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N Shimozawa

Showing results (61-70 of 167) with videos related to

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Human Molecular Genetics|August 13, 1998
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group BK Okumoto, R Itoh, N Shimozawa, et al.
Clinical Genetics|November 1, 1996
Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidationK Inoue, Y Suzuki, S Yajima, et al.
Brain & Development|November 1, 1993
A case of pseudo-Zellweger syndrome with a possible bifunctional enzyme deficiency but detectable enzyme protein. Comparison of two cases of Zellweger syndromeY Nakada, N Hyakuna, Y Suzuki, et al.
Biochimica Et Biophysica Acta|April 20, 2000
Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteinsM Ito, R Ito, Y Huang, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disordersY Suzuki, N Shimozawa, A Imamura, et al.
Prenatal Diagnosis|March 1, 1996
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysisA Imamura, Y Suzuki, X Q Song, et al.
No to Hattatsu = Brain and Development|July 1, 1986
[Central nervous system complications of congenital myotonic dystrophy]N Shimozawa, M Inagaki, T Mito, et al.
Hepato-Gastroenterology|May 3, 2000
Effects of prostaglandin E1 administration during hepatectomy for cirrhotic hepatocellular carcinomaK Hanazaki, S Kajikawa, Y Fujimori, et al.
Journal of Medical Genetics|January 5, 2002
Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disordersA Imamura, N Shimozawa, Y Suzuki, et al.
American Journal of Surgery|July 5, 2001
Hepatic resection for large hepatocellular carcinomaK Hanazaki, S Kajikawa, N Shimozawa, et al.
Pageof 17

Showing results (61-70 of 167) with videos related to

Sort By:
Pageof 17
Human Molecular Genetics|August 13, 1998
Mutations in PEX10 is the cause of Zellweger peroxisome deficiency syndrome of complementation group BK Okumoto, R Itoh, N Shimozawa, et al.
Clinical Genetics|November 1, 1996
Carrier identification of X-linked adrenoleukodystrophy by measurement of very long chain fatty acids and lignoceric acid oxidationK Inoue, Y Suzuki, S Yajima, et al.
Brain & Development|November 1, 1993
A case of pseudo-Zellweger syndrome with a possible bifunctional enzyme deficiency but detectable enzyme protein. Comparison of two cases of Zellweger syndromeY Nakada, N Hyakuna, Y Suzuki, et al.
Biochimica Et Biophysica Acta|April 20, 2000
Rapid isolation and characterization of CHO mutants deficient in peroxisome biogenesis using the peroxisomal forms of fluorescent proteinsM Ito, R Ito, Y Huang, et al.
Journal of Inherited Metabolic Disease|June 19, 2001
Clinical, biochemical and genetic aspects and neuronal migration in peroxisome biogenesis disordersY Suzuki, N Shimozawa, A Imamura, et al.
Prenatal Diagnosis|March 1, 1996
Prenatal diagnosis of adrenoleukodystrophy by means of mutation analysisA Imamura, Y Suzuki, X Q Song, et al.
No to Hattatsu = Brain and Development|July 1, 1986
[Central nervous system complications of congenital myotonic dystrophy]N Shimozawa, M Inagaki, T Mito, et al.
Hepato-Gastroenterology|May 3, 2000
Effects of prostaglandin E1 administration during hepatectomy for cirrhotic hepatocellular carcinomaK Hanazaki, S Kajikawa, Y Fujimori, et al.
Journal of Medical Genetics|January 5, 2002
Temperature sensitive acyl-CoA oxidase import in group A peroxisome biogenesis disordersA Imamura, N Shimozawa, Y Suzuki, et al.
American Journal of Surgery|July 5, 2001
Hepatic resection for large hepatocellular carcinomaK Hanazaki, S Kajikawa, N Shimozawa, et al.
Pageof 17