about
T-cell-expressed proprotein convertase furin is essential for maintenance of peripheral immune toleranceThe lifestyle of naturally occurring CD4+ CD25+ Foxp3+ regulatory T cellsIL-1β promotes Th17 differentiation by inducing alternative splicing of FOXP3.Deletion of Wiskott-Aldrich syndrome protein triggers Rac2 activity and increased cross-presentation by dendritic cells.IL-2 in the tumor microenvironment is necessary for Wiskott-Aldrich syndrome protein deficient NK cells to respond to tumors in vivo.The critical contribution of TGF-beta to the induction of Foxp3 expression and regulatory T cell functionGARP (LRRC32) is essential for the surface expression of latent TGF-beta on platelets and activated FOXP3+ regulatory T cellsTGF-β Affects the Differentiation of Human GM-CSF+ CD4+ T Cells in an Activation- and Sodium-Dependent MannerRegulation of Subunit-Specific Germinal Center B Cell Responses to the HIV-1 Envelope Glycoproteins by Antibody-Mediated Feedback.Foxp3 lacking exons 2 and 7 is unable to confer suppressive ability to regulatory T cells in vivo.Distinct subsets of FoxP3+ regulatory T cells participate in the control of immune responses.Zoledronic acid inhibits NFAT and IL-2 signaling pathways in regulatory T cells and diminishes their suppressive function in patients with metastatic cancer.Guidance Molecule SEMA3A Restricts Tumor Growth by Differentially Regulating the Proliferation of Tumor-Associated Macrophages.Chronic murine Chagas' disease: the impact of host and parasite genotypes.Microglia Induce PDGFRB Expression in Glioma Cells to Enhance Their Migratory CapacityCCR2 upregulated on peripheral T cells in osteoarthritis but not in bone marrowRole of IFN-alpha/beta and IL-12 in the activation of natural killer cells and interferon-gamma production during experimental infection with Trypanosoma cruziCBA/J mice infected with Trypanosoma cruzi: an experimental model for inflammatory myopathiesEnhancement of natural killer (NK) cell cytotoxicity and induction of NK cell-derived interferon-gamma (IFN-gamma) display different kinetics during experimental infection with Trypanosoma cruziAlternative splicing, FOXP3 and cardiovascular diseaseCD4+CD25+ regulatory T cells are activated in vivo by recognition of selfRole of TGF-Beta in the induction of Foxp3 expression and T regulatory cell functionImmunotherapy with tolerogenic apolipoprotein B-100-loaded dendritic cells attenuates atherosclerosis in hypercholesterolemic miceImmunological profiling of haemodialysis patients and young healthy individuals with implications for clinical regulatory T cell sortingAlternative Splicing of FOXP3 Controls Regulatory T Cell Effector Functions and Is Associated With Human Atherosclerotic Plaque StabilityAn intronic deletion in megakaryoblastic leukemia 1 is associated with hyperproliferation of B cells in triplets with Hodgkin lymphomaPeripheral immune biomarkers and neurodegenerative diseases: A prospective cohort study with 20 years of follow-upMulti-faceted inhibition of dendritic cell function by CD4+Foxp3+ regulatory T cellsCD73 immune checkpoint defines regulatory NK cells within the tumor microenvironmentThe FOXP3Δ2 isoform supports Treg cell development and protects against severe IPEX syndrome
P50
Q24656282-4780760D-06D6-4CD4-992D-FA65E145AEA2Q28257250-BF390F69-AB32-4FC4-9E68-0FF47F9DD5C1Q36123262-9F503A04-BD2F-4B6E-BE23-8A0C8EE5FE0AQ37124582-D6822339-C2FA-4CFB-A580-70B617C6A50AQ37141296-88195022-C98B-4120-8BDE-C1294024C53EQ37143002-225A59F1-6934-4BA5-8123-891F1AE82570Q37304003-5DD355F6-73F6-4B38-8FBD-472BA3747D69Q37528532-E89A00F3-03E9-421B-BF1F-EEDEE53275C1Q38656764-61459846-9FE9-4CBC-8763-0C24867ACB60Q50579205-ADCA41AC-F989-428D-BA00-722F1E999D9FQ51975118-39968358-23DE-4262-A9A8-7B392F1EABD5Q52755645-E66A4F11-0955-45DE-9161-E94D82C4B709Q53096435-DD7E5692-6EB1-4C0A-BEAA-10A7C37A32B5Q53937261-EC85DD0B-FFC9-4D16-BC9D-2914FAE53F1AQ58121730-9E3D98F6-9B31-477A-A4F4-DF4C37576EFDQ58580879-6610D15D-1A98-459B-B99D-330A98B176EAQ58845879-9D2F2834-F14F-4CF2-90E6-F8F382631D83Q58846008-03007340-255B-4C65-B73F-892824995A87Q58846725-6B96FA80-C27E-4CDC-8BC0-B67BF429ECBFQ64117728-20BEA96C-3924-4395-A0A5-629AA1ACD5EBQ79974095-47980B4D-8EFD-4DF2-B257-2FF77319AC80Q82037277-D03F56DE-4AAA-4F96-9A01-3C691587A496Q83491273-034944A3-DBF3-4D55-B95E-5DCBA699B9CBQ86863525-E085A443-E94A-4B29-8C83-A4A89EEF2EEEQ88268327-280F5E47-4AC5-4841-B7FD-8E993FDFE0A4Q90466654-385AA020-82C2-4AE5-A432-A6CCED1E9728Q90659345-3A665B88-621D-42D1-BFF8-706B5420620FQ90927914-E2B8AA4E-9E81-4BE1-BF8A-2A428DB04395Q91463459-140028AD-4937-4844-9CC2-4075B8A0D14BQ92573928-CBBB962A-079F-446B-80D4-8301CCB2AAB5
P50
description
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
John Andersson
@ast
John Andersson
@en
John Andersson
@es
John Andersson
@nl
John Andersson
@sl
type
label
John Andersson
@ast
John Andersson
@en
John Andersson
@es
John Andersson
@nl
John Andersson
@sl
prefLabel
John Andersson
@ast
John Andersson
@en
John Andersson
@es
John Andersson
@nl
John Andersson
@sl
P106
P1153
14047763900
P31
P496
0000-0003-2799-6349