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VSX2 gene

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

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
Review
2007
Review
2007
Anophthalmia and microphthalmia describe, respectively, the absence of an eye and the presence of a small eye within the orbit… Expand
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Highly Cited
2006
Highly Cited
2006
Recent molecular genetic studies suggest that the expression of transcription factors in the developing spinal cord helps… Expand
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Highly Cited
2003
Highly Cited
2003
Mice in which all members of the Hox10 or Hox11 paralogous group are disrupted provide evidence that these Hox genes are involved… Expand
Highly Cited
2002
Highly Cited
2002
We have reported previously that neurotoxic damage to the chicken retina causes Müller glia to dedifferentiate, proliferate… Expand
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Highly Cited
2000
Highly Cited
2000
Isolated human microphthalmia/anophthalmia, a cause of congenital blindness, is a clinically and genetically heterogeneous… Expand
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Highly Cited
1999
Highly Cited
1999
Sonic hedgehog (Shh) specifies the identity of both motor neurons (MNs) and interneurons with morphogen-like activity. Here, we… Expand
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Highly Cited
1996
Highly Cited
1996
Ocular retardation (or) is a murine eye mutation causing microphthalmia, a thin hypocellular retina and optic nerve aplasia. Here… Expand
Review
1996
Review
1996
  • J. Graw
  • Developmental genetics
  • 1996
  • Corpus ID: 37453197
The vertebrate eye comprises tissues from different embryonic origins, e.g., iris and ciliary body are derived from the wall of… Expand
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Highly Cited
1994
Highly Cited
1994
Dilysine motifs in cytoplasmic domains of transmembrane proteins are signals for their continuous retrieval from the Golgi back… Expand
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Highly Cited
1994
Highly Cited
1994
Few potential regulatory proteins of vertebrate retinal development have been identified. We describe a 39 kDa murine polypeptide… Expand