gene complex的例句大全

Two simple methods for estimation of RH gene complex frequencies

估计Rh基因组合体频率的两种简易方法

Filaggrin gene is a member of epidermal differentiation complex, and it closely relates to the formation of cell membrane and terminal differentiation of epidermis.

中间丝蛋白基因是表皮分化复合物基因簇的成员之一，与细胞膜形成及表皮终末分化密切相关。

Ternary complex factor Net regulates transcription of c-fos gene

三元复合因子Net对c-fos基因转录的调节作用

Background and Aim: Carcinoma is a type of multi-gene disease, and a complex process involved multi-factor, multi-stage and multi-gene mutation, which caused by activation of telomerase and cancer gene, devitalization of suppressor gene.

背景和目的：研究表明，肿瘤是一类多基因疾病，是由于端粒酶激活、癌基因激活或抑癌基因失活等引发的多因素、多阶段及多基因变异的综合病变过程。

Among genetic factors implicated in autoimmunity, Autoimmune Regulator gene ( AIRE) is one of the candidates to better understand the complex scenario of autoimmune manifestations.

目前对于AIRE蛋白的详细的亚细胞分布、表达调节以及AIRE基因与常见的自身免疫病中的作用还不是很清楚。

LAPP is a data modeling and different from traditional computational method of modeling gene logic networks. This computational approach identifies logic relationships of the elements ( or components) in complex networks through the logic analysis of their expression data.

LAPP和传统建立基因逻辑网络模型的方法不同，它给出了一个从复杂网络的元素（或部件）的表达数据出发，通过逻辑分析，找到元素之间的逻辑关联性的建模方法。

HFE gene is a major histocompatibility complex class ⅰ-like gene, which was identified as a candidate gene for hemochromatosis in 1996. The proposed role for HFE is its part in the regulation of the interaction of the transferrin receptor with transferrin.

HFE基因发现于1996年，属于HLA类样基因，是遗传性血色素沉着症候选基因。HFE分子的功能可能是参与调节转铁蛋白与转铁蛋白受体间的相互作用。

It is well known that TTG1/ GL3/ GL1 protein complex activates the expression of downstream gene GL2, ultimately leading such epidermal cells to differentiating into trichomes.

研究发现，在拟南芥表皮毛分化的过程中，TTG1/GL3/GL1等组成蛋白复合体，激活下游GL2的表达，最终使表皮细胞分化为表皮毛。

Gene Algorithm is an intelligent optimization algorithm, which solves complex combination and optimization problem by simulating the process of natural anagenesis and using simple code and gene operation.

遗传算法是一种新的智能优化算法，通过模拟自然进化过程，利用简单的编码技术和遗传操作高效地解决复杂的组合优化问题。

The gene chip is precisely to solve the inadequacies of the traditional research methods, its large-scale and high-throughput method to study thousands of gene expression under physiological and pathological conditions, to predict their function and the complex between their mutual regulation relationship.

而基因芯片恰恰能解决传统研究方法的不足之处，其以大规模高通量的方法研究成千上万的基因在不同状态下的表达，预测他们的功能，预测他们之间的复杂的相互调控关系。

There are multiple molecular mechanisms that can cause genetic disorders such as point mutations, splicing site mutation, insertion/ deletion mutations, gene duplication, complex rearrangements and gene copy number abnormalities.

引起遗传性疾病的分子机制有多种，常见的有点突变、小片段插入/缺失突变、拼接位点突变、外显子缺失/重复突变、基因重复和复杂重排及基因拷贝数异常等。

Single nucleotide polymorphism in studying complex diseases susceptibility gene

单核苷酸多态性在复杂性状疾病易感基因研究中的应用

Objective To study the characteristic of mutation and polymorphism in exon 4 of tuberous sclerosis complex gene ( TSC1) in Chinese.

目的探讨中国人结节性硬化症（Tuberous Sclerosis Complex，TSC）基因（TSC1）外显子4的基因突变特征及多态现象。

Gene Mutation Analysis of Duchenne Muscular Dystrophy and Tuberous Sclerosis Complex

杜氏肌营养不良症和结节性硬化症的基因突变分析

Objective To analyze the mutation of TSC gene in two sporadic patients with tuberous sclerosis complex ( TSC).

目的检测两例中国汉族结节性硬化症散发病例的基因突变位点。

Cancer is a kind of multi-faceted and complex disease involved in multi-genes and proteins.

恶性肿瘤是一种多种基因和蛋白质参与的复杂疾病。

fully explicating the complex interplay among these enzymes and the molecules they manage has been a primary goal for scientists seeking to understand the mechanisms governing gene control.

充分阐明这些酶和它们管理的蛋白分子间复杂的相互作用已成为科学家们了解基因调控机制的首要目标。

the molecular genetics and mutation profile of the cftr gene are complex, with a wide range of phenotypic consequences.

分子遗传学和基因突变的CFTR基因配置是复杂的，具有广泛的表型后果。

the molecular genetics and mutation profile of the cftr gene are complex, with a wide range of phenotypic consequences.

分子遗传学和基因突变的CFTR基因配置是复杂的，具有广泛的表型后果。

the molecular genetics and mutation profile of the cftr gene are complex, with a wide range of phenotypic consequences.

分子遗传学和基因突变的CFTR基因配置是复杂的，具有广泛的表型后果。