Shimizu N - Search Results

1

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. Among authors: shimizu n. Biochem Biophys Res Commun. 1998 Aug 28;249(3):754-8. doi: 10.1006/bbrc.1998.9134. Biochem Biophys Res Commun. 1998. PMID: 9731209

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. Among authors: shimizu n. 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

Genomic organization and complete nucleotide sequence of the TMEM1 gene on human chromosome 21q22.3.

Nagamine K, Kudoh J, Kawasaki K, Minoshima S, Asakawa S, Ito F, Shimizu N. Nagamine K, et al. Among authors: shimizu n. Biochem Biophys Res Commun. 1997 Jun 9;235(1):185-90. doi: 10.1006/bbrc.1997.6758. Biochem Biophys Res Commun. 1997. PMID: 9196060

4

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: shimizu n. Nature. 1998 Apr 9;392(6676):605-8. doi: 10.1038/33416. Nature. 1998. PMID: 9560156

5

Molecular genetic analysis of a novel Parkin gene in Japanese families with autosomal recessive juvenile parkinsonism: evidence for variable homozygous deletions in the Parkin gene in affected individuals.

Hattori N, Kitada T, Matsumine H, Asakawa S, Yamamura Y, Yoshino H, Kobayashi T, Yokochi M, Wang M, Yoritaka A, Kondo T, Kuzuhara S, Nakamura S, Shimizu N, Mizuno Y. Hattori N, et al. Among authors: shimizu n. Ann Neurol. 1998 Dec;44(6):935-41. doi: 10.1002/ana.410440612. Ann Neurol. 1998. PMID: 9851438

6

Polymorphism in the parkin gene in sporadic Parkinson's disease.

Wang M, Hattori N, Matsumine H, Kobayashi T, Yoshino H, Morioka A, Kitada T, Asakawa S, Minoshima S, Shimizu N, Mizuno Y. Wang M, et al. Among authors: shimizu n. Ann Neurol. 1999 May;45(5):655-8. doi: 10.1002/1531-8249(199905)45:5<655::aid-ana15>3.0.co;2-g. Ann Neurol. 1999. PMID: 10319889

7

Immunohistochemical and subcellular localization of Parkin protein: absence of protein in autosomal recessive juvenile parkinsonism patients.

Shimura H, Hattori N, Kubo S, Yoshikawa M, Kitada T, Matsumine H, Asakawa S, Minoshima S, Yamamura Y, Shimizu N, Mizuno Y. Shimura H, et al. Among authors: shimizu n. Ann Neurol. 1999 May;45(5):668-72. doi: 10.1002/1531-8249(199905)45:5<668::aid-ana19>3.0.co;2-z. Ann Neurol. 1999. PMID: 10319893

8

[Cloning of Parkin gene and its function].

Shimizu N, Minoshima S, Asakawa S. Shimizu N, et al. No To Shinkei. 1999 Jun;51(6):487-91. No To Shinkei. 1999. PMID: 10423750 Review. Japanese. No abstract available.

9

Molecular cloning, gene expression, and identification of a splicing variant of the mouse parkin gene.

Kitada T, Asakawa S, Minoshima S, Mizuno Y, Shimizu N. Kitada T, et al. Among authors: shimizu n. Mamm Genome. 2000 Jun;11(6):417-21. doi: 10.1007/s003350010080. Mamm Genome. 2000. PMID: 10818204

10

Familial Parkinson disease gene product, parkin, is a ubiquitin-protein ligase.

Shimura H, Hattori N, Kubo Si, Mizuno Y, Asakawa S, Minoshima S, Shimizu N, Iwai K, Chiba T, Tanaka K, Suzuki T. Shimura H, et al. Among authors: shimizu n. Nat Genet. 2000 Jul;25(3):302-5. doi: 10.1038/77060. Nat Genet. 2000. PMID: 10888878

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