Skip to search formSkip to main contentSkip to account menu

RS1 gene

Known as: Retinoschisis (X-Linked, Juvenile) 1 Gene, RETINOSCHISIN, RS1 
This gene is involved in development, aging, and cell-cell adhesion in the retina.
National Institutes of Health

Related topics

Related topics

5 relations
AgingBiologic DevelopmentCell AdhesionRetinoschisin Protein

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2013
2013
Influence of Iron Oxide Nanoparticles on Innate and Genetically Modified Secretion Profiles of Mesenchymal Stem Cells
Mesenchymal stem cells (MSCs) have well-established paracrine effects that are proving to be therapeutically useful. This… 
2008
2008
Retina‐Specific mRNA in the Assessment of Diabetic Retinopathy
In a previous study we demonstrated the presence and diagnostic usefulness of circulating rhodopsin mRNA in the assessment of… 
2008
2008
Molecular analysis of the XLRS1 gene in 4 females affected with X-linked juvenile retinoschisis.
BACKGROUND X-linked juvenile retinoschisis (XLRS) is the most common cause of juvenile macular degeneration in males. Because of… 
2006
2006
An unusual X-linked retinoschisis phenotype and biochemical characterization of the W112C RS1 mutation
2006
2006
Identification and characterization of two mature isoforms of retinoschisin in murine retina.
2006
2006
Unusual Phenotypic Expression of an XLRS1 Mutation in X-Linked Juvenile Retinoschisis
X-linked juvenile retinoschisis is a rare progressive vitreoretinal degenerative process that appears in early childhood, results… 
2004
2004
Novel 473-bp deletion in XLRS1 gene in a Japanese family with X-linked juvenile retinoschisis
PurposeTo present the clinical features of two brothers with molecularly confirmed X-linked juvenile retinoschisis (xlRS) but… 
2003
2003
Three Novel Mutations in the X-Linked Juvenile Retinoschisis (XLRS1) Gene in 6 Japanese Patients, 1 of Whom Had Turner’s Syndrome
We examined the XLRS1 gene for mutations in 6 Japanese patients with X-linked juvenile retinoschisis from a total of three… 
1999
1999
A Colombian family with X-linked juvenile retinoschisis with three affected females finding of a frameshift mutation.
X-linked retinoschisis (XLRS) is a vitreoretinal disease responsible for most cases of juvenile macular degeneration in males… 
1999
1999
Recurrent missense (R197C) and nonsense (Y89X) mutations in the XLRS1 gene in families with X-linked retinoschisis.
Congenital retinoschisis (RS) is a hereditary eye disorder characterized by intraretinal schisis and central and peripheral… 
By clicking accept or continuing to use the site, you agree to the terms outlined in our Privacy Policy (opens in a new tab), Terms of Service (opens in a new tab), and Dataset License (opens in a new tab)