Works matching AU Salah, Eidarus
Results: 21
JmjC catalysed histone H2a N-methyl arginine demethylation and C4-arginine hydroxylation reveals importance of sequence-reactivity relationships.
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- Communications Biology, 2024, v. 7, n. 1, p. 1, doi. 10.1038/s42003-024-07183-5
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- Article
Innenrücktitelbild: A Small‐Molecule Inhibitor of Factor Inhibiting HIF Binding to a Tyrosine‐Flip Pocket for the Treatment of Obesity (Angew. Chem. 40/2024).
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- Angewandte Chemie, 2024, v. 136, n. 40, p. 1, doi. 10.1002/ange.202414504
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- Article
A Small‐Molecule Inhibitor of Factor Inhibiting HIF Binding to a Tyrosine‐Flip Pocket for the Treatment of Obesity.
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- Angewandte Chemie, 2024, v. 136, n. 40, p. 1, doi. 10.1002/ange.202410438
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- Article
Conformational plasticity of the ULK3 kinase domain.
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- Biochemical Journal, 2021, v. 478, n. 14, p. 2811, doi. 10.1042/BCJ20210257
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- Article
Lessons from LIMK1 enzymology and their impact on inhibitor design.
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- Biochemical Journal, 2019, v. 476, n. 21, p. 3197, doi. 10.1042/BCJ20190517
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- Article
The catalytic domains of all human KDM5 JmjC demethylases catalyse N‐methyl arginine demethylation.
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- FEBS Letters, 2023, v. 597, n. 7, p. 933, doi. 10.1002/1873-3468.14586
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- Article
Stereospecific targeting of MTH1 by (S)-crizotinib as an anticancer strategy.
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- Nature, 2014, v. 508, n. 7495, p. 222, doi. 10.1038/nature13194
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- Article
2-Oxoglutarate derivatives can selectively enhance or inhibit the activity of human oxygenases.
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- Nature Communications, 2021, v. 12, n. 1, p. 1, doi. 10.1038/s41467-021-26673-2
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- Article
Inside Back Cover: A Small‐Molecule Inhibitor of Factor Inhibiting HIF Binding to a Tyrosine‐Flip Pocket for the Treatment of Obesity (Angew. Chem. Int. Ed. 40/2024).
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- Angewandte Chemie International Edition, 2024, v. 63, n. 40, p. 1, doi. 10.1002/anie.202414504
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- Article
A Small‐Molecule Inhibitor of Factor Inhibiting HIF Binding to a Tyrosine‐Flip Pocket for the Treatment of Obesity.
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- Angewandte Chemie International Edition, 2024, v. 63, n. 40, p. 1, doi. 10.1002/anie.202410438
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- Article
Structure of the CaMKIIδ/Calmodulin Complex Reveals the Molecular Mechanism of CaMKII Kinase Activation.
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- PLoS Biology, 2010, v. 8, n. 7, p. 1, doi. 10.1371/journal.pbio.1000426
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- Article
Crystallographic and Selectivity Studies on the Approved HIF Prolyl Hydroxylase Inhibitors Desidustat and Enarodustat.
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- ChemMedChem, 2024, v. 19, n. 24, p. 1, doi. 10.1002/cmdc.202400504
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- Article
Structure‐Activity Studies Reveal Scope for Optimisation of Ebselen‐Type Inhibition of SARS‐CoV‐2 Main Protease.
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- ChemMedChem, 2022, v. 17, n. 4, p. 1, doi. 10.1002/cmdc.202100582
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- Article
Synthesis of Novel Pyridine‐Carboxylates as Small‐Molecule Inhibitors of Human Aspartate/Asparagine‐β‐Hydroxylase.
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- ChemMedChem, 2020, v. 15, n. 13, p. 1139, doi. 10.1002/cmdc.202000147
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- Article
Cyclic β²,³-amino acids improve the serum stability of macrocyclic peptide inhibitors targeting the SARS-CoV-2 main protease.
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- Bulletin of the Chemical Society of Japan, 2024, v. 97, n. 5, p. 1, doi. 10.1093/bulcsj/uoae018
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Formaldehyde reacts with N-terminal proline residues to give bicyclic aminals.
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- Communications Chemistry, 2023, v. 6, n. 1, p. 1, doi. 10.1038/s42004-022-00801-5
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- Article
Reading and erasing of the phosphonium analogue of trimethyllysine by epigenetic proteins.
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- Communications Chemistry, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42004-022-00640-4
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- Article
Reading and erasing of the phosphonium analogue of trimethyllysine by epigenetic proteins.
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- Communications Chemistry, 2022, v. 5, n. 1, p. 1, doi. 10.1038/s42004-022-00640-4
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- Article
Quality control in oocytes by p63 is based on a spring-loaded activation mechanism on the molecular and cellular level.
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- eLife, 2016, p. 1, doi. 10.7554/eLife.13909
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Comprehensive characterization of the Published Kinase Inhibitor Set.
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- Nature Biotechnology, 2016, v. 34, n. 1, p. 95, doi. 10.1038/nbt.3374
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- Article
Substrate selectivity and inhibition of the human lysyl hydroxylase JMJD7.
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- Protein Science: A Publication of the Protein Society, 2024, v. 33, n. 10, p. 1, doi. 10.1002/pro.5162
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- Article