大部分的寄主感病基因还是未知。
血色病基因可引起铁的过量蓄积而致病，也会影响到铅的吸收。
Hemochromatosis gene, associated with a disease that leads to excessive iron accumulation, may also influence the absorption of lead.
但是正常的朊病基因被完全敲除后到底发生了什么并没有完全搞清楚。
But it is not entirely clear what happens when the gene for normal prions is completely removed.
苗期选用20个白粉菌株，21个鉴别寄主，根据基因对基因学说推导已知抗白粉病基因。
Seedling test was performed with 20 isolates and 21 tester lines carrying known genes. Resistance genes were postulated based on the application of gene-for-gene concept.
但由于致病菌小种分化多，而且不断变异进化，寻找新的高抗广谱抗白叶枯病基因仍是热点研究领域。
But, for the reason of kinds of bacteria and variation, a new resistance gene with high resistance and broad-spectrum is still the hot spot researchers interested in.
研究表明，对该家系听力资料和遗传资料的完整收集为下一步聋病基因定位克隆工作奠定了良好的基础。
The full collections of both blood samples and physiological hearing assessments of this family have provided the solid basis for future study on identifying disease causing gene.
结论四个基因片段为与细胞的增殖与分化相关的已知基因，有一个基因片段可能为新的功能性的白血病基因。
Conclusion the four gene fragments were amplified from known genes involved in cell proliferation and differentiation, while the one unknown gene fragment maybe from a new functional leukemia gene.
本研究对野生二粒小麦21449中的白粉病抗性进行了遗传分析并定位了所携带的一个隐性抗白粉病基因。
In this study, genetic analysis of a wild emmer wheat accession 21449 was carried out, and one recessive resistance gene in 21449 was mapped with microsatellite markers.
伦敦大学学院下属英国朊病毒研究中心的西蒙·米德表示，抗库鲁病基因的发现，是人类还在不断进化最有说服力的证据。
Simon Mead of the British prion research centre at University College London says the discovery of an "anti-kuru" gene is the most clear-cut evidence yet of human evolution in action.
最后，本文对白血病基因表达谱进行了实验，并且和其他文献进行了比较，结果得出本方法是可行的、有效的。
Finally, we carry out experiments on gene expression profiles of leukemia. Through the comparison with other papers, the results show that our method is Feasible and effective.
这些片断高度同源于1号和14号人类染色体上的某些区域，但功能目前尚不清楚，有可能与抑糖尿病基因有关。
They were selected for sequencing and hybridization. They showed highly homologous to some regions of Human chromosome 1 and 14, but the fragments functions are unknown.
利用抗病分离群体，我们在野生二粒小麦2B染色体上发现了多个抗白粉病基因，并利用SSR分子标记进行了定位。
Several powdery mildew resistance genes derived from wild emmer accessions have been mapped on the short and long arms of chromosome 2B by SSR marker.
在自闭症群体中，遗传因素导致的占相当一部分。基因突变引发的孤独症、合并癫痫和智力发育迟缓有很多相同的共病基因。
Genetic etiology play a part of role in ASD, and genes mutated causing autism and epileptic encephalopathy and mental retardation have an overlap.
将该种模型运用于公开的白血病基因表达数据集进行实验，实验表明该方法能自动获取基因表达数据的聚类数，并得到较高的分类准确率。
We applied the model to analyze the expression data set of leukaemia. The experimental result proved that this model can get cluster Numbers automatically and a high accuracy of classification.
例如，因为突变的基因可以提高铁的吸收效率，所以遗传性血色素沉着病突变可以保护带菌者不缺铁。
For example, the hereditary hemochromatosis mutation protects carriers from iron-deficiency because the mutated gene allows increased efficiency of iron absorption.
哮喘病的基因已被识别。
对艾滋病病毒进行基因编辑是一个“好主意”，丘奇对美联社说道。
Using gene editing for HIV is "a good idea", Church told AP.
具有等位基因4的个体，其较薄的内嗅皮层会增加阿耳茨海默（氏）病的风险。
The thinner entorhinal cortex in individuals with the 4 alleles might contribute to the risk of Alzheimer's disease.
提取能导致苯丙酮尿症（PKU）的基因突变.患这种病的人不能分解氨基酸苯丙氨酸，这会导致严重的认知损坏。
Take the gene mutation that causes phenylketonuria, or PKU. People with the disease can't break down the amino acid phenylalanine, a problem that can lead to severe cognitive damage.
全世界近5%的健康人口携带有镰状细胞病或地中海贫血的基因。
Approximately 5% of the world's population are healthy carriers of a gene for sickle-cell disease or thalassaemia.
马凡氏综合症是基因型结缔组织病。
Marfan's Syndrome is a genetic disorder that affects the connective tissue in the body.
它说最大的希望在于一种可能的“治愈”艾滋病的基因疗法。
The strongest hope lies in a potential "cure" based on gene therapy, it says.
心脏病不是有紧张或基因引起的，它是由西方饮食的加工油、乳制品和肉制品引起的。
It has not been stress, or genes. It is their western diet of processed oil, dairy, and meat.
流行病学调查和基因型分型均已确认在这一区域多个国家和美洲有麻疹病毒传播。
Epidemiological investigations and genotyping have confirmed transmission of measles virus among several countries in the Region and to the Americas.
流感病毒尤其容易产生这种重组，一些流行病就是因为这种基因混合所产生的。
Flu viruses are especially prone to this and some pandemics have emerged because of this genetic mixing.
例如，有些基因与高血压与糖尿病的低发病率有关，而另一个基因则能降低老年痴呆症的发病风险。
For example, some profiles were associated with lower rates of hypertension and diabetes, while another was linked to a reduced risk of dementia.
他说，“在很远的未来(才能治愈艾滋病)，现在还做不到，但是基因疗法为治疗艾滋病提供了一个可能的思路。”
"It is way into the future and it is not something that is available now but gene therapy offers a potential avenue to dealing with the HIV epidemic," he said.
那些知道家族内有基因遗传病风险的人们可以寻求医疗干预，或者改变生活习惯以降低患病风险。
Families who learn they are at genetic risk might seek medical intervention sooner. Others may adopt lifestyle changes to try to lower their risk.
那些知道家族内有基因遗传病风险的人们可以寻求医疗干预，或者改变生活习惯以降低患病风险。
Families who learn they are at genetic risk might seek medical intervention sooner. Others may adopt lifestyle changes to try to lower their risk.
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