Jess Moore

@jlmoore.bsky.social

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

So happy to share this angle of my postdoctoral work! The skin epidermis keeps on keeping on, even when we deplete a majority of dermal fibroblasts.

Journal of Cell Biology@jcb.org · 2mo ago

@isabella-gaeta.bsky.social, @shuangshuangdu.bsky.social, @valentatormenta.bsky.social et al. show that the epidermal stem cell layer retains its capacity for proliferation despite significant fibroblast depletion during both adult and neonatal stages in vivo. rupress.org/jcb/article/... #StemCells

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.

Exclusive: NSF puts new research grants to top universities on hold

US science funder once again restricts awards to Harvard University and other research institutions.

nature.com

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...

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

biorxiv.org

🎉 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

bioRxiv Immunology@biorxiv-immuno.bsky.social · 3mo ago

Selective Treg recruitment to bone remodeling niches is required for digit tip regeneration https://www.biorxiv.org/content/10.64898/2026.05.04.722813v1

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.

(Left panels) Modeling of nuclei organization at 11 and 16 days of corneal development in an avian embryo. (Right panels) IHC for N-cadherin (yellow) and ZO-1 in 3D reconstruction of corneal cells at days 11 and 16. Nuclei are magenta.
bioRxiv Developmental Biology@biorxiv-devbio.bsky.social · 3mo ago

Quantitative imaging of corneal endothelial development reveals dynamic but resilient monolayer https://www.biorxiv.org/content/10.64898/2026.05.01.722310v1

Posting for Vibhu Sahni: Due to unforeseen circumstances the Burke Neurological Institute will have to terminate its research operations 5/22. There are international postdocs on visas who are looking for new homes. Please reach out to Vibhu if you can help

Our PhD student Kennedy Orwa, who studies applications of AI to health care, was hastily deported today to Kenya along with his 13-year-old son without opportunity to speak to legal counsel. King 5 reports that he held a valid visa that was rescinded without explanation.

UW graduate student deported through SEA as protesters demand answers

A union representing University of Washington graduate student workers says Kennedy Orwa’s student visa was rescinded without explanation.

king5.com