about
Permuting the PGF Signature Motif Blocks both Archaeosortase-Dependent C-Terminal Cleavage and Prenyl Lipid Attachment for the Haloferax volcanii S-Layer GlycoproteinAnalyses of Histone Proteoforms Using Front-end Electron Transfer Dissociation-enabled Orbitrap Instruments.Low Resolution Data-Independent Acquisition in an LTQ-Orbitrap Allows for Simplified and Fully Untargeted Analysis of Histone Modifications.High resolution is not a strict requirement for characterization and quantification of histone post-translational modifications.Bottom-up and middle-down proteomics have comparable accuracies in defining histone post-translational modification relative abundance and stoichiometry.Sequential Window Acquisition of all Theoretical Mass Spectra (SWATH) Analysis for Characterization and Quantification of Histone Post-translational Modifications.Complete Workflow for Analysis of Histone Post-translational Modifications Using Bottom-up Mass Spectrometry: From Histone Extraction to Data AnalysisA Novel Quantitative Mass Spectrometry Platform for Determining Protein O-GlcNAcylation Dynamics.Identification and interrogation of combinatorial histone modifications.Metabolic labeling in middle-down proteomics allows for investigation of the dynamics of the histone code.Monitoring proteolytic processing events by quantitative mass spectrometry.Identification and Quantification of Histone PTMs Using High-Resolution Mass Spectrometry.PARP-1 Activation Requires Local Unfolding of an Autoinhibitory Domain.Rapid proteomic responses to a near-lethal heat stress in the salt marsh mussel Geukensia demissa.Hydrogen-Deuterium Exchange Coupled to Top- and Middle-Down Mass Spectrometry Reveals Histone Tail Dynamics before and after Nucleosome AssemblyLatitudinal variation in protein expression after heat stress in the salt marsh mussel Geukensia demissaRegulation of nuclear epigenome by mitochondrial DNA heteroplasmy
P50
Q27321892-57C3305E-B001-46D0-8C37-16981C7F6910Q30277719-713682BC-11C0-42C5-B7FD-0A4C6A9DE391Q31011752-BAB27997-5147-4CBF-A3E3-3AD233285185Q34669483-8D558F98-0F24-4BBF-B876-B919C1A8ADECQ35568158-8B0A7307-7F4C-4FFD-B40E-43046218B477Q36040391-5B5A0662-9B77-40EE-8AE9-B7A36AAEEEA6Q36048559-33C0BF17-7BA1-4915-A25B-3808E1510B3DQ37076909-78E3AE9F-B179-49D9-AA85-211E8333B5F0Q38175981-F354A982-D8A1-4B41-8436-F64F8F05AD4FQ38690638-6AA3933E-D70E-4F46-96D1-71FCE24F53BDQ41048038-F3BB61BE-D675-42BF-A4DC-D271713E9FD1Q41641594-FD47F817-D753-4A56-9D67-842BD6651398Q42095016-FD03E189-3FFF-4204-B83E-C0A34A246462Q46528509-27CD7AA7-2FAF-4B89-9564-ACDFC354471EQ57192811-01104296-A63F-4F9A-A661-B5151273D14DQ84236683-475461CA-0EF3-4111-8166-5188953550B4Q93115569-8E349E45-2F79-4A9F-8B40-2632C2419E0E
P50
description
investigador
@es
researcher
@en
wetenschapper
@nl
name
Kelly R Karch
@en
Kelly R Karch
@nl
type
label
Kelly R Karch
@en
Kelly R Karch
@nl
prefLabel
Kelly R Karch
@en
Kelly R Karch
@nl
P31
P496
0000-0002-6350-3217