about
TI-VAMP/VAMP7 is required for optimal phagocytosis of opsonised particles in macrophagesEndosomal WASH and exocyst complexes control exocytosis of MT1-MMP at invadopodia.A WASp-VASP complex regulates actin polymerization at the plasma membrane.ARF6-JIP3/4 regulate endosomal tubules for MT1-MMP exocytosis in cancer invasion.αTAT1 catalyses microtubule acetylation at clathrin-coated pits.Golgi-localized GAP for Cdc42 functions downstream of ARF1 to control Arp2/3 complex and F-actin dynamicsDifferential properties of D4/LyGDI versus RhoGDI: phosphorylation and rho GTPase selectivityMembrane trafficking. Nucleoside diphosphate kinases fuel dynamin superfamily proteins with GTP for membrane remodelingARF proteins: roles in membrane traffic and beyondARF1-mediated actin polymerization produces movement of artificial vesicles.Control of MT1-MMP transport by atypical PKC during breast-cancer progression.Regulated delivery of molecular cargo to invasive tumour-derived microvesiclesProtein interaction mapping: a Drosophila case study.[An array of microfabricated pillars to study cell migration].Molecular cloning of YPT1/SEC4-related cDNAs from an epithelial cell lineThe advantage of channeling nucleotides for very processive functionsCdc42 localization and cell polarity depend on membrane trafficSegment-specific expression of a zinc-finger gene in the developing nervous system of the mouse.Signaling and membrane dynamics during phagocytosis: many roads lead to the phagos(R)ome.AP-1 and ARF1 control endosomal dynamics at sites of FcR mediated phagocytosis.ADP ribosylation factor 6 is activated and controls membrane delivery during phagocytosis in macrophages.Impaired PRC2 activity promotes transcriptional instability and favors breast tumorigenesisAMOTL1 Promotes Breast Cancer Progression and Is Antagonized by MerlinLIN7A is a major determinant of cell-polarity defects in breast carcinomasThe interaction of IQGAP1 with the exocyst complex is required for tumor cell invasion downstream of Cdc42 and RhoA.Cytokinesis arrest and redistribution of actin-cytoskeleton regulatory components in cells expressing the Rho GTPase CDC42Hs.LIMK Regulates Tumor-Cell Invasion and Matrix Degradation Through Tyrosine Phosphorylation of MT1-MMP.RAB2A controls MT1-MMP endocytic and E-cadherin polarized Golgi trafficking to promote invasive breast cancer programs.Endocytic traffic in animal cell cytokinesis.Matrix invasion by tumour cells: a focus on MT1-MMP trafficking to invadopodia.Toward a structural understanding of arf family:effector specificity.Cell polarity during motile processes: keeping on track with the exocyst complex.p63/MT1-MMP axis is required for in situ to invasive transition in basal-like breast cancer.Cellular and Molecular Mechanisms of MT1-MMP-Dependent Cancer Cell Invasion.ATAT1/MEC-17 acetyltransferase and HDAC6 deacetylase control a balance of acetylation of alpha-tubulin and cortactin and regulate MT1-MMP trafficking and breast tumor cell invasion.Implication of metastasis suppressor NM23-H1 in maintaining adherens junctions and limiting the invasive potential of human cancer cells.MT1-MMP-dependent invasion is regulated by TI-VAMP/VAMP7.A role for mammalian diaphanous-related formins in complement receptor (CR3)-mediated phagocytosis in macrophages.An immunologist's look at the Rho and Rab GTP-binding proteins.The N-terminal domain of a rab protein is involved in membrane-membrane recognition and/or fusion.
P50
Q24306564-A17F296E-A4D6-43CE-8EB6-FA1BBC85A1AAQ24313584-3BF93946-E565-40CA-A147-E1E9FDA89754Q24535834-1F5DB33A-D493-4E38-AD1C-59EA85E3F080Q27309213-FE747F86-E419-4BC3-9862-211A7AF357F9Q28000142-5352F4C3-934D-488E-8C22-3D4F09E8AB63Q28241896-BE2F4B03-7CCF-4150-B1FF-4E62894E6A14Q28263808-1002B2C3-2977-42B5-B9F9-70B1E10D423DQ28390881-031F7AC1-A14D-4098-8566-202F1218377FQ29618078-ACE50085-D2EC-4AD0-80B0-289C33F06A08Q30480259-36C12F8A-7D1F-4301-93DB-137AFDDAAC57Q30577989-E1B8CEB4-EF24-41D7-8082-4C1543D648FEQ30657298-93E60689-9250-4450-B0F2-D045B8F834C9Q33211911-FF4E94D7-547B-412B-80CF-5345506CD616Q33222094-50AD838D-CCA5-49A2-AF31-06A4A6FA068CQ33792963-8C8F672E-EAB2-4D07-B764-DC113769342BQ33806597-68154F5F-11EE-43D2-AB3F-92B47E22569FQ34439671-CA81AD5D-0EEC-4185-8581-165B0EC158FAQ34561526-DA1416F4-21D2-41F6-ABE4-D820206AAC65Q35840137-AC26F6C5-12B9-4720-8DD3-5755E4C85A60Q36173885-665FF30E-03B2-43A0-921A-501F6878604AQ36323565-A40B93AA-CFB5-4EF2-93CD-358834FB91F9Q36424889-44AA2D8A-47A6-4983-9382-1CC8337BE465Q36527910-CC3C3BB7-1173-479F-A6BB-1629450C1A9FQ36588092-94CB35BB-07B3-462E-B9C2-28F536DC5545Q36718374-2F93EDE3-9986-4FE2-90BE-A446C6475CDDQ36823371-2F4BFDB7-9DE1-490E-B139-10B795EF2B6FQ36841533-43442AFD-A538-460D-84BC-A8DA1BCF1C04Q37061758-A18BB9AE-DA61-4472-ABF8-FA3866C4436FQ37160165-CE4B9C0F-CEA1-4938-8B33-1BD90D324071Q37582684-19414F46-3067-4751-8EAF-1972726C0799Q37816647-5879C302-C55A-43DC-B1D4-442CFFEFBE18Q37828620-D7A3AE5F-CE67-45B7-B528-086F36153C19Q38884681-44101EA2-E0C5-49FB-BCEC-CBB2ECA10DCBQ38921801-E17A9427-9804-41FA-A5F3-D806489BECEDQ39295604-8D396619-B7DA-40F5-95A6-B11D31950F0FQ39655946-96423BE6-9101-47B5-8DDA-870DD86BA59EQ39969514-38F842A9-B556-43C8-ABF6-59A727AFEDE3Q40348488-4FE5BCFE-AC0D-414D-9FDC-5B705B46302CQ40769606-EED14326-B5D5-437D-953C-96F945B4264BQ40790386-155AD0E2-2571-443E-9FCE-B3A01184A37F
P50
description
researcher ORCID ID = 0000-0002-7351-733X
@en
wetenschapper
@nl
name
Philippe Chavrier
@ast
Philippe Chavrier
@en
Philippe Chavrier
@es
Philippe Chavrier
@nl
type
label
Philippe Chavrier
@ast
Philippe Chavrier
@en
Philippe Chavrier
@es
Philippe Chavrier
@nl
prefLabel
Philippe Chavrier
@ast
Philippe Chavrier
@en
Philippe Chavrier
@es
Philippe Chavrier
@nl
P106
P31
P496
0000-0002-7351-733X