ResearcherEötvös Loránd UniversityActive in the last 2 years
Gábor Mező
Matched on ORCID iD 0000-0002-7618-7954; OpenAlex author ID A5079755467.
Their work
- Papers
- 3 (first author 1, last author 1)
- Trials
- 0
- Grants
- 0
- Collaborators
- 4
2019: 1 paper · 2020: 1 paper · 2021: none · 2022: none · 2023: none · 2024: 1 paper
Papers 3
- Characterisation of the cell and molecular biological effect of peptide-based daunorubicin conjugates developed for targeting pancreatic adenocarcinoma (PANC-1… Co-author DOI 10.1016/j.biopha.2024.116293↗
- Phage Display-Based Homing Peptide-Daunomycin Conjugates for Selective Drug Targeting to PANC-1 Pancreatic Cancer. Last author DOI 10.3390/pharmaceutics12060576↗
- [Comparison of therapeutic peptides targeting pancreatic cancer]. First author PMID 31821385↗
Closest collaborators
The 4 strongest of 4 ranked by shared papers, trials and grants, with recent and small-team work weighing most.
- Eszter Lajkó · 3 shared papers, 2019–2024
- Paper Characterisation of the cell and molecular biological effect of peptide-based daunorubicin conjugates developed for tar… DOI 10.1016/j.biopha.2024.116293↗
- Paper Phage Display-Based Homing Peptide-Daunomycin Conjugates for Selective Drug Targeting to PANC-1 Pancreatic Cancer. DOI 10.3390/pharmaceutics12060576↗
- Paper [Comparison of therapeutic peptides targeting pancreatic cancer]. PMID 31821385↗
- László Kőhidai · 3 shared papers, 2019–2024
- Paper Characterisation of the cell and molecular biological effect of peptide-based daunorubicin conjugates developed for tar… DOI 10.1016/j.biopha.2024.116293↗
- Paper Phage Display-Based Homing Peptide-Daunomycin Conjugates for Selective Drug Targeting to PANC-1 Pancreatic Cancer. DOI 10.3390/pharmaceutics12060576↗
- Paper [Comparison of therapeutic peptides targeting pancreatic cancer]. PMID 31821385↗
- Zsófia A. Szász · 2 shared papers, 2019–2024
- Levente Endre Dókus · 2 shared papers, 2019–2020
How to reach this person
A chain of introductions through people who have published, run trials or held grants together (the fewest links first, then the links with the most shared work). Built from public records only; no contact details are kept.