Shimizu N - Search Results

1

A mutation in the ceruloplasmin gene is associated with systemic hemosiderosis in humans.

Yoshida K, Furihata K, Takeda S, Nakamura A, Yamamoto K, Morita H, Hiyamuta S, Ikeda S, Shimizu N, Yanagisawa N. Yoshida K, et al. Among authors: shimizu n. Nat Genet. 1995 Mar;9(3):267-72. doi: 10.1038/ng0395-267. Nat Genet. 1995. PMID: 7539672

2

HD-PTP: A novel protein tyrosine phosphatase gene on human chromosome 3p21.3.

Toyooka S, Ouchida M, Jitsumori Y, Tsukuda K, Sakai A, Nakamura A, Shimizu N, Shimizu K. Toyooka S, et al. Among authors: shimizu k, shimizu n. Biochem Biophys Res Commun. 2000 Nov 30;278(3):671-8. doi: 10.1006/bbrc.2000.3870. Biochem Biophys Res Commun. 2000. PMID: 11095967

3

Identification of the spinocerebellar ataxia type 2 gene using a direct identification of repeat expansion and cloning technique, DIRECT.

Sanpei K, Takano H, Igarashi S, Sato T, Oyake M, Sasaki H, Wakisaka A, Tashiro K, Ishida Y, Ikeuchi T, Koide R, Saito M, Sato A, Tanaka T, Hanyu S, Takiyama Y, Nishizawa M, Shimizu N, Nomura Y, Segawa M, Iwabuchi K, Eguchi I, Tanaka H, Takahashi H, Tsuji S. Sanpei K, et al. Among authors: shimizu n. Nat Genet. 1996 Nov;14(3):277-84. doi: 10.1038/ng1196-277. Nat Genet. 1996. PMID: 8896556

4

Richner-Hanhart's syndrome. Electron microscopic study of the skin lesion.

Shimizu N, Ito M, Ito K, Nakamura A, Sato Y, Maruyama T. Shimizu N, et al. Arch Dermatol. 1990 Oct;126(10):1342-6. doi: 10.1001/archderm.126.10.1342. Arch Dermatol. 1990. PMID: 2145811

5

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

6

Enhancement of Satellite Cell Transplantation Efficiency by Leukemia Inhibitory Factor.

Ito N, Shimizu N, Tanaka H, Takeda S. Ito N, et al. Among authors: shimizu n. J Neuromuscul Dis. 2016 May 27;3(2):201-207. doi: 10.3233/JND-160156. J Neuromuscul Dis. 2016. PMID: 27854222 Free PMC article.

7

Autosomal dominant retinitis pigmentosa. A mutation in codon 181 (Glu-->Lys) of the rhodopsin gene in a Japanese family.

Saga M, Mashima Y, Akeo K, Oguchi Y, Kudoh J, Shimizu N. Saga M, et al. Among authors: shimizu n. Ophthalmic Genet. 1994 Jun;15(2):61-7. doi: 10.3109/13816819409098865. Ophthalmic Genet. 1994. PMID: 7850270

8

Structure of human holocarboxylase synthetase gene and mutation spectrum of holocarboxylase synthetase deficiency.

Yang X, Aoki Y, Li X, Sakamoto O, Hiratsuka M, Kure S, Taheri S, Christensen E, Inui K, Kubota M, Ohira M, Ohki M, Kudoh J, Kawasaki K, Shibuya K, Shintani A, Asakawa S, Minoshima S, Shimizu N, Narisawa K, Matsubara Y, Suzuki Y. Yang X, et al. Among authors: shimizu n. Hum Genet. 2001 Nov;109(5):526-34. doi: 10.1007/s004390100603. Epub 2001 Oct 5. Hum Genet. 2001. PMID: 11735028

9

A rapid monitoring system of human herpesviruses reactivation by LightCycler in stem cell transplantation.

Aritaki K, Ohyashiki JH, Suzuki A, Ojima T, Abe K, Shimizu N, Yamamoto K, Ohyashiki K, Hoshika A. Aritaki K, et al. Among authors: shimizu n. Bone Marrow Transplant. 2001 Nov;28(10):975-80. doi: 10.1038/sj.bmt.1703266. Bone Marrow Transplant. 2001. PMID: 11753554

10

Charcot-Marie-Tooth neuropathy type 1B is associated with mutations of the myelin P0 gene.

Hayasaka K, Himoro M, Sato W, Takada G, Uyemura K, Shimizu N, Bird TD, Conneally PM, Chance PF. Hayasaka K, et al. Among authors: shimizu n. Nat Genet. 1993 Sep;5(1):31-4. doi: 10.1038/ng0993-31. Nat Genet. 1993. PMID: 7693129

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