Abstract
The age-related increase in aneuploidy has been observed in both humans and mice. Therefore, mice have the potential to be a useful model system to study the origins, etiology, and mechanisms of human aneuploidy and serve as a system to develop new therapeutic strategies. To further establish relevance to this model system, this study aims to validate a method capable of mitochondrial (mt)DNA quantitation in the mouse blastocyst and evaluate putative association with aneuploidy.
Sign-in/Register to access full text options 
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
