about
Impact of notch signaling on inflammatory responses in cardiovascular disordersThe adaptor molecule Lnk negatively regulates tumor necrosis factor-alpha-dependent VCAM-1 expression in endothelial cells through inhibition of the ERK1 and -2 pathwaysAnti-adenovirus immune responses in rats are enhanced by interleukin 4 but not interleukin 10 produced by recombinant adenovirusAntigraft antibody-mediated expression of metalloproteinases on endothelial cells. Differential expression of TIMP-1 and ADAM-10 depends on antibody specificity and isotype.Notch2 signaling sensitizes endothelial cells to apoptosis by negatively regulating the key protective molecule survivin.HLA-E-restricted cross-recognition of allogeneic endothelial cells by CMV-associated CD8 T cells: a potential risk factor following transplantation.Extract from Mimosa pigra attenuates chronic experimental pulmonary hypertension.Bortezomib, C1-inhibitor and plasma exchange do not prolong the survival of multi-transgenic GalT-KO pig kidney xenografts in baboonsLNK (SH2B3) is a key regulator of integrin signaling in endothelial cells and targets α-parvin to control cell adhesion and migration.Differential sensitivity of endothelial cells of various species to apoptosis induced by gene transfer of Fas ligand: role of FLIP levels.Rapid selection of differentially expressed genes in TNF[alpha]-activated endothelial cells.Rabbit antithymocyte globulin-induced serum sickness disease and human kidney graft survival.Protection against hyperacute xenograft rejection of transgenic rat hearts expressing human decay accelerating factor (DAF) transplanted into primates.Early rise in circulating endothelial protein C receptor correlates with poor outcome in severe sepsisTribbles-1 as a novel biomarker of chronic antibody-mediated rejection.Long-term IgG response to porcine Neu5Gc antigens without transmission of PERV in burn patients treated with porcine skin xenografts.Transcriptional and posttranscriptional regulation of alpha 1,3-galactosyltransferase in activated endothelial cells results in decreased expression of Gal alpha 1,3Gal.Expression of MHC class I-related molecules MICA, HLA-E and EPCR shape endothelial cells with unique functions in innate and adaptive immunity.Pathogenesis of non-HLA antibodies in solid organ transplantation: Where do we stand?Endothelial cell activation and proliferation modulate NKG2D activity by regulating MICA expression and shedding.The C-type lectin-like receptor CLEC-1, expressed by myeloid cells and endothelial cells, is up-regulated by immunoregulatory mediators and moderates T cell activation.MICA Mutant A5.1 Influences BK Polyomavirus Reactivation and Associated Nephropathy After Kidney Transplantation.Cytomegalovirus-Infected Primary Endothelial Cells Trigger NKG2C+ Natural Killer Cells.Intracellular expression in pig cells of anti-alpha1,3galactosyltransferase single-chain FV antibodies reduces Gal alpha1,3Gal expression and inhibits cytotoxicity mediated by anti-Gal xenoantibodies.Cloned ovarian cells from sheep: Cholesterol dependency in progesterone synthesis.Protection of rat endothelial cells from primate complement-mediated lysis by expression of human CD59 and/or decay-accelerating factor.Advanced glycation inhibition and protection against endothelial dysfunction induced by coumarins and procyanidins from Mammea neurophylla.Notch signaling triggered via the ligand DLL4 impedes M2 macrophage differentiation and promotes their apoptosis.The disintegrin and metalloproteinase ADAM10 mediates a canonical Notch-dependent regulation of IL-6 through Dll4 in human endothelial cells.HCMV triggers frequent and persistent UL40-specific unconventional HLA-E-restricted CD8 T-cell responses with potential autologous and allogeneic peptide recognition.Elevated soluble Flt1 mediates an anti-angiogenic state in patients with ANCA-associated vasculitis.An early increase in endothelial protein C receptor is associated with excess mortality in pneumococcal pneumonia with septic shock in the ICUXenotransplantation of Galactosyl-Transferase Knockout, CD55, CD59, CD39, and Fucosyl-Transferase Transgenic Pig Kidneys Into BaboonsEarly induction of TIMP-1 in endothelial cells in response to human xenoreactive IgGAdenovirus-mediated gene transfer in rat liver of interleukin 4 but not interleukin 10 produces severe acute hepatitisXenoreactivity in the pig islet to human combination: feasibility of adenovirus-mediated gene transfer into pig islets[Rapid collection of swine lymphocyte subpopulations in large quantity]Assessment of hyperacute rejection in a rat-to-primate cardiac xenograft modelPermanent expression of human CD59 and/or decay-accelerating factor by rat endothelial cells confers protection from human complement-mediated lysisNon-HLA-type endothelial cell reactive alloantibodies in pre-transplant sera of kidney recipients trigger apoptosis
P50
Q26851816-C3AB9303-C25E-4AD6-824C-942B5FD60839Q28236956-DC93A91A-F66B-463C-A147-C5C46B4F2007Q28571536-FBA4EFE9-F07E-4FF1-B3B0-8F7D7EEFDAE0Q32069292-57806C7C-C9EF-479F-BC95-0AAD65EC3062Q33518506-BD46F8CD-1D8C-4E9E-9815-018F835618D3Q34506165-9B98A260-D13C-493F-94BD-3E07C87676F4Q34667266-7ADBDBA9-315F-40D3-AE4F-A1F56774C1E0Q35012361-4E2D0E7F-290F-4310-A368-0275A3984AA3Q35987858-216FF398-9805-4006-A3F7-144047B0FC3CQ36087917-015A31C2-E817-43C7-83BE-FE108F728741Q36088119-FBF6F635-F4F8-4110-B764-D65FC3A54725Q36335918-887B479A-8A3C-4275-90D0-57E799247F6CQ36438512-D62C78E5-2733-4E29-94A9-46B5BACB26F4Q36487830-AE0D7121-1188-4619-BE47-E2C084CBB731Q36677655-9A61E031-A416-4D72-8D80-2AEF6B5CE6FEQ37196570-D9A52C55-C9B0-4D7E-8416-E217AEFD029BQ38337401-723B5E6C-0A8F-47BC-B8F9-A396166F1392Q38750805-15C1D6EB-F0F0-4B45-8787-A9604DC89D75Q38847336-D41A6C90-30A6-4B29-9CC1-8CDA3B254871Q39125039-E7406D58-5C5F-47A2-8FE8-8A4ED7D2B5F7Q39814557-6652F062-ABFA-4C02-AA09-408B18D4B2B1Q40693315-23FD158F-E21C-4153-A295-F1A9D66CA82DQ40698451-290BED88-B552-43B2-B4FD-61DBC0D56023Q40985492-F8D4AD07-8E9A-4705-9D66-6F84A6B3B62DQ41734647-E4962D99-D750-4016-8430-9BDE678F7CDBQ44992535-C60FA1F1-9DC3-4E64-B6E3-98D54B4451BBQ46905750-A908658C-07DD-49EC-97F6-C62DF561EE96Q48268613-456125D2-B607-458A-B59D-FFA728BE7183Q54194488-CF1BF7F0-802E-4363-A327-605804735F42Q55002157-6922B4D3-196C-48D2-8815-B78243072B16Q55461384-E8EDC21C-5FA3-45B6-BB3D-2AA49BFDAB45Q57021510-FCE23016-F9F1-4E68-9B0F-BD31A205A5DCQ60405540-D498C061-3D12-44D0-B63B-ED6CD04D65E7Q62607159-A967E517-075C-434D-BEF6-58FAFFE7EF0CQ64382202-AEB07598-49E5-4831-B44C-951387E3ACADQ64382893-65674879-8BB4-4BE6-A9D9-1EF8FBFABF13Q69437348-C46DAC74-F2F1-4240-9AAD-7A506ED65083Q71075824-19B39E7A-384A-4012-A033-5691E8D442F0Q71678076-6FED573D-ABDD-4247-8415-1FBCF3835D17Q73041731-E57C95DB-7E47-4747-A441-3802EEB7623C
P50
description
researcher
@en
wetenschapper
@nl
name
Beatrice Charreau
@en
Charreau B
@ast
Charreau B
@nl
type
label
Beatrice Charreau
@en
Charreau B
@ast
Charreau B
@nl
altLabel
Charreau B
@en
prefLabel
Beatrice Charreau
@en
Charreau B
@ast
Charreau B
@nl
P106
P31
P496
0000-0001-5870-4615