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Items: 1 to 20 of 97

1.

The spinal muscular atrophy disease protein SMN is linked to the Golgi network.

Ting CH, Wen HL, Liu HC, Hsieh-Li HM, Li H, Lin-Chao S.

PLoS One. 2012;7(12):e51826. doi: 10.1371/journal.pone.0051826. Epub 2012 Dec 17.

2.

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.

J Neurosci. 2003 Jul 23;23(16):6627-37.

3.

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, Rossoll W, Lorson CL, Bao ZZ, Androphy EJ.

Hum Mol Genet. 2011 May 1;20(9):1701-11. doi: 10.1093/hmg/ddr046. Epub 2011 Feb 7.

4.

A role for complexes of survival of motor neurons (SMN) protein with gemins and profilin in neurite-like cytoplasmic extensions of cultured nerve cells.

Sharma A, Lambrechts A, Hao le T, Le TT, Sewry CA, Ampe C, Burghes AH, Morris GE.

Exp Cell Res. 2005 Sep 10;309(1):185-97.

PMID:
15975577
5.

HuD interacts with survival motor neuron protein and can rescue spinal muscular atrophy-like neuronal defects.

Hubers L, Valderrama-Carvajal H, Laframboise J, Timbers J, Sanchez G, Côté J.

Hum Mol Genet. 2011 Feb 1;20(3):553-79. doi: 10.1093/hmg/ddq500. Epub 2010 Nov 18.

PMID:
21088113
6.

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, Lladó J, Comella JX, Soler RM.

Neurobiol Dis. 2011 Jun;42(3):415-26. doi: 10.1016/j.nbd.2011.02.003. Epub 2011 Feb 16.

PMID:
21333739
7.

Co-regulation of survival of motor neuron and Bcl-xL expression: implications for neuroprotection in spinal muscular atrophy.

Anderton RS, Price LL, Turner BJ, Meloni BP, Mitrpant C, Mastaglia FL, Goh C, Wilton SD, Boulos S.

Neuroscience. 2012 Sep 18;220:228-36. doi: 10.1016/j.neuroscience.2012.06.042. Epub 2012 Jun 23.

PMID:
22732506
8.

Stathmin, a microtubule-destabilizing protein, is dysregulated in spinal muscular atrophy.

Wen HL, Lin YT, Ting CH, Lin-Chao S, Li H, Hsieh-Li HM.

Hum Mol Genet. 2010 May 1;19(9):1766-78. doi: 10.1093/hmg/ddq058. Epub 2010 Feb 22.

PMID:
20176735
9.

Analysis of SMN-neurite granules: Core Cajal body components are absent from SMN-cytoplasmic complexes.

Todd AG, Morse R, Shaw DJ, Stebbings H, Young PJ.

Biochem Biophys Res Commun. 2010 Jul 2;397(3):479-85. doi: 10.1016/j.bbrc.2010.05.139. Epub 2010 May 31.

PMID:
20515655
10.

Spinal muscular atrophy and the antiapoptotic role of survival of motor neuron (SMN) protein.

Anderton RS, Meloni BP, Mastaglia FL, Boulos S.

Mol Neurobiol. 2013 Apr;47(2):821-32. doi: 10.1007/s12035-013-8399-5. Epub 2013 Jan 13. Review.

PMID:
23315303
11.

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, Bühler D, Wirth B, Sendtner M, Fischer U.

Hum Mol Genet. 2001 Mar 1;10(5):497-505.

PMID:
11181573
12.

Specific interaction of Smn, the spinal muscular atrophy determining gene product, with hnRNP-R and gry-rbp/hnRNP-Q: a role for Smn in RNA processing in motor axons?

Rossoll W, Kröning AK, Ohndorf UM, Steegborn C, Jablonka S, Sendtner M.

Hum Mol Genet. 2002 Jan 1;11(1):93-105.

PMID:
11773003
13.

Dilysine motifs in exon 2b of SMN protein mediate binding to the COPI vesicle protein α-COP and neurite outgrowth in a cell culture model of spinal muscular atrophy.

Custer SK, Todd AG, Singh NN, Androphy EJ.

Hum Mol Genet. 2013 Oct 15;22(20):4043-52. doi: 10.1093/hmg/ddt254. Epub 2013 May 31.

14.

α-COP binding to the survival motor neuron protein SMN is required for neuronal process outgrowth.

Li H, Custer SK, Gilson T, Hao le T, Beattie CE, Androphy EJ.

Hum Mol Genet. 2015 Dec 20;24(25):7295-307. doi: 10.1093/hmg/ddv428. Epub 2015 Oct 13.

15.
16.

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.

J Neurosci. 2006 Aug 16;26(33):8622-32.

17.

Subcellular distribution of survival motor neuron (SMN) protein: possible involvement in nucleocytoplasmic and dendritic transport.

Béchade C, Rostaing P, Cisterni C, Kalisch R, La Bella V, Pettmann B, Triller A.

Eur J Neurosci. 1999 Jan;11(1):293-304.

PMID:
9987032
18.

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.

Mol Cell Biol. 2005 Jul;25(13):5543-51.

19.

SMN deficiency reduces cellular ability to form stress granules, sensitizing cells to stress.

Zou T, Yang X, Pan D, Huang J, Sahin M, Zhou J.

Cell Mol Neurobiol. 2011 May;31(4):541-50. doi: 10.1007/s10571-011-9647-8. Epub 2011 Jan 15.

PMID:
21234798
20.

Proteomic assessment of a cell model of spinal muscular atrophy.

Wu CY, Whye D, Glazewski L, Choe L, Kerr D, Lee KH, Mason RW, Wang W.

BMC Neurosci. 2011 Mar 8;12:25. doi: 10.1186/1471-2202-12-25.

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