1、

Two other mutations have been found among the Beja people of northeastern Sudan and tribes of the same language family in northern Kenya.

另外两种突变基因也已在苏丹东北部的贝贾人和肯尼亚北部讲贝贾语的部落中发现。

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2、

The gene has previously been linked to neurological disease, but these specific mutations have not.

该基因此前被认为与神经系统疾病有关, 但是这种特定突变则不然.

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3、

Clinical, magnetic resonance image features and detection of pantothenate kinase 2 gene mutations in Chinese patients with Hallervorden-Spatz syndrome

Hallervorden-Spatz综合征的临床、磁共振成像特征及泛酸激酶2基因的突变检测

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4、

Results The gene mutations of 9 SCA families were MJD among which 6 asymptomatic MJD had been detected in 2 SCA families.

结果检出9个家系为MJD,其中2个MJD家系检测到6例症状前MJD。

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5、

Effects of Space Flight on Genetic Mutations& The Drosophila Melanogaster Sex-Linked Recessive Lethal Assay

卫星空间飞行对遗传影响的研究&果蝇伴性隐性致死试验

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6、

The mutations of VHL gene were irrespective of the age and pathological grade and stage of patients.

结论:国人非遗传性肾透明细胞癌中存在VHL基因的突变,且与患者年龄,肿瘤分期、分级无相关性。

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7、

Somatic mutations of VHL gene and HIF-1 α expression in primary renal clear cell carcinomas

肾透明细胞癌中VHL基因突变与缺氧诱导因子-1α表达的研究

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8、

Central nervous system hyperexcitability associated with glutamate dehydrogenase gain of function mutations

中枢神经系统兴奋性过高与谷氨酸脱氢酶获得性功能突变

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9、

BMPR-IB gene is one of the major gene for fecundity of sheep, point mutations ( A746G) called FecB gene can be used as the molecular genetic marker for the selection of multiple births strain of sheep.

BMPR-IB基因是绵羊产羔数的主效基因,点突变基因即FecB基因(A746G)可以用于对绵羊多胎品系的选择。

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10、

FecB for testing, although have found mutations, but for some of the low incidence, group in low-alcohol polymorphism.

对FecBH进行检测,虽然发现有突变为点,但发生率极低,对整个群体处于低度多态性。

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11、

Dr Cox and his colleagues were therefore able to make a statistical comparison of Indonesian and Malagasy mitochondrial genomes knowing that any changes which had occurred since they separated would be the result of rare mutations. These can be spotted and accounted for.

Cox博士和他的同事们因此能进行印尼人和马达加斯加人线粒体基因组的数据比对,从而推断出原本相同的线粒体DNA天各一方后发生的任何遗传变化都是源于一些罕见的基因突变。

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12、

Objective : To investigate the clinical characteristics and mutations of GCH I gene of patients with DRD.

目的: 研究DRD患者的临床特点和GCH基因突变.

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13、

Study on LPL Gene Mutations

脂蛋白脂肪酶基因突变的研究

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Mitochondrial DNA mutations in patients with chronic progressive external ophthalmoplegia and Kearns-Sayre syndrome

慢性进行性眼外肌瘫痪和Kearns-Sayre综合征的线粒体DNA突变分析

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16、

Effects of garlicin on MMS-and Cy-induced sex-linked recessive lethal mutations in Drosophila melanogaster

大蒜素对甲基磺酸甲酯和环磷酰胺诱发果蝇伴性隐性致死的影响

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17、

They first looked for mutations in 22 cancerous breast and colorectal tumors.

它们首先在22中癌变的乳腺和结直肠肿瘤中寻找突变.

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18、

Mild mutations in XPF cause the cancer-prone syndrome xeroderma pigmentosum.

XPF轻微突变导致致癌倾向综合征着色性干皮病.

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19、

Conclusions Mutations in the genes encoding telomerase components can appear as familial idiopathic pulmonary fibrosis.

结论:端粒酶组分的编码基因发生突变时,能以家庭性特发性肺纤维变性的形式出现.

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20、

Germ line mutations in BRCA 1 predispose women to early onset, familial breast and ovarian cancers.

人类乳癌易感基因1(BRCA1)的生殖细胞突变会导致早发性妇女乳腺癌, 遗传性乳腺癌和遗传性卵巢癌.

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