scholarly article | Q13442814 |
P50 | author | Hans-Jürgen Wester | Q128303541 |
Carlos Mas-Moruno | Q38323013 | ||
Elisabetta A Cavalcanti-Adam | Q40380112 | ||
P2093 | author name string | Horst Kessler | |
Benjamin Geiger | |||
Ute Reuning | |||
Florian Rechenmacher | |||
Stefanie Neubauer | |||
Oleg V Maltsev | |||
Joachim Spatz | |||
Johannes Notni | |||
Tobias G Kapp | |||
Revital Zarka | |||
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Non-peptide fibrinogen receptor antagonists. 1. Discovery and design of exosite inhibitors | Q28236317 | ||
Force fluctuations within focal adhesions mediate ECM-rigidity sensing to guide directed cell migration | Q28508256 | ||
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Cell attachment activity of fibronectin can be duplicated by small synthetic fragments of the molecule | Q29616413 | ||
Integrin alpha v beta 3 antagonists promote tumor regression by inducing apoptosis of angiogenic blood vessels | Q29619679 | ||
N-Methylated cyclic RGD peptides as highly active and selective alpha(V)beta(3) integrin antagonists | Q30580638 | ||
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Novel RGD lipopeptides for the targeting of liposomes to integrin-expressing endothelial and melanoma cells | Q31087982 | ||
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Cilengitide combined with standard treatment for patients with newly diagnosed glioblastoma with methylated MGMT promoter (CENTRIC EORTC 26071-22072 study): a multicentre, randomised, open-label, phase 3 trial | Q33417361 | ||
A heterodimeric [RGD-Glu-[(64)Cu-NO2A]-6-Ahx-RM2] αvβ3/GRPr-targeting antagonist radiotracer for PET imaging of prostate tumors | Q33616878 | ||
Ligand binding to integrins | Q33912940 | ||
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Increasing αvβ3 selectivity of the anti-angiogenic drug cilengitide by N-methylation. | Q34030885 | ||
The extracellular matrix at a glance | Q34152843 | ||
RGD modified polymers: biomaterials for stimulated cell adhesion and beyond | Q34223126 | ||
Signal transduction by cell adhesion receptors and the cytoskeleton: functions of integrins, cadherins, selectins, and immunoglobulin-superfamily members | Q34504056 | ||
Biselectivity of isoDGR peptides for fibronectin binding integrin subtypes α5β1 and αvβ6: conformational control through flanking amino acids | Q34567390 | ||
The glycophorin A transmembrane sequence within integrin αvβ3 creates a non-signaling integrin with low basal affinity that is strongly adhesive under force | Q34751810 | ||
Pharmacophoric modifications lead to superpotent αvβ3 integrin ligands with suppressed α5β1 activity | Q35127140 | ||
Therapeutic antagonists and conformational regulation of integrin function | Q35209992 | ||
Phase II study of cilengitide (EMD 121974, NSC 707544) in patients with non-metastatic castration resistant prostate cancer, NCI-6735. A study by the DOD/PCF prostate cancer clinical trials consortium | Q35218871 | ||
PET Imaging of Integrin Positive Tumors Using F Labeled Knottin Peptides | Q35641937 | ||
Overview of the matrisome--an inventory of extracellular matrix constituents and functions | Q35645897 | ||
Cilengitide: the first anti-angiogenic small molecule drug candidate design, synthesis and clinical evaluation | Q35701298 | ||
Two cilengitide regimens in combination with standard treatment for patients with newly diagnosed glioblastoma and unmethylated MGMT gene promoter: results of the open-label, controlled, randomized phase II CORE study | Q35788615 | ||
A cell surface receptor complex for collagen type I recognizes the Arg-Gly-Asp sequence | Q36216437 | ||
Targeting RGD recognizing integrins: drug development, biomaterial research, tumor imaging and targeting | Q36570185 | ||
Nanoparticles coated with the tumor-penetrating peptide iRGD reduce experimental breast cancer metastasis in the brain | Q36729317 | ||
The integrins | Q36837362 | ||
Tumor targeting with RGD peptide ligands-design of new molecular conjugates for imaging and therapy of cancers | Q36952035 | ||
RGDN peptide interaction with endothelial alpha5beta1 integrin causes sustained endothelin-dependent vasoconstriction of rat skeletal muscle arterioles | Q37372789 | ||
The role of thiols and disulfides on protein stability. | Q37524089 | ||
Integrin-TGF-beta crosstalk in fibrosis, cancer and wound healing | Q37675931 | ||
Targeting alphavbeta3 integrin: design and applications of mono- and multifunctional RGD-based peptides and semipeptides | Q37694643 | ||
Integrins as therapeutic targets: lessons and opportunities | Q37795552 | ||
Integrins as therapeutic targets. | Q38013361 | ||
Tumor Targeting via Integrin Ligands | Q38134759 | ||
Integrin modulators: a patent review | Q38139612 | ||
Strategies to inhibit tumor associated integrin receptors: rationale for dual and multi-antagonists. | Q38191051 | ||
Stable Peptides Instead of Stapled Peptides: Highly Potent αvβ6-Selective Integrin Ligands | Q38811936 | ||
αvβ3- or α5β1-Integrin-Selective Peptidomimetics for Surface Coating | Q38852942 | ||
Comparison of biological properties of (111)In-labeled dimeric cyclic RGD peptides | Q38933771 | ||
Preparation and preclinical evaluation of (66)Ga-DOTA-E(c(RGDfK))2 as a potential theranostic radiopharmaceutical | Q38947780 | ||
Benefits of NOPO as chelator in gallium-68 peptides, exemplified by preclinical characterization of (68)Ga-NOPO-c(RGDfK). | Q39011647 | ||
Functionalizing αvβ3- or α5β1-selective integrin antagonists for surface coating: a method to discriminate integrin subtypes in vitro | Q39205680 | ||
The RGD motif in fibronectin is essential for development but dispensable for fibril assembly | Q39743726 | ||
Cilengitide restrains the osteoclast-like bone resorbing activity of myeloma plasma cells | Q40147550 | ||
Structure-function analysis of Arg-Gly-Asp helix motifs in alpha v beta 6 integrin ligands | Q40179951 | ||
Antitumor effect of RGD-4C-GG-D(KLAKLAK)2 peptide in mouse B16(F10) melanoma model. | Q40201435 | ||
Interface Immobilization Chemistry of cRGD-based Peptides Regulates Integrin Mediated Cell Adhesion | Q41157466 | ||
Comparison of disintegrins with limited variation in the RGD loop in their binding to purified integrins alpha IIb beta 3, alpha V beta 3 and alpha 5 beta 1 and in cell adhesion inhibition | Q41425538 | ||
Metabolism and disposition of the αv-integrin ß3/ß5 receptor antagonist cilengitide, a cyclic polypeptide, in humans | Q41434182 | ||
Orally active non-peptide fibrinogen receptor (GpIIb/IIIa) antagonists: identification of 4-[4-[4-(aminoiminomethyl)phenyl]-1-piperazinyl]-1-piperidineacetic acid as a long-acting, broad-spectrum antithrombotic agent | Q42282530 | ||
Influence of length and flexibility of spacers on the binding affinity of divalent ligands | Q42522246 | ||
Phase I trial of the positron-emitting Arg-Gly-Asp (RGD) peptide radioligand 18F-AH111585 in breast cancer patients | Q43788666 | ||
Inhibition of integrin alpha5beta1 function with a small peptide (ATN-161) plus continuous 5-FU infusion reduces colorectal liver metastases and improves survival in mice | Q44313688 | ||
Docking studies on alphavbeta3 integrin ligands: pharmacophore refinement and implications for drug design | Q44604117 | ||
Activation of integrin function by nanopatterned adhesive interfaces | Q44832858 | ||
A molecular toolkit for the functionalization of titanium-based biomaterials that selectively control integrin-mediated cell adhesion | Q44965368 | ||
Human alphavbeta3 integrin potency and specificity of TA138 and its DOTA conjugated form (89)Y-TA138. | Q45226958 | ||
Spontaneous formation of L-isoaspartate and gain of function in fibronectin. | Q45862901 | ||
Ligands for mapping alphavbeta3-integrin expression in vivo. | Q45986254 | ||
Breaking the dogma of the metal-coordinating carboxylate group in integrin ligands: introducing hydroxamic acids to the MIDAS to tune potency and selectivity | Q46062883 | ||
Ligand binding analysis for human alpha5beta1 integrin: strategies for designing new alpha5beta1 integrin antagonists | Q46563136 | ||
Design of potent and specific integrin antagonists. Peptide antagonists with high specificity for glycoprotein IIb-IIIa | Q46581809 | ||
Rational design of highly active and selective ligands for the alpha5beta1 integrin receptor | Q46594811 | ||
Multiple N-methylation by a designed approach enhances receptor selectivity | Q46921733 | ||
Pharmacophore refinement of gpIIb/IIIa antagonists based on comparative studies of antiadhesive cyclic and acyclic RGD peptides | Q49177235 | ||
Small Cause, Great Impact: Modification of the Guanidine Group in the RGD Motif Controls Integrin Subtype Selectivity. | Q50902764 | ||
Selective imaging of the angiogenic relevant integrins α5β1 and αvβ3. | Q53092366 | ||
Arg-Gly-Asp constrained within cyclic pentapeptides. Strong and selective inhibitors of cell adhesion to vitronectin and laminin fragment P1. | Q53686513 | ||
Radioligand Binding Assays and Their Analysis | Q56987865 | ||
Selective recognition of cyclic RGD peptides of NMR defined conformation by alpha IIb beta 3, alpha V beta 3, and alpha 5 beta 1 integrins | Q57189889 | ||
Adhesion articulated | Q58057878 | ||
Receptor-Bound Conformation of Cilengitide Better Represented by Its Solution-State Structure than the Solid-State Structure | Q58855681 | ||
Conformational Control of Integrin-Subtype Selectivity in isoDGR Peptide Motifs: A Biological Switch | Q58855726 | ||
Probing Integrin Selectivity: Rational Design of Highly Active and Selective Ligands for the α5β1 and αvβ3 Integrin Receptor | Q58856002 | ||
Definition of Two Angiogenic Pathways by Distinct alpha(v) Integrins | Q61764268 | ||
3,4,6-Tri-O-acetyl-2-deoxy-2-[18F]fluoroglucopyranosyl Phenylthiosulfonate: A Thiol-Reactive Agent for the Chemoselective18F-Glycosylation of Peptides | Q64030207 | ||
Echistatin. A potent platelet aggregation inhibitor from the venom of the viper, Echis carinatus | Q67980883 | ||
Surface coating with cyclic RGD peptides stimulates osteoblast adhesion and proliferation as well as bone formation | Q76645267 | ||
NC-100717: a versatile RGD peptide scaffold for angiogenesis imaging | Q79135180 | ||
Design and synthesis of a new class of selective integrin alpha5beta1 antagonists | Q80578744 | ||
Selective RGD-Mediated Adhesion of Osteoblasts at Surfaces of Implants | Q88521460 | ||
P407 | language of work or name | English | Q1860 |
P304 | page(s) | 39805 | |
P577 | publication date | 2017-01-11 | |
P1433 | published in | Scientific Reports | Q2261792 |
P1476 | title | A Comprehensive Evaluation of the Activity and Selectivity Profile of Ligands for RGD-binding Integrins | |
P478 | volume | 7 |
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