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染色体

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Objective To investigate the relationship between polymorphism of C-106T at promotor region of aldose reductase gene in chromosome 7q35 and nephropathy with type 2 diabetes in north China.

目的探讨染色体7q35区醛糖还原酶基因启动子区C-106T多态性与2型糖尿病肾病相关性。

Blue Aleurone Gene ; Wheat ; Translocation Chromosome

蓝粒基因;小麦;易位染色体

For example one could be an allele for Black coat and one for Gold coat.

(在1个染色体上的两个基因)它可以一个黑色基因另一个是金色基因。

Allele One of the possible forms of a given gene.

等位基因:在同源染色体上占据相同座位的两个不同形式的基因。

In plants this is sometimes overcome by the doubling of the chromosome number, giving an allopolyploid.

在植物中,这种不育现象有时可因为染色体数目加倍而抵消,产生同源多倍体。

In plants and algae that undergo alternation of generations, a gametophyte is the multicellular structure, or phase, that is haploid, containing a single set of chromosomes, and has its own information on genetic expression.

在植物世代交替的生活史中,配子体是产生配子和具有单倍数染色体的植物体,并且有自己的遗传表达信息。

The reason for primary amenorrhea is very complicated. One of the main causes is chromosome anomalies.

原发性闭经是一种原因复杂的疾病,染色体异常则是发病的主要原因。

Karyotype analysis of two patients with X-autosome translocations indicated that Xp11.2 and Xq22 may be associated with primary amenorrhea.

通过对2例X-常染色体易位携带者的分析,认为Xp11.2和Xq22区域可能与原发性闭经有关。

Chromosome abnormalities are the important cause children amentia as well as sterility and miscarriage in adults,and so that developing the heredity consultation, making prenatal detection and prenatal diagnoses for intervention.

染色体畸变是儿童智力低下,成人不孕不育、流产,性征异常的一个重要原因,要实现优生优育,必需积极开展遗传咨询,产前检查和产前诊断。

Studies showed that the Giemsa-C banding patterns of Ae.tauschii- H.vulgare amphidiploid is much in accord with that of its two parents, and this further proved that the regenerated plants from embryo callus of hybrids between Ae.tauschii and H.vulgare (2n=28) were spontaneously chromosal doubling amphidiploid.

分析表明,节节麦-大麦双二倍体Giemsa--C带核型与两个亲本的带型基本一致,这证明了节节麦-大麦双二倍体的染色体组成。

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