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Items: 1 to 20 of 104

1.

Polymorphisms in the GluR2 gene are not associated with amyotrophic lateral sclerosis.

Bogaert E, Goris A, Van Damme P, Geelen V, Lemmens R, van Es MA, van den Berg LH, Sleegers K, Verpoorten N, Timmerman V, De Jonghe P, Van Broeckhoven C, Traynor BJ, Landers JE, Brown RH Jr, Glass JD, Al-Chalabi A, Shaw CE, Birve A, Andersen PM, Slowik A, Tomik B, Melki J, Robberecht W, Van Den Bosch L.

Neurobiol Aging. 2012 Feb;33(2):418-20. doi: 10.1016/j.neurobiolaging.2010.03.007. Epub 2010 Apr 20.

2.

Deficient RNA editing of GluR2 and neuronal death in amyotropic lateral sclerosis.

Kwak S, Kawahara Y.

J Mol Med (Berl). 2005 Feb;83(2):110-20. Epub 2004 Dec 29. Review.

PMID:
15624111
3.

Screening of VCP mutations in Chinese amyotrophic lateral sclerosis patients.

Zou ZY, Liu MS, Li XG, Cui LY.

Neurobiol Aging. 2013 May;34(5):1519.e3-4. doi: 10.1016/j.neurobiolaging.2012.10.002. Epub 2012 Oct 24.

PMID:
23102936
4.

De novo FUS gene mutations are associated with juvenile-onset sporadic amyotrophic lateral sclerosis in China.

Zou ZY, Cui LY, Sun Q, Li XG, Liu MS, Xu Y, Zhou Y, Yang XZ.

Neurobiol Aging. 2013 Apr;34(4):1312.e1-8. doi: 10.1016/j.neurobiolaging.2012.09.005. Epub 2012 Oct 6.

PMID:
23046859
5.

Mutation analysis of PFN1 in familial amyotrophic lateral sclerosis patients.

Daoud H, Dobrzeniecka S, Camu W, Meininger V, Dupré N, Dion PA, Rouleau GA.

Neurobiol Aging. 2013 Apr;34(4):1311.e1-2. doi: 10.1016/j.neurobiolaging.2012.09.001. Epub 2012 Oct 10.

PMID:
23062600
6.

Rare and common paraoxonase gene variants in amyotrophic lateral sclerosis patients.

van Blitterswijk M, Blokhuis A, van Es MA, van Vught PW, Rowicka PA, Schelhaas HJ, van der Kooi AJ, de Visser M, Veldink JH, van den Berg LH.

Neurobiol Aging. 2012 Aug;33(8):1845.e1-3. doi: 10.1016/j.neurobiolaging.2012.01.007. Epub 2012 Feb 11.

PMID:
22330174
7.
8.

Novel deletion mutations of OPTN in amyotrophic lateral sclerosis in Japanese.

Iida A, Hosono N, Sano M, Kamei T, Oshima S, Tokuda T, Nakajima M, Kubo M, Nakamura Y, Ikegawa S.

Neurobiol Aging. 2012 Aug;33(8):1843.e19-24. doi: 10.1016/j.neurobiolaging.2011.12.037. Epub 2012 Mar 7.

PMID:
22402017
9.

Calcium-permeable AMPA receptors promote misfolding of mutant SOD1 protein and development of amyotrophic lateral sclerosis in a transgenic mouse model.

Tateno M, Sadakata H, Tanaka M, Itohara S, Shin RM, Miura M, Masuda M, Aosaki T, Urushitani M, Misawa H, Takahashi R.

Hum Mol Genet. 2004 Oct 1;13(19):2183-96. Epub 2004 Aug 4.

10.

H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis.

van Rheenen W, Diekstra FP, van Doormaal PT, Seelen M, Kenna K, McLaughlin R, Shatunov A, Czell D, van Es MA, van Vught PW, van Damme P, Smith BN, Waibel S, Schelhaas HJ, van der Kooi AJ, de Visser M, Weber M, Robberecht W, Hardiman O, Shaw PJ, Shaw CE, Morrison KE, Al-Chalabi A, Andersen PM, Ludolph AC, Veldink JH, van den Berg LH.

Neurobiol Aging. 2013 May;34(5):1517.e5-7. doi: 10.1016/j.neurobiolaging.2012.07.020. Epub 2012 Oct 11.

PMID:
23063643
11.

Progranulin genetic variability contributes to amyotrophic lateral sclerosis.

Sleegers K, Brouwers N, Maurer-Stroh S, van Es MA, Van Damme P, van Vught PW, van der Zee J, Serneels S, De Pooter T, Van den Broeck M, Cruts M, Schymkowitz J, De Jonghe P, Rousseau F, van den Berg LH, Robberecht W, Van Broeckhoven C.

Neurology. 2008 Jul 22;71(4):253-9. doi: 10.1212/01.wnl.0000289191.54852.75. Epub 2008 Jan 9.

PMID:
18184915
12.

A novel optineurin truncating mutation and three glaucoma-associated missense variants in patients with familial amyotrophic lateral sclerosis in Germany.

Weishaupt JH, Waibel S, Birve A, Volk AE, Mayer B, Meyer T, Ludolph AC, Andersen PM.

Neurobiol Aging. 2013 May;34(5):1516.e9-15. doi: 10.1016/j.neurobiolaging.2012.09.007. Epub 2012 Oct 10.

PMID:
23062601
13.

No association between DNA repair gene XRCC1 and amyotrophic lateral sclerosis.

Fang F, Umbach DM, Xu Z, Ye W, Sandler DP, Taylor JA, Kamel F.

Neurobiol Aging. 2012 May;33(5):1015.e25-6. doi: 10.1016/j.neurobiolaging.2010.07.004. Epub 2010 Aug 16.

14.

Increased incidence of FMO1 gene single nucleotide polymorphisms in sporadic amyotrophic lateral sclerosis.

Cereda C, Gabanti E, Corato M, de Silvestri A, Alimonti D, Cova E, Malaspina A, Ceroni M.

Amyotroph Lateral Scler. 2006 Dec;7(4):227-34.

PMID:
17127561
15.

Genetic analysis and SOD1 mutation screening in Iranian amyotrophic lateral sclerosis patients.

Alavi A, Nafissi S, Rohani M, Zamani B, Sedighi B, Shamshiri H, Fan JB, Ronaghi M, Elahi E.

Neurobiol Aging. 2013 May;34(5):1516.e1-8. doi: 10.1016/j.neurobiolaging.2012.09.006. Epub 2012 Oct 9.

PMID:
23062701
16.

Chromosome 9p21 in amyotrophic lateral sclerosis in Finland: a genome-wide association study.

Laaksovirta H, Peuralinna T, Schymick JC, Scholz SW, Lai SL, Myllykangas L, Sulkava R, Jansson L, Hernandez DG, Gibbs JR, Nalls MA, Heckerman D, Tienari PJ, Traynor BJ.

Lancet Neurol. 2010 Oct;9(10):978-85. doi: 10.1016/S1474-4422(10)70184-8.

17.

Association between metallothionein genes polymorphisms and sporadic amyotrophic lateral sclerosis in a Japanese population.

Hayashi Y, Hashizume T, Wakida K, Satoh M, Uchida Y, Watabe K, Matsuyama Z, Kimura A, Inuzuka T, Hozumi I.

Amyotroph Lateral Scler. 2006 Mar;7(1):22-6.

PMID:
16546755
18.

CGG-repeat expansion in FMR1 is not associated with amyotrophic lateral sclerosis.

Groen EJ, van Rheenen W, Koppers M, van Doormaal PT, Vlam L, Diekstra FP, Dooijes D, Pasterkamp RJ, van den Berg LH, Veldink JH.

Neurobiol Aging. 2012 Aug;33(8):1852.e1-3. doi: 10.1016/j.neurobiolaging.2012.03.007. Epub 2012 Apr 15.

PMID:
22507827
19.

Astrocytes regulate GluR2 expression in motor neurons and their vulnerability to excitotoxicity.

Van Damme P, Bogaert E, Dewil M, Hersmus N, Kiraly D, Scheveneels W, Bockx I, Braeken D, Verpoorten N, Verhoeven K, Timmerman V, Herijgers P, Callewaert G, Carmeliet P, Van Den Bosch L, Robberecht W.

Proc Natl Acad Sci U S A. 2007 Sep 11;104(37):14825-30. Epub 2007 Sep 5.

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