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N Shimozawa

Showing results (71-80 of 125) with videos related to

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Human Mutation|January 1, 1996
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsA Yamagishi, S Tomatsu, S Fukuda, et al.
Biochemical and Biophysical Research Communications|October 19, 2001
Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 geneR Ito, Y Huang, C Yao, et al.
Reproduction (Cambridge, England)|November 3, 2001
Production of cloned mice from embryonic stem cells arrested at metaphaseY Ono, N Shimozawa, K Muguruma, et al.
Acta Paediatrica Japonica : Overseas Edition|May 15, 1998
Magnetic resonance imaging of acute cerebellar ataxia: report of a case with gadolinium enhancement and review of the literatureZ Kato, N Shimozawa, J Kokuzawa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group IS Tamura, K Okumoto, R Toyama, et al.
Genomics|March 1, 1994
Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking regionY Nakashima, S Tomatsu, T Hori, et al.
Human Genetics|March 1, 1992
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cellsS Yajima, Y Suzuki, N Shimozawa, et al.
Journal of Human Genetics|May 17, 2001
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6N Matsumoto, S Tamura, A Moser, et al.
Human Molecular Genetics|August 11, 1999
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutantsR Toyama, S Mukai, A Itagaki, et al.
Biochemical and Biophysical Research Communications|January 28, 1994
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.
Pageof 13

Showing results (71-80 of 125) with videos related to

Sort By:
Pageof 13
Human Mutation|January 1, 1996
Mucopolysaccharidosis type I: identification of common mutations that cause Hurler and Scheie syndromes in Japanese populationsA Yamagishi, S Tomatsu, S Fukuda, et al.
Biochemical and Biophysical Research Communications|October 19, 2001
Temperature-sensitive phenotype of Chinese hamster ovary cells defective in PEX5 geneR Ito, Y Huang, C Yao, et al.
Reproduction (Cambridge, England)|November 3, 2001
Production of cloned mice from embryonic stem cells arrested at metaphaseY Ono, N Shimozawa, K Muguruma, et al.
Acta Paediatrica Japonica : Overseas Edition|May 15, 1998
Magnetic resonance imaging of acute cerebellar ataxia: report of a case with gadolinium enhancement and review of the literatureZ Kato, N Shimozawa, J Kokuzawa, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 16, 1998
Human PEX1 cloned by functional complementation on a CHO cell mutant is responsible for peroxisome-deficient Zellweger syndrome of complementation group IS Tamura, K Okumoto, R Toyama, et al.
Genomics|March 1, 1994
Mucopolysaccharidosis IV A: molecular cloning of the human N-acetylgalactosamine-6-sulfatase gene (GALNS) and analysis of the 5'-flanking regionY Nakashima, S Tomatsu, T Hori, et al.
Human Genetics|March 1, 1992
Complementation study of peroxisome-deficient disorders by immunofluorescence staining and characterization of fused cellsS Yajima, Y Suzuki, N Shimozawa, et al.
Journal of Human Genetics|May 17, 2001
The peroxin Pex6p gene is impaired in peroxisomal biogenesis disorders of complementation group 6N Matsumoto, S Tamura, A Moser, et al.
Human Molecular Genetics|August 11, 1999
Isolation, characterization and mutation analysis of PEX13-defective Chinese hamster ovary cell mutantsR Toyama, S Mukai, A Itagaki, et al.
Biochemical and Biophysical Research Communications|January 28, 1994
Identification of a nonsense mutation in ALD protein cDNA from a patient with adrenoleukodystrophyA Uchiyama, Y Suzuki, X Q Song, et al.
Pageof 13