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unspecified retinal defect

Known as: Retinal Defect, Retinal defect, unspecified, retinal defects 
An imperfection of the retina of the eye.
National Institutes of Health

Related topics

Related topics

4 relations
EyeRetina

Broader (1)

Retinal Diseases

Narrower (1)

Retinal Perforations

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Highly Cited
2015
Highly Cited
2015
TYPE 3 NEOVASCULARIZATION: Evolution, Association With Pigment Epithelial Detachment, and Treatment Response as Revealed by Spectral Domain Optical Coherence Tomography
Purpose: To demonstrate the evolution and treatment response of Type 3 neovascularization using spectral domain optical coherence… 
Highly Cited
2004
Highly Cited
2004
Control of late off-center cone bipolar cell differentiation and visual signaling by the homeobox gene Vsx1.
Retinal bipolar cells are interneurons that transmit visual signals from photoreceptors to ganglion cells. Although the visual… 
Highly Cited
2003
Highly Cited
2003
Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signaling.
Highly Cited
2001
Highly Cited
2001
PAX2 mutations in oligomeganephronia.
BACKGROUND Oligomeganephronia (OMN) is a rare congenital and usually sporadic anomaly. It is characterized by bilateral renal… 
Highly Cited
2000
Highly Cited
2000
Disruption of the Olfactoretinal Centrifugal Pathway May Relate to the Visual System Defect in night blindness bMutant Zebrafish
We describe here a dominant mutation, night blindness b (nbb), which causes an age-related visual system defect in zebrafish. At… 
Highly Cited
1999
Highly Cited
1999
Retinal sparing by selective retinal pigment epithelial photocoagulation.
OBJECTIVE To investigate whether photocoagulation of the retinal pigment epithelium is possible with sparing of the… 
Highly Cited
1998
Highly Cited
1998
Pax2 expression and retinal morphogenesis in the normal and Krd mouse.
The Kidney and retinal defects (Krd) mouse carries a 7-cM transgene-induced deletion on chromosome 19 that includes the Pax2… 
Highly Cited
1996
Highly Cited
1996
Human Usher 1B/mouse shaker-1: the retinal phenotype discrepancy explained by the presence/absence of myosin VIIA in the photoreceptor cells.
Usher syndrome type 1 (USH1) associates severe congenital deafness, vestibular dysfunction and progressive retinitis pigmentosa… 
Highly Cited
1994
Highly Cited
1994
Kidney and retinal defects (Krd), a transgene-induced mutation with a deletion of mouse chromosome 19 that includes the Pax2 locus.
The semidominant mutation Krd (kidney and retinal defects) was identified in transgenic line Tg8052. Krd/+ mice have a high… 
Highly Cited
1993
Highly Cited
1993
TGF alpha deficiency results in hair follicle and eye abnormalities in targeted and waved-1 mice.
To explore the physiological roles of transforming growth factor alpha (TGF alpha), we disrupted the mouse gene by homologous… 
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