Claudia Bagni - Publications

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93 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2023 Longo F, Aryal S, Anastasiades PG, Maltese M, Baimel C, Albanese F, Tabor J, Zhu JD, Oliveira MM, Gastaldo D, Bagni C, Santini E, Tritsch NX, Carter AG, Klann E. Cell-type-specific disruption of cortico-striatal circuitry drives repetitive patterns of behavior in fragile X syndrome model mice. Cell Reports. 42: 112901. PMID 37505982 DOI: 10.1016/j.celrep.2023.112901  0.305
2023 Mercaldo V, Vidimova B, Gastaldo D, Fernández E, Lo AC, Cencelli G, Pedini G, De Rubeis S, Longo F, Klann E, Smit AB, Grant SGN, Achsel T, Bagni C. Altered striatal actin dynamics drives behavioral inflexibility in a mouse model of fragile X syndrome. Neuron. PMID 36996810 DOI: 10.1016/j.neuron.2023.03.008  0.655
2021 Carotti S, Zingariello M, Francesconi M, D'Andrea L, Latasa MU, Colyn L, Fernandez-Barrena MG, Flammia RS, Falchi M, Righi D, Pedini G, Pantano F, Bagni C, Perrone G, Rana RA, et al. Fragile X mental retardation protein in intrahepatic cholangiocarcinoma: regulating the cancer cell behavior plasticity at the leading edge. Oncogene. PMID 34017076 DOI: 10.1038/s41388-021-01824-3  0.341
2021 Lo AC, Rajan N, Gastaldo D, Telley L, Hilal ML, Buzzi A, Simonato M, Achsel T, Bagni C. Absence of RNA-binding protein FXR2P prevents prolonged phase of kainate-induced seizures. Embo Reports. e51404. PMID 33779029 DOI: 10.15252/embr.202051404  0.307
2020 Di Grazia A, Marafini I, Pedini G, Di Fusco D, Laudisi F, Dinallo V, Rosina E, Stolfi C, Franzè E, Sileri P, Sica G, Monteleone G, Bagni C, Monteleone I. The Fragile X Mental Retardation Protein regulates RIP1K and colorectal cancer resistance to necroptosis. Cellular and Molecular Gastroenterology and Hepatology. PMID 33091622 DOI: 10.1016/j.jcmgh.2020.10.009  0.316
2020 Agote-Aran A, Schmucker S, Jerabkova K, Jmel Boyer I, Berto A, Pacini L, Ronchi P, Kleiss C, Guerard L, Schwab Y, Moine H, Mandel JL, Jacquemont S, Bagni C, Sumara I. Spatial control of nucleoporin condensation by fragile X-related proteins. The Embo Journal. e104467. PMID 32706158 DOI: 10.15252/Embj.2020104467  0.32
2020 Kanellopoulos AK, Mariano V, Spinazzi M, Woo YJ, McLean C, Pech U, Li KW, Armstrong JD, Giangrande A, Callaerts P, Smit AB, Abrahams BS, Fiala A, Achsel T, Bagni C. Aralar Sequesters GABA into Hyperactive Mitochondria, Causing Social Behavior Deficits. Cell. 180: 1178-1197.e20. PMID 32200800 DOI: 10.1016/J.Cell.2020.02.044  0.49
2019 Domínguez-Iturza N, Lo AC, Shah D, Armendáriz M, Vannelli A, Mercaldo V, Trusel M, Li KW, Gastaldo D, Santos AR, Callaerts-Vegh Z, D'Hooge R, Mameli M, Van der Linden A, Smit AB, ... ... Bagni C, et al. The autism- and schizophrenia-associated protein CYFIP1 regulates bilateral brain connectivity and behaviour. Nature Communications. 10: 3454. PMID 31371726 DOI: 10.1038/S41467-019-11203-Y  0.316
2018 Fernández E, Gennaro E, Pirozzi F, Baldo C, Forzano F, Turolla L, Faravelli F, Gastaldo D, Coviello D, Grasso M, Bagni C. FXS-Like Phenotype in Two Unrelated Patients Carrying a Methylated Premutation of the Gene. Frontiers in Genetics. 9: 442. PMID 30450110 DOI: 10.3389/Fgene.2018.00442  0.311
2018 Comhair J, Devoght J, Morelli G, Harvey RJ, Briz V, Borrie SC, Bagni C, Rigo JM, Schiffmann SN, Gall D, Brône B, Molchanova SM. Alpha2-Containing Glycine Receptors Promote Neonatal Spontaneous Activity of Striatal Medium Spiny Neurons and Support Maturation of Glutamatergic Inputs. Frontiers in Molecular Neuroscience. 11: 380. PMID 30374290 DOI: 10.3389/Fnmol.2018.00380  0.356
2018 Jacquemont S, Pacini L, Jønch AE, Cencelli G, Rozenberg I, He Y, D'Andrea L, Pedini G, Eldeeb M, Willemsen R, Gasparini F, Tassone F, Hagerman R, Gomez-Mancilla B, Bagni C. Protein synthesis levels are increased in a subset of individuals with fragile X syndrome. Human Molecular Genetics. PMID 30107584 DOI: 10.1093/Hmg/Ddy291  0.396
2018 Jacquemont S, Pacini L, Jønch AE, Cencelli G, Rozenberg I, He Y, D'Andrea L, Pedini G, Eldeeb M, Willemsen R, Gasparini F, Tassone F, Hagerman R, Gomez-Mancilla B, Bagni C. Protein synthesis levels are increased in a subset of individuals with Fragile X syndrome. Human Molecular Genetics. PMID 29590342 DOI: 10.1093/hmg/ddy099  0.362
2017 Zalfa F, Panasiti V, Carotti S, Zingariello M, Perrone G, Sancillo L, Pacini L, Luciani F, Roberti V, D'Amico S, Coppola R, Abate SO, Rana RA, De Luca A, Fiers M, ... ... Bagni C, et al. The fragile X mental retardation protein regulates tumor invasiveness-related pathways in melanoma cells. Cell Death & Disease. 8: e3169. PMID 29144507 DOI: 10.1038/Cddis.2017.521  0.382
2017 Santini E, Huynh TN, Longo F, Koo SY, Mojica E, D'Andrea L, Bagni C, Klann E. Reducing eIF4E-eIF4G interactions restores the balance between protein synthesis and actin dynamics in fragile X syndrome model mice. Science Signaling. 10. PMID 29114037 DOI: 10.1126/Scisignal.Aan0665  0.476
2017 Fernández E, Collins MO, Frank RAW, Zhu F, Kopanitsa MV, Nithianantharajah J, Lemprière SA, Fricker D, Elsegood KA, McLaughlin CL, Croning MDR, Mclean C, Armstrong JD, Hill WD, Deary IJ, ... ... Bagni C, et al. Arc Requires PSD95 for Assembly into Postsynaptic Complexes Involved with Neural Dysfunction and Intelligence. Cell Reports. 21: 679-691. PMID 29045836 DOI: 10.1016/J.Celrep.2017.09.045  0.375
2017 Borrie SC, Brems H, Legius E, Bagni C. Cognitive Dysfunctions in Intellectual Disabilities: The Contributions of the Ras-MAPK and PI3K-AKT-mTOR Pathways. Annual Review of Genomics and Human Genetics. 18: 115-142. PMID 28859574 DOI: 10.1146/Annurev-Genom-091416-035332  0.373
2017 Briz V, Restivo L, Pasciuto E, Juczewski K, Mercaldo V, Lo AC, Baatsen P, Gounko NV, Borreca A, Girardi T, Luca R, Nys J, Poorthuis RB, Mansvelder HD, Fisone G, ... ... Bagni C, et al. The non-coding RNA BC1 regulates experience-dependent structural plasticity and learning. Nature Communications. 8: 293. PMID 28819097 DOI: 10.1038/S41467-017-00311-2  0.385
2017 Filippini A, Bonini D, Lacoux C, Pacini L, Zingariello M, Sancillo L, Bosisio D, Salvi V, Mingardi J, La Via L, Zalfa F, Bagni C, Barbon A. Absence of the Fragile X Mental Retardation Protein results in defects of RNA editing of neuronal mRNAs in mouse. Rna Biology. 0. PMID 28640668 DOI: 10.1080/15476286.2017.1338232  0.465
2017 Geuens T, De Winter V, Rajan N, Achsel T, Mateiu L, Almeida-Souza L, Asselbergh B, Bouhy D, Auer-Grumbach M, Bagni C, Timmerman V. Mutant HSPB1 causes loss of translational repression by binding to PCBP1, an RNA binding protein with a possible role in neurodegenerative disease. Acta Neuropathologica Communications. 5: 5. PMID 28077174 DOI: 10.1186/S40478-016-0407-3  0.455
2016 Sabanov V, Braat S, D'Andrea L, Willemsem R, Zeidler S, Rooms L, Bagni C, Kooy RF, Balschun D. Impaired GABAergic inhibition in the hippocampus of Fmr1 knockout mice. Neuropharmacology. PMID 28012946 DOI: 10.1016/J.Neuropharm.2016.12.010  0.35
2016 Borrie SC, Bagni C. Neurons acetylate their way to migration. Embo Reports. PMID 27797856 DOI: 10.15252/Embr.201643427  0.322
2016 Juczewski K, von Richthofen H, Bagni C, Celikel T, Fisone G, Krieger P. Somatosensory map expansion and altered processing of tactile inputs in a mouse model of fragile X syndrome. Neurobiology of Disease. PMID 27616423 DOI: 10.1016/J.Nbd.2016.09.007  0.317
2016 Achsel T, Bagni C. Cooperativity in RNA-protein interactions: the complex is more than the sum of its partners. Current Opinion in Neurobiology. 39: 146-151. PMID 27352301 DOI: 10.1016/J.Conb.2016.06.007  0.471
2015 Achsel T, Doms R, Bagni C, Renzi F. Sm-like proteins in the pathogenesis of Spinal Muscular Atrophy. Springerplus. 4: L53. PMID 27386216 DOI: 10.1186/2193-1801-4-S1-L53  0.409
2015 Stepniak B, Kästner A, Poggi G, Mitjans M, Begemann M, Hartmann A, Van der Auwera S, Sananbenesi F, Krueger-Burg D, Matuszko G, Brosi C, Homuth G, Völzke H, Benseler F, Bagni C, et al. Accumulated common variants in the broader fragile X gene family modulate autistic phenotypes. Embo Molecular Medicine. PMID 26612855 DOI: 10.15252/Emmm.201505696  0.333
2015 Di Marino D, Chillemi G, De Rubeis S, Tramontano A, Achsel T, Bagni C. MD and Docking Studies Reveal That the Functional Switch of CYFIP1 is Mediated by a Butterfly-like Motion. Journal of Chemical Theory and Computation. 11: 3401-10. PMID 26575774 DOI: 10.1021/Ct500431H  0.672
2015 Pasciuto E, Ahmed T, Wahle T, Gardoni F, D'Andrea L, Pacini L, Jacquemont S, Tassone F, Balschun D, Dotti CG, Callaerts-Vegh Z, D'Hooge R, Müller UC, Di Luca M, De Strooper B, ... Bagni C, et al. Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to Synaptic Deficits in Fragile X Syndrome. Neuron. 87: 382-98. PMID 26182420 DOI: 10.1016/J.Neuron.2015.06.032  0.43
2015 Fernández E, Li KW, Rajan N, De Rubeis S, Fiers M, Smit AB, Achsel T, Bagni C. FXR2P Exerts a Positive Translational Control and Is Required for the Activity-Dependent Increase of PSD95 Expression. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 9402-8. PMID 26109663 DOI: 10.1523/Jneurosci.4800-14.2015  0.752
2015 Di Marino D, D'Annessa I, Tancredi H, Bagni C, Gallicchio E. A unique binding mode of the eukaryotic translation initiation factor 4E for guiding the design of novel peptide inhibitors. Protein Science : a Publication of the Protein Society. 24: 1370-82. PMID 26013047 DOI: 10.1002/Pro.2708  0.392
2015 Braat S, D'Hulst C, Heulens I, De Rubeis S, Mientjes E, Nelson DL, Willemsen R, Bagni C, Van Dam D, De Deyn PP, Kooy RF. The GABAA Receptor is an FMRP Target with Therapeutic Potential in Fragile X Syndrome. Cell Cycle (Georgetown, Tex.). 0. PMID 25790165 DOI: 10.4161/15384101.2014.989114  0.665
2015 Rossi S, Serrano A, Gerbino V, Giorgi A, Di Francesco L, Nencini M, Bozzo F, Schininà ME, Bagni C, Cestra G, Carrì MT, Achsel T, Cozzolino M. Nuclear accumulation of mRNAs underlies G4C2-repeat-induced translational repression in a cellular model of C9orf72 ALS. Journal of Cell Science. 128: 1787-99. PMID 25788698 DOI: 10.1242/Jcs.165332  0.47
2015 Pasciuto E, Ahmed T, Wahle T, Gardoni F, D'Andrea L, Pacini L, Jacquemont S, Tassone F, Balschun D, Dotti CG, Callaerts-Vegh Z, D'Hooge R, Müller UC, Di Luca M, De Strooper B, ... Bagni C, et al. Errata to Dysregulated ADAM10-Mediated Processing of APP during a Critical Time Window Leads to SynapticDeficits in Fragile X Syndrome [Neuron, 87, (2015), 382-398] Neuron. 87: 908. DOI: 10.1016/J.Neuron.2015.08.010  0.319
2014 Panja D, Kenney JW, D'Andrea L, Zalfa F, Vedeler A, Wibrand K, Fukunaga R, Bagni C, Proud CG, Bramham CR. Two-stage translational control of dentate gyrus LTP consolidation is mediated by sustained BDNF-TrkB signaling to MNK. Cell Reports. 9: 1430-45. PMID 25453757 DOI: 10.1016/J.Celrep.2014.10.016  0.384
2014 La Fata G, Gärtner A, Domínguez-Iturza N, Dresselaers T, Dawitz J, Poorthuis RB, Averna M, Himmelreich U, Meredith RM, Achsel T, Dotti CG, Bagni C. FMRP regulates multipolar to bipolar transition affecting neuronal migration and cortical circuitry. Nature Neuroscience. 17: 1693-700. PMID 25402856 DOI: 10.1038/Nn.3870  0.353
2014 Pasciuto E, Bagni C. SnapShot: FMRP interacting proteins. Cell. 159: 218-218.e1. PMID 25259928 DOI: 10.1016/J.Cell.2014.08.036  0.416
2014 Santos AR, Kanellopoulos AK, Bagni C. Learning and behavioral deficits associated with the absence of the fragile X mental retardation protein: what a fly and mouse model can teach us. Learning & Memory (Cold Spring Harbor, N.Y.). 21: 543-55. PMID 25227249 DOI: 10.1101/Lm.035956.114  0.459
2014 Pasciuto E, Bagni C. SnapShot: FMRP mRNA targets and diseases. Cell. 158: 1446-1446.e1. PMID 25215498 DOI: 10.1016/J.Cell.2014.08.035  0.479
2014 Hsia HE, Kumar R, Luca R, Takeda M, Courchet J, Nakashima J, Wu S, Goebbels S, An W, Eickholt BJ, Polleux F, Rotin D, Wu H, Rossner MJ, Bagni C, et al. Ubiquitin E3 ligase Nedd4-1 acts as a downstream target of PI3K/PTEN-mTORC1 signaling to promote neurite growth. Proceedings of the National Academy of Sciences of the United States of America. 111: 13205-10. PMID 25157163 DOI: 10.1073/Pnas.1400737111  0.332
2014 Di Marino D, Achsel T, Lacoux C, Falconi M, Bagni C. Molecular dynamics simulations show how the FMRP Ile304Asn mutation destabilizes the KH2 domain structure and affects its function. Journal of Biomolecular Structure & Dynamics. 32: 337-50. PMID 23527791 DOI: 10.1080/07391102.2013.768552  0.393
2014 Lucá R, Averna M, Zalfa F, Vecchi M, Bianchi F, La Fata G, Del Nonno F, Nardacci R, Bianchi M, Nuciforo P, Munck S, Parrella P, Moura R, Signori E, Alston R, ... ... Bagni C, et al. The Fragile X Protein binds mRNAs involved in cancer progression and modulates metastasis formation [EMBO Mol Med, 5, (2013) 1523-1536, DOI: 10.1002/emmm.201302847] Embo Molecular Medicine. 6: 567-568. DOI: 10.1002/Emmm.201470030  0.43
2013 Janusz A, Milek J, Perycz M, Pacini L, Bagni C, Kaczmarek L, Dziembowska M. The Fragile X mental retardation protein regulates matrix metalloproteinase 9 mRNA at synapses. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 33: 18234-41. PMID 24227732 DOI: 10.1523/Jneurosci.2207-13.2013  0.412
2013 Fernández E, Rajan N, Bagni C. The FMRP regulon: from targets to disease convergence. Frontiers in Neuroscience. 7: 191. PMID 24167470 DOI: 10.3389/Fnins.2013.00191  0.513
2013 Bagni C, Oostra BA. Fragile X syndrome: From protein function to therapy. American Journal of Medical Genetics. Part A. 161: 2809-21. PMID 24115651 DOI: 10.1002/Ajmg.A.36241  0.512
2013 Lucá R, Averna M, Zalfa F, Vecchi M, Bianchi F, La Fata G, Del Nonno F, Nardacci R, Bianchi M, Nuciforo P, Munck S, Parrella P, Moura R, Signori E, Alston R, ... ... Bagni C, et al. The fragile X protein binds mRNAs involved in cancer progression and modulates metastasis formation. Embo Molecular Medicine. 5: 1523-36. PMID 24092663 DOI: 10.1002/Emmm.201302847  0.39
2013 De Rubeis S, Pasciuto E, Li KW, Fernández E, Di Marino D, Buzzi A, Ostroff LE, Klann E, Zwartkruis FJ, Komiyama NH, Grant SG, Poujol C, Choquet D, Achsel T, Posthuma D, ... ... Bagni C, et al. CYFIP1 coordinates mRNA translation and cytoskeleton remodeling to ensure proper dendritic spine formation. Neuron. 79: 1169-82. PMID 24050404 DOI: 10.1016/J.Neuron.2013.06.039  0.718
2013 Iannilli F, Zalfa F, Gartner A, Bagni C, Dotti CG. Cytoplasmic TERT Associates to RNA Granules in Fully Mature Neurons: Role in the Translational Control of the Cell Cycle Inhibitor p15INK4B. Plos One. 8: e66602. PMID 23825548 DOI: 10.1371/Journal.Pone.0066602  0.362
2013 Charalambous DC, Pasciuto E, Mercaldo V, Pilo Boyl P, Munck S, Bagni C, Santama N. KIF1Bβ transports dendritically localized mRNPs in neurons and is recruited to synapses in an activity-dependent manner. Cellular and Molecular Life Sciences : Cmls. 70: 335-56. PMID 22945799 DOI: 10.1007/S00018-012-1108-0  0.386
2012 Bagni C, Tassone F, Neri G, Hagerman R. Fragile X syndrome: causes, diagnosis, mechanisms, and therapeutics. The Journal of Clinical Investigation. 122: 4314-22. PMID 23202739 DOI: 10.1172/Jci63141  0.396
2012 De Rubeis S, Fernández E, Buzzi A, Di Marino D, Bagni C. Molecular and cellular aspects of mental retardation in the Fragile X syndrome: from gene mutation/s to spine dysmorphogenesis. Advances in Experimental Medicine and Biology. 970: 517-51. PMID 22351071 DOI: 10.1007/978-3-7091-0932-8_23  0.728
2012 Till SM, Wijetunge LS, Seidel VG, Harlow E, Wright AK, Bagni C, Contractor A, Gillingwater TH, Kind PC. Altered maturation of the primary somatosensory cortex in a mouse model of fragile X syndrome. Human Molecular Genetics. 21: 2143-56. PMID 22328088 DOI: 10.1093/Hmg/Dds030  0.401
2012 Lacoux C, Di Marino D, Boyl PP, Zalfa F, Yan B, Ciotti MT, Falconi M, Urlaub H, Achsel T, Mougin A, Caizergues-Ferrer M, Bagni C. BC1-FMRP interaction is modulated by 2'-O-methylation: RNA-binding activity of the tudor domain and translational regulation at synapses. Nucleic Acids Research. 40: 4086-96. PMID 22238374 DOI: 10.1093/Nar/Gkr1254  0.439
2012 Miroci H, Schob C, Kindler S, Ölschläger-Schütt J, Fehr S, Jungenitz T, Schwarzacher SW, Bagni C, Mohr E. Makorin ring zinc finger protein 1 (MKRN1), a novel poly(A)-binding protein-interacting protein, stimulates translation in nerve cells. The Journal of Biological Chemistry. 287: 1322-34. PMID 22128154 DOI: 10.1074/Jbc.M111.315291  0.506
2011 De Rubeis S, Bagni C. Regulation of molecular pathways in the Fragile X Syndrome: insights into Autism Spectrum Disorders. Journal of Neurodevelopmental Disorders. 3: 257-69. PMID 21842222 DOI: 10.1007/S11689-011-9087-2  0.748
2011 Tassone F, De Rubeis S, Carosi C, La Fata G, Serpa G, Raske C, Willemsen R, Hagerman PJ, Bagni C. Differential usage of transcriptional start sites and polyadenylation sites in FMR1 premutation alleles. Nucleic Acids Research. 39: 6172-85. PMID 21478165 DOI: 10.1093/Nar/Gkr100  0.673
2011 De Rubeis S, Bagni C. Identification and characterization of protein complexes from total brain and synaptoneurosomes: Heterogeneity of molecular complexes in distinct subcellular domains Neuromethods. 57: 69-79. DOI: 10.1007/978-1-61779-111-6_6  0.621
2010 Maccarrone M, Rossi S, Bari M, De Chiara V, Rapino C, Musella A, Bernardi G, Bagni C, Centonze D. Abnormal mGlu 5 receptor/endocannabinoid coupling in mice lacking FMRP and BC1 RNA. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. 35: 1500-9. PMID 20393458 DOI: 10.1038/Npp.2010.19  0.554
2010 De Rubeis S, Bagni C. Fragile X mental retardation protein control of neuronal mRNA metabolism: Insights into mRNA stability. Molecular and Cellular Neurosciences. 43: 43-50. PMID 19837168 DOI: 10.1016/J.Mcn.2009.09.013  0.745
2009 Zukin RS, Richter JD, Bagni C. Signals, synapses, and synthesis: how new proteins control plasticity. Frontiers in Neural Circuits. 3: 14. PMID 19838324 DOI: 10.3389/Neuro.04.014.2009  0.51
2009 Fazi B, Melino S, De Rubeis S, Bagni C, Paci M, Piacentini M, Di Sano F. Acetylation of RTN-1C regulates the induction of ER stress by the inhibition of HDAC activity in neuroectodermal tumors. Oncogene. 28: 3814-24. PMID 19668229 DOI: 10.1038/Onc.2009.233  0.643
2009 di Penta A, Mercaldo V, Florenzano F, Munck S, Ciotti MT, Zalfa F, Mercanti D, Molinari M, Bagni C, Achsel T. Dendritic LSm1/CBP80-mRNPs mark the early steps of transport commitment and translational control. The Journal of Cell Biology. 184: 423-35. PMID 19188494 DOI: 10.1083/Jcb.200807033  0.487
2008 Napoli I, Mercaldo V, Boyl PP, Eleuteri B, Zalfa F, De Rubeis S, Di Marino D, Mohr E, Massimi M, Falconi M, Witke W, Costa-Mattioli M, Sonenberg N, Achsel T, Bagni C. The fragile X syndrome protein represses activity-dependent translation through CYFIP1, a new 4E-BP. Cell. 134: 1042-54. PMID 18805096 DOI: 10.1016/J.Cell.2008.07.031  0.74
2008 Bagni C. On BC1 RNA and the fragile X mental retardation protein. Proceedings of the National Academy of Sciences of the United States of America. 105: E19. PMID 18417446 DOI: 10.1073/Pnas.0801034105  0.393
2008 Centonze D, Rossi S, Mercaldo V, Napoli I, Ciotti MT, De Chiara V, Musella A, Prosperetti C, Calabresi P, Bernardi G, Bagni C. Abnormal striatal GABA transmission in the mouse model for the fragile X syndrome. Biological Psychiatry. 63: 963-73. PMID 18028882 DOI: 10.1016/J.Biopsych.2007.09.008  0.529
2007 Centonze D, Rossi S, Napoli I, Mercaldo V, Lacoux C, Ferrari F, Ciotti MT, De Chiara V, Prosperetti C, Maccarrone M, Fezza F, Calabresi P, Bernardi G, Bagni C. The brain cytoplasmic RNA BC1 regulates dopamine D2 receptor-mediated transmission in the striatum. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 8885-92. PMID 17699670 DOI: 10.1523/Jneurosci.0548-07.2007  0.541
2007 Zalfa F, Eleuteri B, Dickson KS, Mercaldo V, De Rubeis S, di Penta A, Tabolacci E, Chiurazzi P, Neri G, Grant SG, Bagni C. A new function for the fragile X mental retardation protein in regulation of PSD-95 mRNA stability. Nature Neuroscience. 10: 578-87. PMID 17417632 DOI: 10.1038/Nn1893  0.74
2007 Tassone F, Beilina A, Carosi C, Albertosi S, Bagni C, Li L, Glover K, Bentley D, Hagerman PJ. Elevated FMR1 mRNA in premutation carriers is due to increased transcription. Rna (New York, N.Y.). 13: 555-62. PMID 17283214 DOI: 10.1261/Rna.280807  0.463
2007 Ferrari F, Mercaldo V, Piccoli G, Sala C, Cannata S, Achsel T, Bagni C. The fragile X mental retardation protein-RNP granules show an mGluR-dependent localization in the post-synaptic spines. Molecular and Cellular Neurosciences. 34: 343-54. PMID 17254795 DOI: 10.1016/J.Mcn.2006.11.015  0.495
2006 Florenzano F, Viscomi MT, Mercaldo V, Longone P, Bernardi G, Bagni C, Molinari M, Carrive P. P2X2R purinergic receptor subunit mRNA and protein are expressed by all hypothalamic hypocretin/orexin neurons. The Journal of Comparative Neurology. 498: 58-67. PMID 16856176 DOI: 10.1002/Cne.21013  0.329
2006 Zalfa F, Achsel T, Bagni C. mRNPs, polysomes or granules: FMRP in neuronal protein synthesis. Current Opinion in Neurobiology. 16: 265-9. PMID 16707258 DOI: 10.1016/J.Conb.2006.05.010  0.502
2006 Paronetto MP, Zalfa F, Botti F, Geremia R, Bagni C, Sette C. The nuclear RNA-binding protein Sam68 translocates to the cytoplasm and associates with the polysomes in mouse spermatocytes. Molecular Biology of the Cell. 17: 14-24. PMID 16221888 DOI: 10.1091/Mbc.E05-06-0548  0.442
2005 Restivo L, Ferrari F, Passino E, Sgobio C, Bock J, Oostra BA, Bagni C, Ammassari-Teule M. Enriched environment promotes behavioral and morphological recovery in a mouse model for the fragile X syndrome. Proceedings of the National Academy of Sciences of the United States of America. 102: 11557-62. PMID 16076950 DOI: 10.1073/Pnas.0504984102  0.383
2005 Zalfa F, Adinolfi S, Napoli I, Kühn-Hölsken E, Urlaub H, Achsel T, Pastore A, Bagni C. Fragile X mental retardation protein (FMRP) binds specifically to the brain cytoplasmic RNAs BC1/BC200 via a novel RNA-binding motif. The Journal of Biological Chemistry. 280: 33403-10. PMID 16006558 DOI: 10.1074/Jbc.M504286200  0.475
2005 Bagni C, Greenough WT. From mRNP trafficking to spine dysmorphogenesis: the roots of fragile X syndrome. Nature Reviews. Neuroscience. 6: 376-87. PMID 15861180 DOI: 10.1038/nrn1667  0.4
2005 Zalfa F, Bagni C. Another view of the role of FMRP in translational regulation. Cellular and Molecular Life Sciences : Cmls. 62: 251-2. PMID 15666096 DOI: 10.1007/S00018-004-4521-1  0.356
2005 Baldini PM, De Vito P, Vismara D, Bagni C, Zalfa F, Minieri M, Di Nardo P. Atrial natriuretic peptide effects on intracellular pH changes and ROS production in HEPG2 cells: role of p38 MAPK and phospholipase D. Cellular Physiology and Biochemistry : International Journal of Experimental Cellular Physiology, Biochemistry, and Pharmacology. 15: 77-88. PMID 15665518 DOI: 10.1159/000083640  0.319
2004 Veneri M, Zalfa F, Bagni C. FMRP and its target RNAs: fishing for the specificity. Neuroreport. 15: 2447-50. PMID 15538171 DOI: 10.1097/00001756-200411150-00002  0.494
2004 Zalfa F, Bagni C. Molecular insights into mental retardation: multiple functions for the Fragile X mental retardation protein? Current Issues in Molecular Biology. 6: 73-88. PMID 15119819  0.452
2003 Zalfa F, Giorgi M, Primerano B, Moro A, Di Penta A, Reis S, Oostra B, Bagni C. The fragile X syndrome protein FMRP associates with BC1 RNA and regulates the translation of specific mRNAs at synapses. Cell. 112: 317-27. PMID 12581522 DOI: 10.1016/S0092-8674(03)00079-5  0.539
2002 Primerano B, Tassone F, Hagerman RJ, Hagerman P, Amaldi F, Bagni C. Reduced FMR1 mRNA translation efficiency in fragile X patients with premutations. Rna (New York, N.Y.). 8: 1482-8. PMID 12515381 DOI: 10.1017/S1355838202020642  0.68
2001 Signori E, Bagni C, Papa S, Primerano B, Rinaldi M, Amaldi F, Fazio VM. A somatic mutation in the 5'UTR of BRCA1 gene in sporadic breast cancer causes down-modulation of translation efficiency. Oncogene. 20: 4596-600. PMID 11494157 DOI: 10.1038/Sj.Onc.1204620  0.649
2001 Schenck A, Bardoni B, Moro A, Bagni C, Mandel JL. A highly conserved protein family interacting with the fragile X mental retardation protein (FMRP) and displaying selective interactions with FMRP-related proteins FXR1P and FXR2P. Proceedings of the National Academy of Sciences of the United States of America. 98: 8844-9. PMID 11438699 DOI: 10.1073/Pnas.151231598  0.455
2000 Bagni C, Mannucci L, Dotti CG, Amaldi F. Chemical stimulation of synaptosomes modulates alpha -Ca2+/calmodulin-dependent protein kinase II mRNA association to polysomes. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 20: RC76. PMID 10783400 DOI: 10.1523/Jneurosci.20-10-J0004.2000  0.66
1999 Mariottini P, Shah ZH, Toivonen JM, Bagni C, Spelbrink JN, Amaldi F, Jacobs HT. Expression of the gene for mitoribosomal protein S12 is controlled in human cells at the levels of transcription, RNA splicing, and translation. The Journal of Biological Chemistry. 274: 31853-62. PMID 10542210 DOI: 10.1074/jbc.274.45.31853  0.673
1999 Adinolfi S, Bagni C, Musco G, Gibson T, Mazzarella L, Pastore A. Dissecting FMR1, the protein responsible for fragile X syndrome, in its structural and functional domains. Rna (New York, N.Y.). 5: 1248-58. PMID 10496225 DOI: 10.1017/S1355838299990647  0.414
1999 Adinolfi S, Bagni C, Castiglione Morelli MA, Fraternali F, Musco G, Pastore A. Novel RNA-binding motif: the KH module. Biopolymers. 51: 153-64. PMID 10397799 DOI: 10.1002/(Sici)1097-0282(1999)51:2<153::Aid-Bip5>3.0.Co;2-6  0.424
1998 Bagni C, Lapeyre B. Gar1p binds to the small nucleolar RNAs snR10 and snR30 in vitro through a nontypical RNA binding element. The Journal of Biological Chemistry. 273: 10868-73. PMID 9556561 DOI: 10.1074/Jbc.273.18.10868  0.373
1993 Bagni C, Mariottini P, Annesi F, Amaldi F. Human ribosomal protein L4: cloning and sequencing of the cDNA and primary structure of the protein. Biochimica Et Biophysica Acta. 1216: 475-8. PMID 8268230 DOI: 10.1016/0167-4781(93)90017-8  0.666
1993 Mariottini P, Bagni C, Francesconi A, Cecconi F, Serra MJ, Chen QM, Loreni F, Annesi F, Amaldi F. Sequence of the gene coding for ribosomal protein S8 of Xenopus laevis. Gene. 132: 255-60. PMID 8224872 DOI: 10.1016/0378-1119(93)90204-G  0.719
1992 Bagni C, Mariottini P, Terrenato L, Amaldi F. Individual variability in the translational regulation of ribosomal protein synthesis in Xenopus laevis. Molecular & General Genetics : Mgg. 234: 60-4. PMID 1495485 DOI: 10.1007/Bf00272345  0.69
1992 Chen QM, Mariottini P, Bagni C, Amaldi F. The pyrimidine sequence encompassing the transcription start point of Xenopus laevis ribosomal-protein-encoding genes is not obligatory for activity in oocytes. Gene. 119: 283-6. PMID 1398110 DOI: 10.1016/0378-1119(92)90284-V  0.663
1990 Bagni C, Mariottini P, Annesi F, Amaldi F. Structure of Xenopus laevis ribosomal protein L32 and its expression during development. Nucleic Acids Research. 18: 4423-6. PMID 2388827 DOI: 10.1093/Nar/18.15.4423  0.683
1989 Cardinali B, Bagni C, Amaldi F, Campioni N, Mariottini P, Pierandrei-Amaldi P. Translational regulation of ribosomal protein synthesis during xenopus development Cell Differentiation and Development. 27: 219. DOI: 10.1016/0922-3371(89)90661-8  0.661
1988 Mariottini P, Bagni C, Annesi F, Amaldi F. Isolation and nucleotide sequences of cDNAs for Xenopus laevis ribosomal protein S8: similarities in the 5' and 3' untranslated regions of mRNAs for various r-proteins. Gene. 67: 69-74. PMID 2843441 DOI: 10.1016/0378-1119(88)90009-1  0.688
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