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. 2014 Apr 27;9:14. doi: 10.1186/1750-1326-9-14

Table 2.

Temporal classification of down-regulated retinal gene cluster changes following ONC

Gene ontology Clusters Time point P value
Molecular function
Structural eye lens protein
7 dpc
3.80E-15
 
Structural eye lens protein
28 dpc
2.60E-14
 
Pattern binding
28 dpc
3.80E-02
Biological process
Chromatin assembly
7 dpc
4.80E-04
 
Regulation of axonogenesis
21 dpc
7.40E-03
 
G-protein coupled receptor signaling pathway
21 dpc
2.00E-04
 
Neurological system process
21 dpc
7.10E-03
 
Intermediate filament bundle process
21 dpc
6.40E-05
 
Microtubule based process
21 dpc
5.10E-03
 
Axonogenesis
21 dpc
1.70E-02
 
Neuron projection morphogenesis
21 dpc
2.00E-02
 
Neuron differentiation
21 dpc
4.20E-02
 
Cell morphogenesis involved in differentiation
28 dpc
1.20E-02
Cellular component
Nucleosome
7 dpc
7.50E-05
 
Neuron projection
21 dpc
5.00E-05
 
Axon
21 dpc
6.50E-05
 
Neurofilament
21 dpc
1.60E-04
 
Intrinsic to membrane
21 dpc
1.30E-02
 
Neuron projection
28 dpc
9.90E-03
  Chromosome 28 dpc 3.10E-02

Gene expression fold-change values were grouped individually from naïve eyes and ONC eyes out to 28 days post crush (dpc). Genes were highlighted based on fold values for down-regulated (≤ −1.5) retinal datasets. The selected genes were analyzed by gene ontology (GO) based cluster identification at each time point using DAVID. Significance was determined using the Benjamini multiple test correction, GO enrichment score χ2 test and Fishers Exact test (p < 0.05).