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.
Review
2014
Review
2014
Diabetic retinopathy: loss of neuroretinal adaptation to the diabetic metabolic environment.
Diabetic retinopathy (DR) impairs vision of patients with type 1 and type 2 diabetes, associated with vascular dysfunction and… (More)
  • figure 1
  • table 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
Highly Cited
2006
Highly Cited
2006
SOX2 is a dose-dependent regulator of retinal neural progenitor competence.
Approximately 10% of humans with anophthalmia (absent eye) or severe microphthalmia (small eye) show haploid insufficiency due to… (More)
Is this relevant?
Highly Cited
2005
Highly Cited
2005
Heterozygous mutations of OTX2 cause severe ocular malformations.
Major malformations of the human eye, including microphthalmia and anophthalmia, are examples of phenotypes that recur in… (More)
Is this relevant?
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… (More)
  • figure 1
  • figure 2
  • figure 4
  • figure 5
  • figure 6
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Cortical and retinal defects caused by dosage-dependent reductions in VEGF-A paracrine signaling.
To determine the function of VEGF-A in nervous system development, we have utilized the Nestin promoter-driven Cre recombinase… (More)
Is this relevant?
Highly Cited
2003
Highly Cited
2003
Types of macular hole closure and their clinical implications.
AIMS To evaluate the clinical significance of macular hole closure types assessed by optical coherence tomography (OCT… (More)
  • figure 1
  • figure 2
  • table 1
  • figure 3
  • table 2
Is this relevant?
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… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
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… (More)
Is this relevant?
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… (More)
Is this relevant?
Highly Cited
1969
Highly Cited
1969
Retinal dystrophy in the rat--a pigment epithelial disease.
Rod outer segment renewal rate was studied by autoradiographic technique in both the Wistar rat (control) and the Royal College… (More)
  • figure 1
  • table I
  • table II
  • figure 2
  • figure 3
Is this relevant?