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线粒体

与 线粒体 相关的网络例句 [注:此内容来源于网络,仅供参考]

To date, only the structures of prokaryotic succinate:ubiquinone oxidoreductases, which share a similar enzymatic function with mitochondrial SQR, have been reported, including QFR from E.coli, QFR from Wolinella succinogenes and SQR from E.coli.

在此之前,只有原核生物的琥珀酸泛醌氧化还原酶的结构得到了解析,这包括大肠杆菌的 QFR , Wolinella succinogenes 细菌中的 QFR 和大肠杆菌的 SQR ,这些蛋白有着与线粒体复合物 II 相类似的酶功能。

First discover that mitochondria are "phaged" by chloroplast in Taraxacum mongolicum and Anapha1is lactea.

首次在蒲公英和乳白香青的叶肉细胞中发现了叶绿体&吞噬&线粒体的现象。

Long-PCR amplification, clone and primer-walking sequencing methods were employed in determine the complete sequence of mitochondrial genome of tokay.

还采用长PCR扩增等方法,测定了大壁虎线粒体基因组全序列。

Studies using fluorescent tracers revealed that MAVS was present in the mitochondria of cells.

研究使用荧光示踪物揭示出MAVS存在于细胞的线粒体中。

Toxocara; Toxascaris; mitochondrial DNA; nad1; PCR; SSCP; sequence analysis

弓首蛔虫;狮弓蛔虫;线粒体DNA;nad1基因;PCR;单链构象多态性分析;序列分析

The objectives of the present study was to examine sequence variation in a portion of the mitochondrial NADH dehydrogenase subunit 1 gene (pnad1) within and among Toxocara canis, T. cati, T. malaysiensis, T. vitulorum and Toxascaris leonina, and to study their systematics and population genetics.

本研究旨在对弓首属犬弓首蛔虫、猫弓首蛔虫、马来西亚弓首蛔虫、牛弓首蛔虫和狮弓属狮弓蛔虫线粒体DNA中烟酰胺脱氢酶亚基I(nad1)基因部分序列(pnad1)进行比较研究,分析它们之间的序列差异和种群遗传关系。

AIM: To study the changes of mitochondrial membrane potential in mouse thymocytes stimulated by dexamethasone.

目的:研究地塞米松刺激小鼠胸腺细胞过程中线粒体膜电势的变化。

S tatus: Three of the 13 proteins have been expressed from the nucleus and shown to work (allowing oxygen utilisation when the mitochondrial counterpart was mutant).

现状:13种蛋白质中的3种已从细胞核表达,并被证明能起作用(当线粒体的对应拷贝发生突变时能利用氧气)。

Transfer cells are active cells containing many mitochondria, and are concerned with short-distance transport of solutes.

传递细胞具有很多的线粒体,与细胞中溶质分子的短途运输有关。

The frequency of three mitochondriai point mutations,1555A→G,3243A→G,7445A→G,was examined using restriction fragment length polymorphism annlysis in 262 Chinese patients with NSHL,con- sisting of 168 sporadic cases,69 sib pairs,and 25 families with affected subjects in more than one generation.

方法收集非综合征型神经性耳聋病例262例,其中散发病例168例,69例同代有耳聋患者,25例不止1代有耳聋患者,采用限制性片段长度多态性分析线粒体基因中的下列3个点突变:1555A→G,3243A→G,7445A→G。

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