查询词典 chromosomal

Results:the preservativecan increase significantly the frequency of micronuclei which were significantly different in comparison with control group;it can not increase significantly the frequencies of chromosomal aber...

结果山梨酸钾可明显引起微核率的上升，与对照组差异显著(P05)或极显著(P01)，不引起染色体畸变率的明显上升。3种物质均可降低山梨酸钾诱发的微核率和染色体畸变率。

Objective To investigate the relationship between sperm anomalies and chromosomal aberrance and to further understand the pathological changes of anomalous spermatozoa.

目的 探讨精子畸形与精子染色体异常的关系，了解畸形精子的病理学改变。

A protein,produced by specialized ameloblast cells,found in tooth enamel.Distinctive in that the genes for it can be found on both the X and the Y chromosome.Chromosomal location:Xp22.1-22.3 and Y.

一种蛋白质，有特定的成釉细胞细胞制造，可以在牙齿的珐琅中找到，特别之处在于它的基因可以在X和Y染色体中找到，染色体位置：Xp22.1-22.3和Y。

A protein,produced by specialized ameloblast cells,found in tooth enamel.Distinctive in that the genes for it can be found on both the X and the Y chromosome.Chromosomal 本地:Xp22.1-22.3 and Y.

一种蛋白质，有特定的成釉细胞细胞制造，可以在牙齿的珐琅中找到，特别之处在于它的基因可以在X和Y染色体中找到，染色体位置：Xp22.1-22.3和Y。

RT-PCR detection of SYT-SSX mRNA can be used in formalin-fixed, paraffin-embedded tissues as a sensitive and specific technique in the diagnosis and differential diagnosis of synovial sarcoma. 2. The SYT-SSX fusion type is related to histological type and cell proliferative activity of synovial sarcoma. 3. Some characteristic sequence motifs flank genomic breakpoints of chromosomal translocation of synovial sarcoma, including Alu sequences, Translin recognition sequences, topoisomerase Ⅱ recognition sites and palindromic sequences, which may be associated with chromosomal translocation of synovial sarcoma.

1、RT-PCR技术检测SYT-SSX mRNA表达可用于福尔马林固定、石蜡包埋组织，敏感性和特异性高，可用于滑膜肉瘤诊断和鉴别诊断。2、SYT-SSX融合基因类型与滑膜肉瘤组织学分型及细胞增殖活性相关。3、滑膜肉瘤染色体易位断裂点旁存在一些特征性序列，包括Alu序列、易位素识别序列、拓扑异构酶Ⅱ识别位点、回文序列等，可能与其染色体易位发生机制有关。

Keywords: Carnivores; Chromosome painting; Comparative chromosomal maps; Chromosomal evolution: Karyotypic phylogeny

中文关键词：食肉目；染色体涂色；比较染色体图谱；染色体进化；核型系统发生

According to An International System for Human Cytogenetic Nomenclature (ISCN 1995), only the case in which two metaphases with the same chromosomal gain or structural rearrangement, or three cells with the same chromosomal loss was defined the presence of an abnormal clone.

根据《人类细胞遗传学命名国际体制(ISCN 1995)》规定：至少2个细胞有同样的染色体增加或结构异常或3个细胞有一致的染色体丢失方称为克隆性染色体异常。

The rest reside among the populations. and that about 80.98% of 12 double chromosomal variability in arm ratio existed within the populations. The rest reside among the populations. Nested random effects analysis of variance for variable the relative length, arm ratio of chromosome, the mean of ratio (largest/smallest), mean ratio of ann. As. K. and actual length of genome of chromosome. As a resuit, chromosomal structure variations was 96.36% within the populations.

结果］在相付长度方面，香水百合12对染色体变异约有88.91%来源于居群内，约有11.09%来源于居群间；在臂比方面，香水百合12对染色体变异约有80.98%来源于居群内，约有19.02%来源于居群间；在染色体长度比、平均臂比、核型不对称系数和染色体组实际长度方面，香水百合染色体变异约有96.36%来源于居群内，约有3.64%来源于居群间。

In this study, we therefore define a new OG order distance that is based on more biologically accurate rearrangements (e.g., reversals, transpositions and translocations) rather than breakpoints and that is applicable to both uni-chromosomal and multi-chromosomal genomes.

因此，在这篇论文中，我们定义了一个新的重叠基因距离，它是根据较有生物正确性的基因重组(例如：翻转、移位与易位)而不是断点所定义出来的，而且它能同时应用在单一染色体与多染色体的基因体上。

Results The bone marrow slides showed faggot auer body stained Alcian blue positive in 8 of 21 patients contrast to none in the other 13 ones. Chromosomal abnormality of t(15; 17) and PML-RARa fusion gene were found in the bone marrow of the 8 patients, and among them 3 had additional chromosomal abnormality.

结果 阿利新蓝染色检测柴捆状Auer小体阳性8例，遗传学检查均显示t(15； 17)和PML-RARa融合基因，其中附加其他染色体异常3例。

In the United States, chronic alcoholism and hepatitis C are the most common ones.

在美国，慢性酒精中毒，肝炎是最常见的。

If you have any questions, you can contact me anytime.

如果有任何问题，你可以随时联系我。