mortality/aging
• 6 of 18 mice die at P0
|
• 4 of 18 mice die by P2
• however, mice exhibit normal survival beyond P2
|
• fewer than expected mice are present at E18.5
|
reproductive system
azoospermia
(
J:230053
)
• in some mice
• however, some mice exhibit normal mature spermatozoa
|
• variable testicular vacuolation
• mice exhibit accumulation of disordered proteins in the testes unlike wild-type mice
• however, mice exhibit normal epithelium and interstitial Leydig cells
|
• degeneration and atrophic ranging from mild and focal vacuolation of the basal layer of spermatogonia to a marked decrease in tubule diameter with diffuse tubular atrophy, vacuolation of the basal layer of spermatogonia
|
cellular
N |
• mouse embryonic fibroblasts exhibit normal cell tolerability to DNA interstrand cross-linking
• skin-derived fibroblasts exhibit normal response to various cytotoxic stressors
|
azoospermia
(
J:230053
)
• in some mice
• however, some mice exhibit normal mature spermatozoa
|
integument
• at P0, more distinct cell borders granules in the granular cell layer compared to in wild-type mice
• however, adult mice exhibit normal epidermal structure
|
• at P0, dorsal skin exhibits loss of granules in the granular cell layer compared with wild-type mice
|
endocrine/exocrine glands
• variable testicular vacuolation
• mice exhibit accumulation of disordered proteins in the testes unlike wild-type mice
• however, mice exhibit normal epithelium and interstitial Leydig cells
|
• degeneration and atrophic ranging from mild and focal vacuolation of the basal layer of spermatogonia to a marked decrease in tubule diameter with diffuse tubular atrophy, vacuolation of the basal layer of spermatogonia
|
hematopoietic system
immune system