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2. Phosphacan acts as a repulsive cue in murine and rat cerebellar granule cells in a TAG‐1/GD3 rafts‐dependent manner

4. PKCδ deficiency inhibits fetal development and is associated with heart elastic fiber hyperplasia and lung inflammation in adult PKCδ knockout mice

7. Binding parameters and thermodynamics of the interaction of imino sugars with a recombinant human acid α-glucosidase (alglucosidase alfa): Insight into the complex formation mechanism

8. Use of a modified [alpha]-N-acetylgalactosaminidase in the development of enzyme replacement therapy for Fabry disease

28. Production of recombinant [beta]-hexosaminidase A, a potential enzyme for replacement therapy for Tay-Sachs and Sandhoff diseases, in the methylotrophic yeast Ogataea minuta

33. 高感度酵素抗体法を用いたRett症候群および他の神経疾患における髄液ガングリオシド分析

35. Fabry disease: Biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution

38. Highly phosphomannosylated enzyme replacement therapy for GM2 gangliosidosis

40. Use of a Modified α-N-Acetylgalactosaminidase in the Development of Enzyme Replacement Therapy for Fabry Disease

41. Molecular interaction of imino sugars with human α-galactosidase: Insight into the mechanism of complex formation and pharmacological chaperone action in Fabry disease

42. Antibody responses to ganglio-series gangliosides in different strains of inbred mice

45. Production of Recombinant β-Hexosaminidase A, a Potential Enzyme for Replacement Therapy for Tay-Sachs and Sandhoff Diseases, in the Methylotrophic Yeast Ogataea minuta

46. Comparison of the effects of agalsidase alfa and agalsidase beta on cultured human Fabry fibroblasts and Fabry mice

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