about
Morphine decreases clopidogrel concentrations and effects: a randomized, double-blind, placebo-controlled trial.Pharmacogenetics guided anticoagulation.Leptin induces endothelin-1 in endothelial cells in vitro.Interaction of CD31 with a heterophilic counterreceptor involved in downregulation of human T cell responses.Characterization of patients at high risk of melanoma in Austria.CD99 engagement on human peripheral blood T cells results in TCR/CD3-dependent cellular activation and allows for Th1-restricted cytokine production.Ligand-induced conformational change within the CD2 ectodomain accompanies receptor clustering: implication for molecular lattice formation.Identification of a homozygous PSTPIP1 mutation in a patient with a PAPA-like syndrome responding to canakinumab treatment.The C-reactive protein (+)1444C/T alteration modulates the inflammation and coagulation response in human endotoxemia.Differential impact of cytochrome 2C9 allelic variants on clopidogrel-mediated platelet inhibition determined by five different platelet function tests.Inhibitor development in two patients with mild haemophilia A - spontaneous disappearance and no recurrence of the inhibitor after re-challenge.Identification of an ancient haemophilia A splice site mutation.CYP2C9 genotype and association with bone mineral density: a pilot study.Influence of functional haplotypes in the drug transporter gene ABCB1 on central nervous system drug distribution in humans.Pharmacoresistance in epilepsy: a pilot PET study with the P-glycoprotein substrate R-[(11)C]verapamil.Clinical restenosis after coronary stent implantation is associated with the heme oxygenase-1 gene promoter polymorphism and the heme oxygenase-1 +99G/C variant.In vitro and in vivo activated T cells display increased sensitivity to PGE2.The association of PC-1 (ENPP1) K121Q polymorphism with metabolic syndrome in patients with coronary heart disease.Simultaneous analysis of MDR1 C3435T, G2677T/A, and C1236T genotypes by multiplexed mutagenically separated PCR.The K121Q polymorphism in the plasma cell membrane glycoprotein 1 gene predisposes to early myocardial infarction.The effect of p22-PHOX (CYBA) polymorphisms on premature coronary artery disease (≤ 40 years of age).CD2 signaling in T cells involves tyrosine phosphorylation and activation of the Tec family kinase, EMT/ITK/TSK.Influence of cytochrome P450 2C9*2 and 2C9*3 variants on the risk of ischemic stroke: a cross-sectional case-control study.Influence of proton pump inhibitors andVKORC1mutations on CYP2C9-mediated dose requirements of vitamin K antagonist therapy: a pilot studyAre inherited thrombotic risk factors associated with fibrostenosis in Crohnʼs disease?Evaluation of the PC-1 K121Q and G2906C variants as independent risk factors for ischaemic strokeCYP2C9*2 and CYP2C9*3 Alleles Confer a Lower Risk for Myocardial InfarctionIs Low Serum Bilirubin an Independent Risk Factor for Coronary Artery Disease in Men but Not in Women?Association of an ABCB1 gene haplotype with pharmacoresistance in temporal lobe epilepsyA microsatellite polymorphism in the heme oxygenase-1 gene promoter is associated with increased bilirubin and HDL levels but not with coronary artery diseaseA p56lck-independent Pathway of CD2 Signaling Involves Jun KinaseFunctional analysis of immunoreceptor tyrosinebased activation motif (ITAM)-mediated signal transduction: the two YxxL segments within a single CD3ζITAM are functionally distinctSingle human T cells stimulated in the absence of feeder cells transcribe interleukin-2 and undergo long-term clonal growth in response to defined monoclonal antibodies and cytokine stimulationCrosslinking of CD27 in the Presence of CD28 Costimulation Results in T Cell Proliferation and Cytokine ProductionHigh IL-4 production is a stable phenotype of CD8negCD45RAnegCD27neg T cells[Regulation of cytokine production by human T-lymphocytes in allergic immune response]A critical role for p59(fyn) in CD2-based signal transduction
P50
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P50
description
Austrian medical researcher
@en
investigadora médica austriaca
@ast
medisch onderzoeker uit Oostenrijk
@nl
taighdeoir leighis Ostarach
@ga
name
Raute Sunder-Plassmann
@ast
Raute Sunder-Plassmann
@ca
Raute Sunder-Plassmann
@en
Raute Sunder-Plassmann
@es
Raute Sunder-Plassmann
@fr
Raute Sunder-Plassmann
@ga
Raute Sunder-Plassmann
@nl
Raute Sunder-Plassmann
@sl
Raute Sunder-Plassmann
@sq
type
label
Raute Sunder-Plassmann
@ast
Raute Sunder-Plassmann
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Raute Sunder-Plassmann
@en
Raute Sunder-Plassmann
@es
Raute Sunder-Plassmann
@fr
Raute Sunder-Plassmann
@ga
Raute Sunder-Plassmann
@nl
Raute Sunder-Plassmann
@sl
Raute Sunder-Plassmann
@sq
altLabel
Raute Sunder-Plaßmann
@en
prefLabel
Raute Sunder-Plassmann
@ast
Raute Sunder-Plassmann
@ca
Raute Sunder-Plassmann
@en
Raute Sunder-Plassmann
@es
Raute Sunder-Plassmann
@fr
Raute Sunder-Plassmann
@ga
Raute Sunder-Plassmann
@nl
Raute Sunder-Plassmann
@sl
Raute Sunder-Plassmann
@sq
P2038
Raute_Sunder-Plassmann
P21
P27
P31
P496
0000-0002-8297-118X