about
sameAs
TMPRSS2 and ADAM17 cleave ACE2 differentially and only proteolysis by TMPRSS2 augments entry driven by the severe acute respiratory syndrome coronavirus spike proteinDifferential N-linked glycosylation of human immunodeficiency virus and Ebola virus envelope glycoproteins modulates interactions with DC-SIGN and DC-SIGNRHepatitis C virus glycoproteins interact with DC-SIGN and DC-SIGNRDC-SIGNR, a DC-SIGN homologue expressed in endothelial cells, binds to human and simian immunodeficiency viruses and activates infection in transDC-SIGN and CLEC-2 mediate human immunodeficiency virus type 1 capture by plateletsThe Role of Phlebovirus Glycoproteins in Viral Entry, Assembly and ReleaseDiscovery and optimization of a natural HIV-1 entry inhibitor targeting the gp41 fusion peptideThe role of DC-SIGN and DC-SIGNR in HIV and Ebola virus infection: can potential therapeutics block virus transmission and dissemination?Diversity of receptors binding HIV on dendritic cell subsetsNatural proteolytic processing of hemofiltrate CC chemokine 1 generates a potent CC chemokine receptor (CCR)1 and CCR5 agonist with anti-HIV propertiesFunctional comparison of mouse CIRE/mouse DC-SIGN and human DC-SIGNInfluenza and SARS-coronavirus activating proteases TMPRSS2 and HAT are expressed at multiple sites in human respiratory and gastrointestinal tractsProteolytic activation of the SARS-coronavirus spike protein: cutting enzymes at the cutting edge of antiviral research.Cellular entry of HIV: Evaluation of therapeutic targets.Tmprss2 is essential for influenza H1N1 virus pathogenesis in mice.Rhesus macaque IFITM3 gene polymorphisms and SIV infection.Inhibition of proprotein convertases abrogates processing of the middle eastern respiratory syndrome coronavirus spike protein in infected cells but does not reduce viral infectivity.DESC1 and MSPL activate influenza A viruses and emerging coronaviruses for host cell entry.Tetherin Sensitivity of Influenza A Viruses Is Strain Specific: Role of Hemagglutinin and Neuraminidase.pH Optimum of Hemagglutinin-Mediated Membrane Fusion Determines Sensitivity of Influenza A Viruses to the Interferon-Induced Antiviral State and IFITMs.A novel mechanism for LSECtin binding to Ebola virus surface glycoprotein through truncated glycans.Severe fever with thrombocytopenia virus glycoproteins are targeted by neutralizing antibodies and can use DC-SIGN as a receptor for pH-dependent entry into human and animal cell linesEvidence that Processing of the Severe Fever with Thrombocytopenia Syndrome Virus Gn/Gc Polyprotein Is Critical for Viral Infectivity and Requires an Internal Gc Signal Peptide.Differential downregulation of ACE2 by the spike proteins of severe acute respiratory syndrome coronavirus and human coronavirus NL63.Non-human primate orthologues of TMPRSS2 cleave and activate the influenza virus hemagglutinin.Simian immunodeficiency virus utilizes human and sooty mangabey but not rhesus macaque STRL33 for efficient entry.DC-SIGN interactions with human immunodeficiency virus type 1 and 2 and simian immunodeficiency virusHuman coronavirus NL63 employs the severe acute respiratory syndrome coronavirus receptor for cellular entry.Functional and antigenic characterization of human, rhesus macaque, pigtailed macaque, and murine DC-SIGN.A single asparagine-linked glycosylation site of the severe acute respiratory syndrome coronavirus spike glycoprotein facilitates inhibition by mannose-binding lectin through multiple mechanisms.The SARS-coronavirus-host interactome: identification of cyclophilins as target for pan-coronavirus inhibitorsHemofiltrate CC chemokine 1[9-74] causes effective internalization of CCR5 and is a potent inhibitor of R5-tropic human immunodeficiency virus type 1 strains in primary T cells and macrophagesTMPRSS2 and TMPRSS4 facilitate trypsin-independent spread of influenza virus in Caco-2 cells.How Ebola virus counters the interferon system.The role of DC-SIGN and DC-SIGNR in HIV and SIV attachment, infection, and transmission.Expression of DC-SIGN by dendritic cells of intestinal and genital mucosae in humans and rhesus macaques.Influenza A virus does not encode a tetherin antagonist with Vpu-like activity and induces IFN-dependent tetherin expression in infected cellsThe clinically approved drugs amiodarone, dronedarone and verapamil inhibit filovirus cell entry.Sensitivity of HIV-1 to entry inhibitors correlates with envelope/coreceptor affinity, receptor density, and fusion kineticsA novel Syk-dependent mechanism of platelet activation by the C-type lectin receptor CLEC-2.
P50
Q24339582-BDD170AB-EEEE-4063-8E7B-185E2D44A7BCQ24541155-3311DA32-38AC-41AA-98D6-257EF62DF8DEQ24551041-990BA49B-FBD5-412B-B89E-E77CF8383EBDQ24601035-89FBD158-90F6-48CA-A323-6C0D4EB70FE9Q24673797-E211474D-594D-4307-974A-2AC9A3EA8E6CQ26700101-2C1F87FF-D92B-47AB-A99B-9D18F9028414Q27644536-A4D029A2-5AEA-46C2-A9F1-172D04231A58Q28201093-BCC326FF-6AA3-4ED7-A23D-727FF242AB3EQ28204326-4332173E-083C-42A2-B4F4-77BD17C6F2BAQ28344956-4C907CCB-4155-4F81-A5C1-DBABC5C4919BQ28590922-ECFFCB90-F5F2-4DAB-8BA9-B0E4617C7AEDQ28730201-6010BE8E-9208-4201-84E7-7834F1CECEABQ30354466-3583F24E-50B2-404E-9D20-D1BB52DD947CQ30355034-EAB58F18-A28B-471F-97E0-EE4BC05BBC25Q30356975-40961ACC-5B73-4948-B94A-612300DAE024Q30361340-5F399CC7-887F-4F4A-B4B1-D7A7ED34BB8BQ30365060-41858A93-EF88-4964-80BD-07C077073031Q30365699-C61893EC-F541-4E2D-86C5-A586293F54D8Q30376050-11D09692-7536-4374-BCD5-C5239C5251E6Q30400470-930731BF-7899-475C-B383-BC5F8525D9B1Q33305051-F3A3291A-4E80-4AF0-8D55-4A33A1EA6416Q33405724-1C7B4220-BC4F-4D64-9448-13732EB6F9B7Q33436837-F4360FA3-FBC3-424A-9121-183E747587D3Q33558501-35128EA5-31CC-476C-8F06-905B1A99DF7DQ33663432-E30C04B1-90F5-40C6-ACAF-0B642AAE727DQ33787066-1A7A6968-CFFD-49FE-AE24-43885B1A8272Q33840771-9895984F-352B-4FBD-BD52-D788ACAFC035Q33841118-70623CBB-C7CD-4358-900A-411F69F4D408Q33847871-4BE05A48-5E76-49C3-A61B-5C943AD37395Q34055469-4001DA37-1057-41F8-88AF-61E54BC595B0Q34064211-51C340BD-A2EE-4037-9A03-E210A3E2F269Q34106131-451C617E-C23A-47C2-95B7-4122CF4B012AQ34120814-C0AD5067-EC9B-413C-8D56-DB8D6F728AACQ34298213-281F6420-D08C-4386-A57A-898B03E4E0E0Q34305532-A829324E-0C9A-4580-9F7F-79B94C37A631Q34331629-A13DCAC9-93BF-495E-B457-492D24C86E44Q34405097-76569DDD-BE1A-4AAF-AC60-BD6F60422947Q34414075-B1A4B513-A50C-4DB1-9C2A-6639B59F1DDAQ34415921-DC55B385-11CC-4443-AFB8-808BF66579CDQ34452496-1061C8B7-C170-4EE8-AC53-7BFA71EC5557
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Stefan Pöhlmann
@ast
Stefan Pöhlmann
@en
Stefan Pöhlmann
@es
Stefan Pöhlmann
@nl
Stefan Pöhlmann
@sl
type
label
Stefan Pöhlmann
@ast
Stefan Pöhlmann
@en
Stefan Pöhlmann
@es
Stefan Pöhlmann
@nl
Stefan Pöhlmann
@sl
prefLabel
Stefan Pöhlmann
@ast
Stefan Pöhlmann
@en
Stefan Pöhlmann
@es
Stefan Pöhlmann
@nl
Stefan Pöhlmann
@sl
P108
P1053
H-2395-2011
P106
P1153
7003508167
P2038
Stefan_Poehlmann2
P21
P31
P3829
P496
0000-0001-6086-9136