Shimozawa N - Search Results

1

Nonsense and temperature-sensitive mutations in PEX13 are the cause of complementation group H of peroxisome biogenesis disorders.

Shimozawa N, Suzuki Y, Zhang Z, Imamura A, Toyama R, Mukai S, Fujiki Y, Tsukamoto T, Osumi T, Orii T, Wanders RJ, Kondo N. Shimozawa N, et al. Hum Mol Genet. 1999 Jun;8(6):1077-83. doi: 10.1093/hmg/8.6.1077. Hum Mol Genet. 1999. PMID: 10332040

2

Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cells.

Yajima S, Suzuki Y, Shimozawa N, Yamaguchi S, Orii T, Fujiki Y, Osumi T, Hashimoto T, Moser HW. Yajima S, et al. Among authors: shimozawa n. Hum Genet. 1992 Mar;88(5):491-9. doi: 10.1007/BF00219334. Hum Genet. 1992. PMID: 1372585

3

Animal cell mutants represent two complementation groups of peroxisome-defective Zellweger syndrome.

Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Fujiki Y. Shimozawa N, et al. J Clin Invest. 1992 Nov;90(5):1864-70. doi: 10.1172/JCI116063. J Clin Invest. 1992. PMID: 1430210 Free PMC article.

4

A human gene responsible for Zellweger syndrome that affects peroxisome assembly.

Shimozawa N, Tsukamoto T, Suzuki Y, Orii T, Shirayoshi Y, Mori T, Fujiki Y. Shimozawa N, et al. Science. 1992 Feb 28;255(5048):1132-4. doi: 10.1126/science.1546315. Science. 1992. PMID: 1546315

5

Peroxisome assembly factor-2, a putative ATPase cloned by functional complementation on a peroxisome-deficient mammalian cell mutant.

Tsukamoto T, Miura S, Nakai T, Yokota S, Shimozawa N, Suzuki Y, Orii T, Fujiki Y, Sakai F, Bogaki A, Yasumo H, Osumi T. Tsukamoto T, et al. Among authors: shimozawa n. Nat Genet. 1995 Dec;11(4):395-401. doi: 10.1038/ng1295-395. Nat Genet. 1995. PMID: 7493019

6

Identification of a novel frameshift mutation in a Japanese adrenoleukodystrophy patient.

Song XQ, Fukao T, Suzuki Y, Imamura A, Uchiyama A, Shimozawa N, Kondo N, Orii T. Song XQ, et al. Among authors: shimozawa n. Hum Mol Genet. 1995 Jun;4(6):1093-4. doi: 10.1093/hmg/4.6.1093. Hum Mol Genet. 1995. PMID: 7655465 No abstract available.

7

[Clinical and molecular aspects of peroxisome-deficient disorders].

Suzuki Y, Shimozawa N, Orii T. Suzuki Y, et al. Among authors: shimozawa n. Nihon Rinsho. 1993 Sep;51(9):2353-8. Nihon Rinsho. 1993. PMID: 7692118 Review. Japanese.

8

New Gaucher disease mutations in exon 10: a novel L444R mutation produces a new NciI site the same as L444P.

Uchiyama A, Tomatsu S, Kondo N, Suzuki Y, Shimozawa N, Fukuda S, Sukegawa K, Taki N, Inamori H, Orii T. Uchiyama A, et al. Among authors: shimozawa n. Hum Mol Genet. 1994 Jul;3(7):1183-4. doi: 10.1093/hmg/3.7.1183. Hum Mol Genet. 1994. PMID: 7981693 No abstract available.

9

Mucopolysaccharidosis IVA: four new exonic mutations in patients with N-acetylgalactosamine-6-sulfate sulfatase deficiency.

Tomatsu S, Fukuda S, Yamagishi A, Cooper A, Wraith JF, Hori T, Kato Z, Yamada N, Isogai K, Sukegawa K, Kondo N, Suzuki Y, Shimozawa N, Orii T. Tomatsu S, et al. Among authors: shimozawa n. Am J Hum Genet. 1996 May;58(5):950-62. Am J Hum Genet. 1996. PMID: 8651279 Free PMC article.

10

Correction by gene expression of biochemical abnormalities in fibroblasts from Zellweger patients.

Shimozawa N, Suzuki Y, Tomatsu S, Tsukamoto T, Osumi T, Fujiki Y, Kamijo K, Hashimoto T, Kondo N, Orii T. Shimozawa N, et al. Pediatr Res. 1996 May;39(5):812-5. doi: 10.1203/00006450-199605000-00011. Pediatr Res. 1996. PMID: 8726233

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