摘要: Embryonic cell fate decisions require an integrated symphony of growth factors presented in a specific sequence and discreet locations within the developing embryo. Because species-specific organization cellular topology utero, factor regulation may differ among organisms. Accordingly, better understanding species-conserved requirements necessitates need for precise modeling differentiation movement during construction definitive embryonic tissues. Ideally, this model would allow control production to experimentally dissect relationship between signal decision.
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