-
1
-
-
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. 1995;80(1):155-165.
-
(1995)
Cell
, vol.80
, Issue.1
, pp. 155-165
-
-
Lefebvre, S.1
-
2
-
-
0034007548
-
An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA)
-
DOI 10.1002/(SICI)1098-1004(200003)15:3<228::AID-H
-
Wirth B. An update of the mutation spectrum of the survival motor neuron gene (SMN1) in autosomal recessive spinal muscular atrophy (SMA). Hum Mutat. 2000;15(3):228-237. (Pubitemid 30132157)
-
(2000)
Human Mutation
, vol.15
, Issue.3
, pp. 228-237
-
-
Wirth, B.1
-
3
-
-
67651083390
-
Spinal muscular atrophy: Why do low levels of survival motor neuron protein make motor neurons sick?
-
Burghes AH, Beattie CE. Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick? Nat Rev Neurosci. 2009;10(8):597-609.
-
(2009)
Nat Rev Neurosci
, vol.10
, Issue.8
, pp. 597-609
-
-
Burghes, A.H.1
Beattie, C.E.2
-
4
-
-
80054880080
-
Reversible molecular pathology of skeletal muscle in spinal muscular atrophy
-
Mutsaers CA, et al. Reversible molecular pathology of skeletal muscle in spinal muscular atrophy. Hum Mol Genet. 2011;20(22):4334-4344.
-
(2011)
Hum Mol Genet
, vol.20
, Issue.22
, pp. 4334-4344
-
-
Mutsaers, C.A.1
-
5
-
-
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
-
DOI 10.1093/hmg/ddm367
-
Murray LM, Comley LH, Thomson D, Parkinson N, Talbot K, Gillingwater TH. 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. 2008;17(7):949-962. (Pubitemid 351426029)
-
(2008)
Human Molecular Genetics
, vol.17
, Issue.7
, pp. 949-962
-
-
Murray, L.M.1
Comley, L.H.2
Thomson, D.3
Parkinson, N.4
Talbot, K.5
Gillingwater, T.H.6
-
6
-
-
48249145306
-
Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy
-
Kariya S, et al. Reduced SMN protein impairs maturation of the neuromuscular junctions in mouse models of spinal muscular atrophy. Hum Mol Genet. 2008;17(16):2552-2569.
-
(2008)
Hum Mol Genet
, vol.17
, Issue.16
, pp. 2552-2569
-
-
Kariya, S.1
-
7
-
-
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. Synaptic defects in the spinal and neuromuscular circuitry in a mouse model of spinal muscular atrophy. PLoS One. 2010;5(11):e15457.
-
(2010)
PLoS One
, vol.5
, Issue.11
-
-
Ling, K.K.1
Lin, M.Y.2
Zingg, B.3
Feng, Z.4
Ko, C.P.5
-
8
-
-
79551663958
-
Early functional impairment of sensory-motor connectivity in a mouse model of spinal muscular atrophy
-
Mentis GZ, et al. Early functional impairment of sensory-motor connectivity in a mouse model of spinal muscular atrophy. Neuron. 2011;69(3):453-467.
-
(2011)
Neuron
, vol.69
, Issue.3
, pp. 453-467
-
-
Mentis, G.Z.1
-
9
-
-
84867511739
-
SMN is required for sensory-motor circuit function in Drosophila
-
Imlach WL, Beck ES, Choi BJ, Lotti F, Pellizzoni L, McCabe BD. SMN is required for sensory-motor circuit function in Drosophila. Cell. 2012;151(2):427-439.
-
(2012)
Cell
, vol.151
, Issue.2
, pp. 427-439
-
-
Imlach, W.L.1
Beck, E.S.2
Choi, B.J.3
Lotti, F.4
Pellizzoni, L.5
McCabe, B.D.6
-
10
-
-
84871718500
-
Spinal muscular atrophy: Going beyond the motor neuron
-
Hamilton G, Gillingwater TH. Spinal muscular atrophy: going beyond the motor neuron. Trends Mol Med. 2013;19(1):40-50.
-
(2013)
Trends Mol Med
, vol.19
, Issue.1
, pp. 40-50
-
-
Hamilton, G.1
Gillingwater, T.H.2
-
11
-
-
77957878494
-
SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy
-
Wishart TM, et al. SMN deficiency disrupts brain development in a mouse model of severe spinal muscular atrophy. Hum Mol Genet. 2010;19(21):4216-4228.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.21
, pp. 4216-4228
-
-
Wishart, T.M.1
-
12
-
-
77957729453
-
Cardiac defects contribute to the pathology of spinal muscular atrophy models
-
Shababi M, Habibi J, Yang HT, Vale SM, Sewell WA, Lorson CL. Cardiac defects contribute to the pathology of spinal muscular atrophy models. Hum Mol Genet. 2010;19(20):4059-4071.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.20
, pp. 4059-4071
-
-
Shababi, M.1
Habibi, J.2
Yang, H.T.3
Vale, S.M.4
Sewell, W.A.5
Lorson, C.L.6
-
13
-
-
84859651967
-
Density, calibre and ramification of muscle capillaries are altered in a mouse model of severe spinal muscular atrophy
-
Somers E, Stencel Z, Wishart TM, Gillingwater TH, Parson SH. Density, calibre and ramification of muscle capillaries are altered in a mouse model of severe spinal muscular atrophy. Neuromuscul Disord. 2012;22(5):435-442.
-
(2012)
Neuromuscul Disord
, vol.22
, Issue.5
, pp. 435-442
-
-
Somers, E.1
Stencel, Z.2
Wishart, T.M.3
Gillingwater, T.H.4
Parson, S.H.5
-
14
-
-
80053902729
-
Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model
-
Hua Y, et al. Peripheral SMN restoration is essential for long-term rescue of a severe spinal muscular atrophy mouse model. Nature. 2011;478(7367):123-126.
-
(2011)
Nature
, vol.478
, Issue.7367
, pp. 123-126
-
-
Hua, Y.1
-
15
-
-
84865592642
-
Glucose metabolism and pancreatic defects in spinal muscular atrophy
-
Bowerman M, et al. Glucose metabolism and pancreatic defects in spinal muscular atrophy. Ann Neurol. 2012;72(2):256-268.
-
(2012)
Ann Neurol
, vol.72
, Issue.2
, pp. 256-268
-
-
Bowerman, M.1
-
16
-
-
84885922032
-
Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585
-
Schreml J, et al. Severe SMA mice show organ impairment that cannot be rescued by therapy with the HDACi JNJ-26481585. Eur J Hum Genet. 2013;21(6):643-652.
-
(2013)
Eur J Hum Genet
, vol.21
, Issue.6
, pp. 643-652
-
-
Schreml, J.1
-
17
-
-
43049168361
-
SMN Deficiency Causes Tissue-Specific Perturbations in the Repertoire of snRNAs and Widespread Defects in Splicing
-
DOI 10.1016/j.cell.2008.03.031, PII S0092867408004601
-
Zhang Z, et al. SMN deficiency causes tissue-specific perturbations in the repertoire of snRNAs and widespread defects in splicing. Cell. 2008;133(4):585-600. (Pubitemid 351636302)
-
(2008)
Cell
, vol.133
, Issue.4
, pp. 585-600
-
-
Zhang, Z.1
Lotti, F.2
Dittmar, K.3
Younis, I.4
Wan, L.5
Kasim, M.6
Dreyfuss, G.7
-
18
-
-
74249094999
-
Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy
-
Bäumer D, et al. Alternative splicing events are a late feature of pathology in a mouse model of spinal muscular atrophy. PLoS Genet. 2009;5(12):e1000773.
-
(2009)
PLoS Genet
, vol.5
, Issue.12
-
-
Bäumer, D.1
-
19
-
-
84867555865
-
An SMN-dependent U12 splicing event essential for motor circuit function
-
Lotti F, et al. An SMN-dependent U12 splicing event essential for motor circuit function. Cell. 2012;151(2):440-454.
-
(2012)
Cell
, vol.151
, Issue.2
, pp. 440-454
-
-
Lotti, F.1
-
20
-
-
84863114222
-
A Drosophila model of spinal muscular atrophy uncouples snRNP biogenesis functions of survival motor neuron from locomotion and viability defects
-
Praveen K, Wen Y, Matera AG. A Drosophila model of spinal muscular atrophy uncouples snRNP biogenesis functions of survival motor neuron from locomotion and viability defects. Cell Rep. 2012;1(6):624-631.
-
(2012)
Cell Rep
, vol.1
, Issue.6
, pp. 624-631
-
-
Praveen, K.1
Wen, Y.2
Matera, A.G.3
-
21
-
-
84878883752
-
Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy
-
Neveling K, et al. Mutations in BICD2, which encodes a golgin and important motor adaptor, cause congenital autosomal-dominant spinal muscular atrophy. Am J Hum Genet. 2013;92(6):946-954.
-
(2013)
Am J Hum Genet
, vol.92
, Issue.6
, pp. 946-954
-
-
Neveling, K.1
-
22
-
-
38749120297
-
Rare Missense and Synonymous Variants in UBE1 Are Associated with X-Linked Infantile Spinal Muscular Atrophy
-
DOI 10.1016/j.ajhg.2007.09.009, PII S0002929707000158
-
Ramser J, et al. Rare missense and synonymous variants in UBE1 are associated with X-linked infantile spinal muscular atrophy. Am J Hum Genet. 2008;82(1):188-193. (Pubitemid 351726086)
-
(2008)
American Journal of Human Genetics
, vol.82
, Issue.1
, pp. 188-193
-
-
Ramser, J.1
Ahearn, M.E.2
Lenski, C.3
Yariz, K.O.4
Hellebrand, H.5
Von, R.M.6
Clark, R.D.7
Schmutzler, R.K.8
Lichtner, P.9
Hoffman, E.P.10
Meindl, A.11
Baumbach-Reardon, L.12
-
23
-
-
42549088649
-
Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy
-
DOI 10.1126/science.1155085
-
Oprea GE, et al. Plastin 3 is a protective modifier of autosomal recessive spinal muscular atrophy. Science. 2008;320(5875):524-527. (Pubitemid 351590664)
-
(2008)
Science
, vol.320
, Issue.5875
, 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
Beattie, C.E.8
Wirth, B.9
-
24
-
-
84875236246
-
Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality
-
Ackermann B, et al. Plastin 3 ameliorates spinal muscular atrophy via delayed axon pruning and improves neuromuscular junction functionality. Hum Mol Genet. 2013;22(7):1328-1347.
-
(2013)
Hum Mol Genet
, vol.22
, Issue.7
, pp. 1328-1347
-
-
Ackermann, B.1
-
25
-
-
77955026640
-
PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons
-
Ning K, et al. PTEN depletion rescues axonal growth defect and improves survival in SMN-deficient motor neurons. Hum Mol Genet. 2010;19(16):3159-3168.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.16
, pp. 3159-3168
-
-
Ning, K.1
-
26
-
-
84873044474
-
A novel function for the survival motoneuron protein as a translational regulator
-
Sanchez G, et al. A novel function for the survival motoneuron protein as a translational regulator. Hum Mol Genet. 2013;22(4):668-684.
-
(2013)
Hum Mol Genet
, vol.22
, Issue.4
, pp. 668-684
-
-
Sanchez, G.1
-
27
-
-
2442528179
-
The ubiquitin proteasome system in synaptic and axonal degeneration: A new twist to an old cycle
-
DOI 10.1083/jcb.200311091
-
Korhonen L, Lindholm D. The ubiquitin proteasome system in synaptic axonal degeneration: a new twist to an old cycle. J Cell Biol. 2004;165(1):27-30. (Pubitemid 38649173)
-
(2004)
Journal of Cell Biology
, vol.165
, Issue.1
, pp. 27-30
-
-
Korhonen, L.1
Lindholm, D.2
-
28
-
-
4444240236
-
Degradation of survival motor neuron (SMN) protein is mediated via the ubiquitin/proteasome pathway
-
Chang HC, Hung WC, Chuang YJ, Jong YJ. Degradation of survival motor neuron (SMN) protein is mediated via the ubiquitin/proteasome pathway. Neurochem Int. 2004;45(7):1107-1112.
-
(2004)
Neurochem Int
, vol.45
, Issue.7
, pp. 1107-1112
-
-
Chang, H.C.1
Hung, W.C.2
Chuang, Y.J.3
Jong, Y.J.4
-
29
-
-
61749099937
-
Regulation of SMN protein stability
-
Burnett BG, Muñoz E, Tandon A, Kwon DY, Sumner CJ, Fischbeck KH. Regulation of SMN protein stability. Mol Cell Biol. 2009;29(5):1107-1115.
-
(2009)
Mol Cell Biol
, vol.29
, Issue.5
, pp. 1107-1115
-
-
Burnett, B.G.1
Muñoz, E.2
Tandon, A.3
Kwon, D.Y.4
Sumner, C.J.5
Fischbeck, K.H.6
-
30
-
-
77957754345
-
Ubiquitin carboxyl-terminal hydrolase L1 (UCHL1) regulates the level of SMN expression through ubiquitination in primary spinal muscular atrophy fibroblasts
-
Hsu SH, et al. Ubiquitin carboxyl-terminal hydrolase L1 (UCHL1) regulates the level of SMN expression through ubiquitination in primary spinal muscular atrophy fibroblasts. Clin Chim Acta. 2010;411(23-24):1920-1928.
-
(2010)
Clin Chim Acta
, vol.411
, Issue.23-24
, pp. 1920-1928
-
-
Hsu, S.H.1
-
31
-
-
0038039295
-
Neuromuscular defects in a Drosophila survival motor neuron gene mutant
-
Chan YB, et al. Neuromuscular defects in a Drosophila survival motor neuron gene mutant. Hum Mol Genet. 2003;12(12):1367-1376. (Pubitemid 36758450)
-
(2003)
Human Molecular Genetics
, vol.12
, Issue.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
Van Den, H.M.8
-
32
-
-
77952295831
-
SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy
-
Riessland M, et al. SAHA ameliorates the SMA phenotype in two mouse models for spinal muscular atrophy. Hum Mol Genet. 2010;19(8):1492-1506.
-
(2010)
Hum Mol Genet
, vol.19
, Issue.8
, pp. 1492-1506
-
-
Riessland, M.1
-
33
-
-
0042887389
-
Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding
-
DOI 10.1083/jcb.200303168
-
McWhorter ML, Monani UR, Burghes AH, Beattie CE. Knockdown of the survival motor neuron (Smn) protein in zebrafish causes defects in motor axon outgrowth and pathfinding. J Cell Biol. 2003;162(5):919-931. (Pubitemid 37087731)
-
(2003)
Journal of Cell Biology
, vol.162
, Issue.5
, pp. 919-931
-
-
McWhorter, M.L.1
Monani, U.R.2
Burghes, A.H.M.3
Beattie, C.E.4
-
34
-
-
80355148474
-
Role of ubiquitylation and USP8-dependent deubiquitylation in the endocytosis and lysosomal targeting of plasma membrane KCa3.1
-
Balut CM, Loch CM, Devor DC. Role of ubiquitylation and USP8-dependent deubiquitylation in the endocytosis and lysosomal targeting of plasma membrane KCa3.1. FASEB J. 2011;25(11):3938-3948.
-
(2011)
FASEB J
, vol.25
, Issue.11
, pp. 3938-3948
-
-
Balut, C.M.1
Loch, C.M.2
Devor, D.C.3
-
35
-
-
84856504393
-
TCFs and Wnt/β-catenin signaling: More than one way to throw the switch
-
Cadigan KM. TCFs and Wnt/β-catenin signaling: more than one way to throw the switch. Curr Top Dev Biol. 2012;98:1-34.
-
(2012)
Curr Top Dev Biol
, vol.98
, pp. 1-34
-
-
Cadigan, K.M.1
-
36
-
-
0026465350
-
Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons
-
Cashman NR, et al. Neuroblastoma x spinal cord (NSC) hybrid cell lines resemble developing motor neurons. Dev Dyn. 1992;194(3):209-221.
-
(1992)
Dev Dyn
, vol.194
, Issue.3
, pp. 209-221
-
-
Cashman, N.R.1
-
37
-
-
84879798567
-
Gene regulatory networks mediating canonical Wnt signal directed control of pluripotency and differentiation in embryo stem cells
-
[published online ahead of print March 15, 2013]. doi:10.1002/stem.1371
-
Zhang X, Peterson KA, Liu XS, McMahon AP, Ohba S. Gene regulatory networks mediating canonical Wnt signal directed control of pluripotency and differentiation in embryo stem cells [published online ahead of print March 15, 2013]. Stem Cells. doi:10.1002/stem.1371.
-
Stem Cells
-
-
Zhang, X.1
Peterson, K.A.2
Liu, X.S.3
McMahon, A.P.4
Ohba, S.5
-
38
-
-
0030978351
-
Beta-catenin is a target for the ubiquitin-proteasome pathway
-
Aberle H, Bauer A, Stappert J, Kispert A, Kemler R. Beta-catenin is a target for the ubiquitin-proteasome pathway. EMBO J. 1997;16(13):3797-3804.
-
(1997)
EMBO J
, vol.16
, Issue.13
, pp. 3797-3804
-
-
Aberle, H.1
Bauer, A.2
Stappert, J.3
Kispert, A.4
Kemler, R.5
-
39
-
-
12844274417
-
Quercetin, a potent inhibitor against β-catenin/Tcf signaling in SW480 colon cancer cells
-
DOI 10.1016/j.bbrc.2004.12.151, PII S0006291X04029808
-
Park CH, Chang JY, Hahm ER, Park S, Kim HK, Yang CH. Quercetin, a potent inhibitor against β-catenin/Tcf signaling in SW480 colon cancer cells. Biochem Biophys Res Commun. 2005;328(1):227-234. (Pubitemid 40164659)
-
(2005)
Biochemical and Biophysical Research Communications
, vol.328
, Issue.1
, pp. 227-234
-
-
Park, C.H.1
Chang, J.Y.2
Hahm, E.R.3
Park, S.4
Kim, H.-K.5
Yang, C.H.6
-
40
-
-
58149382600
-
Constitutive activation of the Wnt canonical pathway in mantle cell lymphoma
-
Gelebart P, et al. Constitutive activation of the Wnt canonical pathway in mantle cell lymphoma. Blood. 2008;112(13):5171-5179.
-
(2008)
Blood
, vol.112
, Issue.13
, pp. 5171-5179
-
-
Gelebart, P.1
-
41
-
-
84862001767
-
Urokinase-type plasminogen activator receptor (uPAR)-mediated regulation of WNT/β-catenin signaling is enhanced in irradiated medulloblastoma cells
-
Asuthkar S, Gondi CS, Nalla AK, Velpula KK, Gorantla B, Rao JS. Urokinase-type plasminogen activator receptor (uPAR)-mediated regulation of WNT/β-catenin signaling is enhanced in irradiated medulloblastoma cells. J Biol Chem. 2012;287(24):20576-20589.
-
(2012)
J Biol Chem
, vol.287
, Issue.24
, pp. 20576-20589
-
-
Asuthkar, S.1
Gondi, C.S.2
Nalla, A.K.3
Velpula, K.K.4
Gorantla, B.5
Rao, J.S.6
-
42
-
-
0037014456
-
Depolarization drives beta-catenin into neuronal spines promoting changes in synaptic structure and function
-
DOI 10.1016/S0896-6273(02)00764-X
-
Murase S, Mosser E, Schuman EM. Depolarization drives beta-catenin into neuronal spines promoting changes in synaptic structure and function. Neuron. 2002;35(1):91-105. (Pubitemid 34804325)
-
(2002)
Neuron
, vol.35
, Issue.1
, pp. 91-105
-
-
Murase, S.1
Mosser, E.2
Schuman, E.M.3
-
43
-
-
39749119832
-
Retrograde regulation of motoneuron differentiation by muscle beta-catenin
-
Li XM, et al. Retrograde regulation of motoneuron differentiation by muscle beta-catenin. Nat Neurosci. 2008;11(3):262-268.
-
(2008)
Nat Neurosci
, vol.11
, Issue.3
, pp. 262-268
-
-
Li, X.M.1
-
44
-
-
80051982748
-
Critical role of PI3K/Akt/ GSK3β in motoneuron specification from human neural stem cells in response to FGF2 and EGF
-
Ojeda L, et al. Critical role of PI3K/Akt/ GSK3β in motoneuron specification from human neural stem cells in response to FGF2 and EGF. PLoS One. 2011;6(8):e23414.
-
(2011)
PLoS One
, vol.6
, Issue.8
-
-
Ojeda, L.1
-
45
-
-
0034639645
-
-/- mice and results in a mouse with spinal muscular atrophy
-
-/- mice and results in a mouse with spinal muscular atrophy. Hum Mol Genet. 2000;9(3):333-339.
-
(2000)
Hum Mol Genet
, vol.9
, Issue.3
, pp. 333-339
-
-
Monani, U.R.1
-
46
-
-
0033987669
-
A mouse model for spinal muscular atrophy
-
DOI 10.1038/71709
-
Hsieh-Li HM, et al. A mouse model for spinal muscular atrophy. Nat Genet. 2000;24(1):66-70. (Pubitemid 30041423)
-
(2000)
Nature Genetics
, vol.24
, Issue.1
, pp. 66-70
-
-
Hsieh-Li, H.M.1
Chang, J.-G.2
Jong, Y.-J.3
Wu, M.-H.4
Wang, N.M.5
Tsai, C.H.6
Li, H.7
-
47
-
-
84885547156
-
Label-free proteomics identifies Calreticulin and GRP75/Mortalin as peripherally accessible protein biomarkers for spinal muscular atrophy
-
Mutsaers CA, Lamont DJ, Hunter G, Wishart TM, Gillingwater TH. Label-free proteomics identifies Calreticulin and GRP75/Mortalin as peripherally accessible protein biomarkers for spinal muscular atrophy. Genome Med. 2013;5(10):95.
-
(2013)
Genome Med
, vol.5
, Issue.10
, pp. 95
-
-
Mutsaers, C.A.1
Lamont, D.J.2
Hunter, G.3
Wishart, T.M.4
Gillingwater, T.H.5
-
48
-
-
84866175104
-
Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo
-
Wishart TM, et al. Combining comparative proteomics and molecular genetics uncovers regulators of synaptic and axonal stability and degeneration in vivo. PLoS Genet. 2012;8(8):e1002936.
-
(2012)
PLoS Genet
, vol.8
, Issue.8
-
-
Wishart, T.M.1
-
49
-
-
0034194444
-
The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells
-
DOI 10.1006/excr.2000.4858
-
Young PJ, Le TT, Man NT, Burghes AHM, Morris GE. The relationship between SMN, the spinal muscular atrophy protein, and nuclear coiled bodies in differentiated tissues and cultured cells. Exp Cell Res. 2000;256(2):365-374. (Pubitemid 30244195)
-
(2000)
Experimental Cell Research
, vol.256
, Issue.2
, pp. 365-374
-
-
Young, P.J.1
Le, T.T.2
Thi, M.N.3
Burghes, A.H.M.4
Morris, G.E.5
-
50
-
-
78751627951
-
Leucine-rich repeat kinase LRRK1 regulates endosomal trafficking of the EGF receptor
-
Hanafusa H, et al. Leucine-rich repeat kinase LRRK1 regulates endosomal trafficking of the EGF receptor. Nat Commun. 2011;2:158.
-
(2011)
Nat Commun
, vol.2
, pp. 158
-
-
Hanafusa, H.1
-
51
-
-
73649149401
-
The SMN interactome includes Myb-binding protein 1a
-
Fuller HR, et al. The SMN interactome includes Myb-binding protein 1a. J Proteome Res. 2010;9(1):556-563.
-
(2010)
J Proteome Res
, vol.9
, Issue.1
, pp. 556-563
-
-
Fuller, H.R.1
-
52
-
-
0024423656
-
NMDA and non-NMDA receptors are co-localized at individual excitatory synapses in cultured rat hippocampus
-
DOI 10.1038/341230a0
-
Bekkers JM, Stevens CF. NMDA and non-NMDA receptors are co-localized at individual excitatory synapses in cultured rat hippocampus. Nature. 1989;341(6239):230-233. (Pubitemid 19231722)
-
(1989)
Nature
, vol.341
, Issue.6239
, pp. 230-233
-
-
Bekkers, J.M.1
Stevens, C.F.2
-
53
-
-
27744602432
-
Neuromuscular synapses can form in vivo by incorporation of initially aneural postsynaptic specializations
-
DOI 10.1242/dev.02044
-
Flanagan-Steet H, Fox MA, Meyer D, Sanes JR. Neuromuscular synapses can form in vivo by incorporation of initially aneural postsynaptic specializations. Development. 2005;132(20):4471-4481. (Pubitemid 41632226)
-
(2005)
Development
, vol.132
, Issue.20
, pp. 4471-4481
-
-
Flanagan-Steet, H.1
Fox, M.A.2
Meyer, D.3
Sanes, J.R.4
-
54
-
-
34447642872
-
Abnormal motor phenotype in the SMNDelta7 mouse model of spinal muscular atrophy
-
DOI 10.1016/j.nbd.2007.04.009, PII S0969996107000903
-
Butchbach ME, Edwards JD, Burghes AH. Abnormal motor phenotype in the SMNDelta7 mouse model of spinal muscular atrophy. Neurobiol Dis. 2007;27(2):207-219. (Pubitemid 47088980)
-
(2007)
Neurobiology of Disease
, vol.27
, Issue.2
, pp. 207-219
-
-
Butchbach, M.E.R.1
Edwards, J.D.2
Burghes, A.H.M.3
-
55
-
-
84866934033
-
Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy
-
Lee AJ, Awano T, Park GH, Monani UR. Limited phenotypic effects of selectively augmenting the SMN protein in the neurons of a mouse model of severe spinal muscular atrophy. PLoS One. 2012;7(9):e46353.
-
(2012)
PLoS One
, vol.7
, Issue.9
-
-
Lee, A.J.1
Awano, T.2
Park, G.H.3
Monani, U.R.4
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