M. Salerno

发表

New findings in the study on the intercalation of bisdaunorubicin and its monomeric analogues with naked and nucleus DNA.

H. Kozłowski, W. Priebe, A. Garnier-Suillerot, 2003, Chemico-biological interactions.

Alzheimer's disease: The use of contrast agents for magnetic resonance imaging to detect amyloid beta peptide inside the brain

M. Salerno, Diego Santo Domingo Porqueras, 2016 .

Resistance to Arsenic- and Antimony-Based Drugs

A. Garnier-Suillerot, M. Salerno, 2003, Bioinorganic chemistry and applications.

Accumulation of Eu3+ chelates in cells expressing or not P-glycoprotein: implications for blood-brain barrier crossing.

C. Geraldes, N. Bouchemal, A. Garnier-Suillerot, 2010, Journal of inorganic biochemistry.

Perturbation of membrane microdomains in GLC4 multidrug‐resistant lung cancer cells − modification of ABCC1 (MRP1) localization and functionality

A. Garnier-Suillerot, V. Stierlé, P. Sudwan, 2007, The FEBS journal.

Decrease of P-Glycoprotein Activity in K562/ADR Cells by MβCD and Filipin and Lack of Effect Induced by Cholesterol Oxidase Indicate That This Transporter Is Not Located in Rafts

L. Moyec, A. Garnier-Suillerot, Paiboon Reungpatthanaphong, 2004, Journal of bioenergetics and biomembranes.

PiB-Conjugated, Metal-Based Imaging Probes: Multimodal Approaches for the Visualization of β-Amyloid Plaques.

C. Duyckaerts, D. Guilloteau, C. Geraldes, 2013, ACS medicinal chemistry letters.

Design and synthesis of new potent N,N-bis(arylalkyl)piperazine derivatives as multidrug resistance (MDR) reversing agents.

G. Bartolucci, S. Dei, E. Teodori, 2018, European journal of medicinal chemistry.

New structure-activity relationship studies in a series of N,N-bis(cyclohexanol)amine aryl esters as potent reversers of P-glycoprotein-mediated multidrug resistance (MDR).

S. Dei, E. Teodori, M. Romanelli, 2013, Bioorganic & medicinal chemistry.

Inhibition of P-glycoprotein-mediated Multidrug Resistance (MDR) by N,N-bis(cyclohexanol)amine aryl esters: further restriction of molecular flexibility maintains high potency and efficacy.

S. Dei, E. Teodori, M. Romanelli, 2011, Bioorganic & medicinal chemistry letters.

Impact of intracellular chloride concentration on cisplatin accumulation in sensitive and resistant GLC4 cells

E. Vries, A. Garnier-Suillerot, E. Pereira-Maia, 2008, JBIC Journal of Biological Inorganic Chemistry.

Relation between the ability of some compounds to modulate the MRP1-mediated efflux of glutathione and to inhibit the MRPl-mediated efflux of daunorubicin.

A. Garnier-Suillerot, M. Salerno, C. Saengkhae, 2004, Biochemical pharmacology.

Bis(thiosemicarbazone) copper complexes: mechanism of intracellular accumulation

N. Lièvre, A. Garnier-Suillerot, H. Beraldo, 2012, JBIC Journal of Biological Inorganic Chemistry.

Exploratory chemistry toward the identification of a new class of multidrug resistance reverters inspired by pervilleine and verapamil models.

S. Dei, E. Teodori, M. Romanelli, 2005, Journal of medicinal chemistry.

The MRP1-Mediated Effluxes of Arsenic and Antimony Do Not Require Arsenic–Glutathione and Antimony–Glutathione Complex Formation

A. Garnier-Suillerot, M. Salerno, Maria Petroutsa, 2002, Journal of bioenergetics and biomembranes.

Analysis of drug transport kinetics in multidrug-resistant cells: implications for drug action.

W. Priebe, A. Garnier-Suillerot, I. Fokt, 2001, Current medicinal chemistry.

Mechanism of thioflavin T accumulation inside cells overexpressing P-glycoprotein or multidrug resistance-associated protein: role of lipophilicity and positive charge.

A. Garnier-Suillerot, M. Salerno, Nacira Darghal, 2006, Biochemical and biophysical research communications.

Preferential efflux by P-glycoprotein, but not MRP1, of compounds containing a free electron donor amine.

W. Priebe, A. Garnier-Suillerot, I. Fokt, 2002, Biochemical pharmacology.

Neurodegenerative diseases – Understanding their molecular bases and progress in the development of potential treatments

H. Kozłowski, M. Rowińska-Żyrek, M. Salerno, 2015 .

Bis(thiosemicarbazone) copper complexes: mechanism of intracellular accumulation

N. Lièvre, A. Garnier-Suillerot, H. Beraldo, 2012, JBIC Journal of Biological Inorganic Chemistry.

Preferential Energy- and Potential-Dependent Accumulation of Cisplatin–Gutathione Complexes in Human Cancer Cell Lines (GLC4 and K562): A Likely Role of Mitochondria

L. Moyec, A. Garnier-Suillerot, E. Pereira-Maia, 2006, Journal of bioenergetics and biomembranes.

Design, synthesis and biological evaluation of stereo- and regioisomers of amino aryl esters as multidrug resistance (MDR) reversers.

N. Colabufo, E. Gazzano, C. Riganti, 2019, European journal of medicinal chemistry.

Design and synthesis of aminoester heterodimers containing flavone or chromone moieties as modulators of P-glycoprotein-based multidrug resistance (MDR).

Niccolò Chiaramonte, S. Dei, E. Teodori, 2018, Bioorganic & medicinal chemistry.

N,N-bis(cyclohexanol)amine aryl esters: a new class of highly potent transporter-dependent multidrug resistance inhibitors.

M. Frosini, S. Dei, E. Teodori, 2009, Journal of medicinal chemistry.

Enhanced oral delivery of antimony from meglumine antimoniate/beta-cyclodextrin nanoassemblies.

L. Le Moyec, F. Frézard, C. Demicheli, 2008, International journal of pharmaceutics.

N-alkanol-N-cyclohexanol amine aryl esters: Multidrug resistance (MDR) reversing agents with high potency and efficacy.

G. Bartolucci, S. Dei, E. Teodori, 2017, European journal of medicinal chemistry.

Multidrug resistance (MDR) reversers: High activity and efficacy in a series of asymmetrical N,N-bis(alkanol)amine aryl esters.

G. Bartolucci, S. Dei, E. Teodori, 2014, European journal of medicinal chemistry.

Kinetics of glutathione and daunorubicin efflux from multidrug resistance protein overexpressing small-cell lung cancer cells.

A. Garnier-Suillerot, A Garnier-Suillerot, M Salerno, 2001, European journal of pharmacology.

Modulation of the spacer in N,N-bis(alkanol)amine aryl ester heterodimers led to the discovery of a series of highly potent P-glycoprotein-based multidrug resistance (MDR) modulators.

N. Colabufo, Niccolò Chiaramonte, G. Bartolucci, 2019, European journal of medicinal chemistry.

Evidence against a role of P-glycoprotein in the clearance of the Alzheimer’s disease Aβ1–42 peptides

M. Salerno, Ivan Bello, 2015, Cell Stress and Chaperones.

Ability of carbazole salts, inhibitors of Alzheimer beta-amyloid fibril formation, to cross cellular membranes.

V. Migonney, L. Le Moyec, A. Siove, 2007, European journal of pharmacology.

Trypanosoma cruzi calmodulin: cloning, expression and characterization.

Y. García-Marchán, G. Benaim, F. Sojo, 2009, Experimental parasitology.

Author ' s personal copy Trypanosoma cruzi calmodulin : Cloning , expression and characterization

Y. García-Marchán, G. Benaim, F. Sojo, 2009 .

Inhibition of the P-glycoprotein- and multidrug resistance protein-mediated efflux of anthracyclines and calceinacetoxymethyl ester by PAK-104P.

A. Garnier-Suillerot, A Garnier-Suillerot, P. Quidu, 2000, European journal of pharmacology.

Comparative toxicity evaluation of flower-shaped and spherical gold nanoparticles on human endothelial cells

S. Aștilean, N. Charnaux, H. Hlawaty, 2015, Nanotechnology.

Evidence against a role of P-glycoprotein in the clearance of the Alzheimer’s disease Aβ1–42 peptides

M. Salerno, Ivan Bello, 2015, Cell Stress and Chaperones.

Structure-activity relationships studies in a series of N,N-bis(alkanol)amine aryl esters as P-glycoprotein (Pgp) dependent multidrug resistance (MDR) inhibitors.

S. Dei, E. Teodori, D. Manetti, 2010, Journal of medicinal chemistry.

Decelerate of Amyloid Fibrillation By The Alkaloids Extracted From Stephania Venosa

Krai Daowtak, C. Udomtanakunchai, Wilart Pompimon, 2021, Journal of Associated Medical Sciences.

N,N-bis(cyclohexanol)amine aryl esters: a new class of highly potent transporter-dependent multidrug resistance inhibitors.

M. Frosini, S. Dei, E. Teodori, 2009, Journal of medicinal chemistry.

Intracellular Transport Studies of Picolinate Macrocyclic Copper and Lanthanide Complexes

M. Salerno, Diego Santo Domingo Porqueras, Raphäel Tripier, 2016 .