Gregory H. Hockerman
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
Publications
67
Citations
2,434
Est. group size
~4
Recurring co-author estimate
Active years
43
Publishing since 1983
Gregory H. Hockerman's research focuses on how ion channels—proteins that control the flow of charged particles in and out of cells—regulate cell signaling and function in tissues such as pancreatic insulin-producing cells and skeletal muscle. His work examines calcium and potassium channels and their roles in processes like insulin secretion, muscle wasting (cachexia), and heart electrical activity. This research combines molecular biology, pharmacology, and electrophysiology techniques to understand disease-related changes in cell signaling.
Publication output has remained fairly steady but modest over the last decade, averaging about 1-4 papers per year with a slight recent slowdown in the last two years.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- RyR2 regulates store-operated Ca2+ entry, phospholipase C activity, and electrical excitability in the insulinoma cell line INS-1
Zenodo (CERN European Organization for Nuclear Research) · 2023
- RyR2 regulates store-operated Ca2+ entry, phospholipase C activity, and electrical excitability in the insulinoma cell line INS-1
Zenodo (CERN European Organization for Nuclear Research) · 2023
- The ERG1A K+ Channel Is More Abundant in Rectus abdominis Muscle from Cancer Patients Than that from Healthy Humans
Diagnostics · 2021
- The ERG1 Potassium Channel is Abundant in Cachectic Human Skeletal Muscle
The FASEB Journal · 2020
- The ERG1 Potassium Channel is More Abundant in Skeletal Muscle from Cachectic than Healthy Humans
Research Square (Research Square) · 2020
- The ERG1a K <sup>+</sup> Channel Increases Intracellular Calcium and Calpain Activity in C2C12 Myotubes
The FASEB Journal · 2019
- Calcium Signaling in Skeletal Muscle Atrophy: A Novel Role for the ERG1alpha K^+ Channel
2019
- Molecular Determinants of the Differential Modulation of Cav1.2 and Cav1.3 by Nifedipine and FPL 64176
Molecular Pharmacology · 2018
- Agonists of the γ-aminobutyric acid type B (GABAB) receptor derived from β-hydroxy and β-amino difluoromethyl ketones
Bioorganic & Medicinal Chemistry Letters · 2018
- The FASEB Journal×5
- bioRxiv (Cold Spring Harbor Laboratory)×4
- PLoS ONE×2
- Scientific Reports×2
- Biochemical Pharmacology×2
- Andy Hudmon
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Ana Laura López-Serrano
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Dan J. Bare
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Theodore Cummins
Biochemistry, Genetics and Molecular Biology · Indiana University
- Chen Gu
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 20, 2026.
Claim or correct this profile