| Year |
Citation |
Score |
| 2022 |
Khandjian EW, Robert C, Davidovic L. FMRP, a multifunctional RNA-binding protein in quest of a new identity. Frontiers in Genetics. 13: 976480. PMID 36035132 DOI: 10.3389/fgene.2022.976480 |
0.349 |
|
| 2019 |
Leboucher A, Pisani DF, Martinez-Gili L, Chilloux J, Bermudez-Martin P, Van Dijck A, Ganief T, Macek B, Becker JAJ, Le Merrer J, Kooy RF, Amri EZ, Khandjian EW, Dumas ME, Davidovic L. The translational regulator FMRP controls lipid and glucose metabolism in mice and humans. Molecular Metabolism. PMID 30686771 DOI: 10.1016/J.Molmet.2019.01.002 |
0.415 |
|
| 2016 |
Khalfallah O, Jarjat M, Davidovic L, Nottet N, Cestèle S, Mantegazza M, Bardoni B. Depletion of the fragile X mental retardation protein in embryonic stem cells alters the kinetics of neurogenesis. Stem Cells (Dayton, Ohio). PMID 27664080 DOI: 10.1002/Stem.2505 |
0.412 |
|
| 2016 |
El Fatimy R, Davidovic L, Tremblay S, Jaglin X, Dury A, Robert C, De Koninck P, Khandjian EW. Tracking the Fragile X Mental Retardation Protein in a Highly Ordered Neuronal RiboNucleoParticles Population: A Link between Stalled Polyribosomes and RNA Granules. Plos Genetics. 12: e1006192. PMID 27462983 DOI: 10.1371/Journal.Pgen.1006192 |
0.526 |
|
| 2015 |
Vicario A, Colliva A, Ratti A, Davidovic L, Baj G, Gricman Ł, Colombrita C, Pallavicini A, Jones KR, Bardoni B, Tongiorgi E. Dendritic targeting of short and long 3' UTR BDNF mRNA is regulated by BDNF or NT-3 and distinct sets of RNA-binding proteins. Frontiers in Molecular Neuroscience. 8: 62. PMID 26578876 DOI: 10.3389/Fnmol.2015.00062 |
0.326 |
|
| 2015 |
Maurin T, Melko M, Abekhoukh S, Khalfallah O, Davidovic L, Jarjat M, D'Antoni S, Catania MV, Moine H, Bechara E, Bardoni B. The FMRP/GRK4 mRNA interaction uncovers a new mode of binding of the Fragile X mental retardation protein in cerebellum. Nucleic Acids Research. 43: 8540-50. PMID 26250109 DOI: 10.1093/Nar/Gkv801 |
0.485 |
|
| 2014 |
Matic K, Eninger T, Bardoni B, Davidovic L, Macek B. Quantitative phosphoproteomics of murine Fmr1-KO cell lines provides new insights into FMRP-dependent signal transduction mechanisms. Journal of Proteome Research. 13: 4388-97. PMID 25168779 DOI: 10.1021/Pr5006372 |
0.457 |
|
| 2013 |
Davidovic L, Durand N, Khalfallah O, Tabet R, Barbry P, Mari B, Sacconi S, Moine H, Bardoni B. A novel role for the RNA-binding protein FXR1P in myoblasts cell-cycle progression by modulating p21/Cdkn1a/Cip1/Waf1 mRNA stability. Plos Genetics. 9: e1003367. PMID 23555284 DOI: 10.1371/Journal.Pgen.1003367 |
0.46 |
|
| 2013 |
Zongaro S, Hukema R, D'Antoni S, Davidovic L, Barbry P, Catania MV, Willemsen R, Mari B, Bardoni B. The 3' UTR of FMR1 mRNA is a target of miR-101, miR-129-5p and miR-221: implications for the molecular pathology of FXTAS at the synapse. Human Molecular Genetics. 22: 1971-82. PMID 23390134 DOI: 10.1093/Hmg/Ddt044 |
0.341 |
|
| 2011 |
Davidovic L, Navratil V, Bonaccorso CM, Catania MV, Bardoni B, Dumas ME. A metabolomic and systems biology perspective on the brain of the fragile X syndrome mouse model. Genome Research. 21: 2190-202. PMID 21900387 DOI: 10.1101/Gr.116764.110 |
0.428 |
|
| 2009 |
Bechara EG, Didiot MC, Melko M, Davidovic L, Bensaid M, Martin P, Castets M, Pognonec P, Khandjian EW, Moine H, Bardoni B. A novel function for fragile X mental retardation protein in translational activation. Plos Biology. 7: e16. PMID 19166269 DOI: 10.1371/Journal.Pbio.1000016 |
0.523 |
|
| 2009 |
Bensaid M, Melko M, Bechara EG, Davidovic L, Berretta A, Catania MV, Gecz J, Lalli E, Bardoni B. FRAXE-associated mental retardation protein (FMR2) is an RNA-binding protein with high affinity for G-quartet RNA forming structure. Nucleic Acids Research. 37: 1269-79. PMID 19136466 DOI: 10.1093/Nar/Gkn1058 |
0.503 |
|
| 2008 |
Davidovic L, Sacconi S, Bechara EG, Delplace S, Allegra M, Desnuelle C, Bardoni B. Alteration of expression of muscle specific isoforms of the fragile X related protein 1 (FXR1P) in facioscapulohumeral muscular dystrophy patients. Journal of Medical Genetics. 45: 679-85. PMID 18628314 DOI: 10.1136/Jmg.2008.060541 |
0.473 |
|
| 2007 |
Davidovic L, Jaglin XH, Lepagnol-Bestel AM, Tremblay S, Simonneau M, Bardoni B, Khandjian EW. The fragile X mental retardation protein is a molecular adaptor between the neurospecific KIF3C kinesin and dendritic RNA granules. Human Molecular Genetics. 16: 3047-58. PMID 17881655 DOI: 10.1093/Hmg/Ddm263 |
0.543 |
|
| 2007 |
Bechara E, Davidovic L, Melko M, Bensaid M, Tremblay S, Grosgeorge J, Khandjian EW, Lalli E, Bardoni B. Fragile X related protein 1 isoforms differentially modulate the affinity of fragile X mental retardation protein for G-quartet RNA structure. Nucleic Acids Research. 35: 299-306. PMID 17170008 DOI: 10.1093/Nar/Gkl1021 |
0.539 |
|
| 2006 |
Plante I, Davidovic L, Ouellet DL, Gobeil LA, Tremblay S, Khandjian EW, Provost P. Dicer-derived microRNAs are utilized by the fragile X mental retardation protein for assembly on target RNAs. Journal of Biomedicine & Biotechnology. 2006: 64347. PMID 17057366 DOI: 10.1155/Jbb/2006/64347 |
0.458 |
|
| 2006 |
Bardoni B, Davidovic L, Bensaid M, Khandjian EW. The fragile X syndrome: exploring its molecular basis and seeking a treatment. Expert Reviews in Molecular Medicine. 8: 1-16. PMID 16626504 DOI: 10.1017/S1462399406010751 |
0.511 |
|
| 2006 |
Davidovic L, Bechara E, Gravel M, Jaglin XH, Tremblay S, Sik A, Bardoni B, Khandjian EW. The nuclear microspherule protein 58 is a novel RNA-binding protein that interacts with fragile X mental retardation protein in polyribosomal mRNPs from neurons. Human Molecular Genetics. 15: 1525-38. PMID 16571602 DOI: 10.1093/Hmg/Ddl074 |
0.618 |
|
| 2006 |
Davidovic L, Tremblay S, Gravel M, De Koninck P, Khandjian EW. [The fragile X syndrome: one protein missing and 1001 disoriented mRNAs]. Mã©Decine Sciences : M/S. 22: 41-6. PMID 16386219 DOI: 10.1051/Medsci/200622141 |
0.565 |
|
| 2005 |
Davidovic L, Huot ME, Khandjian EW. Lost once, the Fragile X Mental Retardation protein is now back onto brain polyribosomes. Rna Biology. 2: 1-3. PMID 17132937 DOI: 10.4161/Rna.2.1.1368 |
0.471 |
|
| 2005 |
Huot ME, Bisson N, Davidovic L, Mazroui R, Labelle Y, Moss T, Khandjian EW. The RNA-binding protein fragile X-related 1 regulates somite formation in Xenopus laevis. Molecular Biology of the Cell. 16: 4350-61. PMID 16000371 DOI: 10.1091/Mbc.E05-04-0304 |
0.514 |
|
| 2005 |
Ivanyi-Nagy R, Davidovic L, Khandjian EW, Darlix JL. Disordered RNA chaperone proteins: from functions to disease. Cellular and Molecular Life Sciences : Cmls. 62: 1409-17. PMID 15924259 DOI: 10.1007/s00018-005-5100-9 |
0.389 |
|
| 2005 |
Khandjian EW, Bechara E, Davidovic L, Bardoni B. Fragile X mental retardation protein: Many partners and multiple targets for a promiscuous function Current Genomics. 6: 515-522. DOI: 10.2174/138920205775067701 |
0.427 |
|
| 2004 |
Khandjian EW, Huot ME, Tremblay S, Davidovic L, Mazroui R, Bardoni B. Biochemical evidence for the association of fragile X mental retardation protein with brain polyribosomal ribonucleoparticles. Proceedings of the National Academy of Sciences of the United States of America. 101: 13357-62. PMID 15329415 DOI: 10.1073/Pnas.0405398101 |
0.541 |
|
| 2003 |
Koonin EV, Makarova KS, Rogozin IB, Davidovic L, Letellier MC, Pellegrini L. The rhomboids: a nearly ubiquitous family of intramembrane serine proteases that probably evolved by multiple ancient horizontal gene transfers. Genome Biology. 4: R19. PMID 12620104 DOI: 10.1186/Gb-2003-4-3-R19 |
0.32 |
|
| 2002 |
Koonin EV, Makarova KS, Davidovic L, Pellegrini L. The rhomboids: a near ubiquitous family of intramembrane serine proteases evolved via multiple horizontal gene transfers Genome Biology. 3: 1-26. DOI: 10.1186/Gb-2002-3-11-Preprint0010 |
0.318 |
|
| 2001 |
Davidovic L, Vodenicharov M, Affar EB, Poirier GG. Importance of poly(ADP-ribose) glycohydrolase in the control of poly(ADP-ribose) metabolism. Experimental Cell Research. 268: 7-13. PMID 11461113 DOI: 10.1006/Excr.2001.5263 |
0.333 |
|
| Show low-probability matches. |