Found: 23
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Application of temperature-responsive HIS-tag fluorophores to differential scanning fluorimetry screening of small molecule libraries.
- Published in:
- Frontiers in Pharmacology, 2022, v. 13, p. 1, doi. 10.3389/fphar.2022.1040039
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- Publication type:
- Article
Inhibition of YAP/TAZ-driven TEAD activity prevents growth of NF2-null schwannoma and meningioma.
- Published in:
- Brain: A Journal of Neurology, 2023, v. 146, n. 4, p. 1697, doi. 10.1093/brain/awac342
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- Article
KDM5 histone demethylases repress immune response via suppression of STING.
- Published in:
- PLoS Biology, 2018, v. 16, n. 8, p. 1, doi. 10.1371/journal.pbio.2006134
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- Article
Selective inhibition of 12-lipoxygenase protects islets and beta cells from inflammatory cytokine-mediated beta cell dysfunction.
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- Diabetologia, 2015, v. 58, n. 3, p. 549, doi. 10.1007/s00125-014-3452-0
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- Article
Auranofin targets UBA1 and enhances UBA1 activity by facilitating ubiquitin trans-thioesterification to E2 ubiquitin-conjugating enzymes.
- Published in:
- Nature Communications, 2023, v. 14, n. 1, p. 1, doi. 10.1038/s41467-023-40537-x
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- Article
Discovery of a Novel Dual Fungal CYP51/Human 5-Lipoxygenase Inhibitor: Implications for Anti-Fungal Therapy.
- Published in:
- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0065928
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- Article
Quantitative High-Throughput Screening Identifies 8-Hydroxyquinolines as Cell-Active Histone Demethylase Inhibitors.
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- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0015535
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- Article
Histone Demethylase KDM5B as a Therapeutic Target for Cancer Therapy.
- Published in:
- Cancers, 2020, v. 12, n. 8, p. 2121, doi. 10.3390/cancers12082121
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- Publication type:
- Article
A Novel 2-Carbon-Linked Dimeric Artemisinin With Potent Antileukemic Activity and Favorable Pharmacology.
- Published in:
- Frontiers in Oncology, 2022, v. 11, p. 1, doi. 10.3389/fonc.2021.790037
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- Publication type:
- Article
A 12‐lipoxygenase‐Gpr31 signaling axis is required for pancreatic organogenesis in the zebrafish.
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- FASEB Journal, 2020, v. 34, n. 11, p. 14850, doi. 10.1096/fj.201902308RR
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- Article
Suppression of the FOXM1 transcriptional programme via novel small molecule inhibition.
- Published in:
- Nature Communications, 2014, v. 5, n. 11, p. 5165, doi. 10.1038/ncomms6165
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- Publication type:
- Article
A Genome-Edited ERα-HiBiT Fusion Reporter Cell Line for the Identification of ERα Modulators Via High-Throughput Screening and CETSA.
- Published in:
- Assay & Drug Development Technologies, 2021, v. 19, n. 8, p. 539, doi. 10.1089/adt.2021.059
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- Publication type:
- Article
A 1,536-Well-Based Kinetic HTS Assay for Inhibitors of Schistosoma mansoniThioredoxin Glutathione Reductase.
- Published in:
- Assay & Drug Development Technologies, 2008, v. 6, n. 4, p. 551, doi. 10.1089/adt.2008.149
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- Publication type:
- Article
ART714 is a best-in-class antileukemic 2-carbon-linked dimeric artemisinin derivative.
- Published in:
- Cancer Chemotherapy & Pharmacology, 2023, v. 92, n. 1, p. 39, doi. 10.1007/s00280-023-04539-2
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- Publication type:
- Article
XBP1 variant 1 promotes mitosis of cancer cells involving upregulation of the polyglutamylase TTLL6.
- Published in:
- Human Molecular Genetics, 2022, v. 31, n. 15, p. 2639, doi. 10.1093/hmg/ddac010
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- Article
Targeting the JMJD2 Histone Demethylases to Epigenetically Control Herpesvirus Infection and Reactivation from Latency.
- Published in:
- Science Translational Medicine, 2013, v. 5, n. 167, p. 1, doi. 10.1126/scitranslmed.3005145
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- Article
Correction: A High-Throughput Screen Identifies 2,9-Diazaspiro[5.5]Undecanes as Inducers of the Endoplasmic Reticulum Stress Response with Cytotoxic Activity in 3D Glioma Cell Models.
- Published in:
- 2016
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- Publication type:
- Correction Notice
A High-Throughput Screen Identifies 2,9-Diazaspiro[5.5]Undecanes as Inducers of the Endoplasmic Reticulum Stress Response with Cytotoxic Activity in 3D Glioma Cell Models.
- Published in:
- PLoS ONE, 2016, v. 11, n. 8, p. 1, doi. 10.1371/journal.pone.0161486
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- Publication type:
- Article
Short Report: In vitro Screening of Compounds against Laboratory and Field Isolates of Human Hookworm Reveals Quantitative Differences in Anthelmintic Susceptibility.
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- American Journal of Tropical Medicine & Hygiene, 2014, v. 90, n. 1, p. 71, doi. 10.4269/ajtmh.12-0547
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- Publication type:
- Article
ALDH1A1 promotes PARP inhibitor resistance by enhancing retinoic acid receptor-mediated DNA polymerase θ expression.
- Published in:
- NPJ Precision Oncology, 2023, v. 7, n. 1, p. 1, doi. 10.1038/s41698-023-00411-x
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- Publication type:
- Article
A Cell-Permeable Ester Derivative of the JmjC Histone Demethylase Inhibitor IOX1.
- Published in:
- ChemMedChem, 2014, v. 9, n. 3, p. 566, doi. 10.1002/cmdc.201300428
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- Publication type:
- Article
Rilpivirine analogs potently inhibit drug-resistant HIV-1 mutants.
- Published in:
- Retrovirology, 2016, v. 13, p. 1, doi. 10.1186/s12977-016-0244-2
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- Publication type:
- Article
A comparison of the ability of rilpivirine (TMC278) and selected analogues to inhibit clinically relevant HIV-1 reverse transcriptase mutants.
- Published in:
- Retrovirology, 2012, v. 9, n. 1, p. 99, doi. 10.1186/1742-4690-9-99
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- Publication type:
- Article