1) hereditary retinal degeneration
遗传性视网膜变性
1.
In order to investigate photoreceptor (PRC) apoptosis and gene regulation in hereditary retinal degeneration of Royal College of Surgeon (RCS) rats, the retinal sections of RCS and SD rats at different ages were examined by TUNEL and Fas protein immunohistochemical method.
为了探讨遗传性视网膜变性时感光细胞凋亡及其基因调控机制 ,本研究对出生后 9、15、2 0、2 5、3 0、3 5、40、60 d的 RCS大鼠及同龄 SD大鼠各 4只的视网膜进行了 TU NEL 凋亡检测及 Fas蛋白免疫组织化学反应。
3) autosomal dominant retinitis pigmentosa
常染色体显性遗传视网膜色素变性
1.
Objective To detect mutation in the rhodopsin gene ( RHO ) in a Chinese family with autosomal dominant retinitis pigmentosa (ADRP).
目的 确定常染色体显性遗传视网膜色素变性家系的致病基因及其突变位点,并研究其临床表型。
5) retinal hereditary disease
遗传性视网膜疾病
1.
AIM To compare the characteristic of the visual electrophysiology between normal SD rats and a case of abnormal rat with retinal hereditary disease.
目的 观察正常 SD大鼠和一例患遗传性视网膜疾病大鼠的视觉电生理学特点 。
6) retinal degeneration
视网膜变性
1.
Analysis of ultra structural changes of retinal photoreceptors in animal models with fast retinal degeneration;
快速退变性视网膜变性感光细胞超微结构变化分析
2.
Histological changes of retina in rats of retinal degeneration at different postnatal days;
不同日龄视网膜变性大鼠眼底组织结构学观察
3.
Expression of immediate early gene following N-methyl-N-nitrosourea-induced retinal degeneration in SD rats;
即早基因在N-甲基-N-亚硝脲诱导SD大鼠视网膜变性中的表达
补充资料：视网膜色素变性肥胖多指综合征
视网膜色素变性肥胖多指综合征
病名。即劳-穆-比综合征，详见该条。
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条