Table 6 |
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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:xla00930] |
Caprolactam degradation |
0.006 |
|
[path:xla03030] |
DNA replication |
0.011 |
|
[path:xla00480] |
Glutathione metabolism |
0.016 |
|
[path:xla00561] |
Glycerolipid metabolism |
0.023 |
|
[path:xla03010] |
Ribosome |
0.045 |
|
[path:xla00982] |
Drug metabolism - cytochrome P450 |
0.057 |
|
[path:xla00983] |
Drug metabolism - other enzymes |
0.057 |
|
[path:xla04012] |
ErbB signaling |
0.067 |
|
[path:xla03060] |
Protein export |
0.072 |
|
[path:xla00562] |
Inositol phosphate metabolism |
0.086 |
|
[path:xla04914] |
Progesterone-mediated oocyte maturation |
0.087 |
|
[path:xla04020] |
Calcium signaling pathway |
0.089 |
|
|
||
|
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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