Jeovanna Lowe
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
41
Citations
802
Est. group size
~11
Recurring co-author estimate
Active years
44
Publishing since 1983
Jeovanna Lowe's research focuses on the biology of muscular dystrophy, particularly how inflammation, immune cells, and a hormone-signaling pathway called the mineralocorticoid receptor (MR) contribute to muscle damage and repair. Much of the work uses mouse models of Duchenne muscular dystrophy to study cell-to-cell communication between muscle fibers, fibroblasts, and immune cells, and to test potential treatments such as MR-blocking drugs and gene therapies (like micro-dystrophin) for both skeletal and heart muscle disease.
Publication output has grown steadily over the last decade, rising from occasional papers in the late 2010s to a peak of six publications in 2025.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- Inflammation in a severe model of dystrophic cardiomyopathy contains a high proportion of T cells that contribute to onset of pathology
American Journal of Physiology-Heart and Circulatory Physiology · 2026
- Direct aldosterone stimulation of skeletal muscle fibroblasts changes gene expression and differentially affects fibroblast functions from normal and diseased muscles
Frontiers in Physiology · 2026
- Intercellular communication from myotubes to fibroblasts is differentially impacted by mineralocorticoid receptor signaling and muscular dystrophy
Cell Communication and Signaling · 2025
- Distinct Cellular Communication from Aldosterone-treated Myotubes to Fibroblasts between Wild-type and Dystrophic Skeletal Muscle
Physiology · 2025
- Mineralocorticoid receptor antagonists reduce inflammatory signaling independent of myofiber mineralocorticoid receptor
Endocrine and Metabolic Science · 2025
- Isolation of Immune Cells from Skeletal Muscles for Flow Cytometry
Methods in molecular biology · 2025
- Gene therapy delivered micro-dystrophins co-localize with transgenic utrophin in dystrophic skeletal muscle fibers
Neuromuscular Disorders · 2024
- Cell-type specific effects of mineralocorticoid receptor gene expression suggest intercellular communication regulating fibrosis in skeletal muscle disease
Frontiers in Physiology · 2024
- Efficiency of enhanced capture methods and age-class structure of dispersing boreal woodpeckers
Journal of Field Ornithology · 2024
- Micro-dystrophin gene therapy demonstrates long-term cardiac efficacy in a severe Duchenne muscular dystrophy model
Molecular Therapy — Methods & Clinical Development · 2023
- Mineralocorticoid receptor antagonists and glucocorticoids differentially affect skeletal muscle inflammation and pathology in muscular dystrophy
JCI Insight · 2022
- Myeloid mineralocorticoid receptors contribute to skeletal muscle repair in muscular dystrophy and acute muscle injury
American Journal of Physiology-Cell Physiology · 2022
- Corrigendum: Muscle Twitch Kinetics Are Dependent on Muscle Group, Disease State, and Age in Duchenne Muscular Dystrophy Mouse Models
Frontiers in Physiology · 2022
- Micro-dystrophin gene therapy prevents heart failure in an improved Duchenne muscular dystrophy cardiomyopathy mouse model
JCI Insight · 2021
- Early Inflammation in Muscular Dystrophy Differs between Limb and Respiratory Muscles and Increases with Dystrophic Severity
American Journal Of Pathology · 2021
- Frontiers in Physiology×5
- JCI Insight×2
- Journal of Neuromuscular Diseases×2
- Human Molecular Genetics×2
- American Journal of Physiology-Cell Physiology×2
- Jill A. Rafael‐Fortney
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- James F. Markworth
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Steven S. Welc
Biochemistry, Genetics and Molecular Biology · Indiana University
- Conner C. Earl
Biochemistry, Genetics and Molecular Biology · Indiana University
- Ashok Kumar
Biochemistry, Genetics and Molecular Biology · The Ohio State University
This profile was generated automatically from public scholarly data (OpenAlex). Group size and activity levels are estimates derived from co-authorship patterns.
Last updated Jul 19, 2026.
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