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1 d their in vivo phenotype when placed in the athymic mouse.
2 ut mouse), and absent specific immunity (the athymic mouse), and the appropriate B6,129F2 and C57BL/6
3 B1, derived from a fibrosarcoma formed in an athymic mouse following injection of carcinogen-transfor
4 When grafted beneath the renal capsule of athymic mouse hosts, all of the tumor-derived cell strai
8 s of intraperitoneal ovarian carcinoma in an athymic mouse model demonstrated that a monoclonal antib
9 ne methyl ester for antitumor activity in an athymic mouse model implanted ip with H-ras-transformed
17 y leads to a complete tumor regression in an athymic mouse tumor xenograft model, it fails to do so i
18 eeks of implantation in muscle pouches of an athymic mouse, whereas explanted particles less than 250
19 varian carcinoma and ascites formation in an athymic mouse xenogeneic transplant model of ovarian can
20 o susceptible to ROPV infection by using the athymic mouse xenograft system and adult immunocompetent
24 JG-136 is active over a wide dosage range in athymic mouse xenografts: on a qd x 5 schedule, the maxi
25 human papillomavirus type 11 (HPV11) in the athymic mouse xenograph neutralization assay and bind HP
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