INT283698
From wiki-pain
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Sentences Mentioned In
Key: | Protein | Mutation | Event | Anatomy | Negation | Speculation | Pain term | Disease term |
Our meta-analyses of publicly available data revealed that Lpin1, Id2, and Sox11 were differentially expressed during retinal development and trauma. | |||||||||||||||
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Genetic variability can explain the expression variability and strong linkage of Lpin1, Sox11, AL024210, and Id2 to their gene locations (cis-eQTLs). | |||||||||||||||
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In forebrain, the expression variability of genes Lpin1, Id2, Sox11, and AL024210 mapped within the locus. | |||||||||||||||
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Lpin1, Id2, and Sox11 were expressed in reactive glia of optic nerve heads (Yang et al. 2004) and diabetic retinas (Gerhardinger et al. 2005). | |||||||||||||||
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Using publicly available data on mouse retinal development (Dorrell et al. 2004), we determined that Lpin1, Id2, and Sox11 were expressed by the developing retina and had well defined patterns of expression (Fig. 3E; note that AL024210 levels were below detectable thresholds). | |||||||||||||||
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Sox11 expression in injured BXD retinas did not correlate with the segregating patterns of alleles. | |||||||||||||||
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Together these results documented that Lpin1, Id2, and Sox11 are candidate genes, because they displayed (1) cis-eQTLs in the brain, cerebellum, and striatum; (2) polymorphisms between parental strains; (3) differential expression during retinal development and retinal healing; and (4) moderate to high levels of expression in normal and reactive neural cells. | |||||||||||||||
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Together these results documented that Lpin1, Id2, and Sox11 are candidate genes, because they displayed (1) cis-eQTLs in the brain, cerebellum, and striatum; (2) polymorphisms between parental strains; (3) differential expression during retinal development and retinal healing; and (4) moderate to high levels of expression in normal and reactive neural cells. | |||||||||||||||
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Together these results documented that Lpin1, Id2, and Sox11 are candidate genes, because they displayed (1) cis-eQTLs in the brain, cerebellum, and striatum; (2) polymorphisms between parental strains; (3) differential expression during retinal development and retinal healing; and (4) moderate to high levels of expression in normal and reactive neural cells. | |||||||||||||||
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