» Articles » PMID: 640793

Ocular Retardation (or) in the Mouse

Overview
Specialty Ophthalmology
Date 1978 May 1
PMID 640793
Citations 8
Authors
Affiliations
Soon will be listed here.
Abstract

The ocular retardation (or) mutation in mice has been studied morphologically in serial 1 mu sections. This recessively inherited, fully penetrant mutation is characterized by an early arrest of retinal development, aplasia of the optic nerve, cataractous degeneration of the lens, and microphthalmia. We describe early alterations of normally occurring morphogenetic cell death in the optic cup and aberrations of optic fissure formation which appear to precede the arrest of retinal and optic nerve development. The subsequent disappearance of central retinal vessels and cataract formation are interpreted as secondary phenomena.

Citing Articles

Genetic chimeras reveal the autonomy requirements for Vsx2 in embryonic retinal progenitor cells.

Sigulinsky C, German M, Leung A, Clark A, Yun S, Levine E Neural Dev. 2015; 10:12.

PMID: 25927996 PMC: 4450477. DOI: 10.1186/s13064-015-0039-5.


Deficient FGF signaling causes optic nerve dysgenesis and ocular coloboma.

Cai Z, Tao C, Li H, Ladher R, Gotoh N, Feng G Development. 2013; 140(13):2711-23.

PMID: 23720040 PMC: 3678341. DOI: 10.1242/dev.089987.


Specification of optic nerve oligodendrocyte precursors by retinal ganglion cell axons.

Gao L, Miller R J Neurosci. 2006; 26(29):7619-28.

PMID: 16855089 PMC: 6674293. DOI: 10.1523/JNEUROSCI.0855-06.2006.


Absence of chx10 causes neural progenitors to persist in the adult retina.

Dhomen N, Balaggan K, Pearson R, Bainbridge J, Levine E, Ali R Invest Ophthalmol Vis Sci. 2005; 47(1):386-96.

PMID: 16384989 PMC: 2423807. DOI: 10.1167/iovs.05-0428.


Rat optic nerve oligodendrocytes develop in the absence of viable retinal ganglion cell axons.

Ueda H, Levine J, Miller R, Trapp B J Cell Biol. 1999; 146(6):1365-74.

PMID: 10491397 PMC: 2156117. DOI: 10.1083/jcb.146.6.1365.