| scholarly article | Q13442814 |
| review article | Q7318358 |
| P50 | author | Stephen W Wilson | Q38320460 |
| Florencia Cavodeassi | Q56606118 | ||
| P2860 | cites work | Gene duplication: the genomic trade in spare parts | Q21092829 |
| Mutation of SALL2 causes recessive ocular coloboma in humans and mice | Q24319044 | ||
| Eye morphogenesis and patterning of the optic vesicle | Q24629124 | ||
| Dynamic coupling of pattern formation and morphogenesis in the developing vertebrate retina | Q27327169 | ||
| Yap and Taz regulate retinal pigment epithelial cell fate | Q27345171 | ||
| Eye development and retinogenesis | Q28277172 | ||
| Heterozygous loss-of-function mutations in YAP1 cause both isolated and syndromic optic fissure closure defects | Q28306581 | ||
| Effective targeted gene 'knockdown' in zebrafish | Q29547445 | ||
| Self-organizing optic-cup morphogenesis in three-dimensional culture | Q29616181 | ||
| Zebrafish--on the move towards ophthalmological research | Q30415226 | ||
| Eph/Ephrin signalling maintains eye field segregation from adjacent neural plate territories during forebrain morphogenesis. | Q30547788 | ||
| Morpholino oligos: making sense of antisense? | Q33957798 | ||
| Identification of a large set of rare complete human knockouts | Q34468556 | ||
| Morpholinos: Antisense and Sensibility | Q34499577 | ||
| Self-formation of optic cups and storable stratified neural retina from human ESCs. | Q34639338 | ||
| Controlling morpholino experiments: don't stop making antisense. | Q34769101 | ||
| Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulators | Q34876963 | ||
| Eye morphogenesis driven by epithelial flow into the optic cup facilitated by modulation of bone morphogenetic protein | Q35111530 | ||
| Wnt ligands from the embryonic surface ectoderm regulate 'bimetallic strip' optic cup morphogenesis in mouse | Q35157491 | ||
| The visual system of zebrafish and its use to model human ocular diseases | Q35449573 | ||
| A complex choreography of cell movements shapes the vertebrate eye. | Q35624848 | ||
| Using Light Sheet Fluorescence Microscopy to Image Zebrafish Eye Development | Q36014200 | ||
| In vitro organogenesis in three dimensions: self-organising stem cells | Q38055078 | ||
| An eye on eye development | Q38107712 | ||
| Retinal pigment epithelium development, plasticity, and tissue homeostasis | Q38141303 | ||
| The genetic architecture of microphthalmia, anophthalmia and coloboma | Q38214549 | ||
| Nlcam modulates midline convergence during anterior neural plate morphogenesis | Q38348109 | ||
| Watching eyes take shape | Q38369723 | ||
| Conserved genetic pathways associated with microphthalmia, anophthalmia, and coloboma | Q38517281 | ||
| Development of the Vertebrate Eye and Retina | Q38574395 | ||
| Genetic approaches to retinal research in zebrafish. | Q38662564 | ||
| Genetic compensation: A phenomenon in search of mechanisms. | Q38680916 | ||
| The zebrafish eye-a paradigm for investigating human ocular genetics. | Q38822858 | ||
| Retina regeneration in zebrafish | Q38855773 | ||
| Zebrafish models of human eye and inner ear diseases | Q39106867 | ||
| Robustness, evolvability, and neutrality | Q39217320 | ||
| The hyaloid vasculature facilitates basement membrane breakdown during choroid fissure closure in the zebrafish eye. | Q39383518 | ||
| BMP signaling protects telencephalic fate by repressing eye identity and its Cxcr4-dependent morphogenesis | Q39534177 | ||
| Human knockouts and phenotypic analysis in a cohort with a high rate of consanguinity | Q40244307 | ||
| Relaxation-expansion model for self-driven retinal morphogenesis: a hypothesis from the perspective of biosystems dynamics at the multi-cellular level | Q40669649 | ||
| Genetic compensation induced by deleterious mutations but not gene knockdowns. | Q40744194 | ||
| Genetic redundancy caused by gene duplications and its evolution in networks of transcriptional regulators | Q40938828 | ||
| Fishing for genes controlling development | Q41099993 | ||
| An analysis of cell shape and the neuroepithelial basal lamina during optic vesicle formation in the mouse embryo | Q41323100 | ||
| Precocious acquisition of neuroepithelial character in the eye field underlies the onset of eye morphogenesis | Q41884445 | ||
| Loss of laminin alpha 1 results in multiple structural defects and divergent effects on adhesion during vertebrate optic cup morphogenesis. | Q42174997 | ||
| Concerted action of neuroepithelial basal shrinkage and active epithelial migration ensures efficient optic cup morphogenesis. | Q42292835 | ||
| Early stages of zebrafish eye formation require the coordinated activity of Wnt11, Fz5, and the Wnt/beta-catenin pathway | Q42958376 | ||
| Guidelines for morpholino use in zebrafish. | Q44909173 | ||
| New Developments in CRISPR/Cas-based Functional Genomics and their Implications for Research using Zebrafish | Q46254709 | ||
| FOXE3 mutations: genotype-phenotype correlations. | Q47840495 | ||
| The logic of gene regulatory networks in early vertebrate forebrain patterning | Q48314781 | ||
| Individual cell migration serves as the driving force for optic vesicle evagination. | Q48437679 | ||
| The Pax protein Noi is required for commissural axon pathway formation in the rostral forebrain. | Q48694650 | ||
| The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio. | Q48841437 | ||
| Genes and pathways in optic fissure closure. | Q49340047 | ||
| Coordinated Morphogenetic Mechanisms Shape the Vertebrate Eye. | Q49626351 | ||
| Cell Behaviors during Closure of the Choroid Fissure in the Developing Eye. | Q50420453 | ||
| The Birth of the Eye Vesicle: When Fate Decision Equals Morphogenesis. | Q50420456 | ||
| Specification of the vertebrate eye by a network of eye field transcription factors. | Q52101071 | ||
| TGFβ-facilitated optic fissure fusion and the role of bone morphogenetic protein antagonism. | Q53834248 | ||
| Dynamic Tissue Rearrangements during Vertebrate Eye Morphogenesis: Insights from Fish Models. | Q55113517 | ||
| Role of duplicate genes in determining the tissue-selectivity of hereditary diseases. | Q55290600 | ||
| Leveraging Zebrafish to Study Retinal Degenerations | Q57072514 | ||
| The 100 000 Genomes Project: bringing whole genome sequencing to the NHS | Q57090374 | ||
| Setting Eyes on the Retinal Pigment Epithelium | Q58566391 | ||
| Strain-triggered mechanical feedback in self-organizing optic-cup morphogenesis | Q59339668 | ||
| Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specification | Q61795789 | ||
| Expanding the CRISPR Toolbox in Zebrafish for Studying Development and Disease | Q64067554 | ||
| Detailed analysis of chick optic fissure closure reveals Netrin-1 as an essential mediator of epithelial fusion | Q83232103 | ||
| A Rapid Method for Directed Gene Knockout for Screening in G0 Zebrafish | Q89427380 | ||
| Versatile Genome Engineering Techniques Advance Human Ocular Disease Researches in Zebrafish | Q90543376 | ||
| Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia | Q91569201 | ||
| PTC-bearing mRNA elicits a genetic compensation response via Upf3a and COMPASS components | Q92830452 | ||
| Genetic compensation triggered by mutant mRNA degradation | Q92830480 | ||
| P433 | issue | 8-9 | |
| P921 | main subject | eye disease | Q3041498 |
| P304 | page(s) | 993-1000 | |
| P577 | publication date | 2019-08-17 | |
| P1433 | published in | Human Genetics | Q5937167 |
| P1476 | title | Looking to the future of zebrafish as a model to understand the genetic basis of eye disease | |
| P478 | volume | 138 |
| Q90397910 | Cytotoxic Evaluation and Anti-Angiogenic Effects of Two Furano-Sesquiterpenoids from Commiphora myrrh Resin | cites work | P2860 |
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