The sequence was confirmed as HBV X gene.
基因测序结果证实为乙肝病毒X基因。
Whether or not HBV X gene or X protein could affect the growth of HCC cell?
乙肝病毒X基因或X蛋白是否影响肝癌细胞生长？
Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia.
ALAS2基因的可遗传突变是人类X连锁铁粒幼细胞性贫血的原因。
The disease is autosomal-recessive and linked to the X-chromosome, so that men whose mothers are carriers of the gene manifest the disease.
该病属常染色体隐性遗传，与X-染色体关联，所以，母亲是基因携带者的男性表现为发病。
For example, in a gene therapy trial for X-SCID - or "bubble-boy" disease - inserting a gene in the wrong place triggered cancer in some of the recipients.
比如，在X光免疫缺陷和“泡泡男孩”疾病的基因疗法试验中，就因基因植入错误而引发了试验者的癌症。
Because men have only one X chromosome that they inherit from their mother and thus only one copy of the TEX11 gene, any mutation could theoretically lead to sterility.
因为男性只有一条从母亲那里遗传来的X染色体，因此他们的TEX11基因只有一个拷贝，理论上来说，TEX11基因的任何突变都可以导致不育。
Rhys had acquired a defective gene on the X-chromosome-inherited from his mother.
里斯的X染色体是一个基因有缺陷（这个X 染色体是从母亲那里继承的）。
The dystrophin gene is found on the X chromosome and passed on to children through a mother who is a carrier.
肌营养不良卵白基因位于人类X染色体，携带基因突变的母亲会遗传给婴儿。
Study on the mechanisms of 'escape' is helpful to the understanding of gene regulation by X inactivation.
探讨这些基因逃避X失活的机制有助于理解X染色体失活是如何对基因表达进行调控的。
This phenomenon is mostly seen in imprinted genes and X-chromosome inactivation where DNA methylation of promoter regions leads to repression of gene expression.
这种现象主要在印迹基因和X染色体失活区域看到，这些区域中的启动子区的DNA甲基化导致了基因表达的抑制。
The colour blindness in the monkeys arises because full colour vision requires two versions of the opsin gene, which is carried on the X chromosome.
色盲在猴群中上升是因为全色觉需要两种不同的视蛋白基因，它们存在于X染色体上。
Amelogenin (AML) gene locates on the conservative region of the bovine X and Y chromosomes.
牛牙釉蛋白(AML)基因定位于牛x染色体和Y染色体上的同源区域。
Most likely there are multiple genes that contribute towards MPB, the most important of which appears to be the Androgen Receptor gene, located on the X chromosome (inherited from the mother).
大多数论证认为多基因会引致雄性脱发，而其中最为重要的的是雄激素受体基因，该基因位于X性染色体(对于男性来说遗传自母亲)。
Objective To explore the relationship between X - linked spondyloepiphyseal dysplasia tarda (SEDL) gene escaping X chromosome inactivation( XCI) and SEDL phenotype.
目的探讨X-连锁迟发性脊椎骨骺发育不良（SEDL）基因逃避X染色体失活（XCI）及与临床表型的关系。
There are tolls of basic study of molecular image-forming such as gene recombinant technique. X-ray crystal image-forming.
分子成像基础研究的工具有基因重组技术、X线晶格成像、快速物质波谱分析、计算机和机器人技术。
Objective To analyze the ABCD1 gene mutations in 5 cases of X-linked adrenoleukodystrophy (X-ALD) patients and 2 cases of their mothers.
目的对5例x -连锁肾上腺脑白质营养不良(X -ALD)患儿及其中2例的母亲进行ABCD 1基因突变分析。
The absence of ALAS2 leads to maturation arrest of primitive erythroid cells. Heritable mutations of ALAS2 gene are responsible for the human X-linked sideroblastic anemia (XLSA).
ALAS2的缺失能导致红细胞发育的停滞，ALAS2基因的遗传性突变能引起X-连锁的成高铁红细胞贫血（XLSA）。
Objective To identity the ABCD1 gene mutation in a Chinese family with X-linked adrenoleukodystrophy (ALD).
目的鉴定并分析1个新的肾上腺脑白质营养不良家系的基因突变类型和位点。
The disease can skip a generation until another son inherits the defective gene on the X-chromosome.
这种疾病可以跳过一代，直到另一个儿子继承了有缺陷的基因在X染色体上。
The methylation of histone H3-K27 was proved to be linked to several silencing phenomena including homeotic-gene silencing, X inactivation and genomic imprinting.
组蛋白H3第27位赖氨酸的甲基化与同源盒基因沉默、X染色体失活、基因印记等基因沉默现象有关；
It's plausible that millions of years ago a single mutation resulted in two different versions of the photopigment gene becoming located on the same X chromosome.
鼠类研究的主要作者Jeremy Nathans说，可能在亿万年前一种特别的突变造成感光素基因中两种不同的感光色素基因编码定位于同一个X染色体上。
The gene products encoded by two X chromosomes of female individuals are nearly identical to those encoded by one X chromosome of male individuals.
雌性两条X染色体编码的基因产物，与雄性一条X染色体编码的基因产物基本相同。
In males (who have only one X chromosome), one altered copy of the gene in each cell is sufficient to cause the condition.
男性(谁只有一个染色体)，一个改变复制的基因在每个细胞就足以造成的条件。
Objective to detect mutations of the RP2 gene in two Chinese families with X linked retinitis pigmentosa (XLRP).
目的检测引起2个家系产生X连锁视网膜色素变性的RP2基因突变。
Objective to study the clonality of palmar fibromatosis by molecular genetic analysis of X chromosome inactivation pattern at a polymorphic site of human androgen receptor gene (HUMARA).
目的通过人雄激素受体(HUMARA)基因位点克隆性分析技术确定掌纤维瘤病是否为肿瘤性增生。
Objective To investigate the effect of dual-target antisense RNA of hepatitis B virus (HBV) targeted to X and P region on replication and expression of HBV gene in HBV transgenic mice.
目的探讨针对乙型肝炎病毒（HBV）x、p双靶区反义RNA对乙型肝炎病毒转基因小鼠HBV复制和表达的影响。
Objective To investigate the effect of dual-target antisense RNA of hepatitis B virus (HBV) targeted to X and P region on replication and expression of HBV gene in HBV transgenic mice.
目的探讨针对乙型肝炎病毒（HBV）x、p双靶区反义RNA对乙型肝炎病毒转基因小鼠HBV复制和表达的影响。
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