Similar articles for PMID: 21816949

Year	Number of Results
1994	1
1995	1
1998	3
2000	2
2001	6
2002	7
2003	3
2004	1
2005	4
2006	11
2007	6
2008	4
2009	3
2010	2
2011	7
2012	11
2013	8
2014	6
2015	6
2016	11
2017	4
2018	2
2019	2
2020	4
2021	2
2022	2
2023	2
2024	0

1

The in vivo contribution of motor neuron TrkB receptors to mutant SOD1 motor neuron disease.

Zhai J, Zhou W, Li J, Hayworth CR, Zhang L, Misawa H, Klein R, Scherer SS, Balice-Gordon RJ, Kalb RG. Zhai J, et al. Hum Mol Genet. 2011 Nov 1;20(21):4116-31. doi: 10.1093/hmg/ddr335. Epub 2011 Aug 4. Hum Mol Genet. 2011. PMID: 21816949 Free PMC article.

2

Spinal inhibitory interneuron pathology follows motor neuron degeneration independent of glial mutant superoxide dismutase 1 expression in SOD1-ALS mice.

Hossaini M, Cardona Cano S, van Dis V, Haasdijk ED, Hoogenraad CC, Holstege JC, Jaarsma D. Hossaini M, et al. J Neuropathol Exp Neurol. 2011 Aug;70(8):662-77. doi: 10.1097/NEN.0b013e31822581ac. J Neuropathol Exp Neurol. 2011. PMID: 21760539

3

Neuroprotective effects of the Sigma-1 receptor (S1R) agonist PRE-084, in a mouse model of motor neuron disease not linked to SOD1 mutation.

Peviani M, Salvaneschi E, Bontempi L, Petese A, Manzo A, Rossi D, Salmona M, Collina S, Bigini P, Curti D. Peviani M, et al. Neurobiol Dis. 2014 Feb;62:218-32. doi: 10.1016/j.nbd.2013.10.010. Epub 2013 Oct 16. Neurobiol Dis. 2014. PMID: 24141020

4

Altered terminal Schwann cell morphology precedes denervation in SOD1 mice.

Carrasco DI, Seburn KL, Pinter MJ. Carrasco DI, et al. Exp Neurol. 2016 Jan;275 Pt 1(0 1):172-81. doi: 10.1016/j.expneurol.2015.09.014. Epub 2015 Sep 26. Exp Neurol. 2016. PMID: 26416261 Free PMC article.

5

Motor terminal degeneration unaffected by activity changes in SOD1(G93A) mice; a possible role for glycolysis.

Carrasco DI, Bichler EK, Rich MM, Wang X, Seburn KL, Pinter MJ. Carrasco DI, et al. Neurobiol Dis. 2012 Oct;48(1):132-40. doi: 10.1016/j.nbd.2012.06.017. Epub 2012 Jun 29. Neurobiol Dis. 2012. PMID: 22750521 Free PMC article.

6

Mutant SOD1 causes motor neuron disease independent of copper chaperone-mediated copper loading.

Subramaniam JR, Lyons WE, Liu J, Bartnikas TB, Rothstein J, Price DL, Cleveland DW, Gitlin JD, Wong PC. Subramaniam JR, et al. Nat Neurosci. 2002 Apr;5(4):301-7. doi: 10.1038/nn823. Nat Neurosci. 2002. PMID: 11889469

7

Coincident thresholds of mutant protein for paralytic disease and protein aggregation caused by restrictively expressed superoxide dismutase cDNA.

Wang J, Xu G, Slunt HH, Gonzales V, Coonfield M, Fromholt D, Copeland NG, Jenkins NA, Borchelt DR. Wang J, et al. Neurobiol Dis. 2005 Dec;20(3):943-52. doi: 10.1016/j.nbd.2005.06.005. Epub 2005 Jul 19. Neurobiol Dis. 2005. PMID: 16046140

8

Overview of Impaired BDNF Signaling, Their Coupled Downstream Serine-Threonine Kinases and SNARE/SM Complex in the Neuromuscular Junction of the Amyotrophic Lateral Sclerosis Model SOD1-G93A Mice.

Just-Borràs L, Hurtado E, Cilleros-Mañé V, Biondi O, Charbonnier F, Tomàs M, Garcia N, Lanuza MA, Tomàs J. Just-Borràs L, et al. Mol Neurobiol. 2019 Oct;56(10):6856-6872. doi: 10.1007/s12035-019-1550-1. Epub 2019 Mar 30. Mol Neurobiol. 2019. PMID: 30929165

9

Neuregulin 1 confers neuroprotection in SOD1-linked amyotrophic lateral sclerosis mice via restoration of C-boutons of spinal motor neurons.

Lasiene J, Komine O, Fujimori-Tonou N, Powers B, Endo F, Watanabe S, Shijie J, Ravits J, Horner P, Misawa H, Yamanaka K. Lasiene J, et al. Acta Neuropathol Commun. 2016 Feb 18;4:15. doi: 10.1186/s40478-016-0286-7. Acta Neuropathol Commun. 2016. PMID: 26891847 Free PMC article.

10

Amyloid precursor protein (APP) contributes to pathology in the SOD1(G93A) mouse model of amyotrophic lateral sclerosis.

Bryson JB, Hobbs C, Parsons MJ, Bosch KD, Pandraud A, Walsh FS, Doherty P, Greensmith L. Bryson JB, et al. Hum Mol Genet. 2012 Sep 1;21(17):3871-82. doi: 10.1093/hmg/dds215. Epub 2012 Jun 7. Hum Mol Genet. 2012. PMID: 22678056

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