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Theranostics
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July 12, 2013
Structure-driven design of radionuclide tracers for non-invasive imaging of uPAR and targeted radiotherapy. The tale of a synthetic peptide antagonist
Michael Ploug
Current Pharmaceutical Design
|
July 23, 2003
Structure-function relationships in the interaction between the urokinase-type plasminogen activator and its receptor
Michael Ploug
Current Opinion in Lipidology
|
December 3, 2021
ANGPTL4: a new mode in the regulation of intravascular lipolysis
Michael Ploug
The Journal of Biological Chemistry
|
March 16, 2007
Mapping of the vitronectin-binding site on the urokinase receptor: involvement of a coherent receptor interface consisting of residues from both domain I and the flanking interdomain linker region
Henrik Gårdsvoll, Michael Ploug
Frontiers in Cell and Developmental Biology
|
September 7, 2021
Targeting the Urokinase-Type Plasminogen Activator Receptor (uPAR) in Human Diseases With a View to Non-invasive Imaging and Therapeutic Intervention
Julie Maja Leth, Michael Ploug
Methods in Molecular Biology (Clifton, N.J.)
|
July 23, 2020
Determination of Binding Kinetics of Intrinsically Disordered Proteins by Surface Plasmon Resonance
Julie M Leth, Michael Ploug
Current Pharmaceutical Design
|
July 29, 2004
The urokinase receptor as a potential target in cancer therapy
John Romer, Boye Schnack Nielsen, Michael Ploug
Cancers
|
November 13, 2021
The Urokinase Receptor (uPAR) as a "Trojan Horse" in Targeted Cancer Therapy: Challenges and Opportunities
Virginia Metrangolo, Michael Ploug, Lars H Engelholm
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
February 23, 2011
Expression of C4.4A, a structural uPAR homolog, reflects squamous epithelial differentiation in the adult mouse and during embryogenesis
Mette C Kriegbaum, Benedikte Jacobsen, Andreas Hald, et al.
The Journal of Biological Chemistry
|
February 6, 2010
Structure-based engineering of species selectivity in the interaction between urokinase and its receptor: implication for preclinical cancer therapy
Lin Lin, Henrik Gårdsvoll, Qing Huai, et al.
Page
of 13
Search research articles
Search
Showing results (1-10 of 127) with videos related to
Sort By:
Page
of 13
Theranostics
|
July 12, 2013
Structure-driven design of radionuclide tracers for non-invasive imaging of uPAR and targeted radiotherapy. The tale of a synthetic peptide antagonist
Michael Ploug
Current Pharmaceutical Design
|
July 23, 2003
Structure-function relationships in the interaction between the urokinase-type plasminogen activator and its receptor
Michael Ploug
Current Opinion in Lipidology
|
December 3, 2021
ANGPTL4: a new mode in the regulation of intravascular lipolysis
Michael Ploug
The Journal of Biological Chemistry
|
March 16, 2007
Mapping of the vitronectin-binding site on the urokinase receptor: involvement of a coherent receptor interface consisting of residues from both domain I and the flanking interdomain linker region
Henrik Gårdsvoll, Michael Ploug
Frontiers in Cell and Developmental Biology
|
September 7, 2021
Targeting the Urokinase-Type Plasminogen Activator Receptor (uPAR) in Human Diseases With a View to Non-invasive Imaging and Therapeutic Intervention
Julie Maja Leth, Michael Ploug
Methods in Molecular Biology (Clifton, N.J.)
|
July 23, 2020
Determination of Binding Kinetics of Intrinsically Disordered Proteins by Surface Plasmon Resonance
Julie M Leth, Michael Ploug
Current Pharmaceutical Design
|
July 29, 2004
The urokinase receptor as a potential target in cancer therapy
John Romer, Boye Schnack Nielsen, Michael Ploug
Cancers
|
November 13, 2021
The Urokinase Receptor (uPAR) as a "Trojan Horse" in Targeted Cancer Therapy: Challenges and Opportunities
Virginia Metrangolo, Michael Ploug, Lars H Engelholm
The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society
|
February 23, 2011
Expression of C4.4A, a structural uPAR homolog, reflects squamous epithelial differentiation in the adult mouse and during embryogenesis
Mette C Kriegbaum, Benedikte Jacobsen, Andreas Hald, et al.
The Journal of Biological Chemistry
|
February 6, 2010
Structure-based engineering of species selectivity in the interaction between urokinase and its receptor: implication for preclinical cancer therapy
Lin Lin, Henrik Gårdsvoll, Qing Huai, et al.
Page
of 13