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1. Data from Molecular Basis for the Induction of an Angiogenesis Inhibitor, Thrombospondin-1, by 5-Fluorouracil

2. Supplementary Table 1 from Molecular Basis for the Induction of an Angiogenesis Inhibitor, Thrombospondin-1, by 5-Fluorouracil

8. A positively charged amino acid proximal to the C-terminus of TM17 of MRP1 is indispensable for GSH-dependent binding of substrates and for transport of LTC (sub)4

16. Thymidine catabolism promotes NADPH oxidase-derived reactive oxygen species (ROS) signalling in KB and yumoto cells

17. Expression of the multidrug transporter, P-glycoprotein, in renal and transitional cell carcinomas

18. Thymidine catabolism promotes NADPH oxidase-derived reactive oxygen species (ROS) signalling in KB and yumoto cells

19. Thymidine Catabolism as a Metabolic Strategy for Cancer Survival

21. CRISPR/Cas9n-Mediated Deletion of the Snail 1Gene (SNAI1) Reveals Its Role in Regulating Cell Morphology, Cell-Cell Interactions, and Gene Expression in Ovarian Cancer (RMG-1) Cells

23. Snail modulates cell metabolism in MDCK cells

27. Molecular Basis for the Induction of an Angiogenesis Inhibitor, Thrombospondin-1, by 5-Fluorouracil

29. Isolation and characterization of arsenite-resistant human epidermoid carcinoma KB cells

31. Molecular basis for the involvement of thymidine phosphorylase in cancer invasion

32. 2-Deoxy-d-ribose inhibits hypoxia-induced apoptosis by suppressing the phosphorylation of p38 MAPK

36. GSH Inhibits Trypsinization of the C-terminal Half of Human MRP1

43. Thymidine phosphorylase inhibits apoptosis induced by cisplatin

44. Binding Site(s) on P-Glycoprotein for a Newly Synthesized Photoaffinity Analog of Agosterol A

45. Reversal of P-glycoprotein mediated multidrug resistance by a newly synthesized 1,4-benzothiazipine derivative, JTV-519

47. Targeted Deletion of Both Thymidine Phosphorylase and Uridine Phosphorylase and Consequent Disorders in Mice

48. Molecular Basis for the Inhibition of Hypoxia-Induced Apoptosis by 2-Deoxy-d-ribose

50. Increased sensitivity to vincristine of MDR cells by the leukotriene D4 receptor antagonist, ONO-1078

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