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Spinal muscular atrophy: the role of SMN in axonal mRNA regulation.

Fallini C, Bassell GJ, Rossoll W.

Brain Res. 2012 Jun 26;1462:81-92. doi: 10.1016/j.brainres.2012.01.044. Epub 2012 Jan 28. Review.


Spinal muscular atrophy and a model for survival of motor neuron protein function in axonal ribonucleoprotein complexes.

Rossoll W, Bassell GJ.

Results Probl Cell Differ. 2009;48:289-326. doi: 10.1007/400_2009_4.


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.


Deficiency of the Survival of Motor Neuron Protein Impairs mRNA Localization and Local Translation in the Growth Cone of Motor Neurons.

Fallini C, Donlin-Asp PG, Rouanet JP, Bassell GJ, Rossoll W.

J Neurosci. 2016 Mar 30;36(13):3811-20. doi: 10.1523/JNEUROSCI.2396-15.2016.


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.


Splicing changes in SMA mouse motoneurons and SMN-depleted neuroblastoma cells: evidence for involvement of splicing regulatory proteins.

Huo Q, Kayikci M, Odermatt P, Meyer K, Michels O, Saxena S, Ule J, Schümperli D.

RNA Biol. 2014;11(11):1430-46. doi: 10.1080/15476286.2014.996494.


Spliceosomal small nuclear ribonucleoprotein biogenesis defects and motor neuron selectivity in spinal muscular atrophy.

Workman E, Kolb SJ, Battle DJ.

Brain Res. 2012 Jun 26;1462:93-9. doi: 10.1016/j.brainres.2012.02.051. Epub 2012 Feb 28. Review.


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.


SMN deficiency alters Nrxn2 expression and splicing in zebrafish and mouse models of spinal muscular atrophy.

See K, Yadav P, Giegerich M, Cheong PS, Graf M, Vyas H, Lee SG, Mathavan S, Fischer U, Sendtner M, Winkler C.

Hum Mol Genet. 2014 Apr 1;23(7):1754-70. doi: 10.1093/hmg/ddt567. Epub 2013 Nov 11.


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.

PLoS One. 2007 Sep 26;2(9):e921.


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.


SMN and Gemins: 'we are family' … or are we?: insights into the partnership between Gemins and the spinal muscular atrophy disease protein SMN.

Cauchi RJ.

Bioessays. 2010 Dec;32(12):1077-89. doi: 10.1002/bies.201000088. Epub 2010 Oct 15. Review.


A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy.

Ruggiu M, McGovern VL, Lotti F, Saieva L, Li DK, Kariya S, Monani UR, Burghes AH, Pellizzoni L.

Mol Cell Biol. 2012 Jan;32(1):126-38. doi: 10.1128/MCB.06077-11. Epub 2011 Oct 28.


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.


Spinal muscular atrophy: the RNP connection.

Eggert C, Chari A, Laggerbauer B, Fischer U.

Trends Mol Med. 2006 Mar;12(3):113-21. Epub 2006 Feb 13.


Molecular and functional analysis of intragenic SMN1 mutations in patients with spinal muscular atrophy.

Sun Y, Grimmler M, Schwarzer V, Schoenen F, Fischer U, Wirth B.

Hum Mutat. 2005 Jan;25(1):64-71.


Molecular and cellular basis of spinal muscular atrophy.

Jablonka S, Sendtner M.

Amyotroph Lateral Scler Other Motor Neuron Disord. 2003 Sep;4(3):144-9. Review.


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.


The survival of motor neuron (SMN) protein interacts with the mRNA-binding protein HuD and regulates localization of poly(A) mRNA in primary motor neuron axons.

Fallini C, Zhang H, Su Y, Silani V, Singer RH, Rossoll W, Bassell GJ.

J Neurosci. 2011 Mar 9;31(10):3914-25. doi: 10.1523/JNEUROSCI.3631-10.2011.


SMNDelta7, the major product of the centromeric survival motor neuron (SMN2) gene, extends survival in mice with spinal muscular atrophy and associates with full-length SMN.

Le TT, Pham LT, Butchbach ME, Zhang HL, Monani UR, Coovert DD, Gavrilina TO, Xing L, Bassell GJ, Burghes AH.

Hum Mol Genet. 2005 Mar 15;14(6):845-57. Epub 2005 Feb 9.


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