染色的例句大全

Among 43 cells with abnormal chromosomes , deletion, translocation , dicentrics , csb and inversion were demonstrated in 19,16,4 , 1 and 1 cells.

43个异常核型细胞中,缺失 、 易位、染色体断裂 、 双着丝粒、倒位各有19、16、4 、 1、1个细胞.

Fullness tumor vascular and intense stain could be seen on DSA.

DSA显示瘤内血管丰富,呈血管团样,静脉期染色.

DSA examination in 3 cases presented obvious staining of tumor.

行DSA检查3例,均显示明显的肿瘤染色.

The technique of chromosome in situ hybridization ( CISH) has been extensively applied to genetics and breeding of higher plants.

染色体原位杂交技术近年发展较快，已广泛应用于植物遗传育种实践。

The paper focused on the effect of LTP treatment on dyeing and shrink proof behaviour.

重点论述了LTP技术对羊毛纤维的染色性能和防毡缩性能的影响.

Method It was used by immunohistochemical PAP method.

方法使用常规HE染色及免疫组化PAP法。

Van der Woude syndrome ( VWS, OMIM 119300) is an autosomal dominant craniofacial disorder characterized by pits of the lower lip, hypodontia and cleft lip and/ or cleft palate.

范德伍兹综合征（Van der Woude syndrome，VWS，OMIM119300）是一种常染色体显性遗传病。其特征是家族性下唇瘘复合唇裂或腭裂，1／4的患者伴有缺牙（Hypodontia）。

Background Familial benign chronic pemphigus or Hailey-Hailey disease ( HHD; OMIM 169600) is a rare autosomal dominant cutaneous disorder characterized by recurrent vesicles and erosions mainly in intertriginous areas.

研究背景：家族性慢性良性天疱疮，又称Hailey-Hailey病（HHD，OMIM169600）是一种罕见的常染色体显性遗传性皮肤病。

Osteogenesis imperfecta ( OMIM 166200) is an autosomal dominant disorder characterized by bone fragility and abnormalities of connective tissue.

成骨不全病（OMIM166200）是一种常染色体显性遗传病，其临床表现以骨折及结缔组织异常为特征。

Infarcted sizes in heart were determined by dual staining with Evans-blue and TTC.

以Evans蓝和TTC双重染色方法测量心肌梗死面积.

The expression of Nogo protein-A in the brain of MCAO rats was observed by in situ hybridization and the section was subjected to image analysis to determine the mean staining gray.

原位杂交法观察大脑中动脉闭塞大鼠脑内勿动蛋白-A的表达，并对切片进行图像分析，测定染色平均灰度。

METHODS: MTT assay and immunohistochemical staining method were used to detect the activity of the proliferation and metabolic status of human bladder cancer BIU 87 cells and the expression of proliferating cell nuclear antigen ( PCNA) after the BPD MA were activated by laser.

方法采用亚甲基噻唑蓝（MTT）法和免疫组化染色法检测激光活化BPD-MA后人膀胱癌细胞株BIU-87细胞增殖代谢活性及增殖细胞核抗原（proliferating cell nuclear antigen，PCNA）的表达。

Objective To establish a quick and easy method for SDS-PAGE protein staining.

目的建立一种快速,简易的SDS-PAGE染色方法.

Hepatolenticular degeneration ( HLD ) is an autosomal reoessively inherited disease caused by copper metabolic dysfunction.

肝豆状核变性 ( Hepatolenticulardegeneration,HLD ) 是一种铜代谢紊乱而引起的常染色体隐性遗传的疾病.

A nucleus can have only one y-chromosome.

一个核可以仅有一个y染色体。

This is a Cryptococcus neoformans meningitis stained with GMS to reveal the nuclei.

新型隐球菌脑膜炎GMS染色法显示细胞核.

Histochemical staining showed the temporary expression rate of GUS gene reached more than 70 %.

组织化学染色结果表明:GUS基因的瞬时表达率可以达到70%以上.

Histochemical staining showed the temporary expression rate of GUS gene reached more than 70 %.

组织化学染色结果表明:GUS基因的瞬时表达率可以达到70%以上.

Methods Scale placed on slide KOH, Parker ink was added and observed under microscope.

方法将病损皮屑置于KOH玻片上后, 再加派克墨水染色,显微镜下观察.

After having been treated with VitE and L-NBP, caspase-3-IR neurons in all four groups decreased significantly ( P < 0.01 ).

缺氧组caspase蛳3阳性染色显著增加 ( P<0.01 ).