Keywords: |
leukemia; unclassified drug; gene mutation; aurora kinase inhibitor; clinical trial; review; cancer growth; liver cell carcinoma; nonhuman; solid tumor; paclitaxel; pancreas cancer; cancer staging; antineoplastic agent; neoplasms; colorectal cancer; mitosis; animals; cell viability; dna damage; gene overexpression; ovary cancer; breast cancer; gene amplification; lung non small cell cancer; lung cancer; vincristine; bladder cancer; vinblastine; hodgkin disease; carcinogenesis; chromatid; cell transformation, neoplastic; docetaxel; prostate cancer; gene expression regulation; nonhodgkin lymphoma; neuroblastoma; head and neck cancer; disease progression; colon cancer; uterine cervix cancer; stomach cancer; chromosomal instability; chromosome breakage; anaphase; models, genetic; ependymoma; thyroid carcinoma; kaposi sarcoma; rhabdomyosarcoma; navelbine; esophagus cancer; testis cancer; astrocytoma; aneuploidy; mycosis fungoides; seminoma; metaphase; nephroblastoma; 2 [[3 [4 [5 [2 (3 fluoroanilino) 2 oxoethyl] 1h pyrazol 3 ylamino] 7 quinazolinyloxy]propyl](ethyl)amino]ethyl dihydrogen phosphate; 1 cyclopropyl 3 [3 (5 morpholinomethyl 1h benzimidazol 2 yl) 1h pyrazol 4 yl]urea; 4 (8 cyclopentyl 7 ethyl 5,6,7,8 tetrahydro 5 methyl 6 oxo 2 pteridinylamino) 3 methoxy n (1 methyl 4 piperidinyl)benzamide; arry 520; azd 4877; gsk 923295; ispinesib; mk 0731; mln 8237; on 01910; p 276 00; sb 743921; chromatid aberration
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