A. Pietro

发表

The linker region of breast cancer resistance protein ABCG2 is critical for coupling of ATP-dependent drug transport

S. Bates, R. Robey, S. Ambudkar, 2016, Cellular and Molecular Life Sciences.

Quantitative evaluation of the combination between cytotoxic drug and efflux transporter inhibitors based on a tumour growth inhibition model

J. Guitton, Myléne Honorat, P. Falson, 2014, Fundamental & clinical pharmacology.

A template model for studying anticancer drug efflux transporter inhibitors in vitro

J. Guitton, Myléne Honorat, P. Falson, 2013, Fundamental & clinical pharmacology.

Becatecarin (rebeccamycin analog, NSC 655649) is a transport substrate and induces expression of the ATP-binding cassette transporter, ABCG2, in lung carcinoma cells

Robert W. Robey, Suneet Shukla, S. Bates, 2009, Cancer Chemotherapy and Pharmacology.

Purification of breast cancer resistance protein ABCG2 and role of arginine-482

J. M. Pérez-Victoria, A. Sardo, A. Pietro, 2006, Cellular and Molecular Life Sciences CMLS.

Make azoles active again: chalcones as potent reversal agents of transporters-mediated resistance in Candida albicans.

R. Prasad, P. Falson, A. Pietro, 2018, Future medicinal chemistry.

Recent Advances in the Discovery of Flavonoids and Analogues with High‐Affinity Binding to P‐Glycoprotein Responsible for Cancer Cell Multidrug Resistance

D. Barron, C. Dumontet, A. Pietro, 2002 .

Preparation of highly phosphorylating mitochondria from the yeastSchizosaccharomyces pombe

J. Jault, A. Pietro, D. Gautheron, 1994, Journal of bioenergetics and biomembranes.

Plant Compounds and Derivatives as Inhibitors of Cancer Cell Multidrug Resistance

A. Pietro, E. Fattorusso, V. Lanzotti, 2011 .

Inhibitors of Cancer Cell Multidrug ABC Transporters: Extrapolation to Combat Candida albicans Resistance to Antifungals

A. Pietro, 2017 .

Candidate Molecule Selection Based on In Silico Predicted ADMET Properties of 12 Indenoindole Derivatives

R. Terreux, A. Pietro, M. Gustin, 2016 .

Organolithium mediated synthesis of prenylchalcones as potential inhibitors of chemoresistance

D. Barron, A. Pietro, G. Comte, 1999 .

Vicinal dithiol in pig heart mitochondrial F1-ATPase related to thermal or ATP-dependent conformational changes

F. Penin, A. Pietro, D. Gautheron, 1977, Journal of bioenergetics and biomembranes.

Probing the conformation of the resting state of a bacterial multidrug ABC transporter, BmrA, by a site‐directed spin labeling approach

D. Cafiso, J. Jault, Miyeon Kim, 2009, Protein science : a publication of the Protein Society.

Recombinant N-terminal Nucleotide-binding Domain from Mouse P-glycoprotein

G. Deléage, J. Cortay, J. Jault, 1996, The Journal of Biological Chemistry.

Flavonolignans from Silybum marianum L.

J. M. Pérez-Victoria, D. Barron, F. Gamarro, 2002 .

MDR1 causes resistance to the antitumour drug miltefosine

H. Grunicke, M. Rybczyńska, F. Sharom, 2001, British Journal of Cancer.

Localization of putative binding sites for cyclic guanosine monophosphate and the anti-cancer drug 5-fluoro-2[prime]-deoxyuridine-5[prime]-monophosphate on ABCC11 in silico models

Myléne Honorat, P. Falson, R. Terreux, 2018 .

Cancer Resistance Protein ABCG 2 Breastand Tectochrysin as Potent and Specific Inhibitors of Flavonoid Structure-Activity Studies Identify 6-Prenylchrysin

S. Bates, J. M. Pérez-Victoria, S. Castanys, 2005 .

Dual properties of hispidulin: antiproliferative effects on HepG2 cancer cells and selective inhibition of ABCG2 transport activity

G. Martinez, A. Pietro, G. Valdameri, 2015, Molecular and Cellular Biochemistry.

Organolithium Mediated Synthesis of Prenylchalcones as Potential Inhibitors of Chemoresistance.

D. Barron, A. Pietro, G. Comte, 1999 .

Modulation by flavonoids of cell multidrug resistance mediated by P-glycoprotein and related ABC transporters

A. Goffeau, J. M. Pérez-Victoria, A. di Pietro, 2002, Cellular and Molecular Life Sciences CMLS.

P-glycoprotein-mediated resistance to chemotherapy in cancer cells: using recombinant cytosolic domains to establish structure-function relationships.

T. Krell, A. di Pietro, J. Jault, 1999, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Flavonoids: a class of modulators with bifunctional interactions at vicinal ATP- and steroid-binding sites on mouse P-glycoprotein.

A. di Pietro, D. Barron, J. Jault, 1998, Proceedings of the National Academy of Sciences of the United States of America.

Nucleotide-Free Crystal Structure of Nucleotide-Binding Domain 1 from Human Abcc1 Supports a 'General-Base Catalysis' Mechanism for ATP Hydrolysis.

P. Falson, A. Pietro, S. Magnard, 2014 .

A common mechanism for ATP hydrolysis in ABC transporter and helicase superfamilies.

G. Deléage, C. Geourjon, C. Blanchet, 2001, Trends in biochemical sciences.

Modulation by flavonoids of cell multidrug resistance mediated by P-glycoprotein and related ABC transporters

A. Goffeau, J. M. Pérez-Victoria, D. Barron, 2002, Cellular and Molecular Life Sciences CMLS.

The acridone derivative MBLI-87 sensitizes breast cancer resistance protein-expressing xenografts to irinotecan.

S. Bates, A. di Pietro, E. Matera, 2011, European journal of cancer.

Binding of steroid modulators to recombinant cytosolic domain from mouse P-glycoprotein in close proximity to the ATP site.

A. di Pietro, E. Baulieu, P. Gros, 1997, Biochemistry.