Magdi Elsallab, MD, PhD (@elsallabmagdi) 's Twitter Profile
Magdi Elsallab, MD, PhD

@elsallabmagdi

Instructor @harvard | @marcelamaus lab | GMP process development | CAR-T enthusiast | Pushing innovations through bottlenecks

ID: 1267807153290645505

calendar_today02-06-2020 13:16:06

190 Tweet

214 Followers

544 Following

Xiao Wang (@wangxiaolab) 's Twitter Profile Photo

Why can RNA only be linear or circular? It can be branched! We made multi-tailed mRNA, and we had fun! Here is our story led by brilliant graduate student Hongyu Chen: rdcu.be/dB7ck and his cartoon illustration👇MIT Chemistry Broad Institute

Why can RNA only be linear or circular? It can be branched! We made multi-tailed mRNA, and we had fun! Here is our story led by brilliant graduate student <a href="/HongyuChenChem/">Hongyu Chen</a>: rdcu.be/dB7ck and his cartoon illustration👇<a href="/ChemistryMIT/">MIT Chemistry</a> <a href="/broadinstitute/">Broad Institute</a>
Blood Cancers Today (@blood_cancers) 's Twitter Profile Photo

What is the incidence of T-cell malignancies after CAR-T? Magdi Elsallab, MD, PhD, of Mass General Cancer Center, and Moataz Ellithi, of University of Nebraska Medical Center, stopped by BCT to discuss their FAERS database analysis on T-cell malignancies after CAR-T. 📺 Watch here: buff.ly/4aYtiqu

What is the incidence of T-cell malignancies after CAR-T?

<a href="/ElsallabMagdi/">Magdi Elsallab, MD, PhD</a>, of <a href="/MGHCancerCenter/">Mass General Cancer Center</a>, and <a href="/EllithiMd/">Moataz Ellithi</a>, of <a href="/UNMC/">University of Nebraska Medical Center</a>, stopped by BCT to discuss their FAERS database analysis on T-cell malignancies after CAR-T.

📺 Watch here: buff.ly/4aYtiqu
Dimitrios L. Wagner (@dlwagner13) 's Twitter Profile Photo

🚀 Join Our Team at Baylor College of Medicine! 🧬 We’re looking for passionate technician to join our lab at Center for Cell and Gene Therapy. Help us develop innovative and accessible cell therapies for cancer and autoimmunity using genome editing. Pls RT 🙏 jobs.bcm.edu/job/Research-T…

Magdi Elsallab, MD, PhD (@elsallabmagdi) 's Twitter Profile Photo

Happy to see our work on the cover of @BloodJournal! If you haven’t read it yet, check out our study analyzing FDA adverse event reports for second primary malignancies post-CAR T cells: authors.elsevier.com/a/1j5wZ1UYwnBkJ

Nature Reviews Drug Discovery (@natrevdrugdisc) 's Twitter Profile Photo

The FDA has approved the first telomerase inhibitor, imetelstat, to treat myelodysplastic syndromes following an epic journey for the drug, which has been tested in more than 20 trials over the past 20 years in various cancers. Find out more here bit.ly/4ekijKL

The FDA has approved the first telomerase inhibitor, imetelstat, to treat myelodysplastic syndromes following an epic journey for the drug, which has been tested in more than 20 trials over the past 20 years in various cancers. Find out more here bit.ly/4ekijKL
Dimitrios L. Wagner (@dlwagner13) 's Twitter Profile Photo

Preprint alert 🚨 Up to 90% CAR knock-in rates in primary human T cells - without drug enhancers? 🧐 Single-stranded HDR templates with truncated Cas12a binding sequences improve knock-in efficiencies in primary human T cells biorxiv.org/content/10.110… 🧵👇

Josh Tycko (@joshtycko) 's Twitter Profile Photo

check out Eva Gottwein's new preprint carefully measuring the toxicity of some CRISPRa activation systems. This is an issue today for functional genomics research and potentially for future therapeutics that use synthetic transcriptional activators biorxiv.org/content/10.110…

Harvard-MIT Center for Regulatory Science (@harvardmit_crs) 's Twitter Profile Photo

Harvard-MIT Center for Regulatory Science Director Florence Bourgeois, former CRS fellow Magdi Elsallab, MD, PhD, and former visiting student Sandra Gillner, publish JAMA Internal Medicine study comparing evidence submitted to the FDA and EMA for cell and gene therapies. Find the full study here: jamanetwork.com/journals/jamai…

JAMA Internal Medicine (@jamainternalmed) 's Twitter Profile Photo

Discrepancies in clinical trial evidence reported to the FDA and EMA for cell and gene therapies highlight the need for harmonization in regulatory submissions. ja.ma/421j4Eo