mortality/aging
|
• after doxycycline treatment
|
integument
|
• with increased survival in doxycycline-treated mice
|
|
• in doxycycline-treated mice
|
|
• in doxycycline-treated mice
|
|
• cornified epidermis in affected skin of doxycycline-treated mice
|
|
• in doxycycline-treated mice
|
|
• in doxycycline-treated mice
• however, MMP inhibitor impairs hyperplasia
|
skin lesions
(
J:201145
)
|
• dry and scaly lesions on the affected skin of doxycycline-treated mice
|
|
• in doxycycline-treated mice
|
thick skin
(
J:201145
)
|
• affected skin of doxycycline-treated mice
|
immune system
| N |
• doxycycline-treated mice exhibit normal spleen weight
|
|
• in the skin of doxycycline-treated mice
|
|
• in the skin of doxycycline-treated mice
• however, doxycycline withdrawal restores CD4+ T cell numbers
|
|
• in doxycycline-treated mice
|
neoplasm
|
• doxycycline-treated mice exposed to DMBA/TPA develop papillomas at 8 weeks that become ulcerative at 11 weeks
• however, sulindac treatment reduces the number and size of tumors
|
|
• doxycycline-treated mice exposed to DMBA/TPA develop papillomas at 8 weeks that become ulcerative at 11 weeks
|
growth/size/body
|
• after doxycycline treatment
|
digestive/alimentary system
|
• mild phenotype in doxycycline-treated mice
|
homeostasis/metabolism
|
• doxycycline-treated mice exposed to DMBA/TPA develop papillomas at 8 weeks that become ulcerative at 11 weeks
• however, sulindac treatment reduces the number and size of tumors
|
cellular
|
• with increased survival in doxycycline-treated mice
|
hematopoietic system
|
• in the skin of doxycycline-treated mice
|
|
• in the skin of doxycycline-treated mice
• however, doxycycline withdrawal restores CD4+ T cell numbers
|


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