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1)  autosomal dominant
常染色体显性
1.
Expression of matrix metalloproteinases-1/tissue inhibitor of metalloproteinase-1 in kidney of patients with autosomal dominant polycystic kidney disease;
基质金属蛋白酶1/组织金属蛋白酶抑制因子1在常染色体显性遗传性多囊肾组织中的表达
2.
Sirolimus slows down disease progression in rats with autosomal dominant polycystic kidney disease and renal dysfunction;
西罗莫司延缓肾功能不全常染色体显性遗传性多囊肾病大鼠的疾病进程
3.
Morphologic, mechanical and functional sonographic parameters of arteties in autosomal dominant polycystic kidney disease;
常染色体显性多囊肾病患者动脉形态学、力学与部分功能性参数研究
2)  autosomal dominant inheritance
常染色体显性遗传
1.
Most cases of this disease are proved to be autosomal dominant inheritance.
多囊卵巢综合征是女性常见病和多发病,其发生主要受遗传控制,多数证实本病是常染色体显性遗传,一些基因位点已被提出,包括CYP11A、胰岛素基因以及胰岛素受体附近区域,研究较为深入的是胰岛素受体附近区域,已被两项独立研究证实,但是位于染色体19P13。
2.
According to genetic analysis, this disease is caused by autosomal dominant inheritance.
经过遗传分析,认为该畸形属常染色体显性遗传。
3.
they are autosomal dominant inheritance,autosomal recessive inheriance,x-linked dominant inheritance,x-linked recessive inheritance,holandric inheritance,that is Y-linked inheritance,sex-influenced inheritance,sex-limited inheritance,and etc.
人类单基因病的遗传方式有常染色体显性遗传 ,常染色体隐性遗传 ;X伴性显性遗传 ,X伴性隐性遗传 ,Y伴性遗传 ;从性遗传和限性遗传等。
3)  autosomal dominant
常染色体显性遗传
1.
Relationship between genotype and phenotype of autosomal dominant polycystic kidney disease;
常染色体显性遗传性多囊肾病基因型与临床表型的关系
2.
Progress in the research of disease genes in autosomal dominant retinitis pigmentosa;
常染色体显性遗传视网膜色素变性致病基因的研究进展
3.
To screen mutation hot spots in two Chinese autosomal dominant con-genital cataract pedigrees.
【目的】对2个常染色体显性遗传先天性白内障中国家系进行基因突变热点筛查,以了解这两个家系的先天性白内障是否与文献报道的17个突变热点相关。
4)  Autosomal dominant polycystic kidney disease
常染色体显性多囊肾病
1.
A Chinese autosomal dominant polycystic kidney disease family probably related to?PKD2 gene;
一个可能与PKD2基因连锁的常染色体显性多囊肾病家系
2.
We combined two dimensional liquid chromatography—tandem mass spectrometry (2D LC-MS/MS) with the method of isotope-coded affinity tag (ICAT) to do comparative analysis between the proteomes of urine, serum and cells from ADPKD patients and normal controls, aiming to find as many proteins as possible which get involved in the pathogenesis of Autosomal dominant polycystic kidney disease (ADPKD).
为尽可能多地寻找与常染色体显性多囊肾病(autosomal dominant polycystic kidney disease,ADPKD)发病相关的蛋白质,我们采用同位素编码的亲和标签技术与二维液相色谱-串联质谱相结合的定量比较蛋白组学方法分别对ADPKD患者与正常成人尿液、血清蛋白质组样品,以及囊肿衬里上皮细胞与正常肾小管上皮细胞的蛋白质组样品进行比较。
3.
Objective:To observe the expression of epidermal growth factor(EGF)and its receptor(EGFR)in the body fluids and renal tissues of rats with autosomal dominant polycystic kidney disease(ADPKD)and to explore their roles in the development of the disease.
目的:观察常染色体显性多囊肾病大鼠体液及肾脏组织中表皮生长因子(EGF)及其受体(EGFR)的表达,探讨二者在多囊肾病发病过程中的作用。
5)  Autosomal dominant polycystic kidney
常染色体显性多囊肾
6)  ADPKD
常染色体显性多囊肾病
1.
Objective: To investigate the role of celecoxib in the treatment of autosomal dominant polycystic kidney disease(ADPKD).
目的:研究特异性环氧化酶-2抑制剂塞来昔布治疗类似良性肿瘤的常染色体显性多囊肾病(ADPKD),以阐明该药具有良好的治疗作用。
补充资料:常染色体显性遗传


常染色体显性遗传
aotosomal dominant inheritance

一种性状或遗传病的基因位于常染色体上,这种基因的性质如果是显性的,这种性状或遗传病的遗传方式就叫做常染色体显性遗传。常染色体显性遗传病系谱特点是:①系谱中连续几代可出现患者;②患者的父母中一方是患病的;③患者同胞中约有1/2也是患者,且男女发病机会均等;④如果双亲正常,则子女一般也不患病。
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