致病性

Ataxin-1 is another pathogenic protein which causes a disease called spinocerebellar ataxia, which is also an incurable hereditary nervous disorder.

Ataxin-1是另一种致病蛋白，它能够引起脊髓小脑性共济失调，也是一种不能治愈的遗传性神经系统疾病。

Researches in genodermatoses has rapidly advanced in China in recent ten years. The causative genes involved in multiple familial trichoepithelioma and primary erythermalgia have been found. Two indepen- dent genome-wide scans with DNA markers have been performed to detect genetic linkage related to psoriasis and vitilig...

近几年来我国皮肤遗传病研究也取得了飞速发展，如发现家族性多发性毛发上皮瘤和原发性红斑肢痛症的致病基因，成功进行了汉族人群银屑病和白癜风易感基因的定位，为搜寻其易感基因奠定了坚实基础。

It is caused by mutations in dyskerin-encoding genes, telomerase-encoding RNA component genes and reverse transcriptase genes, as well as other uncharacterized genes. There are three inherited forms, including X-linked, autosomal dominant and autosomal recessive inheritance.

先天性角化不良是与编码角化不良蛋白基因、编码端粒酶的RNA组份基因、编码端粒酶的逆转录酶基因突变及其他未确认的致病基因突变引起的基因病，其遗传方式有：X-性联隐性遗传、常染色体显性遗传及常染色体隐性遗传。

This preliminary case control study reconfirms that TWHf is a very potent herbal remedy to suppress mononuclear expressions of many inflammatory cytokines and pro-inflammatory molecules.

尽管只有少数的研究对象，本篇研究提供了在免疫致病机转上的可能证据来支持雷公藤对於僵直性脊椎炎患者周边血液单核球细胞内的许多发炎性细胞激素及其它和发炎反应有关的分子的基因表现具有强烈的抑制作用的说法。

They analyzed 500,000 one-letter ariations, or single nucleotide polymorphisms, in their DNA to look for commonalities. They then confirmed possible culprits in two separate studies of Germans and French-Canadians.

为了找出共同特征，他们分析了他们DNA中500，000个单基因突变或者单核苷酸多态性，最终在关于德国人和法籍加拿大人的两个独立的研究中确定了可能的致病突变。

The EIAV proviral genomic long-terminal repeat is a eukaryotic promotor, which plays an important regulatory role on transcription and replication of the virus.

反转录病毒前病毒基因组长末端重复序列对病毒复制有重要的调控作用，影响到病毒的繁殖动力学、组织嗜性、致病力等方面。

The EIAV proviral genomic long-terminal repeat is a eukaryotic promotor, which plays an important regulatory role on transcription and replication of the virus.

反转录病毒前病毒基因组长末端重复序列对病毒复制有重要的调控作用，影响到病毒的复制动力学、细胞嗜性、致病力等方面。

Clinical evaluations demonstrated familial apical HCM in 4 probands, and in 3 probands disease-causing mutations were identified.

临床评价显示4个患者为家族性心尖肥厚型心肌病，并在3个患者验明致病基因突变。

There was no deference in the radio between two transverse areas of CSF column and spinal canal in the two groups.

结论椎体后高中点水平脊髓横断面面积与相应水平椎管横断面面积比值的增高是脊髓型颈椎病的发育性致病因素。

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。