about
RAE-1, a novel PHR binding protein, is required for axon termination and synapse formation in Caenorhabditis elegansIdentification of biologic markers of the premature rupture of fetal membranes: proteomic approachComparative large scale characterization of plant versus mammal proteins reveals similar and idiosyncratic N-α-acetylation featuresBlebs produced by actin-myosin contraction during apoptosis release damage-associated molecular pattern proteins before secondary necrosis occursRPM-1 uses both ubiquitin ligase and phosphatase-based mechanisms to regulate DLK-1 during neuronal developmentHydrogen/deuterium exchange for higher specificity of protein identification by peptide mass fingerprinting.Enhanced protein recovery after electrotransfer using square wave alternating voltage.FindPept, a tool to identify unmatched masses in peptide mass fingerprinting protein identification.Cell fate decisions are specified by the dynamic ERK interactome.Downregulation of N-terminal acetylation triggers ABA-mediated drought responses in ArabidopsisIdentification of protein interfaces between α-synuclein, the principal component of Lewy bodies in Parkinson disease, and the molecular chaperones human Hsc70 and the yeast Ssa1p.EnCOUNTer: a parsing tool to uncover the mature N-terminus of organelle-targeted proteins in complex samplesMolecular identification and functional characterization of the first Nα-acetyltransferase in plastids by global acetylome profiling.Extracellular signal-regulated kinase regulates RhoA activation and tumor cell plasticity by inhibiting guanine exchange factor H1 activity.MetAP1 and MetAP2 drive cell selectivity for a potent anti-cancer agent in synergy, by controlling glutathione redox state.Proteome-wide analysis of the amino terminal status of Escherichia coli proteins at the steady-state and upon deformylation inhibition.SILProNAQ: A Convenient Approach for Proteome-Wide Analysis of Protein N-Termini and N-Terminal Acetylation Quantitation.Precursor ion scans for the targeted detection of stable-isotope-labeled peptides.The C-terminal residue of phage Vp16 PDF, the smallest peptide deformylase, acts as an offset element locking the active conformation.Identification of new high mobility group A1 associated proteins.Identification of novel and cell type enriched cofactors of the transcription activation domain of RelA (p65 NF-kappaB).Two N-terminal acetyltransferases antagonistically regulate the stability of a nod-like receptor in Arabidopsis.Plasticity of protein expression during culture of fetal skin cells.Influence of various endogenous and artefact modifications on large-scale proteomics analysis.SLP-2 interacts with prohibitins in the mitochondrial inner membrane and contributes to their stability.Coomassie stains: are they really mass spectrometry compatible?C. elegans RPM-1 regulates axon termination and synaptogenesis through the Rab GEF GLO-4 and the Rab GTPase GLO-1.Dynamics of post-translational modifications and protein stability in the stroma of Chlamydomonas reinhardtii chloroplasts.Analysis of Proteomes Using the Molecular ScannerProteomics application exercise of the Swiss Proteomics Society: Report of the SPS'02 sessionA clinical molecular scanner to study human proteome complexityToward a Clinical Molecular Scanner for Proteome Research: Parallel Protein Chemical Processing before and during Western BlotStructural and genomic decoding of human and plant myristoylomes reveals a definitive recognition patternNatB-Mediated N-Terminal Acetylation Affects Growth and Biotic Stress Responses
P50
Q24305945-BE915EAC-C474-4EE7-BB40-ED9847CE93F6Q28202195-235B0A14-EB92-4058-BF13-D70BA130E22DQ28256849-C0708450-9130-46A9-B822-66BD76B8870CQ28293202-87A24FDC-B671-4189-B992-9B38BE1A9B64Q28538585-4433897F-B97C-48C4-A7E0-831B076C6390Q31040807-64FC5068-8508-4EA8-AF5B-DE17BA690D8CQ31105928-09BA3D2C-340F-4FD0-8F01-5CF21A15B2E1Q31118040-A0D5C767-A265-487F-B16B-7AA5C9147695Q35014377-930CAECE-4A95-4E8A-B270-65FBCB024ACCQ35932997-E0AB96E4-2D57-4981-B19F-F8B017E0466BQ36294832-ED88BB02-B128-4F72-9C2E-63D86E53CD6CQ36315224-9B37795F-D9C4-48BE-A730-917453DE65BFQ36406812-F8F2D00E-FB0E-4FC6-B1A3-8BDBDC2F43BCQ37336565-2ACBE4F1-C20D-44D8-B0D4-D266B5C11103Q37665317-2AE24B3F-2BCA-4D38-8584-3414CE88959BQ38410857-BFC54C06-50F1-4488-B726-D0A3A950E965Q38896692-69CDFC48-BF28-4EBF-9901-06E768E95012Q39785165-6E3ABDA2-C5E6-4EDB-8ABF-60EFC9043FFDQ40050039-05DA185C-D4F4-4626-B3D0-D069693CD940Q40078619-2BB3F065-4A91-43BF-9D87-C38A5AC34322Q40388061-287CD5C0-899C-4E9F-8734-AAEB6B65179DQ40947490-5D843173-EFB2-4E4D-B79A-1FCA9E72739FQ44411856-927B910F-8DC0-49D8-BA37-9949D50580FDQ44494834-00A6DD72-2553-411C-AA08-81B35BDD600EQ44889102-AAEEADB5-A9F5-4553-9A4D-384449013411Q46049268-B6409CBA-2B72-4F16-8E44-10212CDA5644Q46316719-92A2A926-F419-4D1F-B050-F3E4C1426F10Q53256611-BC9C800B-0AC8-4A20-A5C3-2C903E3F74C0Q57205835-56B284AB-CD8D-4B7A-97E5-9BDF64880E2FQ57325409-7DD6E04C-9845-4011-8F22-608E56ABCB07Q57325437-7D98A234-223F-4F41-BC2E-8D80657B52CBQ57325447-F3CC1CA1-8669-415E-8308-4C6731E0F679Q61136552-E4A319E0-AD1C-4677-B43A-E06BC9123CE4Q91344017-91ACBB8C-29BB-44D0-81E4-76B88316DEDF
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Willy Bienvenut
@ast
Willy Bienvenut
@en
Willy Bienvenut
@es
Willy Bienvenut
@nl
type
label
Willy Bienvenut
@ast
Willy Bienvenut
@en
Willy Bienvenut
@es
Willy Bienvenut
@nl
prefLabel
Willy Bienvenut
@ast
Willy Bienvenut
@en
Willy Bienvenut
@es
Willy Bienvenut
@nl
P106
P1153
6602835392
P21
P31
P496
0000-0003-4192-3920