mortality/aging
• some are born live but all die by P2
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reproductive system
• between E9.5 and 10.5, most PGCs are found with in the hindgut and these have abnormal morphology, while in wild-type embryos most PGCs are found in dorsal portions of mesentery
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• at E9.5, PGCs are located primarily in the ventral axis of the hindgut while in wild-type PGCs are found primarily associated with the hindgut epithelium or in the dorsal axis of the hindgut; total PGC number in mutant embryos is 19% of wild-type
• at E10.5, mutants have 4% of the wild-type number of PGCs
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• at E11.5, no alkaline phosphatase-positive primordial germ cells (PGCs) are detected in genital ridges
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• at E10.5, many PGCs in hindgut appear to be disintegrating; abnormal PGCs in hindgut tend to be nonmotile and apoptotic
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• at E10.5, only 31% of total PGCs have migrated from hindgut, compared to 93% in wild-type
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• at E10.5, migratory PGCs in the hindgut are observed to proliferate
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hematopoietic system
• severe at birth
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• significantly lower than wild-type at P1 (RBC count is 17% of wild-type value)
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cellular
• between E9.5 and 10.5, most PGCs are found with in the hindgut and these have abnormal morphology, while in wild-type embryos most PGCs are found in dorsal portions of mesentery
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• at E9.5, PGCs are located primarily in the ventral axis of the hindgut while in wild-type PGCs are found primarily associated with the hindgut epithelium or in the dorsal axis of the hindgut; total PGC number in mutant embryos is 19% of wild-type
• at E10.5, mutants have 4% of the wild-type number of PGCs
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• at E11.5, no alkaline phosphatase-positive primordial germ cells (PGCs) are detected in genital ridges
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• at E10.5, many PGCs in hindgut appear to be disintegrating; abnormal PGCs in hindgut tend to be nonmotile and apoptotic
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• at E10.5, only 31% of total PGCs have migrated from hindgut, compared to 93% in wild-type
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• at E10.5, migratory PGCs in the hindgut are observed to proliferate
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