Elizabeth McNeill

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Assistant Professor

Iowa State University

United States

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Dr. Elizabeth McNeill is an Assistant Professor at Iowa State University, USA. Her research primarily focuses on the effects of microRNAs in synaptic development and aging, particularly utilizing the Drosophila model. Recent publications highlight her work on glial regulation of synaptogenesis and the impact of environmental stressors on microglial function.

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The role of miR-987 in cardiac morphology and function

Open Date: 2016-01-01

Close Date: 2020-04-01

Articles (14)

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2025

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2020

Collaborators (4)

David Landreth Van Vactor, Jr.

Professor

Harvard Medical School

UNITED STATES

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Stephanie Clark

associate and full professor

Iowa State University

UNITED STATES

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Michael Kimber

Associate Professor

Iowa State University

UNITED STATES

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Tudor Fulga

Associate Professor of Genome Biology

University of Oxford

UNITED KINGDOM

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Elizabeth McNeill

Research Interests

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About

Recent Grants

Articles (14)

MiR-92 Controls Synaptic Development Through Glial Vha55 Regulation

Single-Nucleus RNA Sequencing Reveals Enduring Signatures of Acute Stress and Chronic Exercise in Striatal Microglia

Single-nucleus RNA sequencing reveals enduring signatures of acute stress and chronic exercise in striatal microglia

The Fourth Annual Symposium of the Midwest Aging Consortium

The heart of plastic: utilizing the <i>Drosophila</i> model to investigate the effects of micro/nanoplastics on heart function

Highlighting the role of glial-specific miR-92 on synaptogenesis of developing Drosophila melanogaster

Investigating The Role Of Human Conserved Microrna-193 In The Aging <i>Drosophila</i> Heart

RNA Sequencing Reveals Key Metabolic Pathways Are Modified by Short-Term Whole Egg Consumption

Identification of conserved transcriptome features between humans and Drosophila in the aging brain utilizing machine learning on combined data from the NIH Sequence Read Archive

Drosophila model for gut-mediated horizontal transfer of narrow- And broad-host-range plasmids

FOXO Regulates Neuromuscular Junction Homeostasis During Drosophila Aging

Drosophila enabled promotes synapse morphogenesis and regulates active zone form and function.

The conserved microRNA miR-34 regulates synaptogenesis via coordination of distinct mechanisms in presynaptic and postsynaptic cells.

Whole egg consumption increases gene expression within the glutathione pathway in the liver of Zucker Diabetic Fatty rats

Collaborators (4)

David Landreth Van Vactor, Jr.

Stephanie Clark

Michael Kimber

Tudor Fulga

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