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1. Bioinspired Asymmetric Total Synthesis of Emeriones A–C**

6. Low level of antioxidant capacity biomarkers but not target overexpression predicts vulnerability to ROS-inducing drugs

7. A trypanosome-derived immunotherapeutics platform elicits potent high-affinity antibodies, negating the effects of the synthetic opioid fentanyl

8. Target deconvolution of HDAC pharmacopoeia reveals MBLAC2 as common off-target

11. Decrypting lysine deacetylase inhibitor action and protein modifications by dose-resolved proteomics

13. Author Correction: Target deconvolution of HDAC pharmacopoeia reveals MBLAC2 as common off-target

18. Low level of antioxidant capacity biomarkers but not target overexpression predicts vulnerability to ROS-inducing drugs

22. Aza-SAHA Derivatives Are Selective Histone Deacetylase 10 Chemical Probes That Inhibit Polyamine Deacetylation and Phenocopy HDAC10 Knockout

23. Hydropersulfides inhibit lipid peroxidation and ferroptosis by scavenging radicals

24. Regulation of mitochondrial morphology and function by stearoylation of TFR1

25. Chemoproteomic target deconvolution reveals Histone Deacetylases as targets of (R)-lipoic acid.

28. First Fluorescent Acetylspermidine Deacetylation Assay for HDAC10 Identifies Selective Inhibitors with Cellular Target Engagement**

30. An Epitope-Focused Trypanosome-Derived Vaccine Platform Elicits High-Affinity Antibodies and Immunity Against Fentanyl Effects

33. Aza-SAHA Derivatives are Selective Histone Deacetylase 10 Chemical Probes That Inhibit Polyamine Deacetylation

39. First Fluorescent Acetylspermidine Deacetylation Assay for HDAC10 Identifies Inhibitors of Neuroblastoma Cell Colony Growth That Increase Lysosome Accumulation

41. Design and Synthesis of Dihydroxamic Acids as HDAC6/8/10 Inhibitors

46. Synthesis and Structure‐Activity Relationships of N ‐(4‐Benzamidino)‐Oxazolidinones: Potent and Selective Inhibitors of Kallikrein‐Related Peptidase 6

47. Selective Inhibition of Histone Deacetylase 10: Hydrogen Bonding to the Gatekeeper Residue is Implicated

50. Depsipeptides Featuring a Neutral P1 Are Potent Inhibitors of Kallikrein-Related Peptidase 6 with On-Target Cellular Activity

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