207 results on '"Kawashima, Ikuo"'
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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
3. Clot retraction is mediated by factor XIII-dependent fibrin-αIIbβ3-myosin axis in platelet sphingomyelin-rich membrane rafts
4. PKCδ deficiency inhibits fetal development and is associated with heart elastic fiber hyperplasia and lung inflammation in adult PKCδ knockout mice
5. ラクヘイ コテンエンゲキ タンボウ ―コウセイショウ ノ コテンエンゲキブタイ ト デントウチホウゲキ ノ ゲンジョウ ヲ メグッテ―
6. Efficient Uptake of Recombinant α-Galactosidase A Produced with a Gene-Manipulated Yeast by Fabry Mice Kidneys
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
9. Establishment of immortalized Schwann cells from Fabry mice and their low uptake of recombinant α-galactosidase
10. Corrective effect on Fabry mice of yeast recombinant human α-galactosidase with N-linked sugar chains suitable for lysosomal delivery
11. Comparison of the effects of agalsidase alfa and agalsidase beta on cultured human Fabry fibroblasts and Fabry mice
12. オンシュウ シ キョウソン チタイ ノ サイレイ ト ミンカン ゲイノウ -2017ネン ゲンショウセツ ノ タイジュン ケン ホウコク-
13. Cytochemical analysis of storage materials in cultured skin fibroblasts from patients with I-cell disease
14. ペキン シ チュウシン ブ ノ デントウ ゲキ ジョウエン ジョウキョウ
15. Phospholipid storage in the myocardium of a unique Japanese case of idiopathic cardiomyopathy
16. Highly phosphomannosylated enzyme replacement therapy for GM2 gangliosidosis
17. Cover Feature: Systematic Study on the Catalytic Arsa‐Wittig Reaction (Chem. Eur. J. 59/2020)
18. Systematic Study on the Catalytic Arsa‐Wittig Reaction
19. Production of a Recombinant Single-Chain Variable-Fragment (scFv) Antibody against Sulfoglycolipid
20. チュウゴク デントウ チホウゲキ ノ ショソウ キョウゲキ コンキョク エツゲキ コテン エンゲキ ノ ムカシ ト イマ
21. Dibenzoarsepins: Planarization of 8π‐Electron System in the Lowest Singlet Excited State
22. CELL TYPE-SPECIFIC EXPRESSION OF GANGLIOSIDE ANTIGENS IN RAT PRIMARY CULTURES C
23. Peraryl Arsoles: Practical Synthesis, Electronic Structures, and Solid-State Emission Behaviors
24. Cover Feature: Peraryl Arsoles: Practical Synthesis, Electronic Structures, and Solid-State Emission Behaviors (Chem. Eur. J. 35/2018)
25. シャンハイ コウソ コテン ブタイ ジショウ
26. チュウゴク レキシ コテン ゲキ ショウコウ エツゲキ チョウブンカ ケンサイ オ メグッテ
27. ショウコウ コテン エンゲキ タンポウ
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
29. フクシュウギダイ ケンガクキ
30. Multi-mode emission color tuning of dithieno[3,2-b:2′,3′-d]arsoles
31. Differences in cleavage of globotriaosylceramide and its derivatives accumulated in organs of young Fabry mice following enzyme replacement therapy
32. Measurement of glycosphingolipids by means of tandem mass spectrometry and evaluation of them as a biomarker of Fabry disease
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
34. Development of a Highly Sensitive Immuno-PCR Assay for the Measurement of α-Galactosidase A Protein Levels in Serum and Plasma
35. Fabry disease: Biochemical, pathological and structural studies of the α-galactosidase A with E66Q amino acid substitution
36. Lyso-GM2 Ganglioside: A Possible Biomarker of Tay-Sachs Disease and Sandhoff Disease
37. Efficient Uptake of Recombinant α-Galactosidase A Produced with a Gene-Manipulated Yeast by Fabry Mice Kidneys
38. Highly phosphomannosylated enzyme replacement therapy for GM2 gangliosidosis
39. Tissue and plasma globotriaosylsphingosine could be a biomarker for assessing enzyme replacement therapy for Fabry disease
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
43. Uptake of a Recombinant Human .ALPHA.-L-Iduronidase (laronidase) by Cultured Fibroblasts and Osteoblasts
44. Glycosphingolipid Antigens in Neural Tumor Cell Lines and Anti-Glycosphingolipid Antibodies in Sera of Patients with Neural Tumors
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
47. Expansion of natural killer cells in mice transgenic for IgM antibody to ganglioside GD2: demonstration of prolonged survival after challenge with syngeneic tumor cells
48. Carbohydrate-Carbohydrate Binding of Ganglioside to Integrin α5 Modulates α5β1Function
49. Differential Distribution of Glycosphingolipid Antigens in the Central Nervous System.
50. An immunocytochemical technique with monoclonal antibodies to glycosphingolipids in rat primary cerebellar cultures: influence of detergent permeabilization
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