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Correction to: 2‑O, 3‑O desulfated heparin (ODSH) increases bacterial clearance and attenuates lung injury in cystic fibrosis by restoring HMGB1‑compromised macrophage function.
- Published in:
- 2021
- By:
- Publication type:
- Correction Notice
2-O, 3-O desulfated heparin (ODSH) increases bacterial clearance and attenuates lung injury in cystic fibrosis by restoring HMGB1-compromised macrophage function.
- Published in:
- Molecular Medicine, 2021, v. 27, n. 1, p. 1, doi. 10.1186/s10020-021-00334-y
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- Publication type:
- Article
Evaluation of Coumarin and Neoflavone Derivatives as HCV NS5 B Polymerase Inhibitors.
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- Chemical Biology & Drug Design, 2013, v. 81, n. 5, p. 607, doi. 10.1111/cbdd.12105
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- Publication type:
- Article
Design, Synthesis, and Evaluation of 2-(arylsulfonyl)oxiranes as Cell-permeable Covalent Inhibitors of Protein Tyrosine Phosphatases.
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- Chemical Biology & Drug Design, 2012, v. 80, n. 4, p. 489, doi. 10.1111/j.1747-0285.2012.01437.x
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- Publication type:
- Article
Design and Synthesis of N-Substituted Indazole-3-Carboxamides as Poly(ADP-ribose)polymerase-1 (PARP-1) Inhibitors<sup>†</sup>.
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- Chemical Biology & Drug Design, 2012, v. 79, n. 4, p. 488, doi. 10.1111/j.1747-0285.2011.01302.x
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- Publication type:
- Article
CoMSIA Study on Substituted Aryl Alkanoic Acid Analogs as GPR40 Agonists.
- Published in:
- Chemical Biology & Drug Design, 2011, v. 77, n. 5, p. 361, doi. 10.1111/j.1747-0285.2011.01112.x
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- Publication type:
- Article
Etodolac Thiosemicarbazides:A novel class of hepatitis C virus NS5B polymerase inhibitors.
- Published in:
- Marmara Pharmaceutical Journal, 2013, v. 17, n. 2, p. 138
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- Publication type:
- Article
Microwave assisted synthesis of some novel Flurbiprofen hydrazidehydrazones as anti-HCV NS5B and anticancer agents.
- Published in:
- Marmara Pharmaceutical Journal, 2013, v. 17, n. 1, p. 26
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- Publication type:
- Article
Identification and characterization of coumestans as novel HCV NS5B polymerase inhibitors.
- Published in:
- Nucleic Acids Research, 2008, v. 36, n. 5, p. 1482, doi. 10.1093/nar/gkm1178
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- Publication type:
- Article
Thiazole-valine peptidomimetic (TTT-28) antagonizes multidrug resistance in vitro and in vivo by selectively inhibiting the efflux activity of ABCB1.
- Published in:
- Scientific Reports, 2017, p. 42106, doi. 10.1038/srep42106
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- Publication type:
- Article
Bafetinib (INNO-406) reverses multidrug resistance by inhibiting the efflux function of ABCB1 and ABCG2 transporters.
- Published in:
- Scientific Reports, 2016, p. 25694, doi. 10.1038/srep25694
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- Publication type:
- Article
Multiple Transport-Active Binding Sites Are Available for a Single Substrate on Human P-Glycoprotein (ABCB1).
- Published in:
- PLoS ONE, 2013, v. 8, n. 12, p. 1, doi. 10.1371/journal.pone.0082463
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- Publication type:
- Article
BIRB796, the Inhibitor of p38 Mitogen-Activated Protein Kinase, Enhances the Efficacy of Chemotherapeutic Agents in ABCB1 Overexpression Cells.
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- PLoS ONE, 2013, v. 8, n. 1, p. 1, doi. 10.1371/journal.pone.0054181
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- Publication type:
- Article
The Phosphodiesterase-5 Inhibitor Vardenafil Is a Potent Inhibitor of ABCB1/P-Glycoprotein Transporter.
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- PLoS ONE, 2011, v. 6, n. 4, p. 1, doi. 10.1371/journal.pone.0019329
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- Publication type:
- Article
A single deletion at position 134, 135, or 136 in the beta 7-beta 8 loop of the p51 subunit of HIV-1 RT disrupts the formation of heterodimeric enzyme.
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- Journal of Cellular Biochemistry, 2010, v. 109, n. 3, p. 598, doi. 10.1002/jcb.22439
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- Publication type:
- Article
Lamellarin O, a Pyrrole Alkaloid from an Australian Marine Sponge, Ianthella sp., Reverses BCRP Mediated Drug Resistance in Cancer Cells.
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- Marine Drugs, 2014, v. 12, n. 7, p. 3818, doi. 10.3390/md12073818
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- Publication type:
- Article
Design, Synthesis, and Biological Evaluation of ( S)-Valine Thiazole-Derived Cyclic and Noncyclic Peptidomimetic Oligomers as Modulators of Human P-Glycoprotein (ABCB1).
- Published in:
- ChemBioChem, 2014, v. 15, n. 1, p. 157, doi. 10.1002/cbic.201300565
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- Publication type:
- Article
Novel 4-Thiazolidinones as Non-Nucleoside Inhibitors of Hepatitis C Virus NS5B RNA-Dependent RNA Polymerase.
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- Archiv der Pharmazie, 2015, v. 348, n. 1, p. 10, doi. 10.1002/ardp.201400247
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- Publication type:
- Article
Some Hydrazones of 2-Aroylamino-3-methylbutanohydrazide: Synthesis, Molecular Modeling Studies, and Identification as Stereoselective Inhibitors of HIV-1.
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- Archiv der Pharmazie, 2013, v. 346, n. 2, p. 140, doi. 10.1002/ardp.201200311
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- Publication type:
- Article
Nek2 Kinase Signaling in Malaria, Bone, Immune and Kidney Disorders to Metastatic Cancers and Drug Resistance: Progress on Nek2 Inhibitor Development.
- Published in:
- Molecules, 2022, v. 27, n. 2, p. 347, doi. 10.3390/molecules27020347
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- Publication type:
- Article
Destabilization of tRNA3Lys from the primer-binding site of HIV-1 genome by anti-A loop polyamide nucleotide analog.
- Published in:
- Nucleic Acids Research, 2001, v. 29, n. 24, p. 5099, doi. 10.1093/nar/29.24.5099
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- Publication type:
- Article
Small molecule inhibitors of Nek2 kinase using a whole animal Nek2 overexpression model.
- Published in:
- FASEB Journal, 2022, v. 36, p. N.PAG, doi. 10.1096/fasebj.2022.36.S1.L7836
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- Publication type:
- Article
Anti‐cancer Effects of Dual‐action Inhibitors of Nek2 and EGFR Kinases: Investigation of Synergy.
- Published in:
- FASEB Journal, 2022, v. 36, p. N.PAG, doi. 10.1096/fasebj.2022.36.S1.L7801
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- Publication type:
- Article
ARRY-334543 Reverses Multidrug Resistance by Antagonizing the Activity of ATP-Binding Cassette Subfamily G Member 2.
- Published in:
- Journal of Cellular Biochemistry, 2014, v. 115, n. 8, p. 1381, doi. 10.1002/jcb.24787
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- Publication type:
- Article
Novel modifications of PARP inhibitor veliparib increase PARP1 binding to DNA breaks.
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- Biochemical Journal, 2024, v. 481, n. 6, p. 437, doi. 10.1042/BCJ20230406
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- Publication type:
- Article
Structure-based CoMFA and CoMSIA study of indolinone inhibitors of PDK1.
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- Journal of Computer-Aided Molecular Design, 2009, v. 23, n. 1, p. 25, doi. 10.1007/s10822-008-9235-2
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- Publication type:
- Article
Saracatinib (AZD0530) is a potent modulator of ABCB1-mediated multidrug resistance in vitro and in vivo.
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- International Journal of Cancer, 2013, v. 132, n. 1, p. 224, doi. 10.1002/ijc.27649
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- Publication type:
- Article
In Vitro Antibacterial Activity of Rhodanine Derivatives against Pathogenic Clinical Isolates.
- Published in:
- PLoS ONE, 2016, v. 11, n. 10, p. 1, doi. 10.1371/journal.pone.0164227
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- Publication type:
- Article
Synthesis and Characterization of Celecoxib Derivatives as Possible Anti-Inflammatory, Analgesic, Antioxidant, Anticancer and Anti-HCV Agents.
- Published in:
- Molecules, 2013, v. 18, n. 3, p. 3595, doi. 10.3390/molecules18033595
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- Publication type:
- Article
WHI-P154 enhances the chemotherapeutic effect of anticancer agents in ABCG2-overexpressing cells.
- Published in:
- Cancer Science, 2014, v. 105, n. 8, p. 1071, doi. 10.1111/cas.12462
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- Publication type:
- Article