D477G dominant mutation in RPE65 leads to decreased 11-cis-retinal generation and delayed dark-adaptation in knock-in mouse model of retinitis pigmentosa

Moiseyev Gennadiy P.; Shin Younghwa; Charkraborty Dibyendu; Ma Jian-Xing (Jay)

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D477G dominant mutation in RPE65 leads to decreased 11-cis-retinal generation and delayed dark-adaptation in knock-in mouse model of retinitis pigmentosa

机译：RPE65中的D477G主导突变导致11-CIS-视网膜溶解和延迟后爆击鼠标模型的延迟暗对抗肠道炎色素粒子模型

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来源
《Investigative ophthalmology & visual science》 |2017年第8期|共2页
作者
Moiseyev Gennadiy P.; Shin Younghwa; Charkraborty Dibyendu; Ma Jian-Xing (Jay);
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Univ Oklahoma Hlth Sci Ctr Physiol Oklahoma City OK USA;

Univ Oklahoma Hlth Sci Ctr Physiol Oklahoma City OK USA;

Univ Oklahoma Hlth Sci Ctr Physiol Oklahoma City OK USA;

Univ Oklahoma Hlth Sci Ctr Physiol Oklahoma City OK USA;

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正文语种 eng
中图分类眼科学;
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1. D477G dominant mutation in RPE65 leads to decreased 11-cis-retinal generation and delayed dark-adaptation in knock-in mouse model of retinitis pigmentosa [J] . Moiseyev Gennadiy P., Shin Younghwa, Charkraborty Dibyendu, Investigative ophthalmology & visual science . 2017,第8期

机译：RPE65中的D477G主导突变导致11-CIS-视网膜溶解和延迟后爆击鼠标模型的延迟暗对抗肠道炎色素粒子模型
2. Insights into the pathogenesis of dominant retinitis pigmentosa associated with a D477G mutation in RPE65 [J] . Choi Elliot H., Suh Susie, Sander Christopher L., Human Molecular Genetics . 2018,第13期

机译：洞察RPE65中D477G突变的显性视网膜炎的发病机制
3. A Dominant Mutation in Rpe65, D477G, Delays Dark Adaptation and Disturbs the Visual Cycle in the Mutant Knock-In Mice [J] . Younghwa Shin, Gennadiy Moiseyev, Dibyendu Chakraborty, The American journal of pathology. . 2017,第3期

机译：Rpe65，D477G的显性突变，延迟黑暗适应和扰乱突变敲入小鼠的视觉周期。
4. Viability of the inner retina in a novel mouse model of retinitis pigmentosa [C] . OBrien Emily E, Fletcher Erica L, Meffin Hamish, 32nd Annual International Conference of the IEEE Engineering in Medicine and Biology Society . 2010

机译：视网膜色素变性的新型小鼠模型中视网膜内部的活力。
5. Investigating the pathogenicity of mutations in two ubiquitously expressed housekeeping genes that cause autosomal dominant retinitis pigmentosa. [D] . Spellicy, Catherine Jean. 2009

机译：调查导致常染色体显性遗传性视网膜色素变性的两个普遍表达的管家基因突变的致病性。
6. A Dominant Mutation in Rpe65 D477G Delays Dark Adaptation and Disturbs the Visual Cycle in the Mutant Knock-In Mice [O] . Younghwa Shin, Gennadiy Moiseyev, Dibyendu Chakraborty, 2017

机译：Rpe65D477G的显性突变延迟黑暗适应和扰乱突变敲入小鼠的视觉周期。
7. Phenotypic expansion of autosomal dominant retinitis pigmentosa associated with the D477G mutation in RPE65 [O] . Ruben Jauregui, Ahra Cho, Jin Kyun Oh, 2020

机译：与RPE65中的D477G突变相关的常染色体显性视网膜炎的表型扩张
8. Inducing Somatic Pkd1 Mutations in Vivo in a Mouse Model of Autosomal-Dominant Polycystic Kidney Disease. [R] . Cebrian-Ligero, C. 2018

机译：在常染色体显性多囊肾病小鼠模型中体内诱导体细胞pkd1突变。

D477G dominant mutation in RPE65 leads to decreased 11-cis-retinal generation and delayed dark-adaptation in knock-in mouse model of retinitis pigmentosa

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