Ras gene mutation in childhood AML was mainly found in M 2 , M 4 , M 5 subtypes.

AML患儿中ras基因突变多见于M2 、 M4及M5型.

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ConclusionG 71 R gene mutation combined with G 6 PDdeficiency aggravates the degree of neonatal jaundice.

结论G6PD缺乏与G71R基因突变并存加重新生儿黄疸程度.

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Conclusion Abore point mutation is an inherited gene mutation.

结论表明该突变为一遗传性突变.

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Objetive : To detect the gene mutation of a patient with anhidrotic ectodermal dysplasia.

目的: 检测无汗性外胚层发育不全患者的EDA基因 的突变.

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How can a single gene mutation lead to a complex psychiatric phenotype?

点基因突变如何造成复杂的精神疾病表现型?

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Conclusion There is K 14 1 A domain gene mutation in this DM - EBS pedigree.

结论本DM-EBS家系存在K14的基因突变.

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HBV gene mutation along different types of TCM syndrome are detected by microarray assay.

基因芯片检测慢性乙型肝炎不同证候的HBV前 C区基因变异.

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Objective : To detect ED 1 gene mutation in three hypohidrotic ectodermal dysplasia ( HED ) nuclear families.

目的: 研究少汗性外胚叶发育不全引起先天缺牙的ED1基因突变.

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Objective To study the gene mutation in a pedigree with Dowling - Meara type epidermolysis bullosa simplex ( DM - EBS ).

目的研究Dowling-Meara亚型单纯型大疱性表皮松解症 ( DM -EBS ) 一家系的基因突变.

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Variations of flower color are related to gene mutation and pollination pattern and so on.

研究认为,花色变异与基因突变、传粉机制等因素有关.

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Objective : To study the effects of propolis against gene mutation induced by powerful mutagens in mice.

目的: 探讨蜂胶对环磷酰胺等强诱变剂诱发基因突变的抑制作用.

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Cells with Ras gene mutation or transformed by Ras become resistant to p 53 dependent apoptosis.

Ras基因转染或突变的细胞能够对DNA损伤 引起的p53依赖性凋亡产生抗性.

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Objective : To identify gene mutation in a family with Weber - Cockayne type epidermolysis bullosa simplex ( WC - EBS ).

鉴定单纯型大疱性表皮松解症Weber -Cockayne 亚型 一家系中的基因突变位点.

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Objective To detect the activity of transglutaminase 1 ( TGM 1 ) and gene mutation in a family with lamellar ichthyosis.

目的检测一板层状鱼鳞病家系中患者转谷氨酰胺酶1的活性及其编码基因的突变.

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If the suppressor gene mutation may lead to disorders and cancerous cell growth.

如果抑癌基因发生突变,也可导致细胞生长失调而发生癌变.

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