[Retracted] Toxicological and Teratogenic Effect of Various Food Additives: An Updated Review

S Sambu, U Hemaram, R Murugan… - BioMed Research …, 2022 - Wiley Online Library
Scientific evidence is mounting that synthetic chemicals used as food additives may have
harmful impacts on health. Food additives are chemicals that are added to food to keep it …

[HTML][HTML] Cell fate decisions, transcription factors and signaling during early retinal development

R Diacou, P Nandigrami, A Fiser, W Liu… - Progress in retinal and …, 2022 - Elsevier
The development of the vertebrate eyes is a complex process starting from anterior-posterior
and dorso-ventral patterning of the anterior neural tube, resulting in the formation of the eye …

Eye development and retinogenesis

W Heavner, L Pevny - Cold Spring Harbor perspectives …, 2012 - cshperspectives.cshlp.org
Three embryonic tissue sources—the neural ectoderm, the surface ectoderm, and the
periocular mesenchyme—contribute to the formation of the mammalian eye. For this reason …

Genetic regulation of pituitary gland development in human and mouse

D Kelberman, K Rizzoti, R Lovell-Badge… - Endocrine …, 2009 - academic.oup.com
Normal hypothalamopituitary development is closely related to that of the forebrain and is
dependent upon a complex genetic cascade of transcription factors and signaling molecules …

The genetic architecture of microphthalmia, anophthalmia and coloboma

KA Williamson, DR FitzPatrick - European journal of medical genetics, 2014 - Elsevier
Microphthalmia, anophthalmia and coloboma (MAC) are distinct phenotypes that represent
a continuum of structural developmental eye defects. In severe bilateral cases …

Genetics of combined pituitary hormone deficiency: roadmap into the genome era

Q Fang, AS George, ML Brinkmeier… - Endocrine …, 2016 - academic.oup.com
The genetic basis for combined pituitary hormone deficiency (CPHD) is complex, involving
30 genes in a variety of syndromic and nonsyndromic presentations. Molecular diagnosis of …

SOX2 is a dose-dependent regulator of retinal neural progenitor competence

OV Taranova, ST Magness, BM Fagan… - Genes & …, 2006 - genesdev.cshlp.org
Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia
(small eye) show haploid insufficiency due to mutations in SOX2, a SOXB1-HMG box …

Anophthalmia and microphthalmia

AS Verma, DR FitzPatrick - Orphanet journal of rare diseases, 2007 - Springer
Anophthalmia and microphthalmia describe, respectively, the absence of an eye and the
presence of a small eye within the orbit. The combined birth prevalence of these conditions …

The spectrum of ocular phenotypes caused by mutations in the BEST1 gene

CJF Boon, BJ Klevering, BP Leroy, CB Hoyng… - Progress in retinal and …, 2009 - Elsevier
Bestrophin-1 is an integral membrane protein, encoded by the BEST1 gene, which is
located in the basolateral membrane of the retinal pigment epithelium. The bestrophin-1 …

Oculo-auriculo-vertebral spectrum: new genes and literature review on a complex disease

A Tingaud-Sequeira, A Trimouille… - Journal of medical …, 2022 - jmg.bmj.com
Oculo-auriculo-vertebral spectrum (OAVS) or Goldenhar syndrome is due to an abnormal
development of first and second branchial arches derivatives during embryogenesis and is …