24 results on '"Krzyscik, Mateusz A."'
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2. Investigations of membrane protein interactions in cells using fluorescence microscopy
3. Correction: Galectins use N-glycans of FGFs to capture growth factors at the cell surface and fine-tune their signaling
4. Galectins use N-glycans of FGFs to capture growth factors at the cell surface and fine-tune their signaling
5. Targeting HER2 and FGFR-positive cancer cells with a bispecific cytotoxic conjugate combining anti-HER2 Affibody and FGF2
6. Receptor clustering by a precise set of extracellular galectins initiates FGFR signaling
7. Targeting HER2 and FGFR-positive cancer cells with a bispecific cytotoxic conjugate combining anti-HER2 affibody and FGF2
8. Nanodiamonds as “artificial proteins”: Regulation of a cell signalling system using low nanomolar solutions of inorganic nanocrystals
9. Short report galectins use N-glycans of FGFs to capture growth factors at the cell surface and fine-tune their signaling
10. Additional file 1 of Short report galectins use N-glycans of FGFs to capture growth factors at the cell surface and fine-tune their signaling
11. Cyclic and dimeric fibroblast growth factor 2 variants with high biomedical potential
12. Dual-Warhead Conjugate Based on Fibroblast Growth Factor 2 Dimer Loaded with α-Amanitin and Monomethyl Auristatin E Exhibits Superior Cytotoxicity towards Cancer Cells Overproducing Fibroblast Growth Factor Receptor 1.
13. Drug Conjugation via Maleimide–Thiol Chemistry Does Not Affect Targeting Properties of Cysteine-Containing Anti-FGFR1 Peptibodies
14. Peptibody Based on FGFR1-Binding Peptides From the FGF4 Sequence as a Cancer-Targeting Agent
15. Fibroblast Growth Factor 2 Conjugated with Monomethyl Auristatin E Inhibits Tumor Growth in a Mouse Model
16. Dissecting biological activities of fibroblast growth factor receptors by the coiled-coil-mediated oligomerization of FGF1
17. Preparation of Site-Specific Cytotoxic Protein Conjugates via Maleimide-thiol Chemistry and Sortase A-Mediated Ligation
18. FGFR1 clustering with engineered tetravalent antibody improves the efficiency and modifies the mechanism of receptor internalization
19. Stable Fibroblast Growth Factor 2 Dimers with High Pro-Survival and Mitogenic Potential
20. Site-Specific, Stoichiometric-Controlled, PEGylated Conjugates of Fibroblast Growth Factor 2 (FGF2) with Hydrophilic Auristatin Y for Highly Selective Killing of Cancer Cells Overproducing Fibroblast Growth Factor Receptor 1 (FGFR1)
21. Novel Method for Preparation of Site-Specific, Stoichiometric-Controlled Dual Warhead Conjugate of FGF2 via Dimerization Employing Sortase A-Mediated Ligation
22. Highly cytotoxic FGF2-conjugates
23. Cytotoxic Conjugates of Fibroblast Growth Factor 2 (FGF2) with Monomethyl Auristatin E for Effective Killing of Cells Expressing FGF Receptors
24. High-Yield Site-Specific Conjugation of Fibroblast Growth Factor 1 with Monomethylauristatin E via Cysteine Flanked by Basic Residues
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