M. Degardin

发表

Natural-like replication of an unnatural base pair for the expansion of the genetic alphabet and biotechnology applications.

T. Lavergne, F. Romesberg, P. Ordoukhanian, 2014, Journal of the American Chemical Society.

From Peptide Aptamers to Inhibitors of FUR, Bacterial Transcriptional Regulator of Iron Homeostasis and Virulence.

J. Covès, P. Colas, D. Boturyn, 2016, ACS chemical biology.

Development of a selective cell capture and release assay: impact of clustered RGD ligands.

D. Boturyn, R. Richter, L. Coche-Guérente, 2017, Journal of materials chemistry. B.

αVβ3 Integrin-Targeted Radionuclide Therapy with 64Cu-cyclam-RAFT-c(-RGDfK-)4

Ming-Rong Zhang, Y. Fujibayashi, T. Saga, 2016, Molecular Cancer Therapeutics.

Radiotheranostic Agent 64Cu-cyclam-RAFT-c(-RGDfK-)4 for Management of Peritoneal Metastasis in Ovarian Cancer

Ming-Rong Zhang, T. Higashi, D. Boturyn, 2020, Clinical Cancer Research.

Expanding the scope of replicable unnatural DNA: stepwise optimization of a predominantly hydrophobic base pair.

T. Lavergne, F. Romesberg, P. Ordoukhanian, 2013, Journal of the American Chemical Society.

67Cu-Radiolabeling of a multimeric RGD peptide for αVβ3 integrin-targeted radionuclide therapy: stability, therapeutic efficacy, and safety studies in mice.

Ming-Rong Zhang, Y. Fujibayashi, T. Saga, 2017, Nuclear medicine communications.

Structure‐Based Design and Synthesis of a Small Molecule that Exhibits Anti‐inflammatory Activity by Inhibition of MyD88‐mediated Signaling to Bacterial Toxin Exposure

J. Rebek, D. Waag, Sacha Javor, 2015, Chemical biology & drug design.

Multiplexed Imaging Reveals the Spatial Relationship of the Extracellular Acidity-Targeting pHLIP with Necrosis, Hypoxia, and the Integrin-Targeting cRGD Peptide

Atsushi B. Tsuji, D. Boturyn, P. Dumy, 2022, Cells.

Development of the First Oral Bioprecursors of Bis‐alkylguanidine Antimalarial Drugs

H. Vial, T. Durand, M. Maynadier, 2014, ChemMedChem.

Synthesis and recognition studies with a ditopic, photoswitchable deep cavitand.

J. Rebek, J. Lux, Eric Busseron, 2013, Chemical Communications.

Deep cavitands featuring functional acetal-based walls.

J. Rebek, Eric Busseron, M. Degardin, 2012, Chemical communications.

Evaluation of Bis‐Alkylamidoxime O‐Alkylsulfonates as Orally Available Antimalarials

H. Vial, T. Durand, S. Wein, 2012, ChemMedChem.

Uniform intratumoral distribution of radioactivity produced using two different radioagents, 64Cu-cyclam-RAFT-c(-RGDfK-)4 and 64Cu-ATSM, improves therapeutic efficacy in a small animal tumor model

Atsushi B. Tsuji, Y. Fujibayashi, T. Higashi, 2018, EJNMMI Research.

Multivalency: influence of the residence time and the retraction rate on rupture forces measured by AFM.

R. Auzély-Velty, P. Schaaf, P. Lavalle, 2015, Journal of materials chemistry. B.

Heparan sulfate co-immobilized with cRGD ligands and BMP2 on biomimetic platforms promotes BMP2-mediated osteogenic differentiation.

E. A. Cavalcanti-Adam, D. Boturyn, E. Migliorini, 2020, Acta biomaterialia.

N-substituted bis-C-alkyloxadiazolones as dual effectors: efficient intermediates to amidoximes or amidines and prodrug candidates of potent antimalarials.

T. Durand, S. Wein, M. Degardin, 2009, Bioorganic & medicinal chemistry letters.

Rational design of peptide derivatives for inhibition of MyD88‐mediated toll‐like receptor signaling in human peripheral blood mononuclear cells and epithelial cells exposed to Francisella tularensis

J. Rebek, M. Cameron, T. Kissner, 2017, Chemical biology & drug design.

Impact of multimeric ferrocene-containing cyclodecapeptide scaffold on host-guest interactions at a β-cyclodextrin covered surface.

D. Boturyn, J. Dejeu, L. Coche-Guérente, 2021, Chemphyschem : a European journal of chemical physics and physical chemistry.