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Similar articles for PubMed (Select 23063131)


An SMN-dependent U12 splicing event essential for motor circuit function.

Lotti F, Imlach WL, Saieva L, Beck ES, Hao le T, Li DK, Jiao W, Mentis GZ, Beattie CE, McCabe BD, Pellizzoni L.

Cell. 2012 Oct 12;151(2):440-54. doi: 10.1016/j.cell.2012.09.012.


Developmental arrest of Drosophila survival motor neuron (Smn) mutants accounts for differences in expression of minor intron-containing genes.

Garcia EL, Lu Z, Meers MP, Praveen K, Matera AG.

RNA. 2013 Nov;19(11):1510-6. doi: 10.1261/rna.038919.113. Epub 2013 Sep 4.


SMN is required for sensory-motor circuit function in Drosophila.

Imlach WL, Beck ES, Choi BJ, Lotti F, Pellizzoni L, McCabe BD.

Cell. 2012 Oct 12;151(2):427-39. doi: 10.1016/j.cell.2012.09.011.


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.

Cell Rep. 2012 Jun 28;1(6):624-31. doi: 10.1016/j.celrep.2012.05.014. Epub 2012 Jun 21.


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.

Cell. 2008 May 16;133(4):585-600. doi: 10.1016/j.cell.2008.03.031.


The spinal muscular atrophy protein SMN affects Drosophila germline nuclear organization through the U body-P body pathway.

Lee L, Davies SE, Liu JL.

Dev Biol. 2009 Aug 1;332(1):142-55. doi: 10.1016/j.ydbio.2009.05.553. Epub 2009 May 21.


Modeling spinal muscular atrophy in Drosophila links Smn to FGF signaling.

Sen A, Yokokura T, Kankel MW, Dimlich DN, Manent J, Sanyal S, Artavanis-Tsakonas S.

J Cell Biol. 2011 Feb 7;192(3):481-95. doi: 10.1083/jcb.201004016.


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.

J Cell Biol. 2007 Mar 12;176(6):831-41.


Neuromuscular defects in a Drosophila survival motor neuron gene mutant.

Chan YB, Miguel-Aliaga I, Franks C, Thomas N, Trülzsch B, Sattelle DB, Davies KE, van den Heuvel M.

Hum Mol Genet. 2003 Jun 15;12(12):1367-76.


The SMN binding protein Gemin2 is not involved in motor axon outgrowth.

McWhorter ML, Boon KL, Horan ES, Burghes AH, Beattie CE.

Dev Neurobiol. 2008 Feb 1;68(2):182-94.


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.


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.


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.


Delivery of bifunctional RNAs that target an intronic repressor and increase SMN levels in an animal model of spinal muscular atrophy.

Baughan TD, Dickson A, Osman EY, Lorson CL.

Hum Mol Genet. 2009 May 1;18(9):1600-11. doi: 10.1093/hmg/ddp076. Epub 2009 Feb 19.


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.


Optimization of SMN trans-splicing through the analysis of SMN introns.

Shababi M, Lorson CL.

J Mol Neurosci. 2012 Mar;46(3):459-69. doi: 10.1007/s12031-011-9614-3. Epub 2011 Aug 9.


Restoration of SMN function: delivery of a trans-splicing RNA re-directs SMN2 pre-mRNA splicing.

Coady TH, Shababi M, Tullis GE, Lorson CL.

Mol Ther. 2007 Aug;15(8):1471-8. Epub 2007 Jun 5.


Neurodevelopmental consequences of Smn depletion in a mouse model of spinal muscular atrophy.

Liu H, Shafey D, Moores JN, Kothary R.

J Neurosci Res. 2010 Jan;88(1):111-22. doi: 10.1002/jnr.22189.


The Gemin associates of survival motor neuron are required for motor function in Drosophila.

Borg R, Cauchi RJ.

PLoS One. 2013 Dec 31;8(12):e83878. doi: 10.1371/journal.pone.0083878. eCollection 2013.


Behavioral and electrophysiological outcomes of tissue-specific Smn knockdown in Drosophila melanogaster.

Timmerman C, Sanyal S.

Brain Res. 2012 Dec 13;1489:66-80. doi: 10.1016/j.brainres.2012.10.035. Epub 2012 Oct 26.

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