mutation造句

Objective To analyse TBX 5 mutation in Chinese patients with Holt Oram syndrome ( HOS ) .
目的檢測(cè)中國(guó)心手綜合征患者 TBX5 基因突變.

FvL mutation may be a underlying pathogenicity of familial BCS.
FvL突變可能是家族性BCS的內(nèi)因.

Conclusion Introducing aminoglycoside antibiotic resistance mutation is effective in improving pyrrolnitrin productivity.
結(jié)論引入氨基糖苷類抗生素抗性突變,可以有效提高硝吡咯菌的生產(chǎn)能力.

The virus could jump from civet cats to humans through continuous mutation.
該病毒可透過(guò)不斷變種,由果子貍傳往人類.

cells affected by mutation
受到突變影響的細(xì)胞

The mutation was confirmed by allele specific PCR ( ASPCR ).
應(yīng)用等位基因特異性 PCR 驗(yàn)證測(cè)序所發(fā)現(xiàn)的突變.

Objective To analyse the mutation of ADAR gene in a pedigree with dyschromatosis symmetrical hereditaria.
目的探討遺傳性對(duì)稱性色素異常癥(DSH)一家系A(chǔ)DAR基因突變情況.

Objective To study the gene mutation in a pedigree with Dowling - Meara type epidermolysis bullosa simplex ( DM - EBS ).
目的研究Dowling-Meara亞型單純型大皰性表皮松解癥 ( DM -EBS ) 一家系的基因突變.

Objetive : To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.
目的: 檢測(cè)無(wú)汗性外胚層發(fā)育不全患者的EDA基因 的突變.

It is a missense mutation in exon III.
它是位于外顯子III的錯(cuò)義突變.

In non - coding region It'shows mutation of single nucleotide deletion or substitution.
非編碼區(qū)亦存在單個(gè)堿基缺失及置換突變.

Dwarfism Stunted growth. This may be due to genetic mutation, causing GIBBERELLIN deficiency.
矮態(tài):植物生長(zhǎng)受到限制形成的植株形態(tài)矮小, 可能是由于基因突變?cè)斐傻某嗝顾厝狈σ?

Genetics: Color mutation - The Hypo Boa is a Co - dominant or incomplete dominant trait.
遺傳學(xué): 彩色突變 - 該次寶兒是共同主導(dǎo)的或不完整的主要特征.

Technique of mutation breeding in gladiola was studied by means of electron beam.
用電子束輻射唐菖蒲種球,研究唐菖蒲的誘變育種.

Theologically, Luthar was into reorientation mutation.
在神學(xué)方面, 路德從事轉(zhuǎn)向變異.

Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( WC - EBS ).
鑒定單純型大皰性表皮松解癥Weber -Cockayne 亞型 一家系中的基因突變位點(diǎn).

Albino seedling is the typical chlorophyll - deficient mutation in plants.
植物白化苗則是一種典型的葉綠素合成缺陷突變體.

Objective : To detect ED 1 gene mutation in three hypohidrotic ectodermal dysplasia ( HED ) nuclear families.
目的: 研究少汗性外胚葉發(fā)育不全引起先天缺牙的ED1基因突變.

This mutation makes it better adapted than the other four.
這種變異使它具有比其他四只豬為大的適應(yīng)能力.

Scientists have found a genetic mutation that appears to be the cause of Huntington's disease.
科學(xué)家們已經(jīng)發(fā)現(xiàn)了一種可能是引起亨廷頓舞蹈病的基因變異。

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