人类染色体

端粒是人类染色体的端部结构，可以防止DNA损坏。

Telomeres are structures at the ends of human chromosomes that protect DNA from damage .

双参数人类染色体流式分析及分选

Karyotyping and Sorting Human Chromosomes by Dual parameter Flow Cytometry

人类染色体高分辨技术及其G显带研究

The research of high resolution technique and its G-banding on human chromosome

人类染色体G带的光密度识别与分析

Photometric Density Recognition and Analysis for Human G-Banded Chromosomes

人类染色体R显带法改良初探

Preliminary Exploration of Human Chromosome R-banding Improved Method

为了研究X染色体的进化，研究人员首先以前所未有的精确度排序人类染色体。

To study X evolution , researchers first sequenced the human chromosome more accurately than ever before .

创建DNA标志的人类染色体图谱，方便人们发现基因的位置；

The creation of human chromosome maps for DNA markers that would allow the location of genes to be found .

不论如何，当我们检查这些盘卷的DNA的尾部，我们发现每个人类染色体的尾部都有一个叫做端区的特定DNA序列。

Anyway , if we examine these ends of these coils of DNA , we will find a sequence of DNA at each end of every human Chromosome , called a telomere .

分别应用随机引物和SOX基因兼并引物在人类染色体上进行了原位延伸标记。

Here we present the results of random primer and SOX degenerate primer PRINS on human metaphase chromosomes .

岩参诱发NIH小鼠微核、人类染色体畸变和SCE频率的实验研究

Experimental Studies with Bergenia Purpurascens , the Frequency of Micronucleus in NIH Mice , the Frequency of SCE , and Chromosome Aberration in Human Lymphocytes

对引物原位杂交标记（PRINS）方法及在人类染色体疾病研究、诊断应用中的最新进展作一综述。

To present a brief review on primed in situ labeling ( PRINS ) methods and applications .

本文探讨了在不完全了解着丝粒、复制起始点、端粒等人类染色体基本功能单位的情况下构建HAC的三种策略。

The three strategies to construct HAC have been explored without full knowledge of chromosome elements such as centromere , telomere and replication origin .

结果发现4种新的平衡易位的人类染色体异常核型，分别为46，XX，t（1；6）（q31；p25）；

Result : Four new balanced translocation karyotypes were discovered , they are 46 , XX , t ( 1 ; 6 )( q31 ; p25 );

目的已报道人类染色体8p缺失可能与肝癌转移有关，本文应用实时定量聚合酶链反应（RQ-PCR）研究位于8p的DLC-1基因mRNA表达与肝细胞癌侵袭转移的关系。

Objective To study the relationship between the expression level of DLC-1 mRNA ( located in 8p ) and the invasion / metastasis of human hepatocellular carcinoma ( HCC ) .

本文首报7例世界人类染色体异常核型如下：46，XX，t（1；7）（p32；p22）；

Seven cases of new karyotypes of chromosome abnormalities were found which were not reported previously in the world . 46 ,, XX , t ( 1 ; 7 ) ( P32 ; P22 );

通过对患有闭经、自发流产、死胎、死产等患者外周血淋巴细胞染色体检查，发现16种新的罕见人类染色体异常核型，它们是46，XX，t（6；11）（q25；p15）；

By examining the lymphocytic chromosomes of peripheral blood from patients with amenorrhea , spontaneous abortion and stillbirth history , the 16 rare species of human chromosomal abnormal karyotypes were discovered . They were 46 , XX , t ( 6 ; 11 )( q25 ; p15 );

9种新的人类染色体异常核型报告

A Report of Nine New Kinds of Human Chromosomal Abnormal Karyotypes

人类染色体高序结构的扫描电镜观察研究

A scanning electron microscopical study on higher order structure of human chromosome

用平均灰度投影积分分布曲线描述人类染色体的带型特征

A description of human chromosomes banding features using average integrated density profiles

人类染色体850&1000条带的高分辨技术

High Resolution Technique in 850-1000 Bands Stage of Human Chromosomes

人类染色体可分出21个集团，除9至12号染色体外，其余均能被单独分离。

Human chromosomes could be separated into 21 groups .

世界首报两种人类染色体异常核型

First report on two abnormal karyotypes of human chromosome

人类染色体疾病

Chromosome Diseases of Human ⅱ . Sex Chromosome Diseases

人类染色体畸变核型分布特点的研究

Study on the distributed characteristic of the distortion karyotype of the human chromosome

应用微铺展技术在扫描电镜下对人类染色体的高序结构进行了研究。

Application of chromosome painting technique to analysis of structural aberration of human chromosomes ;

用简并寡核苷酸引物构建人类染色体区带特异性探针池的技术

A technique of constructing human chromosomal band specific probe pools using degenerate oligonucleotide primer

人类染色体中的微切割与微克隆技术

Techniques of Microdissection and Microclone in Human Chromosome

对于人类染色体的自动分割一直是染色体识别的一个难题。

Fully automatic human chromosome segmentation is a tough problem of the chromosome recognition .

染色体分析以超二倍体为主，核型显示为人类染色体核型。

Chromosomal analysis of the tumor cells exhibited human origin with a hyperdiploid model .

三种人类染色体异常新核型（附3例报告）

Abnormal new karyotypes of the human chromosome ( a report of 3 cases )