Zebrafish—on the move towards ophthalmological research

J Chhetri, G Jacobson, N Gueven - Eye, 2014 - nature.com
Millions of people are affected by visual impairment and blindness globally, and the
prevalence of vision loss is likely to increase as we are living longer. However, many ocular …

Single-cell reconstruction of developmental trajectories during zebrafish embryogenesis

JA Farrell, Y Wang, SJ Riesenfeld, K Shekhar, A Regev… - Science, 2018 - science.org
INTRODUCTION During embryogenesis, pluripotent cells gradually become specialized
and acquire distinct functions and morphologies. Because much of the specification process …

Toward a better understanding of human eye disease: Insights from the zebrafish, Danio rerio

J Bibliowicz, RK Tittle, JM Gross - Progress in molecular biology and …, 2011 - Elsevier
Visual impairment and blindness is widespread across the human population, and the
development of therapies for ocular pathologies is of high priority. The zebrafish represents …

Complementary domains of retinoic acid production and degradation in the early chick embryo

EC Swindell, C Thaller, S Sockanathan… - Developmental …, 1999 - Elsevier
Excess retinoids as well as retinoid deprivation cause abnormal development, suggesting
that retinoid homeostasis is critical for proper morphogenesis. RALDH-2 and CYP26, two …

Identification of early requirements for preplacodal ectoderm and sensory organ development

HJ Kwon, N Bhat, EM Sweet, RA Cornell… - PLoS genetics, 2010 - journals.plos.org
Preplacodal ectoderm arises near the end of gastrulation as a narrow band of cells
surrounding the anterior neural plate. This domain later resolves into discrete cranial …

FOXE3 mutations predispose to thoracic aortic aneurysms and dissections

SQ Kuang, O Medina-Martinez, D Guo… - The Journal of …, 2016 - Am Soc Clin Investig
The ascending thoracic aorta is designed to withstand biomechanical forces from pulsatile
blood. Thoracic aortic aneurysms and acute aortic dissections (TAADs) occur as a result of …

Mutation update of transcription factor genes FOXE3, HSF4, MAF, and PITX3 causing cataracts and other developmental ocular defects

D Anand, SA Agrawal, A Slavotinek… - Human mutation, 2018 - Wiley Online Library
Mutations in the transcription factor genes FOXE3, HSF4, MAF, and PITX3 cause congenital
lens defects including cataracts that may be accompanied by defects in other components of …

The lens: a classical model of embryonic induction providing new insights into cell determination in early development

L Gunhaga - … Transactions of the Royal Society B …, 2011 - royalsocietypublishing.org
The lens was the first tissue in which the concept of embryonic induction was demonstrated.
For many years lens induction was thought to occur at the time the optic vesicle and lens …

Zebrafish model in ophthalmology to study disease mechanism and drug discovery

Y Hong, Y Luo - Pharmaceuticals, 2021 - mdpi.com
Visual impairment and blindness are common and seriously affect people's work and quality
of life in the world. Therefore, the effective therapies for eye diseases are of high priority …

Congenital anterior segment ocular disorders: genotype-phenotype correlations and emerging novel mechanisms

LM Reis, S Seese, D Costakos, EV Semina - Progress in Retinal and Eye …, 2024 - Elsevier
Development of the anterior segment of the eye requires reciprocal sequential interactions
between the arising tissues, facilitated by numerous genetic factors. Disruption of any of …