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- CTX-Ⅱ CTX - Ⅱ
- CTX-M基因 CTX-M gene
- CTX/药理学 CTX/pharmacology
- HT/CTX细胞 HT/CTX cell
- CTX/治疗应用 CTX / treatment application
- 环磷酰胺(CTX) cyclopho sphamide(CTX)
- CTX-M型β-内酰胺酶 CTX - M - β- lactamase
- CTX-M类β-内酰胺酶 CTX-M-like extended spectrum beta-lactamase
- 低剂量环磷酰胺(CTX) Low- dose cyclopbosphamide (CTX)
- 人Ⅰ型胶原C端肽(CTX-Ⅰ) C-terminal telopeptide of typeⅠ collagen
- CTX从平均31.3%升高到48.9%; The IR of CTX after addition of ECPC was increased from31.3%25 to 48.9%25,and the IR for ADM from 15.2%25 to 45.5%25,q all > 1,showing that the combination ofECPC with these drugs could enhance the antitumor effect.
- 化疗方案为PCP(DDP+CTX+PYM)。 The regimen was Pcp(DDP+CTX+PYM).
- CTX-M-29是一种新基因型ESBLs,基因库登录号为AY267213。 CTX-M-29 is a novel ESBLs and the GenBank accession number is AY267213.
- 目的:探讨环磷酰胺(CTX)冲击治疗难治性肾病综合征(RNS)的疗效及护理方法。 Objective: To explore the effectiveness and methods of nursing care in the treatment of RNS with CTX pulse therapy.
- 新辅助化疗组术前作3周期CTF(CTX+THP+FUDR)化疗,术后补充放疗、化疗; The NACT group received a chemotherapy with the regiman of CTF(CTX+THP+FUDR)for three cycles before operation.
- TEM、SHV、CTX M 1组、CTX M 13组、Toho 1组通用引物检测产ESBL菌株及其转移接合子 ; The partial bla gene of ESBL producing isolates and their transcojugants were detected by PCR using universal primers for TEM, SHV, CTX-M-1group, Toho-1group, CTX-M-13group respectively.
- ADM +VDS +CTX联合化疗方案优于CMF方案 ,尤其在原发灶缩小上有显著差异 (P <0 0 1)。 ADM+VDS+CTX combined chemotherapy regimen was better than CMF regimen. There was a significant difference especially in remission of primary tumor( P <0 01).
- 目的比较CTX、ADM联合CF+5-Fu持续滴注方案与CAF方案治疗晚期乳腺癌的近期疗效与毒性反应。 Objective To compare the efficacy and toxicity of regimen CTX, ADM and continuously intravenous 5-Fu/CF and regimen CAF to treat advanced breast cancer.
- CTX免疫抑制小鼠经 4 8h体内代谢之后 ,CTX基本上消除 ,此时行SRCA ,CTX不会对移植瘤起抗瘤效应。 At 48 hours after mice was pretreated with CTX,serum CTX in CTX Immunosuppressed mice was eliminated and did not act on the tumor cell in SRCA.
- 方法:建立S180荷瘤小鼠模型,分为单用CTX组、CTX+FZQL组、单用FZQL组和生理盐水对照组,比较各组间的差别。 METHODS: The models of S180 tumor bering mice were established . The animals were divided into CTX therapy group, CTX and FZQL combined therapy group, FZQL therapy group and control group. The results were compared among these groups.