Eye development

J Graw - Current topics in developmental biology, 2010 - Elsevier
The vertebrate eye comprises tissues from different embryonic origins: the lens and the
cornea are derived from the surface ectoderm, but the retina and the epithelial layers of the …

Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia

J Plaisancié, F Ceroni, R Holt, C Zazo Seco, P Calvas… - Human Genetics, 2019 - Springer
Eye formation is the result of coordinated induction and differentiation processes during
embryogenesis. Disruption of any one of these events has the potential to cause ocular …

Eye development genes and known syndromes

AM Slavotinek - Molecular genetics and metabolism, 2011 - Elsevier
Anophthalmia and microphthalmia (A/M) are significant eye defects because they can have
profound effects on visual acuity. A/M is associated with non-ocular abnormalities in an …

Clinical and mutation analysis of 51 probands with anophthalmia and/or severe microphthalmia from a single center

C Gerth‐Kahlert, K Williamson, M Ansari… - Molecular genetics & …, 2013 - Wiley Online Library
Clinical evaluation and mutation analysis was performed in 51 consecutive probands with
severe eye malformations–anophthalmia and/or severe microphthalmia–seen in a single …

Mutational screening of CHX10, GDF6, OTX2, RAX and SOX2 genes in 50 unrelated microphthalmia–anophthalmia–coloboma (MAC) spectrum cases

J Gonzalez-Rodriguez, EL Pelcastre… - British journal of …, 2010 - bjo.bmj.com
Background/aims Microphthalmia-anophthalmia-coloboma (MAC) are congenital eye
malformations causing a significant percentage of visually impairments in children. Although …

[HTML][HTML] The role of homeobox genes in retinal development and disease

JL Zagozewski, Q Zhang, VI Pinto, JT Wigle… - Developmental …, 2014 - Elsevier
Homeobox genes are an evolutionarily conserved class of transcription factors that are
critical for development of many organ systems, including the brain and eye. During …

Inherited eye diseases with retinal manifestations through the eyes of homeobox genes

Y Markitantova, V Simirskii - International journal of molecular sciences, 2020 - mdpi.com
Retinal development is under the coordinated control of overlapping networks of signaling
pathways and transcription factors. The paper was conceived as a review of the data and …

Ocular coloboma: Genetic variants reveal a dynamic model of eye development

KH Yoon, SC Fox, R Dicipulo… - American Journal of …, 2020 - Wiley Online Library
Ocular coloboma is a congenital disorder of the eye where a gap exists in the inferior retina,
lens, iris, or optic nerve tissue. With a prevalence of 2–19 per 100,000 live births, coloboma …

FOXE3 plays a significant role in autosomal recessive microphthalmia

LM Reis, RC Tyler, A Schneider… - American Journal of …, 2010 - Wiley Online Library
FOXE3 forkhead transcription factor is essential to lens development in vertebrates. The
eyes of Foxe3/foxe3‐deficient mice and zebrafish fail to develop normally. In humans …

Repeated evolution of eye loss in Mexican cavefish: Evidence of similar developmental mechanisms in independently evolved populations

I Sifuentes‐Romero, E Ferrufino… - … Zoology Part B …, 2020 - Wiley Online Library
Evolution in similar environments often leads to convergence of behavioral and anatomical
traits. A classic example of convergent trait evolution is the reduced traits that characterize …