
Principal Investigator @IFOMresearch and IGM-CNR. Begging to differ.
Milan, Lombardy
Joined February 2011
- Tweets557
- Following682
- Followers1.4K
- Likes1.4K
🚨 Can we kill a cell by targeting DNA that does nothing?
🧬 Our study shows Cas9 can selectively kill cells carrying a non-functional target sequence, sparing cells without it.
Weaponizing CRISPR/Cas9 for selective elimination of cells with an abe… sciencedirect.com/science/ar…
🚨 Can broken DNA generate a new protein?
Our study independently confirms that DSBs trigger transcription from the break—and shows, for the first time, that the resulting RNA can be translated.
Could this generate neoantigens after radio/chemotherapy?
nature.com/articles/s42003-0…
#IPF has no cure. Median survival: 4 years. Lung transplant is the only real option.
Our new paper shows this might be about to change. 🧵
Disclosure: I co-founded TAG Therapeutics, exploring clinical development of this approach — this study was independent academic work.
📄 IPF paper: link.springer.com/article/10…
Fabrizio d'Adda di Fagagna retweeted
Online now!✨Oppezzo et al therapeutically block telomeric DNA damage signalling to restore hematopoietic function in telomerase-deficient and aged mice, while reducing senescence and inflammation
@FdAdF66
@IFOMresearch nature.com/articles/s43587-0…
1/ What if some of the consequences of #aging are not caused by damage itself, but by the alarm signals our cells generate in response to that #damage?
Today, we publish a study in @NatureAging addressing this question.
nature.com/articles/s43587-0…
8/ This journey is now continuing beyond academia.
tag-therapeutics.com/ is advancing this approach toward clinical translation.
Deep gratitude to @Fondaz_Telethon , @ERC_Research, @IFOMresearch, @CNRsocial_, @AGEIT_PE8 and all who supported this work.
Happy to share our deep characterization of #LLPS events modulating the DNA damage response (#DDR) through #53BP1 condensation promoted by #dincRNA: biorxiv.org/content/10.64898…
