FAQ

VSX2 gene

Known as: HOX10, VISUAL SYSTEM HOMEOBOX 2, CHX10 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

1982-2016
024619822016

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2016
2016
Regulation of WNT Signaling by VSX2 During Optic Vesicle Patterning in Human Induced Pluripotent Stem Cells.
Few gene targets of Visual System Homeobox 2 (VSX2) have been identified despite its broad and critical role in the maintenance… (More)
Is this relevant?
2015
2015
Mutual antagonism of the paired-type homeobox genes, vsx2 and dmbx1, regulates retinal progenitor cell cycle exit upstream of ccnd1 expression.
Understanding the mechanisms that regulate the transition between the proliferative and a post-mitotic state of retinal… (More)
Is this relevant?
2015
2015
Lens subluxation and retinal dysfunction in a girl with homozygous VSX2 mutation.
OBJECTIVE To describe a unique lens subluxation phenotype in a child from a consanguineous family and to determine its genetic… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
Is this relevant?
2009
2009
Novel TUTase associates with an editosome-like complex in mitochondria of Trypanosoma brucei.
Expression of mitochondrial genomes in Kinetoplastida protists requires massive uracil insertion/deletion mRNA editing. The… (More)
  • figure 1
  • figure 2
  • figure 3
  • table 1
  • figure 4
Is this relevant?
2005
2005
UTP-dependent turnover of Trypanosoma brucei mitochondrial mRNA requires UTP polymerization and involves the RET1 TUTase.
Trypanosoma brucei mitochondria possess a unique RNA decay pathway in which rapid degradation of polyadenylated mRNAs is… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
2003
2003
A tale of two TUTases.
The insertion and deletion of U residues at specific sites in mRNAs in trypanosome mitochondria is thought to involve 3' terminal… (More)
  • figure 1
  • figure 2
  • figure 3
  • figure 4
  • figure 5
Is this relevant?
Highly Cited
2002
Highly Cited
2002
National study of microphthalmia, anophthalmia, and coloboma (MAC) in Scotland: investigation of genetic aetiology.
We report an epidemiological and genetic study attempting complete ascertainment of subjects with microphthalmia, anophthalmia… (More)
  • table 1
  • table 2
  • figure 1
  • table 3
  • figure 2
Is this relevant?
1998
1998
A locus for autosomal recessive congenital microphthalmia maps to chromosome 14q32.
Congenital microphthalmia (CMIC) (OMIM 309700) may occur in isolation or in association with a variety of systemic malformations… (More)
Is this relevant?
1990
1990
ret1-1, a yeast mutant affecting transcription termination by RNA polymerase III.
In eukaryotes, extended tracts of T residues are known to signal the termination of RNA polymerase III transcription. However, it… (More)
Is this relevant?
1982
1982
Monoclonal antibodies selective for the inner portion of the chick retina.
Five monoclonal antibodies were selected by immunizing mice with embryonic chick optic nerve and screening the resultant… (More)
  • figure 1.4
  • figure 2
  • figure 3
Is this relevant?