遗传学的

Both of these two genes were cloned into Escherichia coli for overexpression.

在生化测定的同时，我们又应用遗传学方法构建突变株分析基因功能。

Thermoanaerobacter tengcongensis is a rod-shaped, Gram-negative, anaerobic eubacterium that was isolated from a fresh water hot spring in Tengchong, China. Using a"whole-genome-shotgun"method, we sequenced its 2, 689, 445-bp genome from an isolate, MB4〓(Genbank Accession Number AE008691). The genome encodes 2, 588 predicted coding sequences . Among them, 1, 764 (68. 2％) are classified according to homology to other documented proteins, and the rest, 824 CDS (31. 8％), are functionally unknown. One of the interesting features of the T. tengcongensis genome is that 86. 7％ of its genes are encoded on the leading strand of DNA replication.

中文题名腾冲嗜热厌氧菌全基因组测序及分析副题名外文题名 A complete sequence of the T.tengcongensis genome 论文作者包其郁导师杨焕明研究员学科专业遗传学研究领域\研究方向学位级别博士学位授予单位中国科学院遗传与发育生物学研究所学位授予日期2002 论文页码总数88页关键词腾冲嗜热厌氧菌基因组嗜热菌馆藏号BSLW /2003 /Q939.1 /33 腾冲嗜热厌氧菌（MB4＇）是分离于我国腾冲地区温泉内的革兰氏阴性厌氧真细菌。

Background: Frontotemporal lobar degeneration is a genetically and pathologically heterogeneous neurodegenerative disorder.

研究背景额颞叶变性是一种在遗传学和病理学上高度多样化的神经退行性病变。

The main agronomic traits and cytology of BC1F2,BC1F3,BC1F4 between Elymus dahuricus, Hordeum brevisubulatum were studied.

研究了披碱草与野大麦BC1F2、BC1F3、BC1F4代的主要农艺及分子细胞遗传学特性。

The present study demonstrates that the utility of morphometric characters for defining stocks of kuruma shrimp is available,but further verification of the stockstructure(e.g.,genetic evidence)is essential.

本研究利用外部形态已成功之判别斑节虾之系群结构，但更进一步之验证如遗传学证据是必须的。

Objective To explore audiological features of matrilineal non-syndromic deafness and its molecular mechanism.

目的 探讨母系遗传性非综合征性耳聋的听力学特征及分子遗传学机制。

There are some overlapped features between basal-like ca and metaplastic ca as Dr. Huang mentioned. There are no good IHC and genetic features to distingush these two for some case.

如Dr。 Huang所说，基底细胞样癌和化生性癌之间有重叠，在很多病例中，两者之间也没有很好的免疫组化和遗传学特征来进行区分。

Objective To collect, protect and study on pedigrees of microtia.

目的：收集和利用先天性小耳畸形家系资源进行相关的遗传学研究。

In 1980s, molecula biology technology had been applied to familial diabetic genetics, a suit of single genes about diabetes was found: insulin gene, insulin receptor gene and so on.

自上个世纪80年代以来，应用分子生物学技术进行家族性糖尿病遗传学研究发现了一系列与糖尿病相关联的单基因，即胰岛素基因和胰岛素受体基因等。

Objective: To investigate the clinical manifestations and to make genetic analysis in a pedigree with myotonic dystrophy disease.

目的：探讨浙江台州地区一个强直性肌营养不良(myotonic dystrophy， DM)汉族家系的临床表现和分子遗传学基础。

The split between the two groups can hardly be papered over.

这两个团体间的分歧难以掩饰。

This approach not only encourages a greater number of responses, but minimizes the likelihood of stale groupthink.

这种做法不仅鼓励了更多的反应，而且减少跟风的可能性。