Hattori N - Search Results

1

The effect of Ndrg2 expression on astroglial activation.

Takeichi T, Takarada-Iemata M, Hashida K, Sudo H, Okuda T, Kokame K, Hatano T, Takanashi M, Funabe S, Hattori N, Kitamura O, Kitao Y, Hori O. Takeichi T, et al. Among authors: hattori n. Neurochem Int. 2011 Aug;59(1):21-7. doi: 10.1016/j.neuint.2011.03.019. Epub 2011 Jun 13. Neurochem Int. 2011. PMID: 21672576

2

Iron accumulation in the substantia nigra of autosomal recessive juvenile parkinsonism (ARJP).

Takanashi M, Mochizuki H, Yokomizo K, Hattori N, Mori H, Yamamura Y, Mizuno Y. Takanashi M, et al. Among authors: hattori n. Parkinsonism Relat Disord. 2001 Oct;7(4):311-314. doi: 10.1016/s1353-8020(00)00050-x. Parkinsonism Relat Disord. 2001. PMID: 11344015

3

Expression patterns of tau mRNA isoforms correlate with susceptible lesions in progressive supranuclear palsy and corticobasal degeneration.

Takanashi M, Mori H, Arima K, Mizuno Y, Hattori N. Takanashi M, et al. Among authors: hattori n. Brain Res Mol Brain Res. 2002 Aug 15;104(2):210-9. doi: 10.1016/s0169-328x(02)00382-0. Brain Res Mol Brain Res. 2002. PMID: 12225876

4

Expression of 8-oxoguanine DNA glycosylase (OGG1) in Parkinson's disease and related neurodegenerative disorders.

Fukae J, Takanashi M, Kubo S, Nishioka K, Nakabeppu Y, Mori H, Mizuno Y, Hattori N. Fukae J, et al. Among authors: hattori n. Acta Neuropathol. 2005 Mar;109(3):256-62. doi: 10.1007/s00401-004-0937-9. Epub 2004 Nov 17. Acta Neuropathol. 2005. PMID: 15841414

5

[A 73-year-old woman with depression, dementia, and parkinsonism].

Hatano T, Takanashi M, Sumino T, Liu Y, Mori H, Hattori N, Mizuno Y. Hatano T, et al. Among authors: hattori n. No To Shinkei. 2005 Oct;57(10):907-14. No To Shinkei. 2005. PMID: 16277238 Japanese.

6

[A 54-year-old man with familial parkinsonism, gaze palsy, and dementia].

Shimura H, Mori H, Komatsuzaki Y, Nakamura K, Takanashi M, Hattori N, Mizuno Y. Shimura H, et al. Among authors: hattori n. No To Shinkei. 2005 Dec;57(12):1104-12. No To Shinkei. 2005. PMID: 16375198 Japanese.

7

Up-regulation of hMUTYH, a DNA repair enzyme, in the mitochondria of substantia nigra in Parkinson's disease.

Arai T, Fukae J, Hatano T, Kubo S, Ohtsubo T, Nakabeppu Y, Mori H, Mizuno Y, Hattori N. Arai T, et al. Among authors: hattori n. Acta Neuropathol. 2006 Aug;112(2):139-45. doi: 10.1007/s00401-006-0081-9. Epub 2006 Jun 14. Acta Neuropathol. 2006. PMID: 16773329

8

Leucine-rich repeat kinase 2 associates with lipid rafts.

Hatano T, Kubo S, Imai S, Maeda M, Ishikawa K, Mizuno Y, Hattori N. Hatano T, et al. Among authors: hattori n. Hum Mol Genet. 2007 Mar 15;16(6):678-90. doi: 10.1093/hmg/ddm013. Epub 2007 Mar 6. Hum Mol Genet. 2007. PMID: 17341485

9

[Clinical molecular genetics for PARK8 (LRRK2)].

Tomiyama H, Hatano T, Hattori N. Tomiyama H, et al. Among authors: hattori n. Brain Nerve. 2007 Aug;59(8):839-50. Brain Nerve. 2007. PMID: 17713120 Review. Japanese.

10

Mutational analysis of fukutin gene in dilated cardiomyopathy and hypertrophic cardiomyopathy.

Arimura T, Hayashi YK, Murakami T, Oya Y, Funabe S, Arikawa-Hirasawa E, Hattori N, Nishino I, Kimura A. Arimura T, et al. Among authors: hattori n. Circ J. 2009 Jan;73(1):158-61. doi: 10.1253/circj.cj-08-0722. Epub 2008 Nov 17. Circ J. 2009. PMID: 19015585 Free article.

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