Similar articles for PMID: 31927482

Year	Number of Results
1998	1
2000	4
2002	1
2003	3
2005	3
2006	2
2007	2
2008	4
2009	1
2010	3
2011	5
2012	2
2013	2
2014	2
2015	1
2016	7
2017	9
2018	7
2019	5
2020	4
2024	0

1

Splicing Defects of the Profilin Gene Alter Actin Dynamics in an S. pombe SMN Mutant.

Antoine M, Patrick KL, Soret J, Duc P, Rage F, Cacciottolo R, Nissen KE, Cauchi RJ, Krogan NJ, Guthrie C, Gachet Y, Bordonné R. Antoine M, et al. iScience. 2020 Jan 24;23(1):100809. doi: 10.1016/j.isci.2019.100809. Epub 2019 Dec 28. iScience. 2020. PMID: 31927482 Free PMC article.

2

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. Sharma A, et al. Exp Cell Res. 2005 Sep 10;309(1):185-97. doi: 10.1016/j.yexcr.2005.05.014. Exp Cell Res. 2005. PMID: 15975577

3

CHP1 reduction ameliorates spinal muscular atrophy pathology by restoring calcineurin activity and endocytosis.

Janzen E, Mendoza-Ferreira N, Hosseinibarkooie S, Schneider S, Hupperich K, Tschanz T, Grysko V, Riessland M, Hammerschmidt M, Rigo F, Bennett CF, Kye MJ, Torres-Benito L, Wirth B. Janzen E, et al. Brain. 2018 Aug 1;141(8):2343-2361. doi: 10.1093/brain/awy167. Brain. 2018. PMID: 29961886 Free PMC article.

4

SMN deficiency attenuates migration of U87MG astroglioma cells through the activation of RhoA.

Caraballo-Miralles V, Cardona-Rossinyol A, Garcera A, Villalonga P, Soler RM, Olmos G, Lladó J. Caraballo-Miralles V, et al. Mol Cell Neurosci. 2012 Mar;49(3):282-9. doi: 10.1016/j.mcn.2011.12.003. Epub 2011 Dec 16. Mol Cell Neurosci. 2012. PMID: 22197680

5

Characterization of the Schizosaccharomyces pombe orthologue of the human survival motor neuron (SMN) protein.

Owen N, Doe CL, Mellor J, Davies KE. Owen N, et al. Hum Mol Genet. 2000 Mar 22;9(5):675-84. doi: 10.1093/hmg/9.5.675. Hum Mol Genet. 2000. PMID: 10749974

6

Spinal Muscular Atrophy: From Defective Chaperoning of snRNP Assembly to Neuromuscular Dysfunction.

Lanfranco M, Vassallo N, Cauchi RJ. Lanfranco M, et al. Front Mol Biosci. 2017 Jun 8;4:41. doi: 10.3389/fmolb.2017.00041. eCollection 2017. Front Mol Biosci. 2017. PMID: 28642865 Free PMC article. Review.

7

The Actin Cytoskeleton in SMA and ALS: How Does It Contribute to Motoneuron Degeneration?

Hensel N, Claus P. Hensel N, et al. Neuroscientist. 2018 Feb;24(1):54-72. doi: 10.1177/1073858417705059. Epub 2017 May 1. Neuroscientist. 2018. PMID: 28459188 Review.

8

Functional interaction between FUS and SMN underlies SMA-like splicing changes in wild-type hFUS mice.

Mirra A, Rossi S, Scaricamazza S, Di Salvio M, Salvatori I, Valle C, Rusmini P, Poletti A, Cestra G, Carrì MT, Cozzolino M. Mirra A, et al. Sci Rep. 2017 May 17;7(1):2033. doi: 10.1038/s41598-017-02195-0. Sci Rep. 2017. PMID: 28515487 Free PMC article.

9

The spinal muscular atrophy disease protein SMN is linked to the Rho-kinase pathway via profilin.

Nölle A, Zeug A, van Bergeijk J, Tönges L, Gerhard R, Brinkmann H, Al Rayes S, Hensel N, Schill Y, Apkhazava D, Jablonka S, O'mer J, Srivastav RK, Baasner A, Lingor P, Wirth B, Ponimaskin E, Niedenthal R, Grothe C, Claus P. Nölle A, et al. Hum Mol Genet. 2011 Dec 15;20(24):4865-78. doi: 10.1093/hmg/ddr425. Epub 2011 Sep 14. Hum Mol Genet. 2011. PMID: 21920940

10

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. See K, et al. Hum Mol Genet. 2014 Apr 1;23(7):1754-70. doi: 10.1093/hmg/ddt567. Epub 2013 Nov 11. Hum Mol Genet. 2014. PMID: 24218366

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