Table 5 |
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|
Enriched X. laevis pathways due to cyclopamine treatment using SEPEA_NT2 |
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|
KEGG pathway ID |
Pathway description |
P-value |
|
|
||
|
[path:xla03022] |
Basal transcription factors |
0.01 |
|
[path:xla04010] |
MAPK signaling |
0.02 |
|
[path:xla00460] |
Cyanoamino acid metabolism |
0.024 |
|
[path:xla00550] |
Peptidoglycan biosynthesis |
0.031 |
|
[path:xla02010] |
ABC transporters |
0.045 |
|
[path:xla03050] |
Proteasome |
0.05 |
|
[path:xla00982] |
Drug metabolism - cytochrome P450 |
0.053 |
|
[path:xla00830] |
Retinol metabolism |
0.059 |
|
[path:xla04630] |
Jak-STAT signaling |
0.07 |
|
[path:xla04012] |
ErbB signaling |
0.1 |
|
|
||
|
Enriched KEGG [44] pathways (with P-value ≤ 0.1) due to cyclopamine treatment of developing X. laevis, designed to inhibit SHH signaling, using microarray data from GEO [45] [GEO:GSE8293]. P-values were obtained using the SEPEA_NT2 analysis with 1,000 randomizations to compute significance. |
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|
Thomas et al. Genome Biology 2009 10:R44 doi:10.1186/gb-2009-10-4-r44 |
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