David R. Hyde

Zebrafish mutagenesis yields eye morphological mutants with retinal and lens defects.

Regulation of light-dependent Gqalpha translocation and morphological changes in fly photoreceptors.

Novel dominant rhodopsin mutation triggers two mechanisms of retinal degeneration and photoreceptor desensitization.

The zebrafish Pard3 ortholog is required for separation of the eye fields and retinal lamination.

Lens opacity and photoreceptor degeneration in the zebrafish lens opaque mutant.

Cre-mediated site-specific recombination in zebrafish embryos.

Molecular cloning of three zebrafish lin7 genes and their expression patterns in the retina.

Retinal regional differences in photoreceptor cell death and regeneration in light-lesioned albino zebrafish.

Inhibition of zebrafish fin regeneration using in vivo electroporation of morpholinos against fgfr1 and msxb.

Expressed sequence tag analysis of zebrafish eye tissues for NEIBank.

Zebrafish foxe3: roles in ocular lens morphogenesis through interaction with pitx3.

Mutations in laminin alpha 1 result in complex, lens-independent ocular phenotypes in zebrafish.

Mitogen-associated protein kinase- and protein kinase A-dependent regulation of rhodopsin promoter expression in zebrafish rod photoreceptor cells.

Two different transgenes to study gene silencing and re-expression during zebrafish caudal fin and retinal regeneration.

Regeneration of inner retinal neurons after intravitreal injection of ouabain in zebrafish.

A mirror-symmetric cell division that orchestrates neuroepithelial morphogenesis.

Time course analysis of gene expression during light-induced photoreceptor cell death and regeneration in albino zebrafish.

Genetic determinants of hyaloid and retinal vasculature in zebrafish.

Generation and characterization of transgenic zebrafish lines using different ubiquitous promoters.

Ganglion cell regeneration following whole-retina destruction in zebrafish.

Inhibition of Müller glial cell division blocks regeneration of the light-damaged zebrafish retina.

Fgf-dependent depletion of microRNA-133 promotes appendage regeneration in zebrafish.

Connexin43 (GJA1) is required in the population of dividing cells during fin regeneration.

Lengsin expression and function during zebrafish lens formation.

The Tg(ccnb1:EGFP) transgenic zebrafish line labels proliferating cells during retinal development and regeneration.

Characterization of Müller glia and neuronal progenitors during adult zebrafish retinal regeneration.

Cellular expression of midkine-a and midkine-b during retinal development and photoreceptor regeneration in zebrafish.

CNTF induces photoreceptor neuroprotection and Müller glial cell proliferation through two different signaling pathways in the adult zebrafish retina.

Stepwise maturation of apicobasal polarity of the neuroepithelium is essential for vertebrate neurulation.

A novel model of retinal ablation demonstrates that the extent of rod cell death regulates the origin of the regenerated zebrafish rod photoreceptors.

The zebrafish galectin Drgal1-l2 is expressed by proliferating Müller glia and photoreceptor progenitors and regulates the regeneration of rod photoreceptors.

Pax6a and Pax6b are required at different points in neuronal progenitor cell proliferation during zebrafish photoreceptor regeneration.

Zebrafish class 1 phosphatidylinositol transfer proteins: PITPbeta and double cone cell outer segment integrity in retina.

The inhibitor of phagocytosis, O-phospho-L-serine, suppresses Müller glia proliferation and cone cell regeneration in the light-damaged zebrafish retina.

The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism.

The loss of vacuolar protein sorting 11 (vps11) causes retinal pathogenesis in a vertebrate model of syndromic albinism.

Phosphatidylinositol synthase is required for lens structural integrity and photoreceptor cell survival in the zebrafish eye.

FGF signaling regulates rod photoreceptor cell maintenance and regeneration in zebrafish.

Müller glia as a source of neuronal progenitor cells to regenerate the damaged zebrafish retina.

Characterization of multiple light damage paradigms reveals regional differences in photoreceptor loss.