mortality/aging
|
• mice die within 1 year following tamoxifen exposure at weaning
|
|
• tamoxifen exposure beginning at weaning results in a progressive and generalized progeroid syndrome
|
cellular
|
• increased incidence of micronucleated cells in MEFs following tamoxifen treatment
• dramatic increase in micronuclei in proliferating tissues following tamoxifen treatment at weaning
|
|
• tamoxifen exposure at E13.5 results in accumulation of mitotic cells in the thymus
|
|
• sister chromatid exchanges and inter-telomeric recombination rates are increased in MEFs following tamoxifen treatmen
|
|
• accumulation of intercellular DNA bridges in MEFs following tamoxifen treatment
|
adipose tissue
|
• following tamoxifen exposure at weaning
|
pigmentation
|
• following tamoxifen exposure at weaning
|
|
• following tamoxifen exposure at weaning
|
digestive/alimentary system
|
• dramatic increase in micronuclei following tamoxifen treatment at weaning
|
embryo
|
• tamoxifen exposure at E13.5 results in intrauterine dwarfism with overall loss of cellularity particularly in some specific organs including the thymus
|
endocrine/exocrine glands
|
• tamoxifen exposure at E13.5 results in accumulation of mitotic cells in the thymus
|
growth/size/body
|
• tamoxifen exposure at E13.5 results in intrauterine dwarfism with overall loss of cellularity particularly in some specific organs including the thymus
|
hematopoietic system
|
• tamoxifen exposure at E13.5 results in accumulation of mitotic cells in the thymus
|
immune system
|
• tamoxifen exposure at E13.5 results in accumulation of mitotic cells in the thymus
|
integument
|
• following tamoxifen exposure at weaning
|
|
• following tamoxifen exposure at weaning
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
| Bloom syndrome | DOID:2717 |
OMIM:210900 |
J:227197 | |


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