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染色体基因

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But in hexaploid triticale x common wheat, they rely on the chromosome breakage and recombination.

而在其反交中,外源基因的导入则更多依赖于染色体的断裂与拼接。

In common wheat ^hexaploid triticale, the exogenous genes are transferred by means of homoeologous chromosome pairing.

在以普通小麦为母本的杂交方式中,部分同源染色体配对可能是外源基因导入普通小麦基础。

Hexaploid wheat has a lot of homoelogous gones in its genomes, and the main objective of wheat breeding is to get good phenotypes.

小麦是异源六倍体,其染色体组中存在着大量的同源基因,其育种的主要目标是获得可遗传的优良性状。

He and his team discovered the gene on chromosome 6, after searching methodically for genetic markers in ten Israeli Holstein bulls and their 1000 female offspring.

伦和他的同事在系统性地搜寻了十头黑白花牛以及它们的一千头后代的遗传标记后,发现位于染色体6的这种基因。

AIM: To investigate the expression of phosphatase and tension homologue deleted on chromosome 10, the tumor suppressor gene PTEN, in ectopic endometrium in patients with endometriosis and to study the role of PTEN in the pathogenesis of the disease.

目的:检测第10号染色体缺失的磷酸酶和张力蛋白同源物基因在子宫内膜异位症中的表达,探讨其在EMS发病机制中的作用。

Meanwhile, when using the deletion as a DNA marker, the result suggested that Cy homozygote be lethal in embryo period.

同时以该缺失作为Cy染色体的DNA标记,通过基因型多态分析,初步证实Cy纯合型可导致果蝇胚胎期死亡。

Results These two patients were confirmed to suffer from DMD. They were characterized by typical features of DMD including typical clinical manifestations, increased serum enzymes, EMG presenting myogenic impairment, HE staining presentation belonging to DMD, negative dystrophin in brother, and inconstantly positive on the sarcolemma of sister. Furthermore, no deletion or duplication was found in the 1-79 exons of dystrophin gene. The suffering brother and sister carried the same maternal X chromosome.

结果 兄妹二人符合DMD诊断,具有典型的DMD临床表现,肌酸激酶、肌酸激酶同工酶、乳酸脱氢酶、羟丁酸脱氢酶和谷草转氨酶的水平均显著高于正常值,肌电图呈肌源性损害,肌肉HE染色符合DMD,男患者的抗肌萎缩蛋白表达阴性,女患者的少量肌纤维仍可见不连续膜阳性,两患者抗肌萎缩蛋白基因的1~79号外显子未见缺失和重复突变,女患者与男患者携带相同的母源性X染色体。

The crossover operation is performed only on the corresponding genes. The mutation and inverse operation is limited within the gene.

摘 要:提出了相邻开关在染色体中相邻以及构成同一环路的开关在同一基因块内的编码方法。

The genes for two of the factors, VIII and IX, are on the X chromosome.

该基因的两个因素,第八和第九,是对X的染色体。

In 3 cases, SRY detection in gonadal tissue correlated with pathological findings but not with blood karyotype.

有3例患者SRY基因检测与性腺病理吻合,而与外周血白细胞染色体核型不符。

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