Rebecca G. Zitnay
Biochemistry, Genetics and Molecular Biology · The Ohio State University
Publications
18
Citations
54
Est. group size
—
Recurring co-author estimate
Active years
6
Publishing since 2021
Rebecca G. Zitnay studies how skin and lung cancer cells change their behavior and appearance over time, using imaging and genetic tools to track processes like pigmentation, cell shape, and mutation patterns. Her recent work focuses heavily on melanoma (skin cancer), including how pigment-producing cells (melanocytes) vary and adapt, and on developing new microscopy and drug-delivery methods to study and potentially treat these changes. Earlier work also examined the mechanical forces involved in lung tumor growth.
Publication output was minimal or absent from 2017–2020, then increased from 2021 onward with a notable rise in 2024–2026.
Generated by claude-sonnet-5 from public bibliographic data · Jul 20, 2026
- QUILPEN decouples pigment absorption and organelle scatter in live melanocytic cells
2026
- Somatic mutations distinguish melanocyte subpopulations in human skin
Nature Cell Biology · 2026
- Detection of growth rate variations and differential drug response among melanoma states using quantitative phase imaging
2026
- Sphere drop mimics tumor outgrowth to evaluate the rate and depth of migratory plasticity via quantitative phase imaging
2026
- <scp>QUILPEN</scp> Provides Independent and Label‐Free Single‐Cell Quantification of Pigmentation Dynamics and Organelle Content
Pigment Cell & Melanoma Research · 2026
- Transdermal delivery of ultradeformable cationic liposomes complexed with miR211–5p (UCL-211) stabilizes BRAFV600E+ melanocytic nevi
Journal of Controlled Release · 2025
- Quantitative Phase Imaging for Assessing Tumor Cell Adaptability
2025
- QUILPEN provides independent and label-free single-cell quantification of pigmentation dynamics and organelle content
bioRxiv (Cold Spring Harbor Laboratory) · 2025
- A BRN2:MYC transcriptional axis regulates interconversion between therapy-resistant and tumorigenic phenotypes in melanoma
Cell Reports · 2025
- Transdermal Delivery of Ultradeformable Cationic Liposomes Complexed with miR211-5p (UCL-211) Stabilizes BRAFV600E+ Melanocytic Nevi
bioRxiv (Cold Spring Harbor Laboratory) · 2024
- 839 The genomic evolution of tumor cell phenotypic plasticity: Can we inhibit skin cancer adaptability itself?
Journal of Investigative Dermatology · 2024
- Mechanics of lung cancer: A finite element model shows strain amplification during early tumorigenesis
PLoS Computational Biology · 2022
- Mechanics of lung cancer: A finite element model shows strain amplification during early tumorigenesis
bioRxiv (Cold Spring Harbor Laboratory) · 2022
- NKX2-1 controls lung cancer progression by inducing DUSP6 to dampen ERK activity
Oncogene · 2021
- NKX2-1 controls lung cancer progression by inducing DUSP6 to dampen ERK activity
bioRxiv (Cold Spring Harbor Laboratory) · 2021
- bioRxiv (Cold Spring Harbor Laboratory)×6
- Oncogene×1
- Journal of Controlled Release×1
- PLoS Computational Biology×1
- Journal of Investigative Dermatology×1
- Daniel E. Conway
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Aritra Chatterjee
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Adriana T. Dawes
Biochemistry, Genetics and Molecular Biology · The Ohio State University
- Ahmad I. M. Athamneh
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
- Daniel M. Suter
Biochemistry, Genetics and Molecular Biology · Purdue University West Lafayette
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.
Claim or correct this profile