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Items: 1 to 20 of 110

1.

RNA dysfunction and aggrephagy at the centre of an amyotrophic lateral sclerosis/frontotemporal dementia disease continuum.

Thomas M, Alegre-Abarrategui J, Wade-Martins R.

Brain. 2013 May;136(Pt 5):1345-60. doi: 10.1093/brain/awt030. Epub 2013 Mar 9. Review.

2.

The clinical and pathological phenotype of C9ORF72 hexanucleotide repeat expansions.

Simón-Sánchez J, Dopper EG, Cohn-Hokke PE, Hukema RK, Nicolaou N, Seelaar H, de Graaf JR, de Koning I, van Schoor NM, Deeg DJ, Smits M, Raaphorst J, van den Berg LH, Schelhaas HJ, De Die-Smulders CE, Majoor-Krakauer D, Rozemuller AJ, Willemsen R, Pijnenburg YA, Heutink P, van Swieten JC.

Brain. 2012 Mar;135(Pt 3):723-35. doi: 10.1093/brain/awr353. Epub 2012 Feb 1.

3.

How do the RNA-binding proteins TDP-43 and FUS relate to amyotrophic lateral sclerosis and frontotemporal degeneration, and to each other?

Baloh RH.

Curr Opin Neurol. 2012 Dec;25(6):701-7. doi: 10.1097/WCO.0b013e32835a269b. Review.

PMID:
23041957
4.

TDP-43 and FUS in amyotrophic lateral sclerosis and frontotemporal dementia.

Mackenzie IR, Rademakers R, Neumann M.

Lancet Neurol. 2010 Oct;9(10):995-1007. doi: 10.1016/S1474-4422(10)70195-2. Review.

PMID:
20864052
5.

C9orf72 amyotrophic lateral sclerosis and frontotemporal dementia: gain or loss of function?

Mizielinska S, Isaacs AM.

Curr Opin Neurol. 2014 Oct;27(5):515-23. doi: 10.1097/WCO.0000000000000130. Review.

6.

Making connections: pathology and genetics link amyotrophic lateral sclerosis with frontotemporal lobe dementia.

Fecto F, Siddique T.

J Mol Neurosci. 2011 Nov;45(3):663-75. doi: 10.1007/s12031-011-9637-9. Epub 2011 Sep 7. Review.

PMID:
21901496
7.

TAR DNA binding protein-43 and fused in sarcoma/translocated in liposarcoma protein in two neurodegenerative diseases.

Wang XN, Cui LY.

Zhongguo Yi Xue Ke Xue Yuan Xue Bao. 2012 Jun;34(3):286-92. doi: 10.3881/j.issn.1000-503X.2012.03.020. Review.

8.

C9orf72 hexanucleotide repeat associated with amyotrophic lateral sclerosis and frontotemporal dementia forms RNA G-quadruplexes.

Fratta P, Mizielinska S, Nicoll AJ, Zloh M, Fisher EM, Parkinson G, Isaacs AM.

Sci Rep. 2012;2:1016. doi: 10.1038/srep01016. Epub 2012 Dec 21.

9.

The ALS-associated proteins FUS and TDP-43 function together to affect Drosophila locomotion and life span.

Wang JW, Brent JR, Tomlinson A, Shneider NA, McCabe BD.

J Clin Invest. 2011 Oct;121(10):4118-26. doi: 10.1172/JCI57883. Epub 2011 Sep 1.

10.

Modeling key pathological features of frontotemporal dementia with C9ORF72 repeat expansion in iPSC-derived human neurons.

Almeida S, Gascon E, Tran H, Chou HJ, Gendron TF, Degroot S, Tapper AR, Sellier C, Charlet-Berguerand N, Karydas A, Seeley WW, Boxer AL, Petrucelli L, Miller BL, Gao FB.

Acta Neuropathol. 2013 Sep;126(3):385-99. doi: 10.1007/s00401-013-1149-y. Epub 2013 Jul 9. Erratum in: Acta Neuropathol. 2014 Jun;127(6):941.

11.

Interaction of amyotrophic lateral sclerosis/frontotemporal lobar degeneration-associated fused-in-sarcoma with proteins involved in metabolic and protein degradation pathways.

Wang T, Jiang X, Chen G, Xu J.

Neurobiol Aging. 2015 Jan;36(1):527-35. doi: 10.1016/j.neurobiolaging.2014.07.044. Epub 2014 Aug 4.

PMID:
25192599
12.

C9ORF72, implicated in amytrophic lateral sclerosis and frontotemporal dementia, regulates endosomal trafficking.

Farg MA, Sundaramoorthy V, Sultana JM, Yang S, Atkinson RA, Levina V, Halloran MA, Gleeson PA, Blair IP, Soo KY, King AE, Atkin JD.

Hum Mol Genet. 2014 Jul 1;23(13):3579-95. doi: 10.1093/hmg/ddu068. Epub 2014 Feb 18.

13.

The disease-associated r(GGGGCC)n repeat from the C9orf72 gene forms tract length-dependent uni- and multimolecular RNA G-quadruplex structures.

Reddy K, Zamiri B, Stanley SY, Macgregor RB Jr, Pearson CE.

J Biol Chem. 2013 Apr 5;288(14):9860-6. doi: 10.1074/jbc.C113.452532. Epub 2013 Feb 19.

14.

TDP-43 and FUS/TLS: cellular functions and implications for neurodegeneration.

Fiesel FC, Kahle PJ.

FEBS J. 2011 Oct;278(19):3550-68. doi: 10.1111/j.1742-4658.2011.08258.x. Epub 2011 Aug 24. Review.

15.

UBQLN2/P62 cellular recycling pathways in amyotrophic lateral sclerosis and frontotemporal dementia.

Fecto F, Siddique T.

Muscle Nerve. 2012 Feb;45(2):157-62. doi: 10.1002/mus.23278.

PMID:
22246868
16.
17.

Pathological hallmarks of amyotrophic lateral sclerosis/frontotemporal lobar degeneration in transgenic mice produced with TDP-43 genomic fragments.

Swarup V, Phaneuf D, Bareil C, Robertson J, Rouleau GA, Kriz J, Julien JP.

Brain. 2011 Sep;134(Pt 9):2610-26. doi: 10.1093/brain/awr159. Epub 2011 Jul 13.

18.

UBQLN2/ubiquilin 2 mutation and pathology in familial amyotrophic lateral sclerosis.

Williams KL, Warraich ST, Yang S, Solski JA, Fernando R, Rouleau GA, Nicholson GA, Blair IP.

Neurobiol Aging. 2012 Oct;33(10):2527.e3-10. doi: 10.1016/j.neurobiolaging.2012.05.008. Epub 2012 Jun 19.

PMID:
22717235
19.

Stress signaling from the endoplasmic reticulum: A central player in the pathogenesis of amyotrophic lateral sclerosis.

Walker AK, Atkin JD.

IUBMB Life. 2011 Sep;63(9):754-63. doi: 10.1002/iub.520. Epub 2011 Aug 10. Review.

20.

FET proteins in frontotemporal dementia and amyotrophic lateral sclerosis.

Mackenzie IR, Neumann M.

Brain Res. 2012 Jun 26;1462:40-3. doi: 10.1016/j.brainres.2011.12.010. Epub 2011 Dec 13. Review.

PMID:
22261247
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