deletion mutation

基本解釋

• 缺失突變

英漢例句

雙語(yǔ)例句

• All of the patients who had parkin gene deletion mutation had tremor, rigidity and bradykinesia, but athetosis and family history of PD were not found.
  所有缺失突變病例均有震顫、僵直和運(yùn)動(dòng)遲緩，但無(wú)異動(dòng)癥和PD家族史；
• Conclusion:This new method of DNA sequence deletion mutation is simple and accurate. It could avoid new mutation in PCR process of traditional DNA manipulation method.
  結(jié)論：該方法操作簡(jiǎn)單、精確，能夠避免引入新突變，為DNA序列的缺失突變提供了一種新方法。
• They examined the genes of the cancer cells in the infant and found a deletion mutation – some DNA missing in the region that controls expression of the major histocompatibility locus (HLA).
  他們檢查了嬰兒體內(nèi)的癌細(xì)胞基因，發(fā)現(xiàn)一個(gè)缺失變異體——控制主要組織相容性位點(diǎn)（HLA）表現(xiàn)的區(qū)位缺失了某種DNA。

• deletion mutation更多例句

詞組短語(yǔ)

短語(yǔ)

• deletion or mutation 缺失和突變
• deletion and insertion mutation 缺失和插入突變
• gene deletion mutation 基因缺失突變
• single -base deletion mutation 單堿基缺失突變
• mutation deletion 基因缺失突變

• deletion mutation更多詞組

專(zhuān)業(yè)釋義

醫(yī)藥科學(xué)

• 缺失突變

  hereditary multiple exostoses (HME);; EXT1;; EXT2;; deletion mutation;acne inversa (AI);; hidradenitis suppurativa (HS);; exomes;; Sequence Capture;; traditional DNA sequencing;; next-generation DNA sequencing;;‘HS19’
  遺傳性多發(fā)性外生性骨疣;; EXT1基因;; EXT2基因;;缺失突變;反常性痤瘡;;化膿性汗腺炎;;外顯子組;; DNA傳統(tǒng)測(cè)序;; Sequence Capture;;高通量測(cè)序;;“HS19”

• 誘導(dǎo)突變

生物學(xué)

• 缺失突變

  The 2-nucleotide deletion mutation induced by EMS results in lethal to drosophila in later embryo stage or first instar-larvae.
  誘變劑EMS(甲基磺酸乙酯)所致Dxl6的2核甘酸缺失突變導(dǎo)致果蠅胚胎后期或1齡幼蟲(chóng)致死。

  農(nóng)業(yè)科學(xué)

• 缺失載體