A missense mutation in ALDH1A3 causes isolated microphthalmia/anophthalmia in nine individuals from an inbred Muslim kindred

ALDH1A3 Mutations Cause Recessive Anophthalmia and Microphthalmia

(2013) Lucas Fares-Taie et al.   AMERICAN JOURNAL OF HUMAN GENETICS

ALDH1A3 loss of function causes bilateral anophthalmia/microphthalmia and hypoplasia of the optic nerve and optic chiasm

(2013) Mani Yahyavi et al.   HUMAN MOLECULAR GENETICS

A paradoxical teratogenic mechanism for retinoic acid

(2012) L. M. Y. Lee et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Retinaldehyde is a substrate for human aldo–keto reductases of the 1C subfamily

(2011) F. Xavier Ruiz et al.   BIOCHEMICAL JOURNAL

The genetics of anophthalmia and microphthalmia

(2011) Tanya M. Bardakjian et al.   CURRENT OPINION IN OPHTHALMOLOGY

Systemic and ophthalmological anomalies in congenital anophthalmic or microphthalmic patients

(2009) M. P. Schittkowski et al.   BRITISH JOURNAL OF OPHTHALMOLOGY

Ethanol induces embryonic malformations by competing for retinaldehyde dehydrogenase activity during vertebrate gastrulation

(2009) H. Kot-Leibovich et al.   Disease Models & Mechanisms

Disease-associated variants of microsomal retinol dehydrogenase 12 (RDH12) are degraded at mutant-specific rates

(2009) Seung-Ah Lee et al.   FEBS LETTERS

Design of anti- and pro-aggregation variants to assess the effects of methionine oxidation in human prion protein

(2009) C. Wolschner et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Keeping an eye on retinoic acid signaling during eye development

(2008) Gregg Duester   CHEMICO-BIOLOGICAL INTERACTIONS