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Schmidt Science Fellow, Cagla Eroglu’s lab @ Duke Studying astrocyte endfeet ⭐️ PhD from Valentina Greco’s lab @ Yale
Jess Moore









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BREAKING: New proposed OMB regulation, applying to all federal grants, requiring grant reviews by senior political appointees and re-emphasizes that "peer review remains advisory and does not replace agency discretion". #standupforscience public-inspection.federalregister.gov/2026-10817.pdf
13d
public-inspection.federalregister.gov
Scoop: NSF has been quietly blocking new funds and grants to four top universities: Duke, Harvard, Princeton, and Yale. Dozens of proposals from PIs at these universities—and their collaborators—have been stuck at the Office of Award Management awaiting finalization for months.
14d
Stand Up for Science!
US science funder once again restricts awards to Harvard University and other research institutions.
www.nature.com
Exclusive: NSF puts new research grants to top universities on hold
Dan Garisto
SIGN YOUR SUPPORT for the Reinstatement of the National Science Board at this link: zurl.co/UPf5g 1/3
1mo
Stand Up for Science!
Live on bioRxiv🎉🧬🧠! We @BhaduriLab use perturb-seq in human cortical tissues to make sense of the shifting molecular trajectories that form the human prefrontal cortex. (1/7) www.biorxiv.org/content/10.6...
26d
Patricia Nano
δ-catenin controls layer-specific transcriptional maturation of astrocytes via Zbtb20 https://www.biorxiv.org/content/10.64898/2026.05.12.724361v1
Grateful to be part of this amazing community that I've looked up to for years!
1d
28d
What’s new in #DevBio? 👀 Our preLighters Theodora, Jawdat, @sristi.bsky.social & @deevithab.bsky.social have handpicked a selection of exciting preprints in this area. Check out the #preList and let us know your favourite, recent DevBio preprint ⬇️: prelights.biologists.com/prelists/pre...
🎉 First preprint from our lab! Regulatory T cells are selectively recruited to regenerating but not scarring mouse digit tips, driving macrophage-mediated bone remodeling essential for regrowth. A new axis of innate/adaptive immune cooperation in mammalian regeneration! #immunology #regeneration
Jess Moore
Please check out our new preprint! Together with @sarathomasy.bsky.social and led by DVM/PhD candidate Raneesh Ramarapu, we used 3D imaging + quantitative analysis to show how the corneal endothelium maintains a stable layer and refines hexagonal packing during development.
bioRxiv Cell Biology
28d
1mo
1mo
We are thrilled to announce the 2026 Zara Weinberg Leading Edge Fellows! 40 remarkable postdocs pursuing transformative research in biological/biomedical sciences. This is the 7th Leading Edge cohort and we are so excited to welcome them! www.leadingedgesymposium.org/fellows/
1d
preLights
What if brain metastatic cells do not act alone, but form #networks to help them grow? In our new #preprint, we show that #brainmetastases form malignant, gap-junction mediated #networks that drive cell cycle progression & neural features through Ca²⁺ signaling. www.biorxiv.org/content/10.6... 🧵👇
Leading Edge Fellows Program
28d
Kai Mesa
Crystal Rogers, PhD
Matthia Karreman
Intrinsic coordination of dynamic molecular signatures shape the human prefrontal cortex
The cerebral cortex drives human cognition through the coordinated activity of discrete cortical areas, each harboring specialized molecular, structural and functional characteristics. Central to this organization is the prefrontal cortex (PFC), a hub for executive function that displays disproportionate expansion in humans and selective vulnerability to neurodevelopmental disorders. Previous work has identified a collection of PFC-enriched marker genes with dynamic expression trajectories, and re-analysis of these datasets converge these markers into 18 distinct molecular signatures of spatiotemporal PFC identity. However, the intrinsic gene networks that coordinate these molecular signatures to shape the human PFC remains unclear. Through pooled CRISPR activation screens in human primary cortical tissues, we have evaluated the ability of PFC-enriched transcription factors to intrinsically pattern PFC molecular identity. Our screens identify novel roles for the neurogenesis regulator, YBX1, in the activation of human PFC fate. In parallel screens and knock-down experiments in human cortical organoids, we define how YBX1 acts in concert with other PFC determinants to activate molecular signatures of PFC identity. Our findings support a model in which PFC patterning is orchestrated by cohorts of intrinsic determinants that initiate, potentiate, and modulate PFC gene signatures, conferring robustness to the development of the human PFC. ### Competing Interest Statement The authors have declared no competing interest. NIH, R00NS111731, R01MH132689, UM1MH130991, RF1MH132662, U24HG002371 Brain & Behavior Research Foundation, https://ror.org/03a63f080, Young Investigator Award Alfred P. Sloan Foundation, https://ror.org/052csg198, Sloan Fellowship Rose Hills Foundation, Innovation Award Esther A. & Joseph Klingenstein Fund, Klingenstein-Simons Fellowship Simons Foundation, https://ror.org/01cmst727, Klingenstein-Simons Fellowship Ablon Trust, Ablon Scholar Award Department of Biological Chemistry, UCLA Zamenhof Scholarship UCLA Eli and Edythe Broad Center of Regenerative Medicine, Innovation Award, Stem Cell Research Training Program University of California, Los Angeles, https://ror.org/046rm7j60, Eugene V. Cota-Robles Award California Institute for Regenerative Medicine, https://ror.org/033m8b439, DISC0-14514, DISC4-16337 National Science Foundation, Graduate Research Fellowship Program
www.biorxiv.org