 25, 7615–7622. doi: 10.1523/jneurosci.1245-05.2005.
-
(2005)
J. Neurosci
, vol.25
, pp. 7615-7622
-
-
Grondard, C.1
Biondi, O.2
Armand, A.S.3
Lécolle, S.4
Della Gaspera, B.5
Pariset, C.6
-
25
-
-
0030953519
-
Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors. Nat
-
Haase, G., Kennel, P., Pettmann, B., Vigne, E., Akli, S., Revah, F., et al. (1997). Gene therapy of murine motor neuron disease using adenoviral vectors for neurotrophic factors. Nat. Med. 3, 429–436. doi: 10.1038/nm0497-429.
-
(1997)
Med
, vol.3
, pp. 429-436
-
-
Haase, G.1
Kennel, P.2
Pettmann, B.3
Vigne, E.4
Akli, S.5
Revah, F.6
-
26
-
-
77955599311
-
MiRNA malfunction causes spinal motor neuron disease
-
Haramati, S., Chapnik, E., Sztainberg, Y., Eilam, R., Zwang, R., Gershoni, N., et al. (2010). miRNA malfunction causes spinal motor neuron disease. Proc. Natl. Acad. Sci. U S A 107, 13111–13116. doi: 10.1073/pnas.1006151107.
-
(2010)
Proc. Natl. Acad. Sci. U S A
, vol.107
, pp. 13111-13116
-
-
Haramati, S.1
Chapnik, E.2
Sztainberg, Y.3
Eilam, R.4
Zwang, R.5
Gershoni, N.6
-
27
-
-
84920266970
-
Spectrum of neuropathophysiology in spinal muscular atrophy type I
-
Harding, B. N., Kariya, S., Monani, U. R., Chung, W. K., Benton, M., Yum, S. W., et al. (2015). Spectrum of neuropathophysiology in spinal muscular atrophy type I. J. Neuropathol. Exp. Neurol. 74, 15–24. doi: 10.1097/NEN.0000000000000144.
-
(2015)
J. Neuropathol. Exp. Neurol
, vol.74
, pp. 15-24
-
-
Harding, B.N.1
Kariya, S.2
Monani, U.R.3
Chung, W.K.4
Benton, M.5
Yum, S.W.6
-
28
-
-
84895542098
-
Injection of a soluble fragment of neural agrin (NT-1654) considerably improves the muscle pathology caused by the disassembly of the neuromuscular junction
-
Hettwer, S., Lin, S., Kucsera, S., Haubitz, M., Oliveri, F., Fariello, R. G., et al. (2014). Injection of a soluble fragment of neural agrin (NT-1654) considerably improves the muscle pathology caused by the disassembly of the neuromuscular junction. PLoS One 9:e88739. doi: 10.1371/journal.pone.0088739.
-
(2014)
Plos One
, vol.9
-
-
Hettwer, S.1
Lin, S.2
Kucsera, S.3
Haubitz, M.4
Oliveri, F.5
Fariello, R.G.6
-
29
-
-
85027941650
-
Adult rat mesenchymal stem cells delay denervated muscle atrophy
-
Jiang, J., Yao, P., Gu, Y., Xu, L., Xu, J., and Tan, H. (2012). Adult rat mesenchymal stem cells delay denervated muscle atrophy. Cell. Mol. Neurobiol. 32, 1287–1298. doi: 10.1007/s10571-012-9853-z.
-
(2012)
Cell. Mol. Neurobiol
, vol.32
, pp. 1287-1298
-
-
Jiang, J.1
Yao, P.2
Gu, Y.3
Xu, L.4
Xu, J.5
Tan, H.6
-
30
-
-
84893819754
-
Requirement of enhanced survival motoneuron protein imposed during neuromuscular junction maturation
-
Kariya, S., Obis, T., Garone, C., Akay, T., Sera, F., Iwata, S., et al. (2014). Requirement of enhanced survival motoneuron protein imposed during neuromuscular junction maturation. J. Clin. Invest. 124, 785–800. doi: 10.1172/JCI72017.
-
(2014)
J. Clin. Invest
, vol.124
, pp. 785-800
-
-
Kariya, S.1
Obis, T.2
Garone, C.3
Akay, T.4
Sera, F.5
Iwata, S.6
-
31
-
-
48249145306
-
Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy
-
Kariya, S., Park, G. H., Maeno-Hikichi, Y., Leykekhman, O., Lutz, C., Arkovitz, M. S., et al. (2008). Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy. Hum. Mol. Genet. 17, 2552–2569. doi: 10.1093/hmg/ddn156.
-
(2008)
Hum. Mol. Genet
, vol.17
, pp. 2552-2569
-
-
Kariya, S.1
Park, G.H.2
Maeno-Hikichi, Y.3
Leykekhman, O.4
Lutz, C.5
Arkovitz, M.S.6
-
32
-
-
84903778434
-
A short antisense oligonucleotide ameliorates symptoms of severe mouse models of spinal muscular atrophy
-
Keil, J. M., Seo, J., Howell, M. D., Hsu, W. H., Singh, R. N., and DiDonato, C. J. (2014). A short antisense oligonucleotide ameliorates symptoms of severe mouse models of spinal muscular atrophy. Mol. Ther. Nucleic Acids 3:e174. doi: 10.1038/mtna.2014.23.
-
(2014)
Mol. Ther. Nucleic Acids
, vol.3
-
-
Keil, J.M.1
Seo, J.2
Howell, M.D.3
Hsu, W.H.4
Singh, R.N.5
Didonato, C.J.6
-
33
-
-
55049092996
-
Lrp4 is a receptor for agrin and forms a complex with MuSK
-
Kim, N., Stiegler, A. L., Cameron, T. O., Hallock, P. T., Gomez, A. M., Huang, J. H., et al. (2008). Lrp4 is a receptor for agrin and forms a complex with MuSK. Cell 135, 334–342. doi: 10.1016/j.cell.2008.10.002.
-
(2008)
Cell
, vol.135
, pp. 334-342
-
-
Kim, N.1
Stiegler, A.L.2
Cameron, T.O.3
Hallock, P.T.4
Gomez, A.M.5
Huang, J.H.6
-
34
-
-
58849103600
-
Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice
-
Kong, L., Wang, X., Choe, D. W., Polley, M., Burnett, B. G., Bosch-Marcé, M., et al. (2009). Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice. J. Neurosci. 29, 842–851. doi: 10.1523/JNEUROSCI.4434-08.2009.
-
(2009)
J. Neurosci
, vol.29
, pp. 842-851
-
-
Kong, L.1
Wang, X.2
Choe, D.W.3
Polley, M.4
Burnett, B.G.5
Bosch-Marcé, M.6
-
35
-
-
84862488270
-
Axonopathy is associated with complex axonal transport defects in a model of multiple sclerosis
-
Kreutzer, M., Seehusen, F., Kreutzer, R., Pringproa, K., Kummerfeld, M., Claus, P., et al. (2012). Axonopathy is associated with complex axonal transport defects in a model of multiple sclerosis. Brain Pathol. 22, 454–471. doi: 10.1111/j.1750-3639.2011.00541.x.
-
(2012)
Brain Pathol
, vol.22
, pp. 454-471
-
-
Kreutzer, M.1
Seehusen, F.2
Kreutzer, R.3
Pringproa, K.4
Kummerfeld, M.5
Claus, P.6
-
36
-
-
0029125140
-
Local neurotrophic repression of gene transcripts encoding fetal AChRs at rat neuromuscular synapses
-
Kues, W. A., Brenner, H. R., Sakmann, B., and Witzemann, V. (1995). Local neurotrophic repression of gene transcripts encoding fetal AChRs at rat neuromuscular synapses. J. Cell Biol. 130, 949–957. doi: 10.1083/jcb.130.4.949.
-
(1995)
J. Cell Biol
, vol.130
, pp. 949-957
-
-
Kues, W.A.1
Brenner, H.R.2
Sakmann, B.3
Witzemann, V.4
-
37
-
-
84893203703
-
The role of miRNA in motor neuron disease. Front. Cell
-
Kye, M. J., and Gonçalves Ido, C. (2014). The role of miRNA in motor neuron disease. Front. Cell. Neurosci. 8:15. doi: 10.3389/fncel.2014.00015.
-
(2014)
Neurosci
, vol.8
-
-
Kye, M.J.1
Gonçalves Ido, C.2
-
38
-
-
84866934033
-
Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy
-
Lee, A. J., Awano, T., Park, G. H., and Monani, U. R. (2012). Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy. PLoS One 7:e46353. doi: 10.1371/journal.pone.0046353.
-
(2012)
Plos One
, vol.7
-
-
Lee, A.J.1
Awano, T.2
Park, G.H.3
Monani, U.R.4
-
39
-
-
79960563254
-
Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons
-
Lee, Y. I., Mikesh, M., Smith, I., Rimer, M., and Thompson, W. (2011). Muscles in a mouse model of spinal muscular atrophy show profound defects in neuromuscular development even in the absence of failure in neuromuscular transmission or loss of motor neurons. Dev. Biol. 356, 432–444. doi: 10.1016/j.ydbio.2011.05.667.
-
(2011)
Dev. Biol
, vol.356
, pp. 432-444
-
-
Lee, Y.I.1
Mikesh, M.2
Smith, I.3
Rimer, M.4
Thompson, W.5
-
40
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre, S., Bürglen, L., Reboullet, S., Clermont, O., Burlet, P., Viollet, L., et al. (1995). Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80, 155–165. doi: 10.1016/0092-8674(95)90460-3.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Bürglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
-
41
-
-
84904464793
-
SMN control of RNP assembly: From post-transcriptional gene regulation to motor neuron disease
-
Li, D. K., Tisdale, S., Lotti, F., and Pellizzoni, L. (2014). SMN control of RNP assembly: from post-transcriptional gene regulation to motor neuron disease. Semin. Cell Dev. Biol. 32, 22–29. doi: 10.1016/j.semcdb.2014.04.026.
-
(2014)
Semin. Cell Dev. Biol
, vol.32
, pp. 22-29
-
-
Li, D.K.1
Tisdale, S.2
Lotti, F.3
Pellizzoni, L.4
-
42
-
-
83455213467
-
Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy
-
Ling, K. K., Gibbs, R. M., Feng, Z., and Ko, C. P. (2012). Severe neuromuscular denervation of clinically relevant muscles in a mouse model of spinal muscular atrophy. Hum. Mol. Genet. 21, 185–195. doi: 10.1093/hmg/ddr453.
-
(2012)
Hum. Mol. Genet
, vol.21
, pp. 185-195
-
-
Ling, K.K.1
Gibbs, R.M.2
Feng, Z.3
Ko, C.P.4
-
43
-
-
78650946814
-
Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy
-
Liu, H., Beauvais, A., Baker, A. N., Tsilfidis, C., and Kothary, R. (2011). Smn deficiency causes neuritogenesis and neurogenesis defects in the retinal neurons of a mouse model of spinal muscular atrophy. Dev. Neurobiol. 2011, 153–169. doi: 10.1002/dneu.20840.
-
(2011)
Dev. Neurobiol
, vol.2011
, pp. 153-169
-
-
Liu, H.1
Beauvais, A.2
Baker, A.N.3
Tsilfidis, C.4
Kothary, R.5
-
44
-
-
84861807017
-
MicroRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice
-
Liu, N., Williams, A. H., Maxeiner, J. M., Bezprozvannaya, S., Shelton, J. M., Richardson, J. A., et al. (2012). microRNA-206 promotes skeletal muscle regeneration and delays progression of Duchenne muscular dystrophy in mice. J. Clin. Invest. 122, 2054–2065. doi: 10.1172/JCI62656.
-
(2012)
J. Clin. Invest
, vol.122
, pp. 2054-2065
-
-
Liu, N.1
Williams, A.H.2
Maxeiner, J.M.3
Bezprozvannaya, S.4
Shelton, J.M.5
Richardson, J.A.6
-
45
-
-
0033033434
-
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
-
Lorson, C. L., Hahnen, E., Androphy, E. J., and Wirth, B. (1999). A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy. Proc. Natl. Acad. Sci. U S A 96, 6307–6311. doi: 10.1073/pnas.96.11.6307.
-
(1999)
Proc. Natl. Acad. Sci. U S A
, vol.96
, pp. 6307-6311
-
-
Lorson, C.L.1
Hahnen, E.2
Rophy, E.J.3
Wirth, B.4
-
46
-
-
84938852273
-
A perturbed MicroRNA expression pattern characterizes embryonic neural stem cells derived from a severe mouse model of Spinal Muscular Atrophy (SMA)
-
Luchetti, A., Ciafrè, S. A., Murdocca, M., Malgieri, A., Masotti, A., Sanchez, M., et al. (2015). A perturbed MicroRNA expression pattern characterizes embryonic neural stem cells derived from a severe mouse model of Spinal Muscular Atrophy (SMA). Int. J. Mol. Sci. 16, 18312–18327. doi: 10.3390/ijms160818312.
-
(2015)
Int. J. Mol. Sci
, vol.16
, pp. 18312-18327
-
-
Luchetti, A.1
Ciafrè, S.A.2
Murdocca, M.3
Malgieri, A.4
Masotti, A.5
Sanchez, M.6
-
47
-
-
33750075811
-
-
2nd Edn. Champaign, IL: Human Kinetics
-
Macintosh, B., Gardiner, P., and McComas, A. (2006). Skeletal Muscle: Form and Function, 2nd Edn. Champaign, IL: Human Kinetics.
-
(2006)
Skeletal Muscle: Form and Function
-
-
Macintosh, B.1
Gardiner, P.2
McComas, A.3
-
48
-
-
0034658289
-
From plaque to pretzel: Fold formation and acetylcholine receptor loss at the developing neuromuscular junction
-
Marques, M. J., Conchello, J. A., and Lichtman, J. W. (2000). From plaque to pretzel: fold formation and acetylcholine receptor loss at the developing neuromuscular junction. J. Neurosci. 20, 3663–3675.
-
(2000)
J. Neurosci
, vol.20
, pp. 3663-3675
-
-
Marques, M.J.1
Conchello, J.A.2
Lichtman, J.W.3
-
49
-
-
84862883258
-
Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy
-
Martinez, T. L., Kong, L., Wang, X., Osborne, M. A., Crowder, M. E., Van Meerbeke, J. P., et al. (2012). Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy. J. Neurosci. 32, 8703–8715. doi: 10.1523/JNEUROSCI.0204-12.2012.
-
(2012)
J. Neurosci
, vol.32
, pp. 8703-8715
-
-
Martinez, T.L.1
Kong, L.2
Wang, X.3
Osborne, M.A.4
Crowder, M.E.5
Van Meerbeke, J.P.6
-
50
-
-
70349389656
-
Stem cells in amyotrophic lateral sclerosis: State of the art
-
Mazzini, L., Vercelli, A., Ferrero, I., Mareschi, K., Boido, M., Servo, S., et al. (2009). Stem cells in amyotrophic lateral sclerosis: state of the art. Expert Opin. Biol. Ther. 9, 1245–1258. doi: 10.1517/14712590903186956.
-
(2009)
Expert Opin. Biol. Ther
, vol.9
, pp. 1245-1258
-
-
Mazzini, L.1
Vercelli, A.2
Ferrero, I.3
Mareschi, K.4
Boido, M.5
Servo, S.6
-
51
-
-
50849110114
-
Embryonic motor axon development in the severe SMA mouse
-
McGovern, V. L., Gavrilina, T. O., Beattie, C. E., and Burghes, A. H. (2008). Embryonic motor axon development in the severe SMA mouse. Hum. Mol. Genet. 17, 2900–2909. doi: 10.1093/hmg/ddn189.
-
(2008)
Hum. Mol. Genet
, vol.17
, pp. 2900-2909
-
-
McGovern, V.L.1
Gavrilina, T.O.2
Beattie, C.E.3
Burghes, A.H.4
-
52
-
-
0025553844
-
The agrin hypothesis. Cold Spring Harb. Symp
-
McMahan, U. J. (1990). The agrin hypothesis. Cold Spring Harb. Symp. Quant. Biol. 55, 407–418. doi: 10.1101/sqb.1990.055.01.041.
-
(1990)
Quant. Biol
, vol.55
, pp. 407-418
-
-
McMahan, U.J.1
-
53
-
-
0345332575
-
Maturation of the acetylcholine receptor in skeletal muscle: Regulation of the AChR gamma-to-epsilon switch
-
Missias, A. C., Chu, G. C., Klocke, B. J., Sanes, J. R., and Merlie, J. P. (1996). Maturation of the acetylcholine receptor in skeletal muscle: regulation of the AChR gamma-to-epsilon switch. Dev. Biol. 179, 223–238. doi: 10.1006/dbio.1996.0253.
-
(1996)
Dev. Biol
, vol.179
, pp. 223-238
-
-
Missias, A.C.1
Chu, G.C.2
Klocke, B.J.3
Sanes, J.R.4
Merlie, J.P.5
-
54
-
-
41149113045
-
Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy
-
Murray, L. M., Comley, L. H., Thomson, D., Parkinson, N., Talbot, K., and Gillingwater, T. H. (2008). Selective vulnerability of motor neurons and dissociation of pre- and post-synaptic pathology at the neuromuscular junction in mouse models of spinal muscular atrophy. Hum. Mol. Genet. 17, 949–962. doi: 10.1093/hmg/ddm367.
-
(2008)
Hum. Mol.Genet
, vol.17
, pp. 949-962
-
-
Murray, L.M.1
Comley, L.H.2
Thomson, D.3
Parkinson, N.4
Talbot, K.5
Gillingwater, T.H.6
-
55
-
-
84893970488
-
Role of exercise in maintaining the integrity of the neuromuscular junction
-
Nishimune, H., Stanford, J. A., and Mori, Y. (2014). Role of exercise in maintaining the integrity of the neuromuscular junction. Muscle Nerve 49, 315–324. doi: 10.1002/mus.24095.
-
(2014)
Muscle Nerve
, vol.49
, pp. 315-324
-
-
Nishimune, H.1
Stanford, J.A.2
Mori, Y.3
-
56
-
-
84884512903
-
Improvement of neuromuscular synaptic phenotypes without enhanced survival and motor function in severe spinal muscular atrophy mice selectively rescued in motor neurons
-
Paez-Colasante, X., Seaberg, B., Martinez, T. L., Kong, L., Sumner, C. J., and Rimer, M. (2013). Improvement of neuromuscular synaptic phenotypes without enhanced survival and motor function in severe spinal muscular atrophy mice selectively rescued in motor neurons. PLoS One 8:e75866. doi: 10.1371/journal.pone.0075866.
-
(2013)
Plos One
, vol.8
-
-
Paez-Colasante, X.1
Seaberg, B.2
Martinez, T.L.3
Kong, L.4
Sumner, C.J.5
Rimer, M.6
-
57
-
-
79952348568
-
Antisense oligonucleotides delivered to the mouse CNS ameliorate symptoms of severe spinal muscular atrophy
-
Passini, M. A., Bu, J., Richards, A. M., Kinnecom, C., Sardi, S. P., Stanek, L. M., et al. (2011). Antisense oligonucleotides delivered to the mouse CNS ameliorate symptoms of severe spinal muscular atrophy. Sci. Transl. Med. 3:72ra18. doi: 10.1126/scitranslmed.3001777.
-
(2011)
Sci. Transl. Med
, vol.3
-
-
Passini, M.A.1
Bu, J.2
Richards, A.M.3
Kinnecom, C.4
Sardi, S.P.5
Stanek, L.M.6
-
58
-
-
84877859235
-
Antisense oligonucleotides for the treatment of spinal muscular atrophy
-
Porensky, P. N., and Burghes, A. H. (2013). Antisense oligonucleotides for the treatment of spinal muscular atrophy. Hum. Gene Ther. 24, 489–498. doi: 10.1089/hum.2012.225.
-
(2013)
Gene Ther
, vol.24
, pp. 489-498
-
-
Porensky, P.N.1
Burghes, A.H.2
-
59
-
-
77954137213
-
Newborn and carrier screening for spinal muscular atrophy
-
Prior, T. W., Snyder, P. J., Rink, B. D., Pearl, D. K., Pyatt, R. E., Mihl, D. C., et al. (2010). Newborn and carrier screening for spinal muscular atrophy. Am. J. Med. Genet. A 152A, 1608–1616. doi: 10.1002/ajmg.a.33474.
-
(2010)
Am. J. Med. Genet. A
, vol.152
, pp. 1608-1616
-
-
Prior, T.W.1
Snyder, P.J.2
Rink, B.D.3
Pearl, D.K.4
Pyatt, R.E.5
Mihl, D.C.6
-
60
-
-
0026633248
-
Agrin released by motor neurons induces the aggregation of acetylcholine receptors at neuromuscular junctions
-
Reist, N. E., Werle, M. J., and McMahan, U. J. (1992). Agrin released by motor neurons induces the aggregation of acetylcholine receptors at neuromuscular junctions. Neuron 8, 865–868. doi: 10.1016/0896-6273(92)90200-w.
-
(1992)
Neuron
, vol.8
, pp. 865-868
-
-
Reist, N.E.1
Werle, M.J.2
McMahan, U.J.3
-
61
-
-
84902577636
-
Defining the therapeutic window in a severe animal model of spinal muscular atrophy.
-
Robbins, K. L., Glascock, J. J., Osman, E. Y., Miller, M. R., and Lorson, C. L. (2014). Defining the therapeutic window in a severe animal model of spinal muscular atrophy. Hum. Mol. Genet. 23, 4559–4568. doi: 10.1093/hmg/ddu169.
-
(2014)
Hum. Mol.Genet
, vol.23
, pp. 4559-4568
-
-
Robbins, K.L.1
Glascock, J.J.2
Osman, E.Y.3
Miller, M.R.4
Lorson, C.L.5
-
62
-
-
0026583243
-
The agrin gene codes for a family of basal lamina proteins that differ in function and distribution
-
Ruegg, M. A., Tsim, K. W., Horton, S. E., Kröger, S., Escher, G., Gensch, E. M., et al. (1992). The agrin gene codes for a family of basal lamina proteins that differ in function and distribution. Neuron 8, 691–699. doi: 10.1016/0896-6273(92)90090-z.
-
(1992)
Neuron
, vol.8
, pp. 691-699
-
-
Ruegg, M.A.1
Tsim, K.W.2
Horton, S.E.3
Kröger, S.4
Escher, G.5
Gensch, E.M.6
-
63
-
-
75749129049
-
Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice
-
Ruiz, R., Casañas, J. J., Torres-Benito, L., Cano, R., and Tabares, L. (2010). Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice. J. Neurosci. 30, 849–857. doi: 10.1523/JNEUROSCI.4496-09.2010.
-
(2010)
J. Neurosci
, vol.30
, pp. 849-857
-
-
Ruiz, R.1
Casañas, J.J.2
Torres-Benito, L.3
Cano, R.4
Tabares, L.5
-
64
-
-
0020369614
-
Postnatal maturation of nerve-muscle junctions in hindlimb muscles of the mouse
-
Slater, C. R. (1982). Postnatal maturation of nerve-muscle junctions in hindlimb muscles of the mouse. Dev. Biol. 94, 11–22. doi: 10.1016/0012-1606(82)90063-x.
-
(1982)
Dev. Biol
, vol.94
, pp. 11-22
-
-
Slater, C.R.1
-
65
-
-
84934780037
-
Mechanisms regulating neuromuscular junction development and function and causes of muscle wasting
-
Tintignac, L. A., Brenner, H. R., and Rüegg, M. A. (2015). Mechanisms regulating neuromuscular junction development and function and causes of muscle wasting. Physiol. Rev. 95, 809–852. doi: 10.1152/physrev.00033.2014.
-
(2015)
Physiol. Rev
, vol.95
, pp. 809-852
-
-
Tintignac, L.A.1
Brenner, H.R.2
Rüegg, M.A.3
-
66
-
-
83455225174
-
Synaptic defects in spinal muscular atrophy animal models
-
Torres-Benito, L., Ruiz, R., and Tabares, L. (2012). Synaptic defects in spinal muscular atrophy animal models. Dev. Neurobiol. 72, 126–133. doi: 10.1002/dneu.20912.
-
(2012)
Dev. Neurobiol
, vol.72
, pp. 126-133
-
-
Torres-Benito, L.1
Ruiz, R.2
Tabares, L.3
-
67
-
-
84862309444
-
Therapy development for spinal muscular atrophy in SMN independent targets
-
Tsai, L. K. (2012). Therapy development for spinal muscular atrophy in SMN independent targets. Neural Plast. 2012:456478. doi: 10.1155/2012/456478.
-
(2012)
Neural Plast
, vol.2012
-
-
Tsai, L.K.1
-
68
-
-
81955167497
-
IGF-1 delivery to CNS attenuates motor neuron cell death but does not improve motor function in type III SMA mice
-
Tsai, L. K., Chen, Y. C., Cheng, W. C., Ting, C. H., Dodge, J. C., Hwu, W. L., et al. (2012). IGF-1 delivery to CNS attenuates motor neuron cell death but does not improve motor function in type III SMA mice. Neurobiol. Dis. 45, 272–279. doi: 10.1016/j.nbd.2011.06.021.
-
(2012)
Neurobiol. Dis
, vol.45
, pp. 272-279
-
-
Tsai, L.K.1
Chen, Y.C.2
Cheng, W.C.3
Ting, C.H.4
Dodge, J.C.5
Hwu, W.L.6
-
69
-
-
54249110856
-
Multiple therapeutic effects of valproic acid in spinal muscular atrophy model mice
-
Tsai, L. K., Tsai, M. S., Ting, C. H., and Li, H. (2008). Multiple therapeutic effects of valproic acid in spinal muscular atrophy model mice. J. Mol. Med. 86, 1243–1254. doi: 10.1007/s00109-008-0388-1.
-
(2008)
J. Mol. Med
, vol.86
, pp. 1243-1254
-
-
Tsai, L.K.1
Tsai, M.S.2
Ting, C.H.3
Li, H.4
-
70
-
-
84899715456
-
The role of muscle microRNAs in repairing the neuromuscular junction
-
Valdez, G., Heyer, M. P., Feng, G., and Sanes, J. R. (2014). The role of muscle microRNAs in repairing the neuromuscular junction. PLoS One 24:e93140. doi: 10.1371/journal.pone.0093140.
-
(2014)
Plos One
, vol.24
-
-
Valdez, G.1
Heyer, M.P.2
Feng, G.3
Sanes, J.R.4
-
71
-
-
77957090460
-
Attenuation of age-related changes in mouse neuromuscular synapses by caloric restriction and exercise
-
Valdez, G., Tapia, J. C., Kang, H., Clemenson, G. D., Jr., Gage, F. H., Lichtman, J. W., et al. (2010). Attenuation of age-related changes in mouse neuromuscular synapses by caloric restriction and exercise. Proc. Natl. Acad. Sci. U S A 107, 14863–14868. doi: 10.1073/pnas.1002220107.
-
(2010)
Proc. Natl. Acad. Sci. U S A
, vol.107
, pp. 14863-14868
-
-
Valdez, G.1
Tapia, J.C.2
Kang, H.3
Clemenson, G.D.4
Gage, F.H.5
Lichtman, J.W.6
-
72
-
-
84990837005
-
Expression of muscle-specific MiRNA 206 in the progression of disease in a murine SMA model
-
Valsecchi, V., Boido, M., De Amicis, E., Piras, A., and Vercelli, A. (2015). Expression of muscle-specific MiRNA 206 in the progression of disease in a murine SMA model. PLoS One 10:e0128560. doi: 10.1371/journal.pone.0128560.
-
(2015)
Plos One
, vol.10
-
-
Valsecchi, V.1
Boido, M.2
De Amicis, E.3
Piras, A.4
Vercelli, A.5
-
73
-
-
41149117385
-
MicroRNAs flex their muscles
-
van Rooij, E., Liu, N., and Olson, E. N. (2008). MicroRNAs flex their muscles. Trends Genet. 24, 159–166. doi: 10.1016/j.tig.2008.01.007.
-
(2008)
Trends Genet
, vol.24
, pp. 159-166
-
-
Van Rooij, E.1
Liu, N.2
Olson, E.N.3
-
74
-
-
84928121510
-
Allogeneic mesenchymal stem cell therapy outcomes for three patients with spinal muscular atrophy type 1
-
Villanova, M., and Bach, J. R. (2015). Allogeneic mesenchymal stem cell therapy outcomes for three patients with spinal muscular atrophy type 1. Am. J. Phys. Med. Rehabil. 94, 410–415. doi: 10.1097/PHM.0000000000000309.
-
(2015)
Am. J. Phys. Med. Rehabil
, vol.94
, pp. 410-415
-
-
Villanova, M.1
Bach, J.R.2
-
75
-
-
41149130101
-
Evidence for muscle-dependent neuromuscular synaptic site determination in mammals
-
Vock, V. M., Ponomareva, O. N., and Rimer, M. (2008). Evidence for muscle-dependent neuromuscular synaptic site determination in mammals. J. Neurosci. 28, 3123–3130. doi: 10.1523/JNEUROSCI.5080-07.2008.
-
(2008)
J. Neurosci
, vol.28
, pp. 3123-3130
-
-
Vock, V.M.1
Ponomareva, O.N.2
Rimer, M.3
-
76
-
-
84871257650
-
Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3
-
Wadman, R. I., Vrancken, A. F., van den Berg, L. H., and van der Pol, W. L. (2012). Dysfunction of the neuromuscular junction in spinal muscular atrophy types 2 and 3. Neurology 79, 2050–2055. doi: 10.1212/WNL.0b013e3182749eca.
-
(2012)
Neurology
, vol.79
, pp. 2050-2055
-
-
Wadman, R.I.1
Vrancken, A.F.2
Van Den Berg, L.H.3
Van Der Pol, W.L.4
-
77
-
-
0037426977
-
In vivo time-lapse imaging of synaptic takeover associated with naturally occurring synapse elimination
-
Walsh, M. K., and Lichtman, J. W. (2003). In vivo time-lapse imaging of synaptic takeover associated with naturally occurring synapse elimination. Neuron 37, 67–73. doi: 10.1016/s0896-6273(02)01142-x.
-
(2003)
Neuron
, vol.37
, pp. 67-73
-
-
Walsh, M.K.1
Lichtman, J.W.2
-
78
-
-
84899427872
-
Survival of motor neuron protein downregulates miR-9 expression in patients with spinal muscular atrophy. Kaohsiung
-
Wang, L. T., Chiou, S. S., Liao, Y. M., Jong, Y. J., and Hsu, S. H. (2014). Survival of motor neuron protein downregulates miR-9 expression in patients with spinal muscular atrophy. Kaohsiung J. Med. Sci. 30, 229–234. doi: 10.1016/j.kjms.2013.12.007.
-
(2014)
J. Med. Sci
, vol.30
, pp. 229-234
-
-
Wang, L.T.1
Chiou, S.S.2
Liao, Y.M.3
Jong, Y.J.4
Hsu, S.H.5
-
79
-
-
0029020311
-
Neurotrophins promote maturation of developing neuromuscular synapses
-
Wang, T., Xie, K., and Lu, B. (1995). Neurotrophins promote maturation of developing neuromuscular synapses. J. Neurosci. 15, 4796–4805.
-
(1995)
J. Neurosci
, vol.15
, pp. 4796-4805
-
-
Wang, T.1
Xie, K.2
Lu, B.3
-
80
-
-
72149131804
-
MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice
-
Williams, A. H., Valdez, G., Moresi, V., Qi, X., McAnally, J., Elliott, J. L., et al. (2009). MicroRNA-206 delays ALS progression and promotes regeneration of neuromuscular synapses in mice. Science 326, 1549–1554. doi: 10.1126/science.1181046.
-
(2009)
Science
, vol.326
, pp. 1549-1554
-
-
Williams, A.H.1
Valdez, G.2
Moresi, V.3
Qi, X.4
McAnally, J.5
Elliott, J.L.6
-
81
-
-
33748935769
-
Development of the neuromuscular junction
-
Witzemann, V. (2006). Development of the neuromuscular junction. Cell Tissue Res. 326, 263–271. doi: 10.1007/s00441-006-0237-x.
-
(2006)
Cell Tissue Res
, vol.326
, pp. 263-271
-
-
Witzemann, V.1
-
82
-
-
77950462859
-
To build a synapse: Signaling pathways in neuromuscular junction assembly
-
Wu, H., Xiong, W. C., and Mei, L. (2010). To build a synapse: signaling pathways in neuromuscular junction assembly. Development 137, 1017–1033. doi: 10.1242/dev.038711.
-
(2010)
Development
, vol.137
, pp. 1017-1033
-
-
Wu, H.1
Xiong, W.C.2
Mei, L.3
-
83
-
-
77958473921
-
Stem cell-derived neurotrophic support for the neuromuscular junction in spinal muscular atrophy
-
Wyatt, T. J., and Keirstead, H. S. (2010). Stem cell-derived neurotrophic support for the neuromuscular junction in spinal muscular atrophy. Expert Opin. Biol. Ther. 10, 1587–1594. doi: 10.1517/14712598.2010.529895.
-
(2010)
Expert Opin. Biol. Ther
, vol.10
, pp. 1587-1594
-
-
Wyatt, T.J.1
Keirstead, H.S.2
-
84
-
-
84933677989
-
Modeling the early phenotype at the neuromuscular junction of spinal muscular atrophy using patient-derived iPSCs
-
Yoshida, M., Kitaoka, S., Egawa, N., Yamane, M., Ikeda, R., Tsukita, K., et al. (2015). Modeling the early phenotype at the neuromuscular junction of spinal muscular atrophy using patient-derived iPSCs. Stem Cell Reports 4, 561–568. doi: 10.1016/j.stemcr.2015.02.010.
-
(2015)
Stem Cell Reports
, vol.4
, pp. 561-568
-
-
Yoshida, M.1
Kitaoka, S.2
Egawa, N.3
Yamane, M.4
Ikeda, R.5
Tsukita, K.6
-
85
-
-
84888375636
-
Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy
-
Zhang, Z., Pinto, A. M., Wan, L., Wang, W., Berg, M. G., Oliva, I., et al. (2013). Dysregulation of synaptogenesis genes antecedes motor neuron pathology in spinal muscular atrophy. Proc. Natl. Acad. Sci. U S A 110, 19348–19353. doi: 10.1073/pnas.1319280110.
-
(2013)
Proc. Natl. Acad. Sci. U S A
, vol.110
, pp. 19348-19353
-
-
Zhang, Z.1
Pinto, A.M.2
Wan, L.3
Wang, W.4
Berg, M.G.5
Oliva, I.6
-
86
-
-
84939857513
-
Combination of agrin and laminin increase acetylcholine receptor clustering and enhance functional neuromuscular junction formation In vitro
-
[Epub ahead of print]
-
Zhang, B. G., Quigley, A. F., Bourke, J. L., Nowell, C. J., Myers, D. E., Choong, P. F., et al. (2015). Combination of agrin and laminin increase acetylcholine receptor clustering and enhance functional neuromuscular junction formation In vitro. Dev. Neurobiol. doi: 10.1002/dneu.22331 [Epub ahead of print].
-
(2015)
Dev. Neurobiol
-
-
Zhang, B.G.1
Quigley, A.F.2
Bourke, J.L.3
Nowell, C.J.4
Myers, D.E.5
Choong, P.F.6
-
87
-
-
84876562225
-
Skeletal muscle calpain acts through nitric oxide and neural miRNAs to regulate acetylcholine release in motor nerve terminals
-
Zhu, H., Bhattacharyya, B. J., Lin, H., and Gomez, C. M. (2013). Skeletal muscle calpain acts through nitric oxide and neural miRNAs to regulate acetylcholine release in motor nerve terminals. J. Neurosci. 33, 7308–7324. doi: 10.1523/JNEUROSCI.0224-13.2013.
-
(2013)
J. Neurosci
, vol.33
, pp. 7308-7324
-
-
Zhu, H.1
Bhattacharyya, B.J.2
Lin, H.3
Gomez, C.M.4
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