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Targeting non-bromodomain chromatin readers.

  • Read more about Targeting non-bromodomain chromatin readers.

Regulation of DGKε Activity and Substrate Acyl Chain Specificity by Negatively Charged Phospholipids.

  • Read more about Regulation of DGKε Activity and Substrate Acyl Chain Specificity by Negatively Charged Phospholipids.

Quinazoline-based anti-virulence compounds selectively target Salmonella PhoP/PhoQ signal transduction system.

  • Read more about Quinazoline-based anti-virulence compounds selectively target Salmonella PhoP/PhoQ signal transduction system.

Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72.

  • Read more about Implementation of an antibody characterization procedure and application to the major ALS/FTD disease gene C9ORF72.

The C-Terminal Domains SnRK2 Box and ABA Box Have a Role in Sugarcane SnRK2s Auto-Activation and Activity.

  • Read more about The C-Terminal Domains SnRK2 Box and ABA Box Have a Role in Sugarcane SnRK2s Auto-Activation and Activity.

Structural basis for the recognition of non-methylated DNA by the CXXC domain.

  • Read more about Structural basis for the recognition of non-methylated DNA by the CXXC domain.

A structure-guided molecular chaperone approach for restoring the transcriptional activity of the p53 cancer mutant Y220C.

  • Read more about A structure-guided molecular chaperone approach for restoring the transcriptional activity of the p53 cancer mutant Y220C.

Lessons from LIMK1 enzymology and their impact on inhibitor design.

  • Read more about Lessons from LIMK1 enzymology and their impact on inhibitor design.

A chemical probe of CARM1 alters epigenetic plasticity against breast cancer cell invasion.

  • Read more about A chemical probe of CARM1 alters epigenetic plasticity against breast cancer cell invasion.

Aspartate/asparagine-β-hydroxylase crystal structures reveal an unexpected epidermal growth factor-like domain substrate disulfide pattern.

  • Read more about Aspartate/asparagine-β-hydroxylase crystal structures reveal an unexpected epidermal growth factor-like domain substrate disulfide pattern.

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