• 目的观察自体角膜上皮移植联合5—嘧啶治疗翼状胬肉疗效。

    Objective to observe the effects of limbal epithelium autograft and using 5-fu in the treatment of pterygium.

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  • 目的评价5%喹莫特乳治疗尖锐湿疣疗效安全性,并2.5%5-嘧啶进行对照

    Objective To observe the clinical efficacy and safety of 5% imiquimod cream in topical treatment of condyloma acuminatum and to compare it with 2.5% fluorouracil(5-FU) cream.

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  • 方法对27例()行自体角膜上皮移植联合5嘧啶处理植床。

    Methods 27 eyes were given limbal epithelium autograft and used 5-fu on the surface of the wound.

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  • 结论自体角膜缘上皮移植联合5嘧啶治疗治疗胬肉良好方法。

    Conclusion Limbal epithelium autograft and using 5-fu is effective treatment of pterygium.

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  • 患者5-嘧啶联合应用治愈。

    The patient was cured by fluconazole in combination with 5-flucytosine.

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  • 结论人参多糖降低复方嘧啶多相质体的毒副作用

    Conclusion: Panax polysaccharide could reduce the toxicity and adverse effect of compound fluorouracil lipid.

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  • 目的探讨5嘧啶(5FU)胰腺外分泌功能影响

    Objective To observe the effect of 5 Fluorouracil (5 FU) on the exocrine pancreas.

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  • 目的:探讨亚叶酸(CF)联合5嘧啶(5FU)转染嘧啶脱氨酶(CD)基因直肠癌细胞的杀伤作用

    Objective to study antitumor effect of calcium folinate (CF) and 5 fluorocytosine (5 FU) on rectal carcinoma cells transfected with cytosine deaminase (CD) gene.

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  • 目的:建立裸鼠h22肝癌移植瘤模型,观察胰岛素是否增强5 -嘧啶(5 - FU)对裸鼠移植瘤化疗疗效探讨机制

    Objective: to observe whether insulin can enhance the chemotherapeutic response of 5-fluorouracil (5-fu) in transplanted H22 liver cancer in nude mice and to investigate the underlying mechanism.

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  • 目的评价全身化疗联合超声雾化吸入5 -嘧啶在治疗晚期肺癌中的价值。

    Objective To evaluate the effect of chemotherapy combined with 5-fluorouracil(5-FU) via ultrasonic atomizing inhalation for advanced lung cancer.

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  • 两性霉素B、制菌霉素、5 -嘧啶敏感性最高,保持了较高的抗菌活性,三种抗菌药仍然是治疗深部真菌感染有效药物

    Amphotericin B, mycomycin and 5-fluorocytosine were most sensitive to the pathogenic fungi and remain to be the most effective drug to cure deep part infection.

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  • 目的观察多西他赛联合顺铂5 -嘧啶方案治疗转移性食管癌近期疗效毒副反应

    Objective to evaluate the recent efficacy and toxicity of docetaxel combined with cisplatin and 5-fu in the treatment of patients with metastatic esophageal cancer.

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  • 基因干细胞中将毒性小的5 -嘧啶(5 -FC)转变5 -FU化疗药物由干细胞进入肿瘤细胞,产生死性的旁观者效应

    This gene can convert a less toxic drug, 5-fluorocytosine (5-fc), to 5-fu inside the stem cells, and the chemotherapy can then seep out into the tumor, producing a lethal by-stander effect.

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  • 口服伊曲康唑5嘧啶有明显效果

    The patient received oral itraconazole and 5 FC and showed favorable effect.

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  • 新型液晶材料5-基-2-(3,5-二苯基)嘧啶合成路线进行了改进

    This paper presents an improved process for the preparation of the novel liquid crystal 5-propyl2-(3,5-difluorophenyl)pyrimidine.

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  • 对照组81给予复方嘧啶多相质液口服。

    The control group(81 patients )received fluorouracil polyphase liposome perorally.

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  • 目的:验证比较注射用脱氧尿苷(5’-DFUR)和5-尿嘧啶(5-FU)抗肿瘤疗效安全性

    Objective: To evaluate the efficacy and safety of 5'-deoxy-5-fluorouridine (5'-DFUR) injection versus 5-fluorouridine (5-FU) for the treatment of patients with advanced malignant carcinoma.

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  • 取代2'3'-二脱氧-5-三甲基尿嘧啶核苷类,它们制备方法以及它们医药方面的应用

    Substituted 2', 3'-dideoxy-5-trifluoromethylur idines, processes for their preparation and their use in medicaments.

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  • 不用杀虫剂筛选对氯氰菊酯抗药性有显著下降下降的速率低于甲基嘧啶磷筛选。

    The strain was selected with no insecticide, could also prohibit resistant development to cyhalothrin, but the ratio of decline was lower than pirimiphos-methyl selected.

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  • 嘧啶脱氨种能够将叫做5 -嘧啶(5 -FC)药物转化活跃化疗药物5 -尿嘧啶的酶,这种情形发生于干细胞紧邻

    This is an enzyme that converts a drug called 5-fluorocytosine (5-fc) into an active chemotherapy drug, 5-fluorouracil (5-fu), but only in the immediate vicinity of the stem cell.

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  • 本文主要报道以2- 氨基-4, 6-二羟基嘧啶氯苯甲酸起始原料合成除草剂磺隆,以及详细地介绍了各个中间体的合成方法

    This paper reports the synthesis of herbicide ofprimisulfuron-methyl, the method uses 2-amino-4,6-dihydroxylpyrimidine and O-chlorobenzoic acid as the raw materials.

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  • 就白念珠菌对类、多类、5-嘧啶白菌素类等真菌药物耐药机制方面的研究进展,作了介绍

    Here, we reviewed the molecular mechanisms of resistance to azoles, polyenes, 5-flucytosine, and echinocand

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  • 就白念珠菌对类、多类、5-嘧啶白菌素类等真菌药物耐药机制方面的研究进展,作了介绍

    Here, we reviewed the molecular mechanisms of resistance to azoles, polyenes, 5-flucytosine, and echinocand

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