NeuroscienceeLifePeer-reviewed
Author
Nicole A. Pannullo
Johns Hopkins UniversityORCID 0000-0002-1061-7157Unclaimed ORCID profile · follow to get notified of new preprints
Biology Disciplines
Click to filter author papersSignature Assays, Organisms & Methods
Click to filter · or open tagActivity by Year
2021-2026 · peak 2/yrCo-Author Collaboration Network
10 top collaborators · 22 mutual co-author linksFocal author (center)Selected co-authorORCID co-authorUnlinked name
Curved chords = mutual co-authorship5 papers
Recent·Most cited
- NeurosciencebioRxivPreprint
Sox8 and Sox9 regulate differentiation and nuclear positioning of retinal Muller glia.
Nicole A. Pannullo, Debarpita Datta, Clayton P. Santiago…·Seth Blackshaw
This study investigates the role of Sox8 and Sox9 in retinal Muller glia differentiation and nuclear positioning using genetic and single-cell multiomic approaches.
- NeuroscienceScientific ReportsPeer-reviewed
Overexpression of Meis factors in late-stage retinal progenitors yields complex effects on temporal patterning and neurogenesis.
Patrick J. Leavey, Lizhi Jiang, Nicole A. Pannullo…·Seth Blackshaw
This study shows that overexpressing Meis1 and Meis2 in postnatal mouse retinal progenitor cells has distinct effects on temporal identity and neurogenesis, without fully reprogramming cell fate.
- NeuroscienceFrontiers in Cell and Developmental BiologyPeer-reviewed
Ectopic insert-dependent neuronal expression of GFAP promoter-driven AAV constructs in adult mouse retina.
Nguyet Le, Haley Appel, Nicole A. Pannullo…·Seth Blackshaw
This study shows that GFAP promoter-driven AAV constructs in adult mouse retina show insert-dependent expression in non-glial cells without evidence of glia-to-neuron conversion.
50 citations - NeurosciencebioRxivPreprint
Ptbp1 deletion does not induce glia-to-neuron conversion in adult mouse retina and brain.
Thanh V. Hoang, Dong Won Kim, Haley Appel…·Seth Blackshaw
This study shows that deleting Ptbp1 in adult retinal Muller glia and brain astrocytes does not convert glia into neurons, using genetic lineage tracing, scRNA-Seq, and electrophysiology.