Nobuyuki Shimozawa
Division of Genomics Research
Life Science Research Center
Gifu University
Japan
Name/email consistency: high
- Molecular and neurologic findings of peroxisome biogenesis disorders. Shimozawa, N., Nagase, T., Takemoto, Y., Funato, M., Kondo, N., Suzuki, Y. J. Child Neurol. (2005)
- Identification of a new complementation group of the peroxisome biogenesis disorders and PEX14 as the mutated gene. Shimozawa, N., Tsukamoto, T., Nagase, T., Takemoto, Y., Koyama, N., Suzuki, Y., Komori, M., Osumi, T., Jeannette, G., Wanders, R.J., Kondo, N. Hum. Mutat. (2004)
- Genetic heterogeneity of peroxisome biogenesis disorders among Japanese patients: evidence for a founder haplotype for the most common PEX10 gene mutation. Shimozawa, N., Nagase, T., Takemoto, Y., Ohura, T., Suzuki, Y., Kondo, N. Am. J. Med. Genet. A (2003)
- Genetic heterogeneity in Japanese patients with peroxisome biogenesis disorders and evidence for a founder haplotype for the most common mutation in PEX10 gene. Shimozawa, N., Nagase, T., Takemoto, Y., Suzuki, Y., Kondo, N. Adv. Exp. Med. Biol. (2003)
- A novel aberrant splicing mutation of the PEX16 gene in two patients with Zellweger syndrome. Shimozawa, N., Nagase, T., Takemoto, Y., Suzuki, Y., Fujiki, Y., Wanders, R.J., Kondo, N. Biochem. Biophys. Res. Commun. (2002)
- Molecular mechanism of detectable catalase-containing particles, peroxisomes, in fibroblasts from a PEX2-defective patient. Shimozawa, N., Zhang, Z., Imamura, A., Suzuki, Y., Fujiki, Y., Tsukamoto, T., Osumi, T., Aubourg, P., Wanders, R.J., Kondo, N. Biochem. Biophys. Res. Commun. (2000)
- Identification of PEX3 as the gene mutated in a Zellweger syndrome patient lacking peroxisomal remnant structures. Shimozawa, N., Suzuki, Y., Zhang, Z., Imamura, A., Ghaedi, K., Fujiki, Y., Kondo, N. Hum. Mol. Genet. (2000)
- A novel nonsense mutation of the PEX7 gene in a patient with rhizomelic chondrodysplasia punctata. Shimozawa, N., Suzuki, Y., Zhang, Z., Miura, K., Matsumoto, A., Nagaya, M., Castillo-Taucher, S., Kondo, N. J. Hum. Genet. (1999)
- 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, R.J., Kondo, N. Hum. Mol. Genet. (1999)
- Functional heterogeneity of C-terminal peroxisome targeting signal 1 in PEX5-defective patients. Shimozawa, N., Zhang, Z., Suzuki, Y., Imamura, A., Tsukamoto, T., Osumi, T., Fujiki, Y., Orii, T., Barth, P.G., Wanders, R.J., Kondo, N. Biochem. Biophys. Res. Commun. (1999)
- Peroxisome biogenesis disorders: identification of a new complementation group distinct from peroxisome-deficient CHO mutants and not complemented by human PEX 13. Shimozawa, N., Suzuki, Y., Zhang, Z., Imamura, A., Tsukamoto, T., Osumi, T., Tateishi, K., Okumoto, K., Fujiki, Y., Orii, T., Barth, P.G., Wanders, R.J., Kondo, N. Biochem. Biophys. Res. Commun. (1998)
