基本释义:

引起突变

网络释义

1)mutagenesis,引起突变

2)zeropoint mutation,起点突变

3)The Upiising Change,崛起的突变

4)Protuberant pathologicalchanges,突起性病变

5)Poverty breeds strife.,贫困引起冲突。

6)megaprimer PCR,大引物突变法

用法和例句

Excision of Large Faucial Protuber ant Pathological Changes by Using Long Self-regulating Scissor and CO_2 Laser

支撑喉镜下应用自制加长圈套器和CO2激光切除大的咽喉部突起性病变

Gaucher (pronounced "go-SHAY") disease is an inherited illness caused by a gene mutation.

戈谢病是一种由基因突变引起的疾病。

Mutation prevalence varies among ethnic groups and may be influenced by founder mutations.

突变患病率在不同种族间有所变化并可能受起始突变的影响。

Nerval pathological changes has axial mutation sex first, afterwards has pith scabbard denaturation.

神经的病变先有轴突变性，继有髓鞘变性。

The Study on the Relationship between Mutant CD59 and Vescular Proliferation of Diabetes;

CD59基因突变与糖尿病血管病变的相关性研究

Studies on the Morphology, Biology and Pathogenicity of Knemidokoptes Mutans;

鸡突变膝螨病病原形态、生物学及致病性研究

but when a new viral mutation combines contagiousness and lethality, a pandemic ?

但是碰到新种的突变病毒把传染性和致命性结合在一起时，结果就会产生大流行──

We describe a 59-year-old woman with a tumor on the right scalp.

病灶表面为红色并突起成圆顶形状，病患因病灶逐渐变大来求诊。

Dementia can also cause sudden mood changes and personality changes.

痴呆症也会引起突然的性情变化和性格变化。

The Clinical Prevelence of FLT3 Mutations in Acute Leukemia;

FLT3突变在急性白血病中的临床意义

The Genetic Analysis of Leber s Hereditary Optic Neuropathy in Chinese Pedigrees with Mitochondrial DNA Mutations;

Leber遗传性视神经病突变位点的研究

The Study of Tyrosine Kinase JAK2V617F Mutation in Human Myeloproliferative Disorders;

骨髓增殖性疾病JAK2V617F点突变研究

Research of FLT3/ITD Mutation in Acute Myelocytic Leukemia;

急性髓细胞白血病FLT3/ITD突变的研究

GATA4 mutations and sporadic congenital heart disease

GATA4基因突变与散发型先天性心脏病

FMS-like Tyrosine Kinase 3 Gene Mutations in Acute Myeloid Leukemia

急性髓系白血病FLT3基因突变研究

Analysis of NPM1 Gene Mutations in Acute Myeloid Leukemia

急性髓系白血病NPM1基因突变的研究

DETECTION OF Parkin GENE MUTATION IN SPORADIC PARKINSON DISEASE

散发性帕金森病Parkin基因突变检测

Heteroplasmy of Leber's hereditary optic neuropathy families with 11778 mutation

Leber遗传性视神经病变11778突变家系异质性的研究