查询词典 genetic disease

The disease is associated with inflammatory bowel disease, and genetic factors may play a causative role.

该病与炎症性肠病、遗传因素可能发挥作用的原因。

OBJECTIVE: To summarize the advances in the genetic susceptibility to coronary artery disease and explore the heritable basis of the disease.

目的：概述冠状动脉粥样硬化性心脏病遗传易感性的研究进展，探讨冠心病的分子遗传学基础。

Recent research has shown that mitochondrial dysfunction read.freeduan.com underlies a broad spectrum of disease, from maternally inherited genetic disorders to metabolism defects, aging, stroke, and neurodegenerative diseases such as Parkinson's, Alzheimer's, and Lou Gehrig's disease.

新近的研究已经表现那mitochondrial 机能失调read.freeduan.com为疾病的宽的范围的基础，从母亲继承的遗传疾病到新陈代谢缺陷，变旧，中风和neurodegenerative疾病，早老性痴呆症和卢·格里克的疾病。

Although many genetic mutations have been suggested as causes or risk factors for Parkinson's disease, the low penetrance of some mutations and the low disease concordance in relatives suggests that there must be interactions between multiple factors.

虽然许多遗传突变已经被认为是帕金森氏病的危险因素，但是一些突变基因的外显率低，家族相关的发病率也低，这说明一定有多因素的交互作用。

A genetic approach that utilizes a binary inducible transgenic system was used to investigate the disease mechanism and to assess preventability and reversibility of disease features in a mouse model of glycogen-storage cardiomyopathy.

利用二元可诱导性转基因系统的遗传方法在糖原贮积型心肌病小鼠模型中研究发病机制以及评估疾病特征的可预防性和可逆性。

It may also be due to a chronic illness, or a genetic or acquired disease (such as thalassaemia or sickle cell disease).

这也可能是由于慢性疾病，或遗传性或后天的疾病（如地中海贫血病或镰状细胞病）。

Accounting for population genetic substructure is important in reducing type 1 errors in genetic studies of complex disease.

在复杂疾病相关基因的遗传研究中人群遗传结构的组成对类型1错误的减少是很重要的。

Presymptomatic genetic screening : Presymptomatic genetic screening may be appropriate for persons with a family history of a dominantly inherited disorder （eg, Huntington's disease, breast cancer）.

症状前遗传筛查适用于家族史中有显性遗传病的人（如遗传性舞蹈病，乳腺癌）。

Presymptomatic genetic screening : Presymptomatic genetic screening may be a ropriate for perso with a family history of a dominantly inherited disorder （eg, Huntington's disease, breast cancer）.

症状前遗传筛查适用于家族史中有显性遗传病的人（如遗传性舞蹈病，乳腺癌）。

Most previous genetic trawls have focused on using the HapMap — a catalogue of common genetic variants shared by most people with a certain disease.

大多数以前的基因拉网式检查注重的是使用HapMap（人类基因组遗传整合图谱）――由许多有特定疾病的人共享出来的常见的遗传变异所构成的目录。

The absorption and distribution of chromium were studied in ryeusing nutrient culture technique and pot experiment.

采用不同浓度K2CrO4(0，0.4，0.8和1.2 mmol/L)的Hoagland营养液处理黑麦幼苗，测定铬在黑麦体内的亚细胞分布、铬化学形态及不同部位的积累。

By analyzing theory foundation of mathematical morphology in the digital image processing, researching morphology arithmetic of the binary Image, discussing two basic forms for the least structure element: dilation and erosion.

通过分析数学形态学在图像中的理论基础，研究二值图像的形态分析算法，探讨最小结构元素的两种基本形态：膨胀和腐蚀；分析了数学形态学复杂算法的基本原理，把数学形态学的部分并行处理理念引入到家实际应用中。