0
Skip to Content
RUNX1 Research Program
RUNX1 Research Program
For Patients
For Researchers
For Clinicians
Take Action
About Us
English
DONATE
RUNX1 Research Program
RUNX1 Research Program
For Patients
For Researchers
For Clinicians
Take Action
About Us
English
DONATE
For Patients
For Researchers
For Clinicians
Take Action
About Us
English
Back
DONATE
  • Research Webinars,
• 5/6/24

Interface guided phenotyping of coding variants in the transcription factor RUNX1 with SEUSS

Dr. Hannah Carter (UCSD) discusses how she and her colleagues employed SEUSS, a Perturb-seq-like methodology, to generate and assay mutations at physical interfaces of the RUNX1 Runt domain.

Previous

An Approach to Screening Drugs for Preventing Disease Progression in Patients with RUNX1-FPD

Next

RUNX1 Attenuates Toll-Like Receptor and Type I Interferon Signaling in Neutrophils

You Might Also Like

Related Embedded Video Item Thumbnail The Berg Family
Related Embedded Video Item Thumbnail RUNX1 Patient Data Hub Demo 3: Patient Tools
Related Embedded Video Item Thumbnail Limiting Cancer Risk Through Physical Activity
Related Embedded Video Item Thumbnail An Approach to Screening Drugs for Preventing Disease Progression in Patients with RUNX1-FPD
Related Embedded Video Item Thumbnail RUNX1 Patient Data Hub Demo 1: Setting Up Your Account

Sign Up For Our Email List!

Enter your information below to receive the
latest RUNX1 news and updates!

Stay In Touch

Email RRP

Newsletter

Policies

Privacy Policy

Cookie Policy

Accessibility Statement

Site Resources

News & Updates

Calendar of Events

RRP Blog

DONATE
SHOP