Author

Jennifer White

Barrow Neurological Institute

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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Neuroscience· 3

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:mouse· 3 Research Focus:cell type annotation· 1 Assay:imaging· 1

Frequent Co-Authors

Junxiang YiniD· 3 shared Michael F. WatersiD· 3 shared Michael WuiD· 3 shared Harry S. NickiD· 2 shared Jerelyn A. NickiD· 2 shared Kyle D. AlleniD· 2 shared Swati Khare· 2 shared Aamir R. ZuberiiD· 1 shared

Activity by Year

2024-2025 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 39 mutual co-author links

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3 shared papersNeuroscience

Junxiang YinORCID

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Author profile →

3 papers

Recent·Most cited

Intra-arterial Deoxyribonuclease therapy improves stroke outcomes in aged mice

Junxiang Yin, Michael Wu, Jennifer White, Ellie StClair, J Mocco, Michael F. Waters

This study shows that intra-arterial DNase therapy improves stroke outcomes in aged mice by enhancing reperfusion and reducing NETs.

CNS Neuroscience & Therapeutics · Jun 1, 2025Peer-reviewedNeuroscience

Association of cerebellar inflammation and neurodegeneration in a novel spinocerebellar ataxia type 13 mouse model

Junxiang Yin, Jennifer White, Swati Khare, Michael Wu, Aamir R. Zuberi, Ming Gao, Jerelyn A. Nick, Cathleen M. Lutz, Kyle D. Allen, Harry S. Nick, Michael F. Waters

This study creates a novel SCA13 mouse model with a R424H mutation, showing motor deficits, Purkinje cell loss, cerebellar inflammation, and atrophy, linking neuroinflammation to neurodegeneration.

bioRxiv · Oct 28, 2024 · PreprintNeuroscience

A Novel Early Onset Spinocerebellar Ataxia 13 BAC Mouse Model with Cerebellar Hypoplasia, Tremor, and Ataxic Gait

Junxiang Yin, Jerelyn A. Nick, Swati Khare, Heidi E. Kloefkorn, Ming Gao, Michael Wu, Jennifer White, James L. Resnick, Kyle D. Allen, Harry S. Nick, Michael F. Waters

This paper presents a novel BAC mouse model of SCA13 with cerebellar hypoplasia, tremor, and ataxic gait, mimicking human disease features.

bioRxiv · Oct 28, 2024 · PreprintNeuroscience