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Results: 1 to 20 of 94

Similar articles for PubMed (Select 21725888)

1.

FUS gene mutations associated with familiar forms of amyotrophic lateral sclerosis affect cellular localization and aggregation properties of the encoded protein.

Shelkovnikova TA, Ustyugov AA, Smirnov AP, Skvortsova VI, Buchman VL, Bachurin SO, Ninkina NN.

Dokl Biochem Biophys. 2011 May-Jun;438:123-6. doi: 10.1134/S1607672911030045. Epub 2011 Jul 3. No abstract available.

PMID:
21725888
2.

FUS mutations in familial amyotrophic lateral sclerosis in the Netherlands.

Groen EJ, van Es MA, van Vught PW, Spliet WG, van Engelen-Lee J, de Visser M, Wokke JH, Schelhaas HJ, Ophoff RA, Fumoto K, Pasterkamp RJ, Dooijes D, Cuppen E, Veldink JH, van den Berg LH.

Arch Neurol. 2010 Feb;67(2):224-30. doi: 10.1001/archneurol.2009.329.

PMID:
20142531
3.

Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis.

Kwiatkowski TJ Jr, Bosco DA, Leclerc AL, Tamrazian E, Vanderburg CR, Russ C, Davis A, Gilchrist J, Kasarskis EJ, Munsat T, Valdmanis P, Rouleau GA, Hosler BA, Cortelli P, de Jong PJ, Yoshinaga Y, Haines JL, Pericak-Vance MA, Yan J, Ticozzi N, Siddique T, McKenna-Yasek D, Sapp PC, Horvitz HR, Landers JE, Brown RH Jr.

Science. 2009 Feb 27;323(5918):1205-8. doi: 10.1126/science.1166066.

4.

Optineurin is co-localized with FUS in basophilic inclusions of ALS with FUS mutation and in basophilic inclusion body disease.

Ito H, Fujita K, Nakamura M, Wate R, Kaneko S, Sasaki S, Yamane K, Suzuki N, Aoki M, Shibata N, Togashi S, Kawata A, Mochizuki Y, Mizutani T, Maruyama H, Hirano A, Takahashi R, Kawakami H, Kusaka H.

Acta Neuropathol. 2011 Apr;121(4):555-7. doi: 10.1007/s00401-011-0809-z. Epub 2011 Feb 17. No abstract available.

PMID:
21327942
5.

The occurrence of mutations in FUS in a Belgian cohort of patients with familial ALS.

Damme PV, Goris A, Race V, Hersmus N, Dubois B, Bosch LV, Matthijs G, Robberecht W.

Eur J Neurol. 2010 May;17(5):754-6. doi: 10.1111/j.1468-1331.2009.02859.x. Epub 2009 Nov 13.

PMID:
19922450
6.

Identification of novel FUS mutations in sporadic cases of amyotrophic lateral sclerosis.

Belzil VV, Daoud H, St-Onge J, Desjarlais A, Bouchard JP, Dupre N, Lacomblez L, Salachas F, Pradat PF, Meininger V, Camu W, Dion PA, Rouleau GA.

Amyotroph Lateral Scler. 2011 Mar;12(2):113-7. doi: 10.3109/17482968.2010.536840. Epub 2011 Jan 24.

PMID:
21261515
7.

Neurons don't appreciate FUSsing in the cytoplasm.

Buratti E, Baralle FE.

EMBO J. 2010 Aug 18;29(16):2769-71. doi: 10.1038/emboj.2010.163. No abstract available.

8.

TDP-43 and FUS/TLS: sending a complex message about messenger RNA in amyotrophic lateral sclerosis?

Strong MJ, Volkening K.

FEBS J. 2011 Oct;278(19):3569-77. doi: 10.1111/j.1742-4658.2011.08277.x. Epub 2011 Sep 6. Review.

PMID:
21810174
9.

Arginine methylation by PRMT1 regulates nuclear-cytoplasmic localization and toxicity of FUS/TLS harbouring ALS-linked mutations.

Tradewell ML, Yu Z, Tibshirani M, Boulanger MC, Durham HD, Richard S.

Hum Mol Genet. 2012 Jan 1;21(1):136-49. doi: 10.1093/hmg/ddr448. Epub 2011 Sep 28.

10.

Analysis of FUS gene mutation in familial amyotrophic lateral sclerosis within an Italian cohort.

Ticozzi N, Silani V, LeClerc AL, Keagle P, Gellera C, Ratti A, Taroni F, Kwiatkowski TJ Jr, McKenna-Yasek DM, Sapp PC, Brown RH Jr, Landers JE.

Neurology. 2009 Oct 13;73(15):1180-5. doi: 10.1212/WNL.0b013e3181bbff05. Epub 2009 Sep 9.

11.

Motor-neuron disease: Rogue gene in the family.

Sleegers K, Van Broeckhoven C.

Nature. 2009 Mar 26;458(7237):415-7. doi: 10.1038/458415a. No abstract available.

PMID:
19325616
12.

Mutations of FUS gene in sporadic amyotrophic lateral sclerosis.

Corrado L, Del Bo R, Castellotti B, Ratti A, Cereda C, Penco S, Sorarù G, Carlomagno Y, Ghezzi S, Pensato V, Colombrita C, Gagliardi S, Cozzi L, Orsetti V, Mancuso M, Siciliano G, Mazzini L, Comi GP, Gellera C, Ceroni M, D'Alfonso S, Silani V.

J Med Genet. 2010 Mar;47(3):190-4. doi: 10.1136/jmg.2009.071027. Epub 2009 Oct 26.

PMID:
19861302
13.

Intranuclear aggregation of mutant FUS/TLS as a molecular pathomechanism of amyotrophic lateral sclerosis.

Nomura T, Watanabe S, Kaneko K, Yamanaka K, Nukina N, Furukawa Y.

J Biol Chem. 2014 Jan 10;289(2):1192-202. doi: 10.1074/jbc.M113.516492. Epub 2013 Nov 26.

14.

Genetics of familial Amyotrophic lateral sclerosis.

Ticozzi N, Tiloca C, Morelli C, Colombrita C, Poletti B, Doretti A, Maderna L, Messina S, Ratti A, Silani V.

Arch Ital Biol. 2011 Mar;149(1):65-82. doi: 10.4449/aib.v149i1.1262. Review.

PMID:
21412717
15.

FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis.

Sproviero W, La Bella V, Mazzei R, Valentino P, Rodolico C, Simone IL, Logroscino G, Ungaro C, Magariello A, Patitucci A, Tedeschi G, Spataro R, Condino F, Bono F, Citrigno L, Monsurrò MR, Muglia M, Gambardella A, Quattrone A, Conforti FL.

Neurobiol Aging. 2012 Apr;33(4):837.e1-5. doi: 10.1016/j.neurobiolaging.2011.10.005. Epub 2011 Nov 4.

PMID:
22055719
16.

Transportin 1 accumulates in FUS inclusions in adult-onset ALS without FUS mutation.

Takeuchi R, Toyoshima Y, Tada M, Shiga A, Tanaka H, Shimohata M, Kimura K, Morita T, Kakita A, Nishizawa M, Takahashi H.

Neuropathol Appl Neurobiol. 2013 Aug;39(5):580-4. doi: 10.1111/nan.12022. No abstract available.

PMID:
23362988
17.

Novel missense and truncating mutations in FUS/TLS in familial ALS.

Waibel S, Neumann M, Rabe M, Meyer T, Ludolph AC.

Neurology. 2010 Aug 31;75(9):815-7. doi: 10.1212/WNL.0b013e3181f07e26. Epub 2010 Jul 21.

PMID:
20660363
18.

Identification of a FUS splicing mutation in a large family with amyotrophic lateral sclerosis.

Belzil VV, St-Onge J, Daoud H, Desjarlais A, Bouchard JP, Dupré N, Camu W, Dion PA, Rouleau GA.

J Hum Genet. 2011 Mar;56(3):247-9. doi: 10.1038/jhg.2010.162. Epub 2010 Dec 16.

PMID:
21160488
19.

P525L FUS mutation is consistently associated with a severe form of juvenile amyotrophic lateral sclerosis.

Conte A, Lattante S, Zollino M, Marangi G, Luigetti M, Del Grande A, Servidei S, Trombetta F, Sabatelli M.

Neuromuscul Disord. 2012 Jan;22(1):73-5. doi: 10.1016/j.nmd.2011.08.003. Epub 2011 Sep 9.

PMID:
21907581
20.

FUS mutations in frontotemporal lobar degeneration with amyotrophic lateral sclerosis.

Broustal O, Camuzat A, Guillot-Noël L, Guy N, Millecamps S, Deffond D, Lacomblez L, Golfier V, Hannequin D, Salachas F, Camu W, Didic M, Dubois B, Meininger V, Le Ber I, Brice A; French clinical and genetic research network on FTD/FTD-MND.

J Alzheimers Dis. 2010;22(3):765-9.

PMID:
21158017
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