1999
DOI: 10.1002/(sici)1097-010x(19990501)283:6<590::aid-jez11>3.0.co;2-l
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Mouse embryos used as a bioassay to determine control of marsupial embryonic diapause

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Cited by 8 publications
(1 citation statement)
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“…Arrest in non-diapausing blastocysts cannot be profitably induced or maintained artificially in vitro, despite potential indications for decelerated embryonic development, possibly caused by suboptimal culture conditions [27,28]. Thus, such an induced-dormancy/mouse-carrier system might offer new advantages to increase the life span of -for example -in vitro fertilized oocytes that -for whatever reason -cannot be transferred within the right timeframe.…”
Section: Diapause-induced Embryo Preservation Offers An Alternative For Cryopreservationmentioning
confidence: 99%
“…Arrest in non-diapausing blastocysts cannot be profitably induced or maintained artificially in vitro, despite potential indications for decelerated embryonic development, possibly caused by suboptimal culture conditions [27,28]. Thus, such an induced-dormancy/mouse-carrier system might offer new advantages to increase the life span of -for example -in vitro fertilized oocytes that -for whatever reason -cannot be transferred within the right timeframe.…”
Section: Diapause-induced Embryo Preservation Offers An Alternative For Cryopreservationmentioning
confidence: 99%