机译:抑制组蛋白伴侣FACT的抗癌候选药物CBL0137在替莫唑胺反应性和耐药性胶质母细胞瘤的临床前原位模型中有效
Roswell Pk Canc Inst, Dept Neurooncol, Elm & Carlton St, Buffalo, NY 14263 USA;
Buffalo Biolabs LLC, Buffalo, NY USA;
Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA;
Buffalo Biolabs LLC, Buffalo, NY USA;
Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA;
Cleveland Biolabs Inc, Buffalo, NY USA|Incuron LLC, Buffalo, NY USA;
Roswell Pk Canc Inst, Dept Cell Stress Biol, Buffalo, NY 14263 USA|Cleveland Biolabs Inc, Buffalo, NY USA;
Roswell Pk Canc Inst, Dept Neurooncol, Elm & Carlton St, Buffalo, NY 14263 USA;
CBL0137; curaxin; Facilitates Chromatin Transcription; glioblastoma; temozolomide;
机译:组蛋白伴侣复合物FACT的药理靶向性可消除胶质母细胞瘤干细胞并延长临床前模型的存活率
机译:胶质母细胞瘤的临床前原位模型概括了人类肿瘤的关键特征,并证明了对MEK和PI3K途径抑制剂联合使用的敏感性
机译:siRNA纳米粒子抑制耐药基因,延长了原位胶质母细胞瘤异种移植小鼠模型中的存活
机译:基于在鸡胚绒膜尿囊膜(CAM)上生长的Caco-2细胞的靶向抗癌药物制剂的临床前测试肿瘤模型的开发
机译:抑制组蛋白伴侣FACT的抗癌候选药物CBL0137是在替莫唑胺反应和耐药的临床前原位模型中有效胶质母细胞瘤
机译:Claxin CBL0137消除耐药性癌症干细胞,并在胰腺癌的临床前模型中提高吉西他滨的疗效