hypermethylation的意思
hypermethylation中文翻譯:
n.超甲基化;過度甲基化
hypermetropia od───遠視
hypermetropic eye───遠視眼
hypermetropia bilateral───雙側遠視
hypermetropia age───遠視年齡
hypermetamorphosis───n.變態過度
hypermetropic people───遠視者
hypermetropic anisometropia───遠視性屈光參差
hypermetropic eye correction───遠視眼矯正術
hypermetropia───n.[眼科]遠視
hypermetropic───adj.遠視的
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,如果早期的虐待真會導致過甲基化,是否有辦法改善它。
hypomethylation and regional hypermethylation are common mechanisms of aberrant expression of gene.───的低甲基化和區域性高甲基化是基因異常表達的常見機制。
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發病機制。
In addition , hypermethylation at a region next to such a critical region might indicate an early signal of carcinogenesis .───另外,緊靠這些臨界區域的超甲基化可能暗示致癌作用的早期信號。
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基因通過甲基化失活在骨髓增生異常綜合征(MDS)發病中的作用。
Global hypomethylation and regional hypermethylation are common mechanisms of aberrant expression of gene.───廣泛的低甲基化和區域性高甲基化是基因異常表達的常見機制。
Objective: To investigate the function of promoter hypermethylation of secreted frizzled-related protein 2(SFRP2) gene in colorectal cancer.───目的:研究分泌型卷曲相關蛋白2(SFRP2)基因啟動子超甲基化與大腸癌的關系。
Objective: To explore the mechanism of hypermethylation pattern of the calcitonin gene in the HL-60 cells.───目的:探討HL-60細胞降鈣素基因高甲基化的發生機制。
The gene silence of XAF1 is related with the hypermethylation of its promotor.───XAF1的基因沉默與其啟動子高甲基化明顯相關。
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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