Daria Babushok Lab

Laboratory of Daria Babushok, physician-scientist at #PennMedicine, investigating pathogenic mechanisms and malignant transformation in bone marrow failure.

[Daria Babushok Lab @BabushokLab]

Excited to share the Predictive Aplastic Score System (PASS)—a simplified, validated tool to diagnose acquired aplastic anemia in adults. A multi-institutional effort led by our team and Dr. Gabriel Aleixo.
Paper: https://t.co/m6hiXw4xYM
Calculator: https://t.co/KotYeoisvw

[Team Telomere @TeamTelomereInc]

This Veterans Day we are highlighting 2 community members.

Lisa Helms-Guba, US Army & Air Force and Nicole Bjerke, US Air Force.

These 2 women served their country & are founding members of DCO now Team Telomere. Thank you!

In loving memory of Lisa ❤️

[Meredith Herman, DO @MeredithKHerman]

How do you determine bone marrow cellularity?…it’s a vibe, or is it? Made this diagram today to help my PGY1 brain solidify the “vibes” of hemepath #hemepath #PathTwitter #pathx #pathstudytips @UMichPath

[Daria Babushok Lab @BabushokLab]

@la_guettler almond extract

[Daria Babushok Lab @BabushokLab]

@MrinalPatnaik @NIH @theNCI @LashoTerra @a_mangaonkar @MoritzBinderMD @Ryan_M_Carr @MayoCancerCare Congratulations!

[Daria Babushok Lab @BabushokLab]

@XimeJordan Congratulations @XimeJordan on receiving the RUNX1 Research Program grant!

[Alexandra Gomez A. @AGomez_MD]

Dr. Babushok describing the role of somatic mutations in HLA Class I genes in aplastic anemia. HLA loss is sufficient for clonal expansion. HLA alleles in different ethnic groups likely correlate w differences in outcomes @BabushokLab #ASH22 #bmfsm https://t.co/UAGmSqwsvZ

[Mathijs Sanders @MathijsSanders]

Thrilled to share our work on the genomic signatures in Fanconi anaemia-associated cancers @Nature . We used short and long-read sequencing to unravel an complex genetic landscape and assessed transcriptional heterogeneity.

https://t.co/2Q0qoQjMVH

https://t.co/E0im0aidB3

[Daria Babushok Lab @BabushokLab]

Our collaborative study reporting a novel targeted treatment approach for a rare genetic blood disease: https://t.co/55HKpaUdN1