hypermethylation信息详情
n.超甲基化;过度甲基化
hypermetropia od───远视
hypermetropic eye───远视眼
hypermetropia bilateral───双侧远视
hypermetropia age───远视年龄
hypermetamorphosis───n.变态过度
hypermetropic people───远视者
hypermetropic anisometropia───远视性屈光参差
hypermetropic eye correction───远视眼矫正术
hypermetropia───n.[眼科]远视
hypermetropic───adj.远视的
More important, though, if abuse in early life has caused hypermethylation, is whether there is any way to undo it.───更重要的是,如果早期的虐待真会导致过甲基化,是否有办法改善它。
hypomethylation and regional hypermethylation are common mechanisms of aberrant expression of gene.───的低甲基化和区域性高甲基化是基因异常表达的常见机制。
Hypermethylation of GNAT1 may not be oncogenic mechanisms of NPC.───GNAT 1基因的甲基化可能不是鼻咽癌的发病机制。
In addition , hypermethylation at a region next to such a critical region might indicate an early signal of carcinogenesis .───另外,紧靠这些临界区域的超甲基化可能暗示致癌作用的早期信号。
Objective: To explore the role of inactivation of P15 gene by means of hypermethylation in the pathogenesis of MDS.───前言:目的:研究P15基因通过甲基化失活在骨髓增生异常综合征(MDS)发病中的作用。
Global hypomethylation and regional hypermethylation are common mechanisms of aberrant expression of gene.───广泛的低甲基化和区域性高甲基化是基因异常表达的常见机制。
Objective: To investigate the function of promoter hypermethylation of secreted frizzled-related protein 2(SFRP2) gene in colorectal cancer.───目的:研究分泌型卷曲相关蛋白2(SFRP2)基因启动子超甲基化与大肠癌的关系。
Objective: To explore the mechanism of hypermethylation pattern of the calcitonin gene in the HL-60 cells.───目的:探讨HL-60细胞降钙素基因高甲基化的发生机制。
The gene silence of XAF1 is related with the hypermethylation of its promotor.───XAF1的基因沉默与其启动子高甲基化明显相关。
Recent research found that the hypermethylation of lung cancer-related genes and the abnormal expression of methyltransferase were closely related to the occurrence of lung cancer.
Objective:To detect the expression of O6-methylguanine-DNA methyltransferase (MGMT), and its effect of promoter hypermethylation on tumorigenesis and progression.
DNA hypermethylation is a major cause of gene inactivation in cancer.
Methods: The hypermethylation was examined by methyl sensitive restrictive DNA endoenzyme analysis in 34 cases of angioreticuloma and the VHL gene mutations detected by PCR SSCP analysis.
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