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monogenic相关的网络例句

查询词典 monogenic

与 monogenic 相关的网络例句 [注:此内容来源于网络,仅供参考]

There is an agreement that autosomal recessive juvenile parkinsonism is a monogenic disease caused by mutation in parkin gene.

一致的观念认为常染色体隐性遗传性青少年型帕金森综合症是parkin基因突变引起的一种单基因遗传病。

Dr Casanova thinks HSE is the first example of a disease that was thought to be purely infectious but which has turned out to be purely monogenic—that is, under the control of a single gene.

Casanova博士认为HSE的是第一个种原本被认为是单纯的传染性疾病,却最终被证明是被一个单一的基因控制的。

With the development of molecular biology,a lot of genes for the inherited endocrine and metabolic diseases have been reported.Meanwhile,more and more endocrine and metabolic diseases caused by monogenic mutations have been discovered.

随着分子生物学技术的发展,相当多的遗传性内分泌代谢病的致病基因相继被报道;同时,越来越多的单基因突变所致的内分泌代谢疾病被发现。

It is found that schizophrenia is not a monogenic disease, but probably a polygenic disease influenced by multiple genes with small or medium risks, and by environment factors as well.

人们还发现精神分裂症并不是单基因遗传病,而可能是多个微效或中效基因共同作用的多基因疾病,并且还受到环境因素的很大影响。

The clinical application of PGD of ACH has accumulated experience for us to developing clinical PGD of other monogenic genetic conditions further.

ACH的临床PGD的实施,为我们进一步开展其它单基因遗传病的临床PGD积累了经验。

Genetic analysis showed the dwarf is controlled by a monogenic recessive gene. We named the dwarf gene Ds.

遗传分析表明,该矮秆性状受隐性单基因控制,我们将其暂定名为Ds。

Monogenic dwarf mutants 91G318,91D27 and 93-597 carried 1 pair of new recessive dwarf genes respectively.

单基因突变品系91G318、91冬27和93-597,各自携带1对新的隐性矮秆基因。

Most families presented evidence against hMLH3 as a monogenic explanation for the familial aggregation of colorectal cancer, and most of the mutations were found in the low risk patients.

因为这些突变与疾病相关,且在散发性食管癌患者和正常对照中几乎没有此项突变的发生。

BACKGROUND: Several cardiac ion channel genes have been implicated in monogenic traits with a high risk of sudden cardiac death. Mutations or rare variants in these genes have been proposed as potential contributors to more common forms of SCD, but this hypothesis has not been assessed systematically.

背景:数种心肌离子通道基因和高危心源性猝死的单基因特性有关,这些基因的罕见突变被认为是SCD更常见的潜在促进因素,但是这一假说没有被系统的评价过。

Osteogenesis imperfecta (01) is a typical monogenic disorder related to bone tissue. Seven different types have been described, in which OI type I is the most common form of OI.

成骨不全(osteogenesis imperfecta,OI)是一种典型的骨骼系统相关的单基因疾病,有七种类型,其中Ⅰ型是最主要的一种类型。

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However, as the name(read-only memory)implies, CD disks cannot be written onorchanged in any way.

然而,正如其名字所指出的那样,CD盘不能写,也不能用任何方式改变其内容。

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