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Bibliografía Científica

Artículos por temáticas

En este apartado encontrará la selección de artículos sobre Trastornos del Movimiento clasificados según los 11 tipos establecidos por International Parkinson & Movement Disorder Society.

Ataxia

408 ARTíCULOS , VIENDO DEL 391 AL 405

PUBMED

Ataxia telangiectasia mutated kinase mediates NF-κB serine 276 phosphorylation and interferon expression via the IRF7-RIG-I amplification loop in paramyxovirus infection.

Fang L, Choudhary S, Tian B, Boldogh I, Yang C, Ivanciuc T, Ma Y, Garofalo RP, Brasier AR.

J Virol. 2015 Mar;89(5):2628-42. doi: 10.1128/JVI.02458-14.

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PUBMED

Caffeine Suppresses Apoptosis of Bladder Cancer RT4 Cells in Response to Ionizing Radiation by Inhibiting Ataxia Telangiectasia Mutated-Chk2-p53 Axis.

Zhang ZW, Xiao J, Luo W, Wang BH, Chen JM.

Chin Med J (Engl). 2015 Nov 5;128(21):2938-45. doi: 10.4103/0366-6999.168065.

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Riluzole in patients with hereditary cerebellar ataxia: a randomised, double-blind, placebo-controlled trial.

Romano S, Coarelli G, Marcotulli C, Leonardi L, Piccolo F, Spadaro M, Frontali M, Ferraldeschi M, Vulpiani MC, Ponzelli F, Salvetti M, Orzi F, Petrucci A, Vanacore N, Casali C, Ristori G.

Lancet Neurol. 2015 Oct;14(10):985-91. doi: 10.1016/S1474-4422(15)00201-X.

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PUBMED

Gait and balance in adults with Friedreich's ataxia.

Stephenson J, Zesiewicz T, Gooch C, Wecker L, Sullivan K, Jahan I, Kim SH.

Gait Posture. 2015 Feb;41(2):603-7. doi: 10.1016/j.gaitpost.2015.01.002.

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Ataxia-telangiectasia mutated (ATM) silencing promotes neuroblastoma progression through a MYCN independent mechanism.

Mandriota SJ, Valentijn LJ, Lesne L, Betts DR, Marino D, Boudal-Khoshbeen M, London WB, Rougemont AL, Attiyeh EF, Maris JM, Hogarty MD, Koster J, Molenaar JJ, Versteeg R, Ansari M, Gumy-Pause F.

Oncotarget. 2015 Jul 30;6(21):18558-76.

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PUBMED

Ataxia telangiectasia-mutated gene polymorphisms and acute normal tissue injuries in cancer patients after radiation therapy: a systematic review and meta-analysis.

Dong L, Cui J, Tang F, Cong X, Han F.

Int J Radiat Oncol Biol Phys. 2015 Apr 1;91(5):1090-8. doi: 10.1016/j.ijrobp.2014.12.041. Review.

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PUBMED

Interaction of Heat Shock Protein Cpn10 with the Cyclin E/Cdk2 Substrate Nuclear Protein Ataxia-Telangiectasia (NPAT) Is Involved in Regulating Histone Transcription.

Ling Zheng L, Wang FY, Cong XX, Shen Y, Rao XS, Huang DS, Fan W, Yi P, Wang XB, Zheng L, Zhou YT, Luo Y.

J Biol Chem. 2015 Dec 4;290(49):29290-300. doi: 10.1074/jbc.M115.659201.

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PUBMED

SNP Analysis and Whole Exome Sequencing: Their Application in the Analysis of a Consanguineous Pedigree Segregating Ataxia.

Nickerson SL, Marquis-Nicholson R, Claxton K, Ashton F, Leong IU, Prosser DO, Love JM, George AM, Taylor G, Wilson C, Gardner RJ, Love DR.

Microarrays (Basel). 2015 Oct 23;4(4):490-502. doi: 10.3390/microarrays4040490.

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[A case of neurologic muscle weakness, ataxia, and retinitis pigmentosa (NARP) syndrome with a novel mitochondrial mutation m.8729 G>A].

Miyawaki T, Koto S, Ishihara H, Goto Y, Nishino I, Kanda F, Toda T.

Rinsho Shinkeigaku. 2015;55(2):91-5. doi: 10.5692/clinicalneurol.55.91. Japanese.

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PUBMED

Crystallographic and Computational Analyses of AUUCU Repeating RNA That Causes Spinocerebellar Ataxia Type 10 (SCA10).

Park H, González ÀL, Yildirim I, Tran T, Lohman JR, Fang P, Guo M, Disney MD.

Biochemistry. 2015 Jun 23;54(24):3851-9. doi: 10.1021/acs.biochem.5b00551.

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PUBMED

Exome Sequencing and Linkage Analysis Identified Novel Candidate Genes in Recessive Intellectual Disability Associated with Ataxia.

Jazayeri R, Hu H, Fattahi Z, Musante L, Abedini SS, Hosseini M, Wienker TF, Ropers HH, Najmabadi H, Kahrizi K.

Arch Iran Med. 2015 Oct;18(10):670-82. doi: 0151810/AIM.007.

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PUBMED

Functional analysis helps to define KCNC3 mutational spectrum in Dutch ataxia cases.

Duarri A, Nibbeling EA, Fokkens MR, Meijer M, Boerrigter M, Verschuuren-Bemelmans CC, Kremer BP, van de Warrenburg BP, Dooijes D, Boddeke E, Sinke RJ, Verbeek DS.

PLoS One. 2015 Mar 10;10(3):e0116599. doi: 10.1371/journal.pone.0116599.

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Reply: Replicating studies of genetic modifiers in spinocerebellar ataxia type 3: can homogeneous cohorts aid?

Tezenas du Montcel S.

Brain. 2015 Dec;138(Pt 12):e399. doi: 10.1093/brain/awv207. No abstract available.

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PUBMED

TORC1 Inhibition by Rapamycin Promotes Antioxidant Defences in a Drosophila Model of Friedreich's Ataxia.

Calap-Quintana P, Soriano S, Llorens JV, Al-Ramahi I, Botas J, Moltó MD, Martínez-Sebastián MJ.

PLoS One. 2015 Jul 9;10(7):e0132376. doi: 10.1371/journal.pone.0132376.

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