| Year |
Citation |
Score |
| 2020 |
Daurat M, Nguyen C, Dominguez Gil S, Sol V, Chaleix V, Charnay C, Raehm L, El Cheikh K, Morère A, Bernasconi M, Timpanaro A, Garcia M, Cunin F, Roessler J, Durand JO, et al. The mannose 6-phosphate receptor targeted with porphyrin-based periodic mesoporous organosilica nanoparticles for rhabdomyosarcoma theranostics. Biomaterials Science. PMID 32469353 DOI: 10.1039/D0Bm00586J |
0.365 |
|
| 2019 |
Bouffard E, Mauriello Jimenez C, El Cheikh K, Maynadier M, Basile I, Raehm L, Nguyen C, Gary-Bobo M, Garcia M, Durand JO, Morère A. Efficient Photodynamic Therapy of Prostate Cancer Cells through an Improved Targeting of the Cation-Independent Mannose 6-Phosphate Receptor. International Journal of Molecular Sciences. 20. PMID 31181759 DOI: 10.3390/Ijms20112809 |
0.323 |
|
| 2017 |
Liu W, Chaix A, Gary-Bobo M, Angeletti B, Masion A, Da Silva A, Daurat M, Lichon L, Garcia M, Morère A, El Cheikh K, Durand JO, Cunin F, Auffan M. Stealth Biocompatible Si-Based Nanoparticles for Biomedical Applications. Nanomaterials (Basel, Switzerland). 7. PMID 28946628 DOI: 10.3390/Nano7100288 |
0.31 |
|
| 2016 |
Chaix A, El Cheikh K, Bouffard E, Maynadier M, Aggad D, Stojanovic V, Knezevic N, Garcia M, Maillard P, Morère A, Gary-Bobo M, Raehm L, Richeter S, Durand JO, Cunin F. Mesoporous silicon nanoparticles for targeted two-photon theranostics of prostate cancer. Journal of Materials Chemistry. B. 4: 3639-3642. PMID 32263302 DOI: 10.1039/C6Tb00690F |
0.306 |
|
| 2016 |
El Cheikh K, Basile I, Da Silva A, Bernon C, Cérutti P, Salgues F, Perez M, Maynadier M, Gary-Bobo M, Caillaud C, Cérutti M, Garcia M, Morère A. Design of Potent Mannose 6-Phosphate Analogues for the Functionalization of Lysosomal Enzymes To Improve the Treatment of Pompe Disease. Angewandte Chemie (International Ed. in English). PMID 27774736 DOI: 10.1002/Anie.201607824 |
0.312 |
|
| 2016 |
Jimenez CM, Rubio YG, Saunier V, Warther D, Stojanovic V, Raehm L, Frochot C, Arnoux P, Garcia M, Morère A, Bettache N, Maynadier M, Maillard P, Gary-Bobo M, Durand JO. 20-nm-sized mesoporous silica nanoparticles with porphyrin photosensitizers for in vitro photodynamic therapy Journal of Sol-Gel Science and Technology. 1-10. DOI: 10.1007/S10971-016-3991-6 |
0.335 |
|
| 2015 |
Vaillant O, El Cheikh K, Warther D, Brevet D, Maynadier M, Bouffard E, Salgues F, Jeanjean A, Puche P, Mazerolles C, Maillard P, Mongin O, Blanchard-Desce M, Raehm L, Rébillard X, et al. Mannose-6-phosphate receptor: a target for theranostics of prostate cancer. Angewandte Chemie (International Ed. in English). 54: 5952-6. PMID 25802144 DOI: 10.1002/Anie.201500286 |
0.307 |
|
| 2013 |
Gallud A, Silva AD, Maynadier M, Basile I, Fontanel S, Lemaire C, Maillard P, Blanchard-Desce M, Mongin O, Morere A, Dur J, Raehm L, Garcia M, Gary-Bobo M. Functionalized Nanoparticles for Drug Delivery, One- and Two-photon Photodynamic Therapy as a Promising Treatment of Retinoblastoma Journal of Clinical & Experimental Ophthalmology. 4: 1-4. DOI: 10.4172/2155-9570.1000288 |
0.304 |
|
| 2013 |
Perrier M, Gary-Bobo M, Lartigue L, Brevet D, Morère A, Garcia M, Maillard P, Raehm L, Guari Y, Larionova J, Durand JO, Mongin O, Blanchard-Desce M. Mannose-functionalized porous silica-coated magnetic nanoparticles for two-photon imaging or PDT of cancer cells Journal of Nanoparticle Research. 15. DOI: 10.1007/S11051-013-1602-9 |
0.323 |
|
| 2006 |
Morère A, Mouffouk F, Leiris S, Leydet A, Montero J. Influence of the Benzyloxycarbonyl Protective Group on Glycosylation with Mannopyranosyl Donors Journal of Carbohydrate Chemistry. 25: 451-459. DOI: 10.1080/07328300600859759 |
0.309 |
|
| 2004 |
Gagnard V, Leydet A, Morère A, Montero JL, Lefèbvre I, Gosselin G, Pannecouque C, De Clercq E. Synthesis and in vitro evaluation of S-acyl-3-thiopropyl prodrugs of Foscarnet. Bioorganic & Medicinal Chemistry. 12: 1393-402. PMID 15018912 DOI: 10.1016/J.Bmc.2004.01.017 |
0.331 |
|
| 2004 |
Mouffouk F, Morère A, Vidal S, Leydet A, Montero J. Selective Removal of Benzyl Carbonate Used as a Protecting Group in Carbohydrate Chemistry Synthetic Communications. 34: 303-307. DOI: 10.1081/Scc-120027267 |
0.517 |
|
| 2003 |
Gagnard V, Leydet A, Le Mellay V, Aubenque M, Morère A, Montero JL. Synthesis and biological evaluation of S-acyl-3-thiopropyl prodrugs of N-phosphonoacetyl-L-aspartate (PALA). European Journal of Medicinal Chemistry. 38: 883-91. PMID 14575935 DOI: 10.1016/J.Ejmech.2003.07.002 |
0.327 |
|
| 2003 |
Vidal S, Morère A, Montero J. A convenient synthetic route to mannose 6-phosphonate-cholesteryl conjugate Heteroatom Chemistry. 14: 241-246. DOI: 10.1002/Hc.10134 |
0.559 |
|
| 2002 |
Vidal S, Garcia M, Montero JL, Morère A. Synthesis and biological evaluation of new mannose 6-phosphate analogues. Bioorganic & Medicinal Chemistry. 10: 4051-6. PMID 12413858 DOI: 10.1016/S0968-0896(02)00264-X |
0.52 |
|
| 2000 |
Vidil C, Vidal S, Morère A, Montero J. SYNTHÈSE DE MANNOSE 6-PHOSPHONATES, ANALOGUES ISOSTÈRES DU MANNOSE 6-PHOSPHATE Phosphorus, Sulfur, and Silicon and the Related Elements. 158: 125-139. DOI: 10.1080/10426500008042080 |
0.536 |
|
| 2000 |
Vidal S, Vidil C, Morère A, Garcia M, Montero J. Synthesis and Biological Evaluation of Two Mannose 6-Phosphate Analogs European Journal of Organic Chemistry. 2000: 3433-3437. DOI: 10.1002/1099-0690(200010)2000:20<3433::Aid-Ejoc3433>3.0.Co;2-I |
0.549 |
|
| 1999 |
Vidil C, Morère A, Garcia M, Barragan V, Hamdaoui B, Rochefort H, Montero J. Synthesis and Biological Activity of Phosphonate Analogs of Mannose 6‐Phosphate (M6P) European Journal of Organic Chemistry. 1999: 447-450. DOI: 10.1002/(Sici)1099-0690(199902)1999:2<447::Aid-Ejoc447>3.0.Co;2-R |
0.361 |
|
| 1997 |
Morère A, Mouffouk F, Chavis C, Montero JL. The benzyloxycarbonyl protective group: A good alternative to the benzyl protective group in the glycopyranoside and glycofuranoside series Tetrahedron Letters. 38: 7519-7522. DOI: 10.1016/S0040-4039(97)10021-1 |
0.319 |
|
| 1996 |
Abdaoui M, Dewynter G, Aouf N, Favre G, Morère A, Montero JL. A new family of potential oncostatics: 2-Chloroethylnitrososulfamides (CENS) - I. Synthesis, structure, and pharmacological evaluation (preliminary results) Bioorganic and Medicinal Chemistry. 4: 1227-1235. PMID 8879544 DOI: 10.1016/0968-0896(96)00118-6 |
0.345 |
|
| 1992 |
Riviére-baudet M, Onyszchuk M, Morére A, Satgé J. Trimesitylgermylamine mes3genh2: Syntheses, structure, propriétés Phosphorus, Sulfur, and Silicon and the Related Elements. 70: 75-90. DOI: 10.1080/10426509208049154 |
0.308 |
|
| 1991 |
Rivière-Baudet M, Morère A. Derives N-diethylgermanies du 3-amino 2-thiophoate de methyle Phosphorus Sulfur and Silicon and the Related Elements. 62: 211-217. DOI: 10.1080/10426509108034478 |
0.314 |
|
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