针对这种明确的单基因疾病有可能开展基因治疗。
It is possible to cure the patients with XLSA by gene therapy because it is a single gene disorder.
但是，单基因疾病研究能从新的方面揭示基因组生物学。
But study of monogenic diseases can reveal new aspects of genomic biology.
GPCR的突变及基因多态性将引发各种疾病，目前已经发现有30多种单基因疾病与此相关。
Mutant GPCR and genetic variation will cause diseases and responsible for more than 30 different human diseases which have been identified to date.
从单基因疾病的基因治疗、肿瘤的基因治疗和AIDS疾病的基因治疗三个方面介绍基因治疗的研究进展及基因治疗在临床上的应用概况。
The article introduces the study advance of the gene therapy and the clinical practical concerns of the gene therapy from the three aspects of gene therapies of solo gene disease, tumour and AIDS.
牛白细胞粘附缺陷病(BLAD)是一种常染色体单基因隐性遗传疾病，病因为白细胞表面整合素cd 18亚单位基因突变所致。
Bovine leukocyte adhesion deficiency (BLAD) is autosomal recessive disease. The pathogeny of BLAD is genic mutation of CD18-integrins on the leukocyte.
目前，使用PGD技术，可以测试出许多种不同的疾病，包括非整倍体，单基因病和染色体易位等。
Currently, we are able to perform PGD for many genetic conditions including single gene disorders and chromosome abnormalities.
Cochran博士认为，德系犹太人也面临着同样的情况，他们的某些基因如果以单组出现就可以提高智力，一旦以双组出现就会引起疾病。
Dr Cochran argues that something similar happened to the Ashkenazim. Genes that promote intelligence in an individual when present as a single copy create disease when present as a double copy.
目前，已有超过200种单基因遗传性疾病被认为是由X染色体连锁遗传引起的，这些疾病只影响男性胎儿。
At present, more than 200 diseases which have been identified are X-linked, these diseases only affect male fetuses.
结论肝癌不符合单基因遗传模式，为一多因子疾病，受遗传与环境的综合影响。
Conclusion Our findings suggested that HCC followed a multifactorial mode rather than single inheritance. An interaction effect of inheritance and environment on HCC was also noticed.
此法不仅适用于疾病研究中的DNA测序，还可制各单链DNA探针，更利于基因结构组成的研究。
This efficient method is suitable for DNA sequence analysis, for the preparation of ssDNA probes, and potentially useful in studies of genomic structural organization.
此法不仅适用于疾病研究中的DNA测序，还可制各单链DNA探针，更利于基因结构组成的研究。
This efficient method is suitable for DNA sequence analysis, for the preparation of ssDNA probes, and potentially useful in studies of genomic structural organization.
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