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Items: 1 to 20 of 114

1.

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.

2.

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.

3.

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.

4.

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.

5.

Dynamics of survival of motor neuron (SMN) protein interaction with the mRNA-binding protein IMP1 facilitates its trafficking into motor neuron axons.

Fallini C, Rouanet JP, Donlin-Asp PG, Guo P, Zhang H, Singer RH, Rossoll W, Bassell GJ.

Dev Neurobiol. 2014 Mar;74(3):319-32. doi: 10.1002/dneu.22111. Epub 2013 Oct 4.

6.

Interaction of survival of motor neuron (SMN) and HuD proteins with mRNA cpg15 rescues motor neuron axonal deficits.

Akten B, Kye MJ, Hao le T, Wertz MH, Singh S, Nie D, Huang J, Merianda TT, Twiss JL, Beattie CE, Steen JA, Sahin M.

Proc Natl Acad Sci U S A. 2011 Jun 21;108(25):10337-42. doi: 10.1073/pnas.1104928108. Epub 2011 Jun 7.

7.

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
8.

Temporal requirement for SMN in motoneuron development.

Hao le T, Duy PQ, Jontes JD, Wolman M, Granato M, Beattie CE.

Hum Mol Genet. 2013 Jul 1;22(13):2612-25. doi: 10.1093/hmg/ddt110. Epub 2013 Mar 3.

9.

Motoneuron development influences dorsal root ganglia survival and Schwann cell development in a vertebrate model of spinal muscular atrophy.

Hao le T, Duy PQ, Jontes JD, Beattie CE.

Hum Mol Genet. 2015 Jan 15;24(2):346-60. doi: 10.1093/hmg/ddu447. Epub 2014 Sep 1.

10.

Spinal muscular atrophy: why do low levels of survival motor neuron protein make motor neurons sick?

Burghes AH, Beattie CE.

Nat Rev Neurosci. 2009 Aug;10(8):597-609. doi: 10.1038/nrn2670. Epub 2009 Jul 8. Review.

11.

Zebrafish survival motor neuron mutants exhibit presynaptic neuromuscular junction defects.

Boon KL, Xiao S, McWhorter ML, Donn T, Wolf-Saxon E, Bohnsack MT, Moens CB, Beattie CE.

Hum Mol Genet. 2009 Oct 1;18(19):3615-25. doi: 10.1093/hmg/ddp310. Epub 2009 Jul 10.

12.

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
13.

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, Kröning AK, Karle K, Monani UR, Sendtner M.

J Cell Biol. 2003 Nov 24;163(4):801-12. Epub 2003 Nov 17.

14.

Survival motor neuron protein in motor neurons determines synaptic integrity in spinal muscular atrophy.

Martinez TL, Kong L, Wang X, Osborne MA, Crowder ME, Van Meerbeke JP, Xu X, Davis C, Wooley J, Goldhamer DJ, Lutz CM, Rich MM, Sumner CJ.

J Neurosci. 2012 Jun 20;32(25):8703-15. doi: 10.1523/JNEUROSCI.0204-12.2012.

15.

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.

16.

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.

J Cell Biol. 2003 Sep 1;162(5):919-31.

17.

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
18.

Restoration of SMN to Emx-1 expressing cortical neurons is not sufficient to provide benefit to a severe mouse model of Spinal Muscular Atrophy.

Taylor AS, Glascock JJ, Rose FF Jr, Lutz C, Lorson CL.

Transgenic Res. 2013 Oct;22(5):1029-36. doi: 10.1007/s11248-013-9702-y. Epub 2013 Mar 20.

19.

Therapeutics development for spinal muscular atrophy.

Sumner CJ.

NeuroRx. 2006 Apr;3(2):235-45. Review.

20.

ALS-associated mutations in FUS disrupt the axonal distribution and function of SMN.

Groen EJ, Fumoto K, Blokhuis AM, Engelen-Lee J, Zhou Y, van den Heuvel DM, Koppers M, van Diggelen F, van Heest J, Demmers JA, Kirby J, Shaw PJ, Aronica E, Spliet WG, Veldink JH, van den Berg LH, Pasterkamp RJ.

Hum Mol Genet. 2013 Sep 15;22(18):3690-704. doi: 10.1093/hmg/ddt222. Epub 2013 May 15.

PMID:
23681068

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