A missing genetic switch at the origin of embryonic malformations

· by · in Biotechnology industry, iPS Cells, Personalized Therapies, Regenerative Medicine. ·


Fluorescence visualization of Pitx1 gene expression in mouse embryos. The absence of Pen, one of the Pitx1 switches (right), results in a loss of fluorescence in developing legs. Credit: © UNIGE / Guillaume Andrey
https://phys.org/news/2021-12-genetic-embryonic-malformations.html

Leave a Reply

Fill in your details below or click an icon to log in:

Gravatar
WordPress.com Logo

You are commenting using your WordPress.com account. ( Log Out /  Change )

Twitter picture

You are commenting using your Twitter account. ( Log Out /  Change )

Facebook photo

You are commenting using your Facebook account. ( Log Out /  Change )

Cancel

Connecting to %s

This site uses Akismet to reduce spam. Learn how your comment data is processed.