Mapping of genetic modifiers affecting the eye phenotype of ocular retardation (Chx10or-J) mice

No abstract is available for this paper.

• Publication year

  2006

• Venue

  Mammalian Genome

• Publication date

  2006-06-12

• Fields of study

  Biology, Medicine

• Identifiers
  DOI 10.1007/s00335-005-0159-zPMID 16783634
• External record

  Open on Semantic Scholar

• Source metadata

  Semantic Scholar, PubMed

• No claims are published for this paper.

• No concepts are published for this paper.

• Transcriptional Activity of the Paired-like Homeodomain Proteins CHX10 and VSX1*

  2005cited by this paper
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  2004influential reference
• Kruppel-like factor 15, a zinc-finger transcriptional regulator, represses the rhodopsin and interphotoreceptor retinoid-binding protein promoters.

  2004influential reference
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• MGD: the Mouse Genome Database

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  2002influential reference
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  2001cited by this paper
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  2001cited by this paper
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  2000cited by this paper
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  2000cited by this paper
• Morphological, physiological, and biochemical changes in rhodopsin knockout mice.

  1999influential reference
• Genetic aspects of embryonic eye development in vertebrates.

  1996cited by this paper
• Ocular retardation mouse caused by Chx10 homeobox null allele: impaired retinal progenitor proliferation and bipolar cell differentiation

  1996cited by this paper
• Genetics and Analysis of Quantitative Traits

  1996cited by this paper
• Empirical threshold values for quantitative trait mapping.

  1994cited by this paper
• A genetic map of the mouse with 4,006 simple sequence length polymorphisms

  1994cited by this paper
• Mapping mendelian factors underlying quantitative traits using RFLP linkage maps.

  1989influential reference
• A simple salting out procedure for extracting DNA from human nucleated cells.

  1988cited by this paper
• Studies on the development of the eye cup and optic nerve in normal mice and in mutants with congenital optic nerve aplasia.

  1979influential reference
• A new allele of ocular retardation: Early development and morphogenetic cell death

  1976influential reference
• Interaction of the genes of ocular retardation and microphthalmia in mice.

  1966cited by this paper
• Interaction of the genes of ocular retardation and microphthalmia in mice.

  1966cited by this paper
• A gene causing ocular retardation in the mouse.

  1962influential reference

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