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The International Journal of Developmental Biology|September 15, 2020
Developmental delay during eye morphogenesis underlies optic cup and neurogenesis defects in <i>mab21l2<sup>u517</sup></i> zebrafish mutantsRebecca Wycliffe, Julie Plaisancie, Sydney Leaman, et al.
Development (Cambridge, England)|July 26, 2015
Yap and Taz regulate retinal pigment epithelial cell fateJoel B Miesfeld, Gaia Gestri, Brian S Clark, et al.
Plos One|January 30, 2019
Abrogation of Stem Loop Binding Protein (Slbp) function leads to a failure of cells to transition from proliferation to differentiation, retinal coloboma and midline axon guidance deficitsKatherine J Turner, Jacqueline Hoyle, Leonardo E Valdivia, et al.
Disease Models & Mechanisms|May 22, 2025
frizzled 5 mutant zebrafish are genetically sensitised to developing microphthalmia and colobomaClinton Monfries, Stephen Carter, Paris Ataliotis, et al.
Elife|January 8, 2021
A simple and effective F0 knockout method for rapid screening of behaviour and other complex phenotypesFrançois Kroll, Gareth T Powell, Marcus Ghosh, et al.
Human Genetics|August 18, 2009
Reduced TFAP2A function causes variable optic fissure closure and retinal defects and sensitizes eye development to mutations in other morphogenetic regulatorsGaia Gestri, Robert J Osborne, Alexander W Wyatt, et al.
Development (Cambridge, England)|February 20, 2016
Antagonism between Gdf6a and retinoic acid pathways controls timing of retinal neurogenesis and growth of the eye in zebrafishLeonardo E Valdivia, Dayna B Lamb, Wilson Horner, et al.
Elife|February 20, 2019
Compensatory growth renders Tcf7l1a dispensable for eye formation despite its requirement in eye field specificationRodrigo M Young, Thomas A Hawkins, Florencia Cavodeassi, et al.
Science (New York, N.Y.)|May 2, 2024
Cachd1 interacts with Wnt receptors and regulates neuronal asymmetry in the zebrafish brainGareth T Powell, Ana Faro, Yuguang Zhao, et al.
Medrxiv : the Preprint Server for Health Sciences|August 16, 2024
Loss-of-function of the Zinc Finger Homeobox 4 (<i>ZFHX4</i>) gene underlies a neurodevelopmental disorderPérez Baca María Del Rocío, María Palomares Bralo, Michiel Vanhooydonck, et al.
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