查询词典 genetic disease

Data from twins, adoptees, and families show that genetic factors play an important role in the etiology of this disease.

大量的双生子、寄养子和家系研究的数据表明在精神分裂症的发病过程中遗传因素有很重要的作用，所以精神分裂症作为一种复杂遗传疾病被纳入遗传学的研究范畴。

This genetic and phenotypic heterogeneity has importantpractical consequences for a number of human interests, includingantibiotic or biocide resistance, the productivity and stabilityof industrial fermentations, the efficacy of food preservatives,and the potential of pathogens to cause disease.

这种遗传和表型异质性已成为部分人类利益的重要性，包括抗生素或生物杀灭剂抗性，工业发酵的产量和稳定性，食品防腐剂的效能和潜在的病原体致病性。

The selective chromosome as genetic marker of minimal residual disease is significant to predict relapse following transplantation at chimerism condition.

选择性染色体作为微小残留病监测的遗传学标志，对分析嵌合状态预测移植后复发具有重要意义。

Comparing with the genetic myopathy, alcoholic myopathy is the only treatable muscle disease, and it has the certain reference value to research the other metabolic myopathy by the studying of the cytes and molecular level of CAM.

国外学者在肌营养不良症和包涵体肌病的研究中发现，一氧化氮合酶(Nitric oxide synthase，NOS)与氧化应激可诱导肌萎缩的发生，且二者具有一定的相关性。

This paper summarized the structure and function of the ERF transcription factors in cotton and other plants, and discussed the significance in enhancing cotton disease resistance and molecular genetic improvement based on the current research progress.

本文主要论述了棉花等植物中ERF的结构与功能特征，当前相关研究进展，及其对棉花抗病性分子遗传改良的意义。

Objective To investigate further the genetic basis of hereditary multiple exostoses and provide useful information for gene diagnosis of the disease.

目的 进一步阐明遗传性多发性外生骨疣(hereditary multiple exostoses，EXT)的发病机理，并为最终防治本病提供依据。

Its longevity is also obtained without genetic modification – its disease-resistant properties come from a gene found in the Asiatic apple malus floribunda.

而且此种苹果没有经过基因改造，它的抗病特性来自于从亚洲多花海棠果提取的基因。

We anticipate that genetic variation in MIF expression may impact on the response of the human heart to ischaemia by the AMPK pathway, and that diagnostic MIF genotyping might predict risk in patients with coronary artery disease.

我们认为，MIF表达的遗传变异可通过AMPK途径影响心脏对缺血的反应，从而通过诊断MIF基因型可预测冠心病患者的危险性。

"Yes." First Affiliated Hospital of Henan College of Traditional Chinese Medicine Obstetrics and Gynecology of a chief physician, said Wang Lina, if both husband and wife blood group incompatibility, the fetus may be obtained from the genetic father of the missing mother of blood group antigen, blood group antigens of red blood cells that once the mother, mother will produce antibodies, which antibodies can enter the fetus via the placenta, the baby will cause the destruction of red blood cell hemolysis, manifested as jaundice, anemia and other serious symptoms may lead to cerebral palsy; If severe intrauterine hemolytic disease will result in miscarriage or stillbirth.

&是的。&河南中医学院一附院妇产科主任医师王丽娜说，如果夫妻双方血型不合，胎儿就可能从父亲身上遗传获得母亲所缺少的血型抗原，这种血型抗原的红细胞一旦进入母体，母体会产生抗体，而这种抗体可经胎盘进入胎儿体内，就会引起宝宝的红细胞被破坏而溶血，表现为黄疸、贫血等，症状严重可能导致脑瘫；如果在宫内出现严重的溶血症，还会导致流产或死胎。

To be sure, we will know much, much more about the genetic causes of death and disease, and it would be surprising indeed if lifespans did not continue to increase.

可以肯定的是，我们将更为了解生老病死的基因上的原因，而且寿命将肯定会延长。

Do you know, i need you to come back

你知道吗，我需要你回来

Yang yinshu、Wang xiangsheng、Li decang,The first discovery of haemaphysalis conicinna.

1〕 杨银书，王祥生，李德昌。安徽省首次发现嗜群血蜱。