1、

A Study of Correlation between the Change of Chromosome Centromeric Dots and Habitual Abortions

染色体着丝点结构变化与习惯性流产的关系

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The SCE frequency in each centromeric region was very high and accordance with the relative length of each chromosome.

着丝粒区的SCE相对很高,按染色体的相对长度分布。

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3、

DNA, respectively. Information DNA Relation between Variation of Centromeric Alpha Satellite DNA on Human X Chromosome and Aneuploidy

人类X染色体着丝粒区α卫星DNA变异与非整倍体关系研究

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Study on chromosomal centromeric dots in couples with spontaneous abortion

自然流产夫妇染色体着丝粒点的研究

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At last, 5 rats of each group were checked with MRI, then they were immolated for myelin staining.

最后的时间点各取5只大鼠,分别行核磁共振扫描,取大脑脚和脊髓进行髓鞘染色进行光镜观察。

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8、

Trypan Blue staining was used to find disabled cells between normal condition and death, combining with the determination of physiological indexes. The paper also discussed relations between the cell death and vacuole leakage or cell membrane rupture.

利用台盼蓝染色,结合生理指标的测定,试图寻找介于正常和死亡之间的伤残细胞,同时探讨了细胞死亡与液泡渗漏或细胞膜破裂的关系。

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9、

Could you explain why you take samples of the blood from the patient? The scientist stained his specimen before examining it under the microscope.

你能解释一下你为什么抽取病人的血样吗?那位科学家先把抽样染色,再置于显微镜下检视。

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10、

Chromosome Studies on a Liver Cancer Patient of a High Incidence Clan

肝癌高发家族中1例患者染色体的研究

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The results of 7 cases of the fibrous histiocytoma of the brain are reported with immunoelectron microscopy, using post-embedding staining and gold labeled protein A method for the first time.

本文首次报告7例脑纤维组织细胞瘤免疫电镜结果。应用包埋后染色、胶体金A蛋白法。

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CD41 specific monoclonal antibody staining was observed by immunofluorescence microscopy.

利用CD41单克隆抗体免疫荧光染色观察培养体系中的细胞情况。

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14、

An Improved Immunofluorescence Microscopy for Observing Microtubule Cytoskeleton in Plant Cells

一种改进的观察植物细胞微管的免疫荧光染色方法

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15、

Rapid detection of numerical sex chromosome abnormality on male gonad agenesis by interphase FISH

用间期细胞FISH技术快速分析性腺发育不全患者的性染色体数目异常

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16、

Diagnosis of sex chromosome aberration using fluorescence in suit hybridization

荧光原位杂交技术诊断性染色体畸变的应用

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17、

Objective To explore the clinical and biological characteristics of 12 cases of t ( 8; 21) acute myeloid leukemia with sex chromosome loss.

目的探讨12例伴有性染色体丢失的t(8;21)急性髓系白血病患者的临床和生物学特征。

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Conclusion The sex chromosome abnormality is one of the major causes of primary azoospermia.

结论性染色体异常是原发性无精子症发生的根本原因之一。

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Conclusion: Turner's syndrome is the most common abnormality of sex chromosome in children.

结论:Turner氏综合征是儿童性染色体异常中最常见的类型。

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20、

Unlike other sex chromosome aneuploidy, there are no general characteristic physical features for triple X patients.

与其他性染色体非整倍体不同,XXX核型的患者并没有显著的身体特征。

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