Hattori N - Search Results

1

Pseudo-heterozygous rearrangement mutation of parkin.

Funayama M, Yoshino H, Li Y, Kusaka H, Tomiyama H, Hattori N. Funayama M, et al. Among authors: hattori n. Mov Disord. 2012 Apr;27(4):552-5. doi: 10.1002/mds.24906. Epub 2012 Feb 5. Mov Disord. 2012. PMID: 22308057

2

Structural organization and chromosomal localization of the human nuclear gene (NDUFV2) for the 24-kDa iron-sulfur subunit of complex I in mitochondrial respiratory chain.

Hattori N, Suzuki H, Wang Y, Minoshima S, Shimizu N, Yoshino H, Kurashima R, Tanaka M, Ozawa T, Mizuno Y. Hattori N, et al. Biochem Biophys Res Commun. 1995 Nov 22;216(3):771-7. doi: 10.1006/bbrc.1995.2688. Biochem Biophys Res Commun. 1995. PMID: 7488192

3

An immunohistochemical study on alpha-ketoglutarate dehydrogenase complex in Parkinson's disease.

Mizuno Y, Matuda S, Yoshino H, Mori H, Hattori N, Ikebe S. Mizuno Y, et al. Among authors: hattori n. Ann Neurol. 1994 Feb;35(2):204-10. doi: 10.1002/ana.410350212. Ann Neurol. 1994. PMID: 8109900

4

Postischemic accumulation of lipid peroxidation products in the rat brain: immunohistochemical detection of 4-hydroxy-2-nonenal modified proteins.

Yoshino H, Hattori N, Urabe T, Uchida K, Tanaka M, Mizuno Y. Yoshino H, et al. Among authors: hattori n. Brain Res. 1997 Aug 29;767(1):81-6. doi: 10.1016/s0006-8993(97)00616-1. Brain Res. 1997. PMID: 9365018

5

Catechol-O-methyltransferase genotype and susceptibility to Parkinson's disease in Japan. Short communication.

Yoritaka A, Hattori N, Yoshino H, Mizuno Y. Yoritaka A, et al. Among authors: hattori n. J Neural Transm (Vienna). 1997;104(11-12):1313-7. doi: 10.1007/BF01294732. J Neural Transm (Vienna). 1997. PMID: 9503277 Clinical Trial.

6

Mutations in the parkin gene cause autosomal recessive juvenile parkinsonism.

Kitada T, Asakawa S, Hattori N, Matsumine H, Yamamura Y, Minoshima S, Yokochi M, Mizuno Y, Shimizu N. Kitada T, et al. Among authors: hattori n. Nature. 1998 Apr 9;392(6676):605-8. doi: 10.1038/33416. Nature. 1998. PMID: 9560156

7

Genotype in the 24-kDa subunit gene (NDUFV2) of mitochondrial complex I and susceptibility to Parkinson disease.

Hattori N, Yoshino H, Tanaka M, Suzuki H, Mizuno Y. Hattori N, et al. Genomics. 1998 Apr 1;49(1):52-8. doi: 10.1006/geno.1997.5192. Genomics. 1998. PMID: 9570948

8

Colocalization of Bcl-2 and 4-hydroxynonenal modified proteins in microglial cells and neurons of rat brain following transient focal ischemia.

Urabe T, Hattori N, Yoshikawa M, Yoshino H, Uchida K, Mizuno Y. Urabe T, et al. Among authors: hattori n. Neurosci Lett. 1998 May 15;247(2-3):159-62. doi: 10.1016/s0304-3940(98)00311-5. Neurosci Lett. 1998. PMID: 9655617

9

Point mutations (Thr240Arg and Gln311Stop) [correction of Thr240Arg and Ala311Stop] in the Parkin gene.

Hattori N, Matsumine H, Asakawa S, Kitada T, Yoshino H, Elibol B, Brookes AJ, Yamamura Y, Kobayashi T, Wang M, Yoritaka A, Minoshima S, Shimizu N, Mizuno Y. Hattori N, et al. Biochem Biophys Res Commun. 1998 Aug 28;249(3):754-8. doi: 10.1006/bbrc.1998.9134. Biochem Biophys Res Commun. 1998. PMID: 9731209

10

Mitochondrial dysfunction in Parkinson's disease.

Mizuno Y, Yoshino H, Ikebe S, Hattori N, Kobayashi T, Shimoda-Matsubayashi S, Matsumine H, Kondo T. Mizuno Y, et al. Among authors: hattori n. Ann Neurol. 1998 Sep;44(3 Suppl 1):S99-109. doi: 10.1002/ana.410440715. Ann Neurol. 1998. PMID: 9749580 Review.

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