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Most zygote isolations were completed using cellulase and pectinase because the enzymes substantially improved this process.
In five zygotes development was delayed and altered.
Here we experimentally enlarged blastomeres to zygote size by enucleation and fusion with blastomeres that were in developmental synchrony with the recipient.
In these models, inbreeding depression is assumed to affect zygote-to-adult viability only.
The survival of a zygote was determined by generating a random number and comparing it with the relative viability value of the zygote.
Only in about 5% of zygotes evaluated were we unable to detect replicating nuclei at all.
In practice, zygote frequencies cannot be observed directly.
The study forms part of a broader investigation aimed at developing alternative ways of producing human zygotes in vitro.
During early events of embryonic development, activated zygotes were compared to in vitro fertilized ones.
The bright spot at the top of the zygote corresponds to injury at the injection site.
These injections interfere with the normal process of chromatin decondensation/recondensation occurring in the zygote after fertilisation.
In sharp contrast, human dignity understood as human equality is perhaps too strong insofar as it would include human zygotes and blastocysts.
One or two minutes after the last exocytotic events the ridges disappear and the surface of the zygote becomes smooth.
The transformation of a zygote into an embryo adheres both to nature and to nurture: not only genetics but also environment determines the outcome.
Independently of the number of pronuclei found, -tubulins were uniformly distributed throughout the cytoplasm of the abnormal zygotes.
