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Results: 1 to 20 of 127

Similar articles for PubMed (Select 22393909)

1.

Reduced brain-derived neurotrophic factor (BDNF) mRNA expression and presence of BDNF-immunoreactive granules in the spinocerebellar ataxia type 6 (SCA6) cerebellum.

Takahashi M, Ishikawa K, Sato N, Obayashi M, Niimi Y, Ishiguro T, Yamada M, Toyoshima Y, Takahashi H, Kato T, Takao M, Murayama S, Mori O, Eishi Y, Mizusawa H.

Neuropathology. 2012 Dec;32(6):595-603. doi: 10.1111/j.1440-1789.2012.01302.x. Epub 2012 Mar 7.

PMID:
22393909
2.

The carboxy-terminal fragment of alpha(1A) calcium channel preferentially aggregates in the cytoplasm of human spinocerebellar ataxia type 6 Purkinje cells.

Ishiguro T, Ishikawa K, Takahashi M, Obayashi M, Amino T, Sato N, Sakamoto M, Fujigasaki H, Tsuruta F, Dolmetsch R, Arai T, Sasaki H, Nagashima K, Kato T, Yamada M, Takahashi H, Hashizume Y, Mizusawa H.

Acta Neuropathol. 2010 Apr;119(4):447-64. doi: 10.1007/s00401-009-0630-0. Epub 2009 Dec 31.

3.

Abundant expression and cytoplasmic aggregations of [alpha]1A voltage-dependent calcium channel protein associated with neurodegeneration in spinocerebellar ataxia type 6.

Ishikawa K, Fujigasaki H, Saegusa H, Ohwada K, Fujita T, Iwamoto H, Komatsuzaki Y, Toru S, Toriyama H, Watanabe M, Ohkoshi N, Shoji S, Kanazawa I, Tanabe T, Mizusawa H.

Hum Mol Genet. 1999 Jul;8(7):1185-93.

4.

Cell-type-specific alternative splicing in spinocerebellar ataxia type 6.

Tsunemi T, Ishikawa K, Jin H, Mizusawa H.

Neurosci Lett. 2008 Dec 5;447(1):78-81. doi: 10.1016/j.neulet.2008.09.065. Epub 2008 Sep 30.

PMID:
18835329
5.

Cytoplasmic and nuclear polyglutamine aggregates in SCA6 Purkinje cells.

Ishikawa K, Owada K, Ishida K, Fujigasaki H, Shun Li M, Tsunemi T, Ohkoshi N, Toru S, Mizutani T, Hayashi M, Arai N, Hasegawa K, Kawanami T, Kato T, Makifuchi T, Shoji S, Tanabe T, Mizusawa H.

Neurology. 2001 Jun 26;56(12):1753-6.

PMID:
11425948
6.

Cytoplasmic location of α1A voltage-gated calcium channel C-terminal fragment (Cav2.1-CTF) aggregate is sufficient to cause cell death.

Takahashi M, Obayashi M, Ishiguro T, Sato N, Niimi Y, Ozaki K, Mogushi K, Mahmut Y, Tanaka H, Tsuruta F, Dolmetsch R, Yamada M, Takahashi H, Kato T, Mori O, Eishi Y, Mizusawa H, Ishikawa K.

PLoS One. 2013;8(3):e50121. doi: 10.1371/journal.pone.0050121. Epub 2013 Mar 7.

7.

The p62 antibody reveals various cytoplasmic protein aggregates in spinocerebellar ataxia type 6.

Seidel K, Brunt ER, de Vos RA, Dijk F, van der Want HJ, Rüb U, den Dunnen WF.

Clin Neuropathol. 2009 Sep-Oct;28(5):344-9.

8.

Splice isoform-specific suppression of the Cav2.1 variant underlying spinocerebellar ataxia type 6.

Tsou WL, Soong BW, Paulson HL, Rodríguez-Lebrón E.

Neurobiol Dis. 2011 Sep;43(3):533-42. doi: 10.1016/j.nbd.2011.04.016. Epub 2011 Apr 29.

9.

Deficit of heat shock transcription factor 1-heat shock 70 kDa protein 1A axis determines the cell death vulnerability in a model of spinocerebellar ataxia type 6.

Li L, Saegusa H, Tanabe T.

Genes Cells. 2009 Nov;14(11):1253-69. doi: 10.1111/j.1365-2443.2009.01348.x. Epub 2009 Oct 8.

PMID:
19817876
10.

The polyglutamine expansion in spinocerebellar ataxia type 6 causes a beta subunit-specific enhanced activation of P/Q-type calcium channels in Xenopus oocytes.

Restituito S, Thompson RM, Eliet J, Raike RS, Riedl M, Charnet P, Gomez CM.

J Neurosci. 2000 Sep 1;20(17):6394-403.

11.

Morphological Purkinje cell changes in spinocerebellar ataxia type 6.

Yang Q, Hashizume Y, Yoshida M, Wang Y, Goto Y, Mitsuma N, Ishikawa K, Mizusawa H.

Acta Neuropathol. 2000 Oct;100(4):371-6.

PMID:
10985694
12.

Direct alteration of the P/Q-type Ca2+ channel property by polyglutamine expansion in spinocerebellar ataxia 6.

Matsuyama Z, Wakamori M, Mori Y, Kawakami H, Nakamura S, Imoto K.

J Neurosci. 1999 Jun 15;19(12):RC14.

13.

Increased expression of alpha 1A Ca2+ channel currents arising from expanded trinucleotide repeats in spinocerebellar ataxia type 6.

Piedras-Renteria ES, Watase K, Harata N, Zhuchenko O, Zoghbi HY, Lee CC, Tsien RW.

J Neurosci. 2001 Dec 1;21(23):9185-93.

14.

Spinocerebellar ataxia type 2: polyQ repeat variation in the CACNA1A calcium channel modifies age of onset.

Pulst SM, Santos N, Wang D, Yang H, Huynh D, Velazquez L, Figueroa KP.

Brain. 2005 Oct;128(Pt 10):2297-303. Epub 2005 Jul 6.

15.

Transcriptional dysregulation of TrkA associates with neurodegeneration in spinocerebellar ataxia type 17.

Shah AG, Friedman MJ, Huang S, Roberts M, Li XJ, Li S.

Hum Mol Genet. 2009 Nov 1;18(21):4141-52. doi: 10.1093/hmg/ddp363. Epub 2009 Jul 30.

16.

Neuropathological and molecular studies of spinocerebellar ataxia type 6 (SCA6).

Sasaki H, Kojima H, Yabe I, Tashiro K, Hamada T, Sawa H, Hiraga H, Nagashima K.

Acta Neuropathol. 1998 Feb;95(2):199-204.

PMID:
9498057
17.

Spinocerebellar ataxia type 6 (SCA6): neurodegeneration goes beyond the known brain predilection sites.

Gierga K, Schelhaas HJ, Brunt ER, Seidel K, Scherzed W, Egensperger R, de Vos RA, den Dunnen W, Ippel PF, Petrasch-Parwez E, Deller T, Schöls L, Rüb U.

Neuropathol Appl Neurobiol. 2009 Oct;35(5):515-27. doi: 10.1111/j.1365-2990.2009.01015.x. Epub 2009 Jan 30.

PMID:
19207264
18.

Development of Purkinje cell degeneration in a knockin mouse model reveals lysosomal involvement in the pathogenesis of SCA6.

Unno T, Wakamori M, Koike M, Uchiyama Y, Ishikawa K, Kubota H, Yoshida T, Sasakawa H, Peters C, Mizusawa H, Watase K.

Proc Natl Acad Sci U S A. 2012 Oct 23;109(43):17693-8. doi: 10.1073/pnas.1212786109. Epub 2012 Oct 10.

19.

Molecular pathogenesis of spinocerebellar ataxia type 6.

Kordasiewicz HB, Gomez CM.

Neurotherapeutics. 2007 Apr;4(2):285-94. Review.

PMID:
17395139
20.

Lentivector-mediated rescue from cerebellar ataxia in a mouse model of spinocerebellar ataxia.

Torashima T, Koyama C, Iizuka A, Mitsumura K, Takayama K, Yanagi S, Oue M, Yamaguchi H, Hirai H.

EMBO Rep. 2008 Apr;9(4):393-9. doi: 10.1038/embor.2008.31. Epub 2008 Mar 14.

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