Follow
Laurent Desaubry
Laurent Desaubry
University of Strasbourg, CNRS, INSERM, TUST
Verified email at unistra.fr - Homepage
Title
Cited by
Cited by
Year
eIF4F is a nexus of resistance to anti-BRAF and anti-MEK cancer therapies
L Boussemart, H Malka-Mahieu, I Girault, D Allard, O Hemmingsson, ...
Nature 513 (7516), 105-109, 2014
3642014
Cytochromes P450 CYP94C1 and CYP94B3 catalyze two successive oxidation steps of plant hormone jasmonoyl-isoleucine for catabolic turnover
T Heitz, E Widemann, R Lugan, L Miesch, P Ullmann, L Désaubry, ...
Journal of Biological Chemistry 287 (9), 6296-6306, 2012
2652012
PHB2 (prohibitin 2) promotes PINK1-PRKN/Parkin-dependent mitophagy by the PARL-PGAM5-PINK1 axis
C Yan, L Gong, L Chen, M Xu, H Abou-Hamdan, M Tang, L Désaubry, ...
Autophagy 16 (3), 419-434, 2020
2432020
Prohibitin ligands in cell death and survival: mode of action and therapeutic potential
F Thuaud, N Ribeiro, CG Nebigil, L Désaubry
Chemistry & biology 20 (3), 316-331, 2013
2182013
Translational control of tumor immune escape via the eIF4F–STAT1–PD-L1 axis in melanoma
M Cerezo, R Guemiri, S Druillennec, I Girault, H Malka-Mahieu, S Shen, ...
Nature medicine 24 (12), 1877-1886, 2018
2052018
Updates in anthracycline-mediated cardiotoxicity
CG Nebigil, L Désaubry
Frontiers in Pharmacology 9, 415242, 2018
1812018
The natural anticancer compounds rocaglamides inhibit the Raf-MEK-ERK pathway by targeting prohibitin 1 and 2
G Polier, J Neumann, F Thuaud, N Ribeiro, C Gelhaus, H Schmidt, ...
Chemistry & biology 19 (9), 1093-1104, 2012
1712012
Wogonin and related natural flavones are inhibitors of CDK9 that induce apoptosis in cancer cells by transcriptional suppression of Mcl-1
G Polier, J Ding, BV Konkimalla, D Eick, N Ribeiro, R Köhler, M Giaisi, ...
Cell death & disease 2 (7), e182-e182, 2011
1662011
Cancer wars: natural products strike back
C Basmadjian, Q Zhao, E Bentouhami, A Djehal, CG Nebigil, RA Johnson, ...
Frontiers in chemistry 2, 20, 2014
1562014
CUG initiation and frameshifting enable production of dipeptide repeat proteins from ALS/FTD C9ORF72 transcripts
R Tabet, L Schaeffer, F Freyermuth, M Jambeau, M Workman, CZ Lee, ...
Nature communications 9 (1), 152, 2018
1452018
Synthetic analogue of rocaglaol displays a potent and selective cytotoxicity in cancer cells: involvement of apoptosis inducing factor and caspase-12
F Thuaud, Y Bernard, G Turkeri, R Dirr, G Aubert, T Cresteil, A Baguet, ...
Journal of medicinal chemistry 52 (16), 5176-5187, 2009
1122009
Recent Advances in the Synthesis of C2‐Functionalized Pyridines and Quinolines Using N‐Oxide Chemistry
D Wang, L Désaubry, G Li, M Huang, S Zheng
Advanced Synthesis & Catalysis 363 (1), 2-39, 2021
1082021
Isozyme-dependent sensitivity of adenylyl cyclases to P-site-mediated inhibition by adenine nucleosides and nucleoside 3′-polyphosphates
RA Johnson, L Désaubry, G Bianchi, I Shoshani, E Lyons, R Taussig, ...
Journal of Biological Chemistry 272 (14), 8962-8966, 1997
1061997
Prokineticin‐2 promotes chemotaxis and alternative A2 reactivity of astrocytes
M Neal, J Luo, DS Harischandra, R Gordon, S Sarkar, H Jin, ...
Glia 66 (10), 2137-2157, 2018
1032018
Molecular pathways: the eIF4F translation initiation complex—new opportunities for cancer treatment
H Malka-Mahieu, M Newman, L Désaubry, C Robert, S Vagner
Clinical Cancer Research 23 (1), 21-25, 2017
972017
Progress in copper complexes as anticancer agents
R Tabti, N Tounsi, C Gaiddon, E Bentouhami, L Désaubry
Med. Chem 7, 875-879, 2017
922017
Flavaglines: potent anticancer drugs that target prohibitins and the helicase eIF4A
C Basmadjian, F Thuaud, N Ribeiro, L Désaubry
Future medicinal chemistry 5 (18), 2185-2197, 2013
792013
The mTOR-S6 kinase pathway promotes stress granule assembly
AP Sfakianos, LE Mellor, YF Pang, P Kritsiligkou, H Needs, ...
Cell Death & Differentiation 25 (10), 1766-1780, 2018
752018
Flavaglines as potent anticancer and cytoprotective agents
N Ribeiro, F Thuaud, Y Bernard, C Gaiddon, T Cresteil, A Hild, EC Hirsch, ...
Journal of medicinal chemistry 55 (22), 10064-10073, 2012
742012
2′, 5′-Dideoxyadenosine 3′-polyphosphates are potent inhibitors of adenylyl cyclases
L Désaubry, I Shoshani, RA Johnson
Journal of Biological Chemistry 271 (5), 2380-2382, 1996
741996
The system can't perform the operation now. Try again later.
Articles 1–20