1、

Multiple carboxylase deficiency ( MCD) is an autosomal recessive disorder of inherited metabolic diseases.

多种羧化酶缺陷症(MCD)是一种常染色体隐性遗传的先天遗传代谢性疾病。

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2、

WD is a common autosomal recessive inherited neuropathy, whose only pathogenic gene is ATP7B.

WD是神经科较为常见的常染色体隐性遗传病,其唯一致病基因为ATP7B基因。

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3、

The pathway of male sexual development in mammals is initiated by SRY, agene on the short arm boundary of Y chromosome.

哺乳动物中位于Y染色体短臂临界区域的SRY基因启动雄性性状的发育。

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4、

Methylmalonic acidemia is one of the most common disorders of congenital organic acid metabolism.

甲基丙二酸血症是一种常染色体隐性遗传的有机酸血症,在先天性有机酸代谢异常中最为常见。

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5、

Positive results were found in 8 out of 50 by sputum acidfast staining, 73 out of 86 by bronchoscopic brushing smears, and 17 out of 56 by bronchial biopsies.

56例痰涂片行抗酸染色者中8例阳性,86例行纤支镜刷片检查者中73例阳性,56例行活组织检查者中17例证实为结核。

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6、

Started with ACO1 ( aconitase I), we got positive clone of ACO1 then obtained 16 clones by chromosome walking. After analysis fingerprinting of 16 BAC clones.

以离ID最近的ACO1(aconitase1,顺乌头酸酶)基因为起点,设计引物筛选含ACO1的BAC克隆,用染色体步行的方法得到16个BAC克隆。

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7、

Objective: To search the relationship between satellite associations in human acrocentric chromosomes and recurrent abortions.

目的:为探讨人近端着丝粒染色体随体联合与自然流产的相关性。

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8、

Acrocentric chromosome ( ophthalmology) inability to focus on near objects.

近端点着丝粒染色体(眼)不能聚焦于近处物体。

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9、

The Satellite Association of Acrocentric Chromosomes from the Patients with Hyperthyroidism

甲亢患者的近端着丝粒染色体随体联合

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10、

The Choice of Process Lines and Conditions in Dyeing Acrylic Fibres with Weakly Acidic Group

弱酸性型腈纶针织物染色工艺路线的选择和工艺条件的制定

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11、

Study on Rare Earth Dyeing of Acrylic Fibres by Photoacoustic Spectroscopy

稀土腈纶染色的光声光谱研究

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12、

The source of the energy for both protoplasmic streaming and migration of the chromatin substance is supplied by ATP ( adenosine triphosphate) which is produced in the process of aerobic respiration.

原生质川流运动和染色质穿壁运动所需要的能源是有氧呼吸所生成的能,通过ATP释放高能磷酸键(~P)的形式供给的。

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13、

Methods: To analyze the chromosome karyotypes of circular lymphocytes in 61 patients with primary amenia.

方法分析61例原发闭经患者外周血淋巴细胞染色体核型。

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14、

[ Results] Positive rate of Amsel was 28%, one step sialidase was 34%, Gram-stain was 30% and amines was 24%.

【结果】Amsel法阳性率28%,组织多胺试验阳性率24%,一步法唾液酸酶活性的检测试验阳性率34%,革兰染色细菌评分法阳性率30%;

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15、

The evaluation of the injury of pulse intense sound to the hair cell in ampullar crest of guinea pig by trypan blue staining

台盼蓝染色法观察脉冲口噪声对豚鼠壶腹嵴毛细胞活力的损伤

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16、

Chromosome count showed that the plants, containing non tetraploid cells besides amphidiploid, were chimeras.

染色体检查发现,除了四倍体之外,还存在其它倍性的细胞,呈嵌合体状态。

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17、

Objective: To analyze abnormal chromosome karyotype and pathogenesis of primary amenia.

前言:目的分析原发闭经患者染色体核型与病因。

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18、

Research on Alizarin Red S simulated dyeing wastewater treatment with electrochemical method

电化学法处理茜素红S模拟染色废水的研究

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19、

Detection of Alien Chromatins Introgressed into Wheat in Mitotic Interphase ALBUMINOUS CELLS

小麦细胞分裂间期外源染色质的检测

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20、

We also studies the cause of hypophrenia and the relation between karyotype and phenotype of aberrational chromsome.

探讨了智力低下的病因及异常染色体核型与表型间的关系。

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