1) polycystic kidney disease.
多囊性肾病
2) Polycystic renal disease
肾脏多囊性疾病
3) polycystic kidney disease
多囊肾病
1.
Morphology of renal tissue in Han:SPRD,a rat model of autosomal dominant polycystic kidney disease;
常染色体显性多囊肾病Han:SPRD大鼠肾脏病理观察及其意义
2.
Gene diagnosis of autosomal dominant polycystic kidney disease type 2 using microsatellite DNA tightly linked to polycystic kidney disease gene 2;
用与PKD2紧密连锁的微卫星DNA对2型常染色体显性多囊肾病进行基因诊断
3.
N-(4-hydroxyphenyl) retinamide induced apoptosis in autosomal dominant polycystic kidney disease cyst-lining epithelial cells;
4-羟苯基维甲酸诱导常染色体显性遗传性多囊肾病囊肿衬里上皮细胞凋亡
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) 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。
6) renal cystic lesion
肾囊性病变
1.
Objective To explore the value of contrast-enhanced ultrasound(CEUS) in the diagnosis of renal cystic lesion.
目的探讨超声造影(CEUS)在肾囊性病变中的应用价值。
补充资料：囊性肾疾病
| 囊性肾疾病 cystic renal diseases 一类有囊肿形成的肾脏疾病。由遗传性、发育性或获得性因素形成。分类方法较多，通常分为孤立性囊肿、先天性多囊肾、肾盂旁囊肿、髓质海绵肾、多囊性肾疾病。无特有临床表现，可长期无症状，亦可因长大、出血、损伤或慢性肾功能衰竭而出现症状。囊肿单个或多个，起源于由肾小球和肾小管组成的肾单位。若囊肿为多数性且直径较大时，可压迫肾实质使肾单位大量减少而发生肾功能衰竭。确切发病机理不明。放射学和超声检查能确诊。CT检查囊肿与周围有明确分界，呈均匀如水的衰减，静脉注射造影剂后密度不变。孤立性肾囊肿最常见，2％～3％伴发恶性肿瘤。若无出血、感染、压迫肾实质或伴发恶性肿瘤时不必手术。 多囊肾是遗传性双肾多数性囊性肾病变，有家族史，肾脏明显肿大且布满大小不等囊肿，成人型系显性遗传，一般于40岁以后出现症状，血尿、高血压及肾功能损害为其主要表现，可伴发结石及感染，大囊肿减压术可减缓对肾实质的压迫，最终需接受透析或肾移植；婴儿型系隐性遗传，出生后不久即出现症状，一般在10岁内死亡。这两型不发生于同一家族。血尿和腹部包块为常见症状。 |
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参考词条