Author

Ashley L. Lennox

Duke Medical Center

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetics· 1 Neuroscience· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 2 Organism:mouse· 2 Research Focus:cell type annotation· 1 Research Focus:cell-cell communication· 1 Organism:human· 1 Assay:proteomics· 1

Frequent Co-Authors

Debra L. SilveriD· 2 shared A. James BarkovichiD· 1 shared Alban C. ZiegleriD· 1 shared Alexandra AfenjariD· 1 shared Allan Micheil InnesiD· 1 shared Amy Sarah Kimball· 1 shared Annalise Bracher· 1 shared Atsushi FujitaiD· 1 shared

Activity by Year

2020-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 37 mutual co-author links

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2 shared papersNeuroscience

Debra L. SilverORCID

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2 papers

Recent·Most cited

Subcellular proteome of radial glia reveals non-muscle myosins control basal endfeet to mediate interneuron organization

Brooke R. D’Arcy, Ashley L. Lennox, Camila Manso Musso, Annalise Bracher, Carla F. Escobar-Tomlienovich, Stephany Perez-Sanchez, Debra L. Silver

The paper uses in vivo proximity labeling to analyze the subcellular proteome of radial glial cells and identifies non-muscle myosins that regulate endfoot structure and interneuron organization.

bioRxiv · Nov 18, 2022 · PreprintNeuroscience

Pathogenic DDX3X mutations impair RNA metabolism and neurogenesis during fetal cortical development

Ashley L. Lennox, Mariah L. Hoye, Ruiji Jiang, Bethany Johnson-Kerner, Lindsey Suit, Srivats Venkataramanan, Charles J. Sheehan, Fernando C. Alsina, Brieana Fregeau, Kimberly A. Aldinger, Ching Moey, Iryna V. Lobach, Alexandra Afenjar, Dusica Babovic‐Vuksanovic, Stéphane Bezieau, , Elliott H. Sherr

This study identifies DDX3X mutations as causing neurodevelopmental disorders by disrupting RNA metabolism and neurogenesis during fetal cortical development.

Neuron · Mar 4, 2020Peer-reviewedGenetics