Development of genotyping method for functionally relevant variants of cytochromes P450 in cynomolgus macaques
Uno, Y., Osada, N., Sakurai, S., Shimozawa, N., Iwata, T., Ikeo, K., Yamazaki, H.
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Published in Journal of veterinary pharmacology and therapeutics (01.02.2018)
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Cloned Mice from Fetal Fibroblast Cells Arrested at Metaphase by a Serial Nuclear Transfer
ONO, Yukiko, SHIMOZAWA, Nobuhiro, ITO, Mamoru, KONO, Tomohiro
Published in Biology of reproduction (01.01.2001)
Published in Biology of reproduction (01.01.2001)
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Association between drusen and blood test results in a colony of 1,174 monkeys
Nishiguchi, K., Yokoyama, Y., Fujii, Y., Furukawa, T., Ono, F., Shimozawa, N., Togo, M., Suzuki, M., Nakazawa, T.
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Published in Acta ophthalmologica (Oxford, England) (01.10.2015)
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Disruption of imprinting in cloned mouse fetuses from embryonic stem cells
Ogawa, H, Ono, Y, Shimozawa, N, Sotomaru, Y, Katsuzawa, Y, Hiura, H, Ito, M, Kono, T
Published in Reproduction (Cambridge, England) (01.10.2003)
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Clinical, biochemical and molecular characterization of peroxisomal diseases in Arabs
Shaheen, R, Al-Dirbashi, OY, Al-Hassnan, ZN, Al-Owain, M, Makhsheed, N, Basheeri, F, Seidahmed, MZ, Salih, MAM, Faqih, E, Zaidan, H, Al-Sayed, M, Rahbeeni, Z, Al-Sheddi, T, Hashem, M, Kurdi, W, Shimozawa, N, Alkuraya, FS
Published in Clinical genetics (01.01.2011)
Published in Clinical genetics (01.01.2011)
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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
Published in Human molecular genetics (12.08.2000)
Published in Human molecular genetics (12.08.2000)
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Retinitis pigmentosa and mucopolysaccharidosis type II: an extremely attenuated phenotype
Suzuki, Y, Aoyama, A, Kato, T, Shimozawa, N, Orii, T
Published in Journal of inherited metabolic disease (01.08.2009)
Published in Journal of inherited metabolic disease (01.08.2009)
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Zellweger syndrome caused by PEX13 deficiency: Report of two novel mutations
Al-Dirbashi, O.Y., Shaheen, R., Al-Sayed, M., Al-Dosari, M., Makhseed, N., Safieh, L. Abu, Santa, T., Meyer, B.F., Shimozawa, N., Alkuraya, F.S.
Published in American journal of medical genetics. Part A (01.06.2009)
Published in American journal of medical genetics. Part A (01.06.2009)
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Baicalein 5,6,7-trimethyl ether activates peroxisomal but not mitochondrial fatty acid β-oxidation
Morita, M., Kanai, M., Mizuno, S., Iwashima, M., Hayashi, T., Shimozawa, N., Suzuki, Y., Imanaka, T.
Published in Journal of inherited metabolic disease (01.06.2008)
Published in Journal of inherited metabolic disease (01.06.2008)
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Production of cloned mice from embryonic stem cells arrested at metaphase
Ono, Y, Shimozawa, N, Muguruma, K, Kimoto, S, Hioki, K, Tachibana, M, Shinkai, Y, Ito, M, Kono, T
Published in Reproduction (Cambridge, England) (01.11.2001)
Published in Reproduction (Cambridge, England) (01.11.2001)
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Isolation, Characterization and Mutation Analysis of PEX13-Defective Chinese Hamster Ovary Cell Mutants
Toyama, Ryusuke, Mukai, Satoru, Itagaki, Atsushi, Tamura, Shigehiko, Shimozawa, Nobuyuki, Suzuki, Yasuyuki, Kondo, Naomi, Wanders, Ronald J. A., Fujiki, Yukio
Published in Human molecular genetics (01.09.1999)
Published in Human molecular genetics (01.09.1999)
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Human peroxisome assembly factor-2 (PAF-2) : A gene responsible for group C peroxisome biogenesis disorder in humans
FUKUDA, S, SHIMOZAWA, N, KUROKI, Y, FUJIKI, Y, ORII, T, KONDO, N, SUZUKI, Y, ZHANG, Z, TOMATSU, S, TSUKAMOTO, T, HASHIGUCHI, N, OSUMI, T, MASUNO, M, IMAIZUMI, K
Published in American journal of human genetics (01.12.1996)
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Published in American journal of human genetics (01.12.1996)
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Bone marrow transplantation for the treatment of X‐linked adrenoleukodystrophy
Suzuki, Y., Isogai, K., Teramoto, T., Tashita, H., Shimozawa, N., Nishimura, M., Asano, T., Oda, M., Kamei, A., Ishiguro, H., Kato, S., Ohashi, T., Kobayashi, H., Eto, Y., Kondo, N.
Published in Journal of inherited metabolic disease (01.07.2000)
Published in Journal of inherited metabolic disease (01.07.2000)
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Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disorders
Suzuki, Y., Shimozawa, N., Imamura, A., Fukuda, S., Zhang, Z., Orii, T., Kondo, N.
Published in Journal of inherited metabolic disease (01.04.2001)
Published in Journal of inherited metabolic disease (01.04.2001)
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Conference Proceeding
Standardization of complementation grouping of peroxisome-deficient disorders and the second Zellweger patient with peroxisomal assembly factor-1 (PAF-1) defect
Shimozawa, N, Suzuki, Y, Orii, T, Moser, A, Moser, H W, Wanders, R J
Published in American journal of human genetics (01.04.1993)
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Published in American journal of human genetics (01.04.1993)
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Epidemiology of X-linked adrenoleukodystrophy in Japan
Takemoto, Yasuhiko, Suzuki, Yasuyuki, Tamakoshi, Akiko, Onodera, Osamu, Tsuji, Shoji, Hashimoto, Takashi, Shimozawa, Nobuyuki, Orii, Tadao, Kondo, Naomi
Published in Journal of human genetics (01.01.2002)
Published in Journal of human genetics (01.01.2002)
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