-
1
-
-
67651140516
-
Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy
-
Acsadi G, Lee I, Li X, Khaidakov M, Pecinova A, Parker GC, Huttemann M. 2009. Mitochondrial dysfunction in a neural cell model of spinal muscular atrophy. J Neurosci Res 87: 2748-2756.
-
(2009)
J Neurosci Res
, vol.87
, pp. 2748-2756
-
-
Acsadi, G.1
Lee, I.2
Li, X.3
Khaidakov, M.4
Pecinova, A.5
Parker, G.C.6
Huttemann, M.7
-
2
-
-
0038360854
-
Colocalization of synapsin and actin during synaptic vesicle recycling
-
Bloom O, Evergren E, Tomilin N, Kjaerulff O, Low P, Brodin L, Pieribone VA, et al. 2003. Colocalization of synapsin and actin during synaptic vesicle recycling. J Cell Biol 161: 737-747.
-
(2003)
J Cell Biol
, vol.161
, pp. 737-747
-
-
Bloom, O.1
Evergren, E.2
Tomilin, N.3
Kjaerulff, O.4
Low, P.5
Brodin, L.6
Pieribone, V.A.7
-
3
-
-
67651004474
-
SMN, profilin IIa and plastin 3: A link between the deregulation of actin dynamics and SMA pathogenesis
-
Bowerman M, Anderson CL, Beauvais A, Boyl PP, Witke W, 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.
-
(2009)
Mol Cell Neurosci
, vol.42
, pp. 66-74
-
-
Bowerman, M.1
Anderson, C.L.2
Beauvais, A.3
Boyl, P.P.4
Witke, W.5
Kothary, R.6
-
4
-
-
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, 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.
-
(2007)
J Mol Neurosci
, vol.32
, pp. 120-131
-
-
Bowerman, M.1
Shafey, D.2
Kothary, R.3
-
5
-
-
57649207934
-
Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan
-
Briese M, Esmaeili B, Fraboulet S, Burt EC, Christodoulou S, Towers PR, Davies KE, et al. 2009. Deletion of smn-1, the Caenorhabditis elegans ortholog of the spinal muscular atrophy gene, results in locomotor dysfunction and reduced lifespan. Hum Mol Genet 18: 97-104.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 97-104
-
-
Briese, M.1
Esmaeili, B.2
Fraboulet, S.3
Burt, E.C.4
Christodoulou, S.5
Towers, P.R.6
Davies, K.E.7
-
6
-
-
67651083390
-
Spinal muscular atrophy: Why do low levels of survival motor neuron protein make motor neurons sick
-
Burghes AH, Beattie CE. 2009. Spinal muscular atrophy: Why do low levels of survival motor neuron protein make motor neurons sick. Nature Rev 10: 597-609.
-
(2009)
Nature Rev
, vol.10
, pp. 597-609
-
-
Burghes, A.H.1
Beattie, C.E.2
-
7
-
-
33751100104
-
Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis
-
Carrel TL, McWhorter ML, Workman E, Zhang H, Wolstencroft EC, Lorson C, Bassell GJ, et al. 2006. Survival motor neuron function in motor axons is independent of functions required for small nuclear ribonucleoprotein biogenesis. J Neurosci 26: 11014-11022.
-
(2006)
J Neurosci
, vol.26
, pp. 11014-11022
-
-
Carrel, T.L.1
McWhorter, M.L.2
Workman, E.3
Zhang, H.4
Wolstencroft, E.C.5
Lorson, C.6
Bassell, G.J.7
-
8
-
-
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 ME, Borra-Cebrian C, Panozzo C, Frugier T, Millet G, et al. 2002. Neurofilament accumulation at the motor endplate and lack of axonal sprouting in a spinal muscular atrophy mouse model. Human Mol Genet 11: 1439-1447.
-
(2002)
Human 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
Millet, G.7
-
9
-
-
0030130574
-
The neurobiology of childhood spinal muscular atrophy
-
Crawford TO, Pardo CA. 1996. The neurobiology of childhood spinal muscular atrophy. Neurobiol Dis 3: 97-110.
-
(1996)
Neurobiol Dis
, vol.3
, pp. 97-110
-
-
Crawford, T.O.1
Pardo, C.A.2
-
10
-
-
0038039295
-
Neuromuscular defects in a Drosophila survival motor neuron gene mutant
-
Chan YB, Miguel-Aliaga I, Franks C, Thomas N, Trulzsch B, Sattelle DB, Davies KE, et al. 2003. Neuromuscular defects in a Drosophila survival motor neuron gene mutant. Hum Mol Genet 12: 1367-1376.
-
(2003)
Hum Mol Genet
, vol.12
, pp. 1367-1376
-
-
Chan, Y.B.1
Miguel-Aliaga, I.2
Franks, C.3
Thomas, N.4
Trulzsch, B.5
Sattelle, D.B.6
Davies, K.E.7
-
11
-
-
66049124365
-
The role of RNP biogenesis in spinal muscular atrophy
-
Chari A, Paknia E, Fischer U. 2009. The role of RNP biogenesis in spinal muscular atrophy. Curr Opin Cell Biol 21: 387-393.
-
(2009)
Curr Opin Cell Biol
, vol.21
, pp. 387-393
-
-
Chari, A.1
Paknia, E.2
Fischer, U.3
-
12
-
-
0141864656
-
RhoA/ROCK regulation of neuritogenesis via profilin IIa-mediated control of actin stability
-
Da Silva JS, Medina M, Zuliani C, Di Nardo A, Witke W, Dotti CG. 2003. RhoA/ROCK regulation of neuritogenesis via profilin IIa-mediated control of actin stability. J Cell Biol 162: 1267-1279.
-
(2003)
J Cell Biol
, vol.162
, pp. 1267-1279
-
-
Da Silva, J.S.1
Medina, M.2
Zuliani, C.3
Di Nardo, A.4
Witke, W.5
Dotti, C.G.6
-
14
-
-
0036647269
-
Survival motor neuron (SMN) protein: Role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development
-
Fan L, Simard LR. 2002. Survival motor neuron (SMN) protein: Role in neurite outgrowth and neuromuscular maturation during neuronal differentiation and development. Hum Mol Genet 11: 1605-1614.
-
(2002)
Hum Mol Genet
, vol.11
, pp. 1605-1614
-
-
Fan, L.1
Simard, L.R.2
-
15
-
-
0030928716
-
The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis
-
Fischer U, Liu Q, Dreyfuss G. 1997. The SMN-SIP1 complex has an essential role in spliceosomal snRNP biogenesis. Cell 90: 1023-1029.
-
(1997)
Cell
, vol.90
, pp. 1023-1029
-
-
Fischer, U.1
Liu, Q.2
Dreyfuss, G.3
-
16
-
-
0034676457
-
Functional genomic analysis of C. elegans chromosome I by systematic RNA interference
-
Fraser AG, Kamath RS, Zipperlen P, Martinez-Campos M, Sohrmann M, Ahringer J. 2000. Functional genomic analysis of C. elegans chromosome I by systematic RNA interference. Nature 408: 325-330.
-
(2000)
Nature
, vol.408
, pp. 325-330
-
-
Fraser, A.G.1
Kamath, R.S.2
Zipperlen, P.3
Martinez-Campos, M.4
Sohrmann, M.5
Ahringer, J.6
-
17
-
-
0028177313
-
An FCCP-sensitive Ca2+ store in bullfrog sympathetic neurons and its participation in stimulus-evoked changes in [Ca2+]i
-
Friel DD, Tsien RW. 1994. An FCCP-sensitive Ca2+ store in bullfrog sympathetic neurons and its participation in stimulus-evoked changes in [Ca2+]i. J Neurosci 14: 4007-4024.
-
(1994)
J Neurosci
, vol.14
, pp. 4007-4024
-
-
Friel, D.D.1
Tsien, R.W.2
-
18
-
-
41549119007
-
Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs
-
Gabanella F, Butchbach ME, Saieva L, Carissimi C, Burghes AH, Pellizzoni L. 2007. Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs. PLo S One 2: e921.
-
(2007)
PLo S One
, vol.2
-
-
Gabanella, F.1
Butchbach, M.E.2
Saieva, L.3
Carissimi, C.4
Burghes, A.H.5
Pellizzoni, L.6
-
19
-
-
79954631444
-
A new model to study spinal muscular atrophy: Neurite degeneration and cell death is counteracted by BCL-X(L) overexpression in motoneurons
-
Garcera A, Mincheva S, Gou-Fabregas M, Caraballo-Miralles V, Llado J, Comella JX, Soler RM. 2011. A new model to study spinal muscular atrophy: Neurite degeneration and cell death is counteracted by BCL-X(L) overexpression in motoneurons. Neurobiol Dis 2011; 42: 415-426.
-
(2011)
Neurobiol Dis
, vol.2011
, Issue.42
, pp. 415-426
-
-
Garcera, A.1
Mincheva, S.2
Gou-Fabregas, M.3
Caraballo-Miralles, V.4
Llado, J.5
Comella, J.X.6
Soler, R.M.7
-
20
-
-
0029147787
-
Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients
-
Gennarelli M, Lucarelli M, Capon F, Pizzuti A, Merlini L, Angelini C, Novelli G, et al. 1995. Survival motor neuron gene transcript analysis in muscles from spinal muscular atrophy patients. Biochem Biophys Res Commun 213: 342-348.
-
(1995)
Biochem Biophys Res Commun
, vol.213
, pp. 342-348
-
-
Gennarelli, M.1
Lucarelli, M.2
Capon, F.3
Pizzuti, A.4
Merlini, L.5
Angelini, C.6
Novelli, G.7
-
21
-
-
77952539315
-
The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons
-
Glinka M, Herrmann T, Funk N, Havlicek S, Rossoll W, Winkler C, Sendtner M. 2010. The heterogeneous nuclear ribonucleoprotein-R is necessary for axonal beta-actin mRNA translocation in spinal motor neurons. Hum Mol Genet 19: 1951-1966.
-
(2010)
Hum Mol Genet
, vol.19
, pp. 1951-1966
-
-
Glinka, M.1
Herrmann, T.2
Funk, N.3
Havlicek, S.4
Rossoll, W.5
Winkler, C.6
Sendtner, M.7
-
22
-
-
79953121904
-
Generation and Characterization of a zebrafish model of SMA carrying the human SMN2 gene
-
Hao LT, Burghes AH, Beattie CE. 2011. Generation and Characterization of a zebrafish model of SMA carrying the human SMN2 gene. Mol Neurodegener 6: 24.
-
(2011)
Mol Neurodegener
, vol.6
, pp. 24
-
-
Hao, L.T.1
Burghes, A.H.2
Beattie, C.E.3
-
23
-
-
33646241740
-
Mitochondrial dysfunction and amyotrophic lateral sclerosis
-
Hervias I, Beal MF, Manfredi G. 2006. Mitochondrial dysfunction and amyotrophic lateral sclerosis. Muscle Nerve 33: 598-608.
-
(2006)
Muscle Nerve
, vol.33
, pp. 598-608
-
-
Hervias, I.1
Beal, M.F.2
Manfredi, G.3
-
24
-
-
0035282740
-
Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy
-
Jablonka S, Bandilla M, Wiese S, Buhler D, Wirth B, Sendtner M, Fischer U. 2001. Co-regulation of survival of motor neuron (SMN) protein and its interactor SIP1 during development and in spinal muscular atrophy. Hum Mol Genet 10: 497-505.
-
(2001)
Hum Mol Genet
, vol.10
, pp. 497-505
-
-
Jablonka, S.1
Bandilla, M.2
Wiese, S.3
Buhler, D.4
Wirth, B.5
Sendtner, M.6
Fischer, U.7
-
25
-
-
35348929982
-
Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy
-
Jablonka S, Beck M, Lechner BD, Mayer C, Sendtner M. 2007. Defective Ca2+ channel clustering in axon terminals disturbs excitability in motoneurons in spinal muscular atrophy. J Cell Biol 179: 139-149.
-
(2007)
J Cell Biol
, vol.179
, pp. 139-149
-
-
Jablonka, S.1
Beck, M.2
Lechner, B.D.3
Mayer, C.4
Sendtner, M.5
-
26
-
-
48249145306
-
Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy
-
Kariya S, Park GH, Maeno-Hikichi Y, Leykekhman O, Lutz C, Arkovitz MS, Landmesser LT, 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.
-
(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
Landmesser, L.T.7
-
27
-
-
58849103600
-
Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice
-
Kong L, Wang X, Choe DW, Polley M, Burnett BG, Bosch-Marce M, Griffin JW, et al. 2009. Impaired synaptic vesicle release and immaturity of neuromuscular junctions in spinal muscular atrophy mice. J Neurosci 29: 842-851.
-
(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-Marce, M.6
Griffin, J.W.7
-
28
-
-
0028797783
-
Identification and characterization of a spinal muscular atrophy-determining gene
-
Lefebvre S, Burglen L, Reboullet S, Clermont O, Burlet P, Viollet L, Benichou B, et al. 1995. Identification and characterization of a spinal muscular atrophy-determining gene. Cell 80: 155-165.
-
(1995)
Cell
, vol.80
, pp. 155-165
-
-
Lefebvre, S.1
Burglen, L.2
Reboullet, S.3
Clermont, O.4
Burlet, P.5
Viollet, L.6
Benichou, B.7
-
29
-
-
78649723966
-
Synaptic defects in the spinal and neuromuscular circuitry in a mouse model of spinal muscular atrophy
-
Ling KK, Lin MY, Zingg B, Feng Z, Ko CP. 2010. Synaptic defects in the spinal and neuromuscular circuitry in a mouse model of spinal muscular atrophy. PLo S One 5: e15457.
-
(2010)
PLo S One
, vol.5
-
-
Ling, K.K.1
Lin, M.Y.2
Zingg, B.3
Feng, Z.4
Ko, C.P.5
-
30
-
-
0030931727
-
The spinal muscular atrophy disease gene product. SMN, and its associated protein SIP1 are in a complex with spliceosomal sn
-
Liu Q, Fischer U, Wang F, Dreyfuss G. 1997. The spinal muscular atrophy disease gene product. SMN, and its associated protein SIP1 are in a complex with spliceosomal sn RNP proteins Cell 90: 1013-1021.
-
(1997)
RNP proteins Cell
, vol.90
, pp. 1013-1021
-
-
Liu, Q.1
Fischer, U.2
Wang, F.3
Dreyfuss, G.4
-
31
-
-
0033033434
-
A single nucleotide in the SMN gene regulates splicing and is responsible for spinal muscular atrophy
-
Lorson CL, Hahnen E, Androphy EJ, 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.
-
(1999)
Proc Natl Acad Sci U S A
, vol.96
, pp. 6307-6311
-
-
Lorson, C.L.1
Hahnen, E.2
Androphy, E.J.3
Wirth, B.4
-
33
-
-
0042887389
-
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
-
McWhorter ML, Monani UR, Burghes AH, Beattie CE. 2003. Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. J Cell Biol 162: 919-931.
-
(2003)
J Cell Biol
, vol.162
, pp. 919-931
-
-
McWhorter, M.L.1
Monani, U.R.2
Burghes, A.H.3
Beattie, C.E.4
-
34
-
-
0035735484
-
A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs
-
Meister G, Buhler D, Pillai R, Lottspeich F, Fischer U. 2001. A multiprotein complex mediates the ATP-dependent assembly of spliceosomal U snRNPs. Nat Cell Biol 3: 945-949.
-
(2001)
Nat Cell Biol
, vol.3
, pp. 945-949
-
-
Meister, G.1
Buhler, D.2
Pillai, R.3
Lottspeich, F.4
Fischer, U.5
-
35
-
-
0032718045
-
The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability
-
Miguel-Aliaga I, Culetto E, Walker DS, Baylis HA, Sattelle DB, Davies KE. 1999. The Caenorhabditis elegans orthologue of the human gene responsible for spinal muscular atrophy is a maternal product critical for germline maturation and embryonic viability. Hum Mol Genet 8: 2133-2143.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 2133-2143
-
-
Miguel-Aliaga, I.1
Culetto, E.2
Walker, D.S.3
Baylis, H.A.4
Sattelle, D.B.5
Davies, K.E.6
-
36
-
-
33645081469
-
Regulation of mitochondria distribution by RhoA and formins
-
Minin AA, Kulik AV, Gyoeva FK, Li Y, Goshima G, Gelfand VI. 2006. Regulation of mitochondria distribution by RhoA and formins. J Cell Sci 119: 659-670.
-
(2006)
J Cell Sci
, vol.119
, pp. 659-670
-
-
Minin, A.A.1
Kulik, A.V.2
Gyoeva, F.K.3
Li, Y.4
Goshima, G.5
Gelfand, V.I.6
-
37
-
-
29144463310
-
Spinal muscular atrophy: A deficiency in a ubiquitous protein; a motor neuron-specific disease
-
Monani UR. 2005. Spinal muscular atrophy: A deficiency in a ubiquitous protein; a motor neuron-specific disease. Neuron 48: 885-896.
-
(2005)
Neuron
, vol.48
, pp. 885-896
-
-
Monani, U.R.1
-
38
-
-
0032799998
-
A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2
-
Monani UR, Lorson CL, Parsons DW, Prior TW, Androphy EJ, Burghes AH, McPherson JD. 1999. A single nucleotide difference that alters splicing patterns distinguishes the SMA gene SMN1 from the copy gene SMN2. Hum Mol Genet 8: 1177-1183.
-
(1999)
Hum Mol Genet
, vol.8
, pp. 1177-1183
-
-
Monani, U.R.1
Lorson, C.L.2
Parsons, D.W.3
Prior, T.W.4
Androphy, E.J.5
Burghes, A.H.6
McPherson, J.D.7
-
39
-
-
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 LM, Comley LH, Thomson D, Parkinson N, Talbot K, Gillingwater TH. 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.
-
(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
-
40
-
-
33747831850
-
The essential role of the mitochondria-dependent death-signaling cascade in chemotherapy-induced potentiation of Apo2L/TRAIL cytotoxicity in cultured thoracic cancer cells: Amplified caspase 8 is indispensable for combination-mediated massive cell death
-
Nguyen DM, Yeow WS, Ziauddin MF, Baras A, Tsai W, Reddy RM, et al. 2006. The essential role of the mitochondria-dependent death-signaling cascade in chemotherapy-induced potentiation of Apo2L/TRAIL cytotoxicity in cultured thoracic cancer cells: Amplified caspase 8 is indispensable for combination-mediated massive cell death. Cancer J 12: 257-273.
-
(2006)
Cancer J
, vol.12
, pp. 257-273
-
-
Nguyen, D.M.1
Yeow, W.S.2
Ziauddin, M.F.3
Baras, A.4
Tsai, W.5
Reddy, R.M.6
-
41
-
-
42549088649
-
Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
-
Oprea GE, Krober S, McWhorter ML, Rossoll W, Muller S, Krawczak M, Bassell GJ, et al. 2008. Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science 320: 524-527.
-
(2008)
Science
, vol.320
, pp. 524-527
-
-
Oprea, G.E.1
Krober, S.2
McWhorter, M.L.3
Rossoll, W.4
Muller, S.5
Krawczak, M.6
Bassell, G.J.7
-
42
-
-
0034096078
-
Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord
-
Pagliardini S, Giavazzi A, Setola V, Lizier C, Di Luca M, DeBiasi S, Battaglia G. 2000. Subcellular localization and axonal transport of the survival motor neuron (SMN) protein in the developing rat spinal cord. Hum Mol Genet 9: 47-56.
-
(2000)
Hum Mol Genet
, vol.9
, pp. 47-56
-
-
Pagliardini, S.1
Giavazzi, A.2
Setola, V.3
Lizier, C.4
Di Luca, M.5
DeBiasi, S.6
Battaglia, G.7
-
43
-
-
34047148903
-
Chaperoning ribonucleoprotein biogenesis in health and disease
-
Pellizzoni L. 2007. Chaperoning ribonucleoprotein biogenesis in health and disease. EMBO Rep 8: 340-345.
-
(2007)
EMBO Rep
, vol.8
, pp. 340-345
-
-
Pellizzoni, L.1
-
44
-
-
2242443509
-
Essential role for the SMN complex in the specificity of snRNP assembly
-
Pellizzoni L, Yong J, Dreyfuss G. 2002. Essential role for the SMN complex in the specificity of snRNP assembly. Science 298: 1775-1779.
-
(2002)
Science
, vol.298
, pp. 1775-1779
-
-
Pellizzoni, L.1
Yong, J.2
Dreyfuss, G.3
-
45
-
-
79954519035
-
The COPI vesicle complex binds and moves with survival motor neuron within axons
-
Peter CJ, Evans M, Thayanithy V, Taniguchi-Ishigaki N, Bach I, Kolpak A, Bassell GJ, et al. 2011. The COPI vesicle complex binds and moves with survival motor neuron within axons. Hum Mol Genet 2011; 20: 1701-1711.
-
(2011)
Hum Mol Genet
, vol.2011
, Issue.20
, pp. 1701-1711
-
-
Peter, C.J.1
Evans, M.2
Thayanithy, V.3
Taniguchi-Ishigaki, N.4
Bach, I.5
Kolpak, A.6
Bassell, G.J.7
-
46
-
-
33947217787
-
A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle
-
Rajendra TK, Gonsalvez GB, Walker MP, Shpargel KB, Salz HK, Matera AG. 2007. A Drosophila melanogaster model of spinal muscular atrophy reveals a function for SMN in striated muscle. J Cell Biol 176: 831-841.
-
(2007)
J Cell Biol
, vol.176
, pp. 831-841
-
-
Rajendra, T.K.1
Gonsalvez, G.B.2
Walker, M.P.3
Shpargel, K.B.4
Salz, H.K.5
Matera, A.G.6
-
47
-
-
57649207936
-
Mitochondrial abnormalities in spinal and bulbar muscular atrophy
-
Ranganathan S, Harmison GG, Meyertholen K, Pennuto M, Burnett BG, Fischbeck KH. 2009. Mitochondrial abnormalities in spinal and bulbar muscular atrophy. Hum Mol Genet 18: 27-42.
-
(2009)
Hum Mol Genet
, vol.18
, pp. 27-42
-
-
Ranganathan, S.1
Harmison, G.G.2
Meyertholen, K.3
Pennuto, M.4
Burnett, B.G.5
Fischbeck, K.H.6
-
48
-
-
0345599021
-
Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons
-
Rossoll W, Jablonka S, Andreassi C, Kroning AK, Karle K, Monani UR, Sendtner M. 2003. Smn, the spinal muscular atrophy-determining gene product, modulates axon growth and localization of beta-actin mRNA in growth cones of motoneurons. J Cell Biol 163: 801-812.
-
(2003)
J Cell Biol
, vol.163
, pp. 801-812
-
-
Rossoll, W.1
Jablonka, S.2
Andreassi, C.3
Kroning, A.K.4
Karle, K.5
Monani, U.R.6
Sendtner, M.7
-
49
-
-
75749129049
-
Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice
-
Ruiz R, Casañas JJ, Torres-Benito L, Cano R, Tabares L. 2010. Altered intracellular Ca2+ homeostasis in nerve terminals of severe spinal muscular atrophy mice. J Neurosci 30: 849-857.
-
(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
-
50
-
-
0032936983
-
Development of the vertebrate neuromuscular junction
-
Sanes JR, Lichtman JW. 1999. Development of the vertebrate neuromuscular junction. Annu Rev Neurosci 22: 389-442.
-
(1999)
Annu Rev Neurosci
, vol.22
, pp. 389-442
-
-
Sanes, J.R.1
Lichtman, J.W.2
-
51
-
-
0037195182
-
Impaired recycling of synaptic vesicles after acute perturbation of the presynaptic actin cytoskeleton
-
Shupliakov O, Bloom O, Gustafsson JS, Kjaerulff O, Low P, Tomilin N, Pieribone VA, et al. 2002. Impaired recycling of synaptic vesicles after acute perturbation of the presynaptic actin cytoskeleton. Proc Natl Acad Sci U S A 99: 14476-14481.
-
(2002)
Proc Natl Acad Sci U S A
, vol.99
, pp. 14476-14481
-
-
Shupliakov, O.1
Bloom, O.2
Gustafsson, J.S.3
Kjaerulff, O.4
Low, P.5
Tomilin, N.6
Pieribone, V.A.7
-
52
-
-
15844431376
-
Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans
-
Sonnichsen B, Koski LB, Walsh A, Marschall P, Neumann B, Brehm M, Alleaume AM, et al. 2005. Full-genome RNAi profiling of early embryogenesis in Caenorhabditis elegans. Nature 434: 462-469.
-
(2005)
Nature
, vol.434
, pp. 462-469
-
-
Sonnichsen, B.1
Koski, L.B.2
Walsh, A.3
Marschall, P.4
Neumann, B.5
Brehm, M.6
Alleaume, A.M.7
-
53
-
-
20744455958
-
The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy
-
Wan L, Battle DJ, Yong J, Gubitz AK, Kolb SJ, Wang J, Dreyfuss G. 2005. The survival of motor neurons protein determines the capacity for snRNP assembly: biochemical deficiency in spinal muscular atrophy. Mol Cell Biol 25: 5543-5551.
-
(2005)
Mol Cell Biol
, vol.25
, pp. 5543-5551
-
-
Wan, L.1
Battle, D.J.2
Yong, J.3
Gubitz, A.K.4
Kolb, S.J.5
Wang, J.6
Dreyfuss, G.7
-
54
-
-
25844461744
-
Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy
-
Winkler C, Eggert C, Gradl D, Meister G, Giegerich M, Wedlich D, Laggerbauer B, et al. 2005. Reduced U snRNP assembly causes motor axon degeneration in an animal model for spinal muscular atrophy. Genes Dev 19: 2320-2330.
-
(2005)
Genes Dev
, vol.19
, pp. 2320-2330
-
-
Winkler, C.1
Eggert, C.2
Gradl, D.3
Meister, G.4
Giegerich, M.5
Wedlich, D.6
Laggerbauer, B.7
-
55
-
-
76549115901
-
Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy
-
Ymlahi-Ouazzani Q, O JB, Paillard E, Ballagny C, Chesneau A, Jadaud A, Mazabraud A, et al. 2010. Reduced levels of survival motor neuron protein leads to aberrant motoneuron growth in a Xenopus model of muscular atrophy. Neurogenetics 11: 27-40.
-
(2010)
Neurogenetics
, vol.11
, pp. 27-40
-
-
Ymlahi-Ouazzani, Q.1
O, J.B.2
Paillard, E.3
Ballagny, C.4
Chesneau, A.5
Jadaud, A.6
Mazabraud, A.7
-
56
-
-
33748186105
-
Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons
-
Zhang H, Xing L, Rossoll W, Wichterle H, Singer RH, Bassell GJ. 2006. Multiprotein complexes of the survival of motor neuron protein SMN with Gemins traffic to neuronal processes and growth cones of motor neurons. J Neurosci 26: 8622-8632.
-
(2006)
J Neurosci
, vol.26
, pp. 8622-8632
-
-
Zhang, H.1
Xing, L.2
Rossoll, W.3
Wichterle, H.4
Singer, R.H.5
Bassell, G.J.6
-
57
-
-
0042202619
-
Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization
-
Zhang HL, Pan F, Hong D, Shenoy SM, Singer RH, Bassell GJ. 2003. Active transport of the survival motor neuron protein and the role of exon-7 in cytoplasmic localization. J Neurosci 23: 6627-6637.
-
(2003)
J Neurosci
, vol.23
, pp. 6627-6637
-
-
Zhang, H.L.1
Pan, F.2
Hong, D.3
Shenoy, S.M.4
Singer, R.H.5
Bassell, G.J.6
-
58
-
-
43049168361
-
SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing
-
Zhang Z, Lotti F, Dittmar K, Younis I, Wan L, Kasim M, Dreyfuss G. 2008. SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing. Cell 133: 585-600.
-
(2008)
Cell
, vol.133
, pp. 585-600
-
-
Zhang, Z.1
Lotti, F.2
Dittmar, K.3
Younis, I.4
Wan, L.5
Kasim, M.6
Dreyfuss, G.7
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