Line 10: | Line 10: | ||
</a> | </a> | ||
</li> | </li> | ||
− | <br | + | <br> |
<!--<h2><br>This diagnostic process can be expedited with synthetic biological tools that sense the following molecular markers in endometrial biopsy samples.</h2>--> | <!--<h2><br>This diagnostic process can be expedited with synthetic biological tools that sense the following molecular markers in endometrial biopsy samples.</h2>--> | ||
<img src="https://static.igem.org/mediawiki/2016/e/e7/T--MIT--HomepageTransition1.svg"> | <img src="https://static.igem.org/mediawiki/2016/e/e7/T--MIT--HomepageTransition1.svg"> | ||
<br> | <br> | ||
− | + | <li> | |
<a href="https://2016.igem.org/Team:MIT/Experiments/Promoters"> | <a href="https://2016.igem.org/Team:MIT/Experiments/Promoters"> | ||
<img src="https://static.igem.org/mediawiki/2016/1/16/T--MIT--synpromobutton.svg" alt="Promoters" > | <img src="https://static.igem.org/mediawiki/2016/1/16/T--MIT--synpromobutton.svg" alt="Promoters" > |
Revision as of 03:45, 17 October 2016
-
Read more about endometriosis
-
Read more about how we created synthetic promoters to respond to this disease marker
-
Read more about how we characterized miRNA profiles in model cells under varying conditions
-
Read more about how we characterized serine integrase TP901 that could give a circuit memory across a cycle
-
Read about a summary of our results and how our sensors interact logically after transfection of
4 to 5-unit genetic circuits into model cell cultures
-
Read about how we worked with other iGEM teams throughout our project
-
Read more about the future of our work through circuit design and clinical application