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Detailed analysis of chick optic fissure closure reveals Netrin-1 as an essential mediator of epithelial fusion.详细分析小鸡视裂闭合过程揭示 Netrin-1 是上皮融合的必需介质。
Elife. 2019 Jun 4;8:e43877. doi: 10.7554/eLife.43877.
2
Genetic compensation triggered by mutant mRNA degradation.突变 mRNA 降解引发的遗传补偿。
Nature. 2019 Apr;568(7751):193-197. doi: 10.1038/s41586-019-1064-z. Epub 2019 Apr 3.
3
PTC-bearing mRNA elicits a genetic compensation response via Upf3a and COMPASS components.PTC 携带的 mRNA 通过 Upf3a 和 COMPASS 成分引发遗传补偿反应。
Nature. 2019 Apr;568(7751):259-263. doi: 10.1038/s41586-019-1057-y. Epub 2019 Apr 3.
4
Expanding the CRISPR Toolbox in Zebrafish for Studying Development and Disease.扩展用于研究发育和疾病的斑马鱼CRISPR工具箱。
Front Cell Dev Biol. 2019 Mar 4;7:13. doi: 10.3389/fcell.2019.00013. eCollection 2019.
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Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification.代偿性生长使得 Tcf7l1a 在眼睛形成中变得可有可无,尽管它在眼区规范中是必需的。
Elife. 2019 Feb 19;8:e40093. doi: 10.7554/eLife.40093.
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Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia.先天性无眼症和小眼球症的遗传学。第 1 部分:非综合征性先天性无眼症/小眼球症。
Hum Genet. 2019 Sep;138(8-9):799-830. doi: 10.1007/s00439-019-01977-y. Epub 2019 Feb 14.
7
Strain-triggered mechanical feedback in self-organizing optic-cup morphogenesis.应变触发的自组织视杯形态发生的机械反馈。
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8
Setting Eyes on the Retinal Pigment Epithelium.聚焦视网膜色素上皮
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Front Cell Dev Biol. 2018 Sep 19;6:110. doi: 10.3389/fcell.2018.00110. eCollection 2018.
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Versatile Genome Engineering Techniques Advance Human Ocular Disease Researches in Zebrafish.多功能基因组工程技术推动斑马鱼人类眼部疾病研究
Front Cell Dev Biol. 2018 Jul 12;6:75. doi: 10.3389/fcell.2018.00075. eCollection 2018.

展望斑马鱼作为一种模型,用于理解眼部疾病的遗传基础。

Looking to the future of zebrafish as a model to understand the genetic basis of eye disease.

机构信息

Institute of Medical and Biomedical Education, St. George's, University of London, Cranmer Terrace, London, SW17 0RE, UK.

Department of Cell and Developmental Biology, Biosciences, UCL, Gower St, London, WC1E 6BT, UK.

出版信息

Hum Genet. 2019 Sep;138(8-9):993-1000. doi: 10.1007/s00439-019-02055-z. Epub 2019 Aug 17.

DOI:10.1007/s00439-019-02055-z
PMID:31422478
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6710215/
Abstract

In this brief commentary, we provide some of our thoughts and opinions on the current and future use of zebrafish to model human eye disease, dissect pathological progression and advance in our understanding of the genetic bases of microphthalmia, andophthalmia and coloboma (MAC) in humans. We provide some background on eye formation in fish and conservation and divergence across vertebrates in this process, discuss different approaches for manipulating gene function and speculate on future research areas where we think research using fish may prove to be particularly effective.

摘要

在这篇简要的评论中,我们就当前和未来使用斑马鱼来模拟人类眼部疾病、剖析病理性进展以及深入了解人类小眼症、无眼症和虹膜脉络膜缺损(MAC)的遗传基础,提出了一些想法和观点。我们介绍了鱼类眼睛形成过程中的背景知识以及这一过程中脊椎动物的保守性和分化,并讨论了不同的基因功能操作方法,推测了我们认为鱼类研究可能特别有效的未来研究领域。