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N Usuda

Showing results (81-90 of 92) with videos related to

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Biochemical and Biophysical Research Communications|September 15, 1993
Inhibition of acid secretion in gastric parietal cells by the Ca2+/calmodulin-dependent protein kinase II inhibitor KN-93N Mamiya, J R Goldenring, Y Tsunoda, et al.
The Journal of Biological Chemistry|May 21, 1999
Absence of spontaneous peroxisome proliferation in enoyl-CoA Hydratase/L-3-hydroxyacyl-CoA dehydrogenase-deficient mouse liver. Further support for the role of fatty acyl CoA oxidase in PPARalpha ligand metabolismC Qi, Y Zhu, J Pan, et al.
Journal of Cell Science|April 1, 1994
Uric acid degrading enzymes, urate oxidase and allantoinase, are associated with different subcellular organelles in frog liver and kidneyN Usuda, S Hayashi, S Fujiwara, et al.
The Journal of Biological Chemistry|April 22, 1994
Amphibian allantoinase. Molecular cloning, tissue distribution, and functional expressionS Hayashi, S Jain, R Chu, et al.
The New England Journal of Medicine|March 10, 2001
High serum IgG4 concentrations in patients with sclerosing pancreatitisH Hamano, S Kawa, A Horiuchi, et al.
Gene Expression|May 4, 2000
Cloning and expression of the mouse deoxyuridine triphosphate nucleotidohydrolase gene: differs from the rat enzyme in that it lacks nuclear receptor interacting LXXLL motifL Kan, S Jain, W Cook, et al.
Journal of Human Genetics|May 13, 1999
Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiencyY Suzuki, Z Zhang, N Shimozawa, et al.
The Journal of Biological Chemistry|June 26, 1999
Peroxisomal and mitochondrial fatty acid beta-oxidation in mice nullizygous for both peroxisome proliferator-activated receptor alpha and peroxisomal fatty acyl-CoA oxidase. Genotype correlation with fatty liver phenotypeT Hashimoto, T Fujita, N Usuda, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Targeted disruption of the peroxisomal fatty acyl-CoA oxidase gene: generation of a mouse model of pseudoneonatal adrenoleukodystrophyC Y Fan, J Pan, R Chu, et al.
The Journal of Biological Chemistry|October 4, 1996
Hepatocellular and hepatic peroxisomal alterations in mice with a disrupted peroxisomal fatty acyl-coenzyme A oxidase geneC Y Fan, J Pan, R Chu, et al.
Pageof 10

Showing results (81-90 of 92) with videos related to

Sort By:
Pageof 10
Biochemical and Biophysical Research Communications|September 15, 1993
Inhibition of acid secretion in gastric parietal cells by the Ca2+/calmodulin-dependent protein kinase II inhibitor KN-93N Mamiya, J R Goldenring, Y Tsunoda, et al.
The Journal of Biological Chemistry|May 21, 1999
Absence of spontaneous peroxisome proliferation in enoyl-CoA Hydratase/L-3-hydroxyacyl-CoA dehydrogenase-deficient mouse liver. Further support for the role of fatty acyl CoA oxidase in PPARalpha ligand metabolismC Qi, Y Zhu, J Pan, et al.
Journal of Cell Science|April 1, 1994
Uric acid degrading enzymes, urate oxidase and allantoinase, are associated with different subcellular organelles in frog liver and kidneyN Usuda, S Hayashi, S Fujiwara, et al.
The Journal of Biological Chemistry|April 22, 1994
Amphibian allantoinase. Molecular cloning, tissue distribution, and functional expressionS Hayashi, S Jain, R Chu, et al.
The New England Journal of Medicine|March 10, 2001
High serum IgG4 concentrations in patients with sclerosing pancreatitisH Hamano, S Kawa, A Horiuchi, et al.
Gene Expression|May 4, 2000
Cloning and expression of the mouse deoxyuridine triphosphate nucleotidohydrolase gene: differs from the rat enzyme in that it lacks nuclear receptor interacting LXXLL motifL Kan, S Jain, W Cook, et al.
Journal of Human Genetics|May 13, 1999
Prenatal diagnosis of peroxisomal D-3-hydroxyacyl-CoA dehydratase/D-3-hydroxyacyl-CoA dehydrogenase bifunctional protein deficiencyY Suzuki, Z Zhang, N Shimozawa, et al.
The Journal of Biological Chemistry|June 26, 1999
Peroxisomal and mitochondrial fatty acid beta-oxidation in mice nullizygous for both peroxisome proliferator-activated receptor alpha and peroxisomal fatty acyl-CoA oxidase. Genotype correlation with fatty liver phenotypeT Hashimoto, T Fujita, N Usuda, et al.
Annals of the New York Academy of Sciences|December 27, 1996
Targeted disruption of the peroxisomal fatty acyl-CoA oxidase gene: generation of a mouse model of pseudoneonatal adrenoleukodystrophyC Y Fan, J Pan, R Chu, et al.
The Journal of Biological Chemistry|October 4, 1996
Hepatocellular and hepatic peroxisomal alterations in mice with a disrupted peroxisomal fatty acyl-coenzyme A oxidase geneC Y Fan, J Pan, R Chu, et al.
Pageof 10