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白血病

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Leukemic or lymphomatous cells in order to identify residual abnormal cells.

聚合酶链反应通过发现白血病细胞或淋巴瘤细胞中

PCR requires a specific DNA abnormality or marker, like an oncogene, in the leukemic or lymphomatous cells in order to identify residual abnormal cells.

为了识别残存的异常细胞,聚合酶链式反应需要一个特殊的DNA或RNA的畸形或标记物,在白血病细胞或淋巴瘤细胞中,如同致癌基因一样。

PCR requires a specific DNA abnormality or marker, like an oncogene, in the leukemic or lymphomatous cells in order to identify residual abnormal cells.

为了识别残存的异常细胞,聚合酶链反应需要在白血病细胞或淋巴瘤细胞中找到一个特定的DNA或RNA的异常点或标记物,如致癌基因。

PCR requires a specific DNA abnormality or marker, like an oncogene, in the leukemic or lymphomatous cells in order to identify residual abnormal cells.

为了识别残留的异常细胞,聚合酶链式反应需要一个特殊的DNA或RNA的畸形或标记物,在白血病细胞或淋巴瘤细胞中,如同致癌基因一样。

PCR requires a specific DNA abnormality or marker, like an oncogene, in the leukemic or lymphomatous cells in order to identify residual abnormal cells.

聚合酶链反应通过发现白血病细胞或淋巴瘤细胞中特定的DNA或RNA的异常点或标记物如致癌基因来识别残存的异常细胞。

AIM: To study the anti-leukemia effect of the extract from Lysimachia clethroides Duby and its primary mechanism.

目的:研究珍珠菜提取物(ZE4)的抗白血病作用,初步探讨其可能的作用机制。

Result] From total 8075 samples, 18 cases were screened as leukaemia, 4 megaloblastic anemia.

结果]在门诊总量8075份标本中筛选出18例白血病,4例巨幼性贫血。

[Objective] To explore more correct and complete method for diagnosing leukaemia and megaloblastic anemia.

[目的]探讨诊断白血病及巨幼性贫血更准确,更全面的方法。

Method] Take hemanalysis instrument and artificial smear simultaneously to coordinate the diagnosis of leukaemia and megaloblastic anemia.

方法]采用血液分析仪和手工涂片同时进行辅助诊断白血病及巨幼性贫血。

We measured the serum sFR and membrane-associated FR ofmorrow cell on megaloblastic anemia,MDS and leukimia,and RBC folic acidwith radio-receptor assay in same time.

本实验应用放射受体技术检测了巨幼细胞贫血、MDS及白血病患者血清sFR和骨髓细胞膜FR水平,同时检测了这些患者红细胞内叶酸水平。

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This one mode pays close attention to network credence foundation of the businessman very much.

这一模式非常关注商人的网络信用基础。

Cell morphology of bacterial ghost of Pasteurella multocida was observed by scanning electron microscopy and inactivation ratio was estimated by CFU analysi.

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双标记神经干细胞的增殖、分化活力与未标记神经干细胞相比无改变。