Shimozawa N - Search Results

1

Enhanced expression of a-series gangliosides in fibroblasts of patients with peroxisome biogenesis disorders.

Tatsumi K, Saito M, Lin B, Iwamori M, Ichiseki H, Shimozawa N, Kamoshita S, Igarashi T, Sakakihara Y. Tatsumi K, et al. Among authors: shimozawa n. Biochim Biophys Acta. 2001 Mar 26;1535(3):285-93. doi: 10.1016/s0925-4439(01)00027-8. Biochim Biophys Acta. 2001. PMID: 11278168 Free article.

2

Accumulation of glycolipids in mutant Chinese hamster ovary cells (Z65) with defective peroxisomal assembly and comparison of the metabolic rate of glycosphingolipids between Z65 cells and wild-type CHO-K1 cells.

Saito M, Iwamori M, Lin B, Oka A, Fujiki Y, Shimozawa N, Kamoshita S, Yanagisawa M, Sakakihara Y. Saito M, et al. Among authors: shimozawa n. Biochim Biophys Acta. 1999 Apr 19;1438(1):55-62. doi: 10.1016/s1388-1981(99)00037-2. Biochim Biophys Acta. 1999. PMID: 10216280

3

[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.

4

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

5

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

6

Restoration of biochemical function of the peroxisome in the temperature-sensitive mild forms of peroxisome biogenesis disorder in humans.

Imamura A, Shimozawa N, Suzuki Y, Zhang Z, Tsukamoto T, Fujiki Y, Orii T, Osumi T, Kondo N. Imamura A, et al. Among authors: shimozawa n. Brain Dev. 2000 Jan;22(1):8-12. doi: 10.1016/s0387-7604(99)00072-8. Brain Dev. 2000. PMID: 10761827

7

Phenotype-genotype relationships in peroxisome biogenesis disorders of PEX1-defective complementation group 1 are defined by Pex1p-Pex6p interaction.

Tamura S, Matsumoto N, Imamura A, Shimozawa N, Suzuki Y, Kondo N, Fujiki Y. Tamura S, et al. Among authors: shimozawa n. Biochem J. 2001 Jul 15;357(Pt 2):417-26. doi: 10.1042/0264-6021:3570417. Biochem J. 2001. PMID: 11439091 Free PMC article.

8

Transformation and characterization of mutant human fibroblasts defective in peroxisome assembly.

Okamoto H, Suzuki Y, Shimozawa N, Yajima S, Masuno M, Orii T. Okamoto H, et al. Among authors: shimozawa n. Exp Cell Res. 1992 Aug;201(2):307-12. doi: 10.1016/0014-4827(92)90278-g. Exp Cell Res. 1992. PMID: 1639130

9

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

10

[Molecular analysis of peroxisomal disorders].

Shimozawa N. Shimozawa N. No To Hattatsu. 1998 Mar;30(2):128-33. No To Hattatsu. 1998. PMID: 9545777 Japanese.

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