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Items: 1 to 20 of 152

1.

Molecular biology of amyotrophic lateral sclerosis: insights from genetics.

Pasinelli P, Brown RH.

Nat Rev Neurosci. 2006 Sep;7(9):710-23. Review.

PMID:
16924260
2.

Determinants of rapid disease progression in ALS.

Yamanaka K, Cleveland DW.

Neurology. 2005 Dec 27;65(12):1859-60. No abstract available.

PMID:
16380607
3.

Rodent Models of Amyotrophic Lateral Sclerosis.

Philips T, Rothstein JD.

Curr Protoc Pharmacol. 2015 Jun 1;69:5.67.1-21. doi: 10.1002/0471141755.ph0567s69. Review.

4.

Fas(t) balls and Lou Gehrig disease. A clue to selective vulnerability of motor neurons?

Xiong ZQ, McNamara JO.

Neuron. 2002 Sep 12;35(6):1011-3. Review.

5.

Mitochondrial involvement in amyotrophic lateral sclerosis: trigger or target?

Bacman SR, Bradley WG, Moraes CT.

Mol Neurobiol. 2006 Apr;33(2):113-31. Review.

PMID:
16603792
6.

Cdk5 sinks into ALS.

Patzke H, Tsai LH.

Trends Neurosci. 2002 Jan;25(1):8-10. Review.

PMID:
11801324
7.

Rapid disease progression correlates with instability of mutant SOD1 in familial ALS.

Sato T, Nakanishi T, Yamamoto Y, Andersen PM, Ogawa Y, Fukada K, Zhou Z, Aoike F, Sugai F, Nagano S, Hirata S, Ogawa M, Nakano R, Ohi T, Kato T, Nakagawa M, Hamasaki T, Shimizu A, Sakoda S.

Neurology. 2005 Dec 27;65(12):1954-7. Epub 2005 Nov 16.

PMID:
16291929
8.

Amyotrophic lateral sclerosis: pathogenesis.

Brown RH Jr, Robberecht W.

Semin Neurol. 2001 Jun;21(2):131-9. Review.

PMID:
11442322
9.

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.

Neurobiol Dis. 2005 Dec;20(3):943-52. Epub 2005 Jul 19.

PMID:
16046140
10.

Pathophysiology of neurodegeneration in familial amyotrophic lateral sclerosis.

Vucic S, Kiernan MC.

Curr Mol Med. 2009 Apr;9(3):255-72. Review.

PMID:
19355908
11.

Superoxide dismutase: the cause of all amyotrophic lateral sclerosis?

Matias-Guiu J, Galan L, Garcia-Ramos R, Barcia JA.

Ann Neurol. 2008 Sep;64(3):356-7; author reply 358. doi: 10.1002/ana.21373. No abstract available.

PMID:
18350588
12.

Increased autophagy in transgenic mice with a G93A mutant SOD1 gene.

Morimoto N, Nagai M, Ohta Y, Miyazaki K, Kurata T, Morimoto M, Murakami T, Takehisa Y, Ikeda Y, Kamiya T, Abe K.

Brain Res. 2007 Sep 5;1167:112-7. Epub 2007 Jul 7.

PMID:
17689501
13.

Familial Amyotrophic Lateral Sclerosis.

Boylan K.

Neurol Clin. 2015 Nov;33(4):807-30. doi: 10.1016/j.ncl.2015.07.001. Epub 2015 Sep 8. Review.

14.

Mutant SOD1-induced neuronal toxicity is mediated by increased mitochondrial superoxide levels.

Zimmerman MC, Oberley LW, Flanagan SW.

J Neurochem. 2007 Aug;102(3):609-18. Epub 2007 Mar 23.

15.
16.

SMN genotypes producing less SMN protein increase susceptibility to and severity of sporadic ALS.

Veldink JH, Kalmijn S, Van der Hout AH, Lemmink HH, Groeneveld GJ, Lummen C, Scheffer H, Wokke JH, Van den Berg LH.

Neurology. 2005 Sep 27;65(6):820-5. Epub 2005 Aug 10.

PMID:
16093455
17.

Histological evidence of protein aggregation in mutant SOD1 transgenic mice and in amyotrophic lateral sclerosis neural tissues.

Watanabe M, Dykes-Hoberg M, Culotta VC, Price DL, Wong PC, Rothstein JD.

Neurobiol Dis. 2001 Dec;8(6):933-41.

PMID:
11741389
18.

Motor neuron disease: The curious ways of ALS.

Polymenidou M, Cleveland DW.

Nature. 2008 Jul 17;454(7202):284-5. doi: 10.1038/454284a. No abstract available.

19.

Mechanisms for neuronal degeneration in amyotrophic lateral sclerosis and in models of motor neuron death (Review).

Martin LJ, Price AC, Kaiser A, Shaikh AY, Liu Z.

Int J Mol Med. 2000 Jan;5(1):3-13. Review.

PMID:
10601567
20.

Mitochondrial dysfunction in amyotrophic lateral sclerosis.

Shi P, Gal J, Kwinter DM, Liu X, Zhu H.

Biochim Biophys Acta. 2010 Jan;1802(1):45-51. doi: 10.1016/j.bbadis.2009.08.012. Epub 2009 Aug 26. Review.

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