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Items: 1 to 20 of 30

1.

Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia.

Deng HX, Chen W, Hong ST, Boycott KM, Gorrie GH, Siddique N, Yang Y, Fecto F, Shi Y, Zhai H, Jiang H, Hirano M, Rampersaud E, Jansen GH, Donkervoort S, Bigio EH, Brooks BR, Ajroud K, Sufit RL, Haines JL, Mugnaini E, Pericak-Vance MA, Siddique T.

Nature. 2011 Aug 21;477(7363):211-5. doi: 10.1038/nature10353.

2.

Ubiquilin 2: a component of the ubiquitin-proteasome system with an emerging role in neurodegeneration.

Zhang KY, Yang S, Warraich ST, Blair IP.

Int J Biochem Cell Biol. 2014 May;50:123-6. doi: 10.1016/j.biocel.2014.02.018. Epub 2014 Feb 28. Review.

PMID:
24589709
3.

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
4.

Molecular basis of amyotrophic lateral sclerosis.

Liscic RM, Breljak D.

Prog Neuropsychopharmacol Biol Psychiatry. 2011 Mar 30;35(2):370-2. doi: 10.1016/j.pnpbp.2010.07.017. Epub 2010 Jul 23. Review.

PMID:
20655970
5.

The neuropathology of FTD associated With ALS.

Mackenzie IR.

Alzheimer Dis Assoc Disord. 2007 Oct-Dec;21(4):S44-9. Review.

PMID:
18090423
6.

State of play in amyotrophic lateral sclerosis genetics.

Renton AE, Chiò A, Traynor BJ.

Nat Neurosci. 2014 Jan;17(1):17-23. doi: 10.1038/nn.3584. Epub 2013 Dec 26. Review.

7.

Sporadic and hereditary amyotrophic lateral sclerosis (ALS).

Ajroud-Driss S, Siddique T.

Biochim Biophys Acta. 2015 Apr;1852(4):679-84. doi: 10.1016/j.bbadis.2014.08.010. Epub 2014 Sep 1. Review.

8.

Recent advances in the genetics of the ALS-FTLD complex.

Morris HR, Waite AJ, Williams NM, Neal JW, Blake DJ.

Curr Neurol Neurosci Rep. 2012 Jun;12(3):243-50. doi: 10.1007/s11910-012-0268-5. Review.

PMID:
22477152
9.

Mutations in TDP-43 link glycine-rich domain functions to amyotrophic lateral sclerosis.

Pesiridis GS, Lee VM, Trojanowski JQ.

Hum Mol Genet. 2009 Oct 15;18(R2):R156-62. doi: 10.1093/hmg/ddp303. Review.

10.

ALS and FTLD: two faces of TDP-43 proteinopathy.

Liscic RM, Grinberg LT, Zidar J, Gitcho MA, Cairns NJ.

Eur J Neurol. 2008 Aug;15(8):772-80. doi: 10.1111/j.1468-1331.2008.02195.x. Review.

11.

Neuronal death in amyotrophic lateral sclerosis (ALS): what can we learn from genetics?

Sreedharan J.

CNS Neurol Disord Drug Targets. 2010 Jul;9(3):259-67. Review.

PMID:
20406185
12.

[Gene mutations in familial amyotrophic lateral sclerosis].

Oda M, Izumi Y, Kaji R.

Brain Nerve. 2011 Feb;63(2):165-70. Review. Japanese.

PMID:
21301041
13.
14.

Converging mechanisms in ALS and FTD: disrupted RNA and protein homeostasis.

Ling SC, Polymenidou M, Cleveland DW.

Neuron. 2013 Aug 7;79(3):416-38. doi: 10.1016/j.neuron.2013.07.033. Review.

15.

Protein aggregation in amyotrophic lateral sclerosis.

Blokhuis AM, Groen EJ, Koppers M, van den Berg LH, Pasterkamp RJ.

Acta Neuropathol. 2013 Jun;125(6):777-94. doi: 10.1007/s00401-013-1125-6. Epub 2013 May 15. Review.

16.

Gene and protein therapies utilizing VEGF for ALS.

Keifer OP Jr, O'Connor DM, Boulis NM.

Pharmacol Ther. 2014 Mar;141(3):261-71. doi: 10.1016/j.pharmthera.2013.10.009. Epub 2013 Oct 29. Review.

17.

Impaired protein degradation in FTLD and related disorders.

Götzl JK, Lang CM, Haass C, Capell A.

Ageing Res Rev. 2016 Dec;32:122-139. doi: 10.1016/j.arr.2016.04.008. Epub 2016 May 7. Review.

PMID:
27166223
18.

Linking RNA Dysfunction and Neurodegeneration in Amyotrophic Lateral Sclerosis.

Barmada SJ.

Neurotherapeutics. 2015 Apr;12(2):340-51. doi: 10.1007/s13311-015-0340-3. Review.

19.

Amyotrophic Lateral Sclerosis Pathogenesis Converges on Defects in Protein Homeostasis Associated with TDP-43 Mislocalization and Proteasome-Mediated Degradation Overload.

Lin G, Mao D, Bellen HJ.

Curr Top Dev Biol. 2017;121:111-171. doi: 10.1016/bs.ctdb.2016.07.004. Epub 2016 Aug 13. Review.

PMID:
28057298
20.

Amyotrophic lateral sclerosis: an update on recent genetic insights.

Iguchi Y, Katsuno M, Ikenaka K, Ishigaki S, Sobue G.

J Neurol. 2013 Nov;260(11):2917-27. doi: 10.1007/s00415-013-7112-y. Epub 2013 Oct 2. Review.

PMID:
24085347

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