Minoshima S - Search Results

1

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: minoshima s. Nat Genet. 2000 Jul;25(3):302-5. doi: 10.1038/77060. Nat Genet. 2000. PMID: 10888878

2

Analysis of eighteen deletion breakpoints in the parkin gene.

Asakawa S, Hattori N, Shimizu A, Shimizu Y, Minoshima S, Mizuno Y, Shimizu N. Asakawa S, et al. Among authors: minoshima s. Biochem Biophys Res Commun. 2009 Nov 6;389(1):181-6. doi: 10.1016/j.bbrc.2009.08.115. Epub 2009 Aug 26. Biochem Biophys Res Commun. 2009. PMID: 19715670

3

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

4

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

5

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: minoshima s. 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

6

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: minoshima s. 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

7

[Cloning of Parkin gene and its function].

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

8

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: minoshima s. Mamm Genome. 2000 Jun;11(6):417-21. doi: 10.1007/s003350010080. Mamm Genome. 2000. PMID: 10818204

9

Progress in the clinical and molecular genetics of familial parkinsonism.

Kitada T, Asakawa S, Matsumine H, Hattori N, Shimura H, Minoshima S, Shimizu N, Mizuno Y. Kitada T, et al. Among authors: minoshima s. Neurogenetics. 2000 Mar;2(4):207-18. doi: 10.1007/s100489900083. Neurogenetics. 2000. PMID: 10983716 Review.

10

PARKIN as a pathogenic gene for autosomal recessive juvenile parkinsonism.

Shimizu N, Asakawa S, Minoshima S, Kitada T, Hattori N, Matsumine H, Yokochi M, Yamamura Y, Mizuno Y. Shimizu N, et al. Among authors: minoshima s. J Neural Transm Suppl. 2000;(58):19-30. doi: 10.1007/978-3-7091-6284-2_2. J Neural Transm Suppl. 2000. PMID: 11128608 Review.

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