It provide an evidence of using this technique for the PGD for ADPKD.
该方法为常染色体显性多囊肾疾病行胚胎植入前遗传学诊断提供了依据。
Conclusions ADPKD cyst-lining epithelial cells synthesize and secret HGF.
结论ADPKD囊肿衬里上皮细胞可合成和分泌hgf。
Objective To study the expression of extracellular matrix and polycystin-1 in ADPKD and their relation to cyst formation.
目的研究常染色体显性遗传型多囊肾病肾组织中细胞外基质和多囊蛋白-1的表达及与囊肿发生的关系。
Objective: to analyze the relationship between the genotype and phenotype of autosomal dominant polycystic kidney disease (ADPKD) in Han nationality in East China.
目的：研究华东地区汉族人常染色体显性遗传性多囊肾病(adpkd)基因型与临床表现型的关系。
CONCLUSION an ADPKD cyst lining epithelial cell line has been established and identified, which can be used in the research of ADPKD cellular and molecular mechanism.
结论：经鉴定，ADPKD囊肿衬里上皮细胞系已建立，可用于ADPKD细胞及分子生物学的研究。
Objective: cyst lining epithelial cell proliferation and apoptosis are implicated in the pathogenesis of cyst formation in autosomal dominant polycystic kidney disease (ADPKD).
目的：研究多囊肾病囊肿衬里上皮的增生与凋亡及相关蛋白表达。
The expression of IGF-1, IGF-1R, IGF-1 mRNA, IGF-1R mR NA were examined in ADPKD kidney tissues and normal kidney tissues using immunohistochemistry and in situ hybridization technique.
应用原位杂交及免疫组织化学染色方法检测IGF-1及其受体（IGF-1R）在正常肾组织及ADPKD囊壁组织中的表达分布；
In the U. S., the number of individuals affected by ADPKD is greater than the number affected by cystic fibrosis, muscular dystrophy, hemophilia, Down's syndrome, and sickle cell anemia combined.
美国患adpkd的人数超过囊性纤维化、肌营养不良、血友病、唐氏综合症、镰刀细胞性贫血数种疾病加起来的患者。
In the U. S., the number of individuals affected by ADPKD is greater than the number affected by cystic fibrosis, muscular dystrophy, hemophilia, Down's syndrome, and sickle cell anemia combined.
美国患adpkd的人数超过囊性纤维化、肌营养不良、血友病、唐氏综合症、镰刀细胞性贫血数种疾病加起来的患者。
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