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Drug screening with zebrafish visual behavior identifies carvedilol as a potential treatment for an autosomal dominant form of retinitis pigmentosa

机译：用斑马鱼视觉行为的药物筛查将卡维地洛视为常染色体定位形式的视网膜炎的潜在治疗

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Logan Ganzen; Mee Jung Ko; Mengrui Zhang; Rui Xie; Yongkai Chen; Liyun Zhang; Rebecca James; Jeff Mumm; Richard M. van Rijn; Wenxuan Zhong; Chi Pui Pang; Mingzhi Zhang; Motokazu Tsujikawa; Yuk Fai Leung;
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1. Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa [J] . Jennifer D. Churchill, Sara J. Bowne, Lori S. Sullivan, Investigative ophthalmology & visual science . 2013,第2期

机译：X连锁视网膜色素变性视网膜蛋白基因RPGR和RP2的突变在8.5％的家庭中发现，并初步诊断为常染色体显性视网膜色素变性。
2. Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5% of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa [J] . Jennifer D. Churchill, Sara J. Bowne, Lori S. Sullivan, Investigative ophthalmology & visual science . 2013,第2期

机译：X连锁视网膜色素变性视网膜蛋白基因RPGR和RP2的突变在8.5％的家庭中发现，并初步诊断为常染色体显性视网膜色素变性。
3. Mutations in the X-linked retinitis pigmentosa genes RPGR and RP2 found in 8.5% of families with a provisional diagnosis of autosomal dominant retinitis pigmentosa [J] . ChurchillJ.D., BowneS.J., SullivanL.S., Investigative ophthalmology & visual science . 2013,第2期

机译：X连锁性视网膜色素变性视网膜基因RPGR和RP2突变在8.5％的家庭中被初步诊断为常染色体显性遗传性视网膜色素变性
4. Automated quantification of Zebrafish tail deformation for high-throughput drug screening [C] . Ishaq O., Negri J., Bray M.-A., IEEE International Symposium on Biomedical Imaging: From Nano to Macro . 2013

机译：自动化定量分析斑马鱼尾巴变形以进行高通量药物筛选
5. Experiences of Individuals Adjusting to a Recent Diagnosis of Autosomal Dominant Retinitis Pigmentosa [D] . Satern, Marissa Lauren. 2017

机译：个人适应性常染色体显性视网膜色素变性的最新诊断的经验。
6. Mutations in the X-Linked Retinitis Pigmentosa Genes RPGR and RP2 Found in 8.5 of Families with a Provisional Diagnosis of Autosomal Dominant Retinitis Pigmentosa [O] . Jennifer D. Churchill, Sara J. Bowne, Lori S. Sullivan, -1

机译：X连锁视网膜色素变性视网膜蛋白基因RPGR和RP2的突变在8.5％的家庭中发现并初步诊断为常染色体显性视网膜色素变性。
7. Mutational screening of splicing factor genes in cases with autosomal dominant retinitis pigmentosa [O] . Benaglio Paola, Fernandez San Jose Patricia, Avila-Fernandez Almudena, 2014

机译：常染色体显性视网膜色素变性病例中剪接因子基因的突变筛选

Drug screening with zebrafish visual behavior identifies carvedilol as a potential treatment for an autosomal dominant form of retinitis pigmentosa

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