Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases-Reference-Cited by-同舟云学术

Co-morbidity of TDP-43 proteinopathy in Lewy body related diseases

Published:2007-07-25 Issue:3 Volume:114 Page:221-229
ISSN:0001-6322
Container-title:Acta Neuropathologica
language:en
Short-container-title:Acta Neuropathol

Author:

Nakashima-Yasuda Hanae,Uryu Kunihiro,Robinson John,Xie Sharon X.,Hurtig Howard,Duda John E.,Arnold Steven E.,Siderowf Andrew,Grossman Murray,Leverenz James B.,Woltjer Randy,Lopez Oscar L.,Hamilton Ronald,Tsuang Debby W.,Galasko Douglas,Masliah Eliezer,Kaye Jeffrey,Clark Christopher M.,Montine Thomas J.,Lee Virginia M. -Y.,Trojanowski John Q.

Publisher

Springer Science and Business Media LLC

Subject

Cellular and Molecular Neuroscience,Clinical Neurology,Pathology and Forensic Medicine

Link

http://link.springer.com/content/pdf/10.1007/s00401-007-0261-2.pdf

Reference31 articles.

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2. Arai T, Hasegawa M, Akiyama H, Ikeda K, Nonaka T, Mori H, Mann D, Tsuchiya K, Yoshida M, Hashizume Y, Oda T (2006) TDP-43 is a component of ubiquitin-positive tau-negative inclusions in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Biochem Biophys Res Commun 351:602–611

3. Buratti E, Dork T, Zuccato E, Pagani F, Romano M, Baralle FE (2001) Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping. EMBO J 20:1774–1784

4. Buratti E, Brindisi A, Pagani F, Baralle FE (2004) Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: a functional link with disease penetrance. Am J Hum Genet 74:1322–1325

5. Cairns NJ, Neumann M, Bigio EH, Holm IE, Troost D, Hatanpaa KJ, Foong C, White CL III, Schneider JA, Kretzschmar HA, Carter D, Paulsmeyer K, Strider J, Gitcho M, Goate AM, Morris JC, Mishra M, Kwong LK, Stieber A, Xu Y, Forman MS, Trojanowski JQ, Lee VM-Y, Mackenzie IR (2007) TDP-43 in Familial and Sporadic Frontotemporal Lobar Degeneration with Ubiquitin Inclusions. Am J Pathol 171:227–240

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