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Results: 1 to 20 of 152

Similar articles for PubMed (Select 23448665)

1.

Abundant FUS-immunoreactive pathology in the skin of sporadic amyotrophic lateral sclerosis.

Oketa Y, Higashida K, Fukasawa H, Tsukie T, Ono S.

Acta Neurol Scand. 2013 Oct;128(4):257-64. doi: 10.1111/ane.12114. Epub 2013 Mar 1.

PMID:
23448665
2.

Subcellular localization and RNAs determine FUS architecture in different cellular compartments.

Yang L, Zhang J, Kamelgarn M, Niu C, Gal J, Gong W, Zhu H.

Hum Mol Genet. 2015 Jun 29. pii: ddv239. [Epub ahead of print]

PMID:
26123490
3.

Decreased Amount of Collagen in The Skin of Amyotrophic Lateral Sclerosis in The Kii Peninsula of Japan.

Tsukie T, Masaki H, Yoshida S, Fujikura M, Ono S.

Acta Neurol Taiwan. 2014 Sep;23(3):82-9.

PMID:
26077179
4.

Amelioration of toxicity in neuronal models of amyotrophic lateral sclerosis by hUPF1.

Barmada SJ, Ju S, Arjun A, Batarse A, Archbold HC, Peisach D, Li X, Zhang Y, Tank EM, Qiu H, Huang EJ, Ringe D, Petsko GA, Finkbeiner S.

Proc Natl Acad Sci U S A. 2015 Jun 23;112(25):7821-6. doi: 10.1073/pnas.1509744112. Epub 2015 Jun 8.

PMID:
26056265
5.

Emerging mechanisms of molecular pathology in ALS.

Peters OM, Ghasemi M, Brown RH Jr.

J Clin Invest. 2015 Jun 1;125(6):2548. doi: 10.1172/JCI82693. Epub 2015 Jun 1. No abstract available.

PMID:
26030230
6.

Measuring change in amyotrophic lateral sclerosis.

Swash M, Kiernan MC.

J Neurol Neurosurg Psychiatry. 2015 May 21. pii: jnnp-2015-311051. doi: 10.1136/jnnp-2015-311051. [Epub ahead of print] No abstract available.

PMID:
25999409
7.

Time to generalisation as a predictor of prognosis in amyotrophic lateral sclerosis.

Tortelli R, Copetti M, Panza F, Cortese R, Capozzo R, D'Errico E, Fontana A, Simone IL, Logroscino G.

J Neurol Neurosurg Psychiatry. 2015 May 20. pii: jnnp-2014-308478. doi: 10.1136/jnnp-2014-308478. [Epub ahead of print] No abstract available.

PMID:
25995485
8.

Early lethality and neuronal proteinopathy in mice expressing cytoplasm-targeted FUS that lacks the RNA recognition motif.

Robinson HK, Deykin AV, Bronovitsky EV, Ovchinnikov RK, Ustyugov AA, Shelkovnikova TA, Kukharsky MS, Ermolkevich TG, Goldman IL, Sadchikova ER, Kovrazhkina EA, Bachurin SO, Buchman VL, Ninkina NN.

Amyotroph Lateral Scler Frontotemporal Degener. 2015 May 20:1-8. [Epub ahead of print]

PMID:
25991062
9.

FUS regulates AMPA receptor function and FTLD/ALS-associated behaviour via GluA1 mRNA stabilization.

Udagawa T, Fujioka Y, Tanaka M, Honda D, Yokoi S, Riku Y, Ibi D, Nagai T, Yamada K, Watanabe H, Katsuno M, Inada T, Ohno K, Sokabe M, Okado H, Ishigaki S, Sobue G.

Nat Commun. 2015 May 13;6:7098. doi: 10.1038/ncomms8098.

10.

Exome sequencing uncovers hidden pathways in familial and sporadic ALS.

Bettencourt C, Houlden H.

Nat Neurosci. 2015 May;18(5):611-3. doi: 10.1038/nn.4012. No abstract available.

PMID:
25919956
11.
12.

TUBA4A gene analysis in sporadic amyotrophic lateral sclerosis: identification of novel mutations.

Pensato V, Tiloca C, Corrado L, Bertolin C, Sardone V, Del Bo R, Calini D, Mandrioli J, Lauria G, Mazzini L, Querin G, Ceroni M, Cantello R, Corti S, Castellotti B, Soldà G, Duga S, Comi GP, Cereda C, Sorarù G, D'Alfonso S, Taroni F, Shaw CE, Landers JE, Ticozzi N, Ratti A, Gellera C, Silani V; SLAGEN Consortium.

J Neurol. 2015 May;262(5):1376-8. doi: 10.1007/s00415-015-7739-y. Epub 2015 Apr 18. No abstract available.

PMID:
25893256
13.

Diagnosing amyotrophic lateral sclerosis (ALS) in ENT.

Harrison L, Wills A, Beasley N.

Clin Otolaryngol. 2013 Dec;38(6):564-5. No abstract available.

PMID:
25741568
14.

R-loops highlight the nucleus in ALS.

Salvi JS, Mekhail K.

Nucleus. 2015;6(1):23-9. doi: 10.1080/19491034.2015.1004952.

PMID:
25587791
15.

Reply: CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Bannwarth S, Ait-El-Mkadem S, Chaussenot A, Genin EC, Lacas-Gervais S, Fragaki K, Berg-Alonso L, Kageyama Y, Serre V, Moore D, Verschueren A, Rouzier C, Le Ber I, Augé G, Cochaud C, Lespinasse F, N'Guyen K, de Septenville A, Brice A, Yu-Wai-Man P, Sesaki H, Pouget J, Paquis-Flucklinger V.

Brain. 2015 Jan 8. pii: awu385. [Epub ahead of print] No abstract available.

PMID:
25576309
16.

CHCHD10 mutations in Italian patients with sporadic amyotrophic lateral sclerosis.

Ronchi D, Riboldi G, Del Bo R, Ticozzi N, Scarlato M, Galimberti D, Corti S, Silani V, Bresolin N, Comi GP.

Brain. 2015 Jan 8. pii: awu384. [Epub ahead of print] No abstract available.

PMID:
25576308
17.

Pincer nail deformity in a patient with amyotrophic lateral sclerosis.

Fujita Y, Fujita T.

Neurol Int. 2014 Dec 11;6(4):5716. doi: 10.4081/ni.2014.5716. eCollection 2014 Oct 23.

18.

Intermediate-length polyglutamine in ATXN2 is a possible risk factor among Eastern Chinese patients with amyotrophic lateral sclerosis.

Lu HP, Gan SR, Chen S, Li HF, Liu ZJ, Ni W, Wang N, Wu ZY.

Neurobiol Aging. 2015 Mar;36(3):1603.e11-4. doi: 10.1016/j.neurobiolaging.2014.10.015. Epub 2014 Oct 16.

PMID:
25457026
19.

Self-assembled FUS binds active chromatin and regulates gene transcription.

Yang L, Gal J, Chen J, Zhu H.

Proc Natl Acad Sci U S A. 2014 Dec 16;111(50):17809-14. doi: 10.1073/pnas.1414004111. Epub 2014 Dec 1.

20.

Characterisation of multiple regulatory domains spanning the major transcriptional start site of the FUS gene, a candidate gene for motor neurone disease.

Khursheed K, Wilm TP, Cashman C, Quinn JP, Bubb VJ, Moss DJ.

Brain Res. 2015 Jan 21;1595:1-9. doi: 10.1016/j.brainres.2014.10.056. Epub 2014 Nov 5.

PMID:
25451114
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