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