Found: 10
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Two-Front War on Cancer—Targeting TAM Receptors in Solid Tumour Therapy.
- Published in:
- Cancers, 2022, v. 14, n. 10, p. 2488, doi. 10.3390/cancers14102488
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- Article
Improved cytotoxicity of novel TRAIL variants produced as recombinant fusion proteins.
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- PEDS: Protein Engineering, Design & Selection, 2018, v. 31, n. 2, p. 37, doi. 10.1093/protein/gzx065
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- Article
A PDE10A inhibitor CPL500036 is a novel agent modulating striatal function devoid of most neuroleptic side-effects.
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- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.999685
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- Article
Evaluation of the hepatotoxicity of the novel GPR40 (FFAR1) agonist CPL207280 in the rat and monkey.
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- PLoS ONE, 2021, v. 16, n. 9, p. 1, doi. 10.1371/journal.pone.0257477
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- Article
Preclinical characterization of CPL302-253, a selective inhibitor of PI3Kδ, as the candidate for the inhalatory treatment and prevention of Asthma.
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- PLoS ONE, 2020, v. 15, n. 7, p. 1, doi. 10.1371/journal.pone.0236159
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- Article
2333-PUB: CPL207-280, a Potent and Safe GPR40 Agonist for the treatment of Type 2 Diabetes.
- Published in:
- Diabetes, 2019, v. 68, p. N.PAG, doi. 10.2337/db19-2333-PUB
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- Article
AD-O53.2-a novel recombinant fusion protein combining the activities of TRAIL/Apo2L and Smac/Diablo, overcomes resistance of human cancer cells to TRAIL/Apo2L.
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- Investigational New Drugs, 2014, v. 32, n. 6, p. 1155, doi. 10.1007/s10637-014-0153-y
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- Article
Correction: Serwotka-Suszczak, A. M. et al. A Conjugate Based on Anti-HER2 Diaffibody and Auristatin E Targets HER2-Positive Cancer Cells. Int. J. Mol. Sci. 2017, 18, 401.
- Published in:
- 2018
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- Correction Notice
A Conjugate Based on Anti-HER2 Diaffibody and Auristatin E Targets HER2-Positive Cancer Cells.
- Published in:
- International Journal of Molecular Sciences, 2017, v. 18, n. 2, p. 401, doi. 10.3390/ijms18020401
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- Article
Novel engineered TRAIL‐based chimeric protein strongly inhibits tumor growth and bypasses TRAIL resistance.
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- International Journal of Cancer, 2020, v. 147, n. 4, p. 1117, doi. 10.1002/ijc.32845
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- Article