Claudia Bagni - Publications

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86 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
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  0.44
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  0.44
2016 Yrigollen CM, Pacini L, Nobile V, Lozano R, Hagerman RJ, Bagni C, Tassone F. Clinical and Molecular Assessment in a Female with Fragile X Syndrome and Tuberous Sclerosis. Journal of Genetic Disorders & Genetic Reports. 5. PMID 28232951 DOI: 10.4172/2327-5790.1000139  0.44
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  0.96
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  0.96
2015 Grant SG, Bagni C, O'Dell TJ. Synaptopathy - From Biology to Therapy. Neuropharmacology. PMID 26292261 DOI: 10.1016/j.neuropharm.2015.08.022  0.96
2015 Pasciuto E, Borrie SC, Kanellopoulos AK, Santos AR, Cappuyns E, D'Andrea L, Pacini L, Bagni C. Autism Spectrum Disorders: Translating human deficits into mouse behavior. Neurobiology of Learning and Memory. 124: 71-87. PMID 26220900 DOI: 10.1016/j.nlm.2015.07.013  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2015 Achsel T, Doms R, Bagni C, Renzi F. Sm-like proteins in the pathogenesis of Spinal Muscular Atrophy Springerplus. 4: 1-32. DOI: 10.1186/2193-1801-4-S1-L53  0.96
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  0.96
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  0.96
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  0.96
2014 Pasciuto E, Bagni C. SnapShot: FMRP interacting proteins. Cell. 159: 218-218.e1. PMID 25259928 DOI: 10.1016/j.cell.2014.08.036  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2013 Trovò L, Ahmed T, Callaerts-Vegh Z, Buzzi A, Bagni C, Chuah M, Vandendriessche T, D'Hooge R, Balschun D, Dotti CG. Low hippocampal PI(4,5)Pâ‚‚ contributes to reduced cognition in old mice as a result of loss of MARCKS. Nature Neuroscience. 16: 449-55. PMID 23434911 DOI: 10.1038/nn.3342  0.96
2013 De Keersmaecker K, Atak ZK, Li N, Vicente C, Patchett S, Girardi T, Gianfelici V, Geerdens E, Clappier E, Porcu M, Lahortiga I, Lucà R, Yan J, Hulselmans G, Vranckx H, ... ... Bagni C, et al. Exome sequencing identifies mutation in CNOT3 and ribosomal genes RPL5 and RPL10 in T-cell acute lymphoblastic leukemia. Nature Genetics. 45: 186-90. PMID 23263491 DOI: 10.1038/ng.2508  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2008 Tabolacci E, Moscato U, Zalfa F, Bagni C, Chiurazzi P, Neri G. Epigenetic analysis reveals a euchromatic configuration in the FMR1 unmethylated full mutations. European Journal of Human Genetics : Ejhg. 16: 1487-98. PMID 18628788 DOI: 10.1038/ejhg.2008.130  0.96
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  0.96
2008 Florenzano F, Carrive P, Viscomi MT, Ferrari F, Latini L, Conversi D, Cabib S, Bagni C, Molinari M. Cortical and subcortical distribution of ionotropic purinergic receptor subunit type 1 (P2X(1)R) immunoreactive neurons in the rat forebrain. Neuroscience. 151: 791-801. PMID 18178317 DOI: 10.1016/j.neuroscience.2007.11.027  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2005 Baldini PM, De Vito P, D'aquilio F, Vismara D, Zalfa F, Bagni C, Fiaccavento R, Di Nardo P. Role of atrial natriuretic peptide in the suppression of lysophosphatydic acid-induced rat aortic smooth muscle (RASM) cell growth. Molecular and Cellular Biochemistry. 272: 19-28. PMID 16010968 DOI: 10.1007/s11010-005-4779-0  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2005 Pietrobono R, Tabolacci E, Zalfa F, Zito I, Terracciano A, Moscato U, Bagni C, Oostra B, Chiurazzi P, Neri G. Molecular dissection of the events leading to inactivation of the FMR1 gene. Human Molecular Genetics. 14: 267-77. PMID 15563507 DOI: 10.1093/hmg/ddi024  0.96
2004 Baldini PM, De Vito P, Antenucci D, Vismara D, D'Aquilio F, Luly P, Zalfa F, Bagni C, Di Nardo P. Atrial natriuretic peptide induces cell death in human hepatoblastoma (HepG2) through the involvement of NADPH oxidase. Cell Death and Differentiation. 11: S210-2. PMID 15565178 DOI: 10.1038/sj.cdd.4401520  0.96
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  0.96
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  0.96
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  0.96
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  0.96
2002 Bagni C, Bray S, Gogos JA, Kafatos FC, Hsu T. The Drosophila zinc finger transcription factor CF2 is a myogenic marker downstream of MEF2 during muscle development. Mechanisms of Development. 117: 265-8. PMID 12204268 DOI: 10.1016/S0925-4773(02)00176-4  0.96
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  0.96
2001 Pepe G, Giusti B, Evangelisti L, Porciani MC, Brunelli T, Giurlani L, Attanasio M, Fattori R, Bagni C, Comeglio P, Abbate R, Gensini GF. Fibrillin-1 (FBN1) gene frameshift mutations in Marfan patients: genotype-phenotype correlation. Clinical Genetics. 59: 444-50. PMID 11453977 DOI: 10.1034/j.1399-0004.2001.590610.x  0.96
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  0.96
2001 Cannata SM, Bagni C, Bernardini S, Christen B, Filoni S. Nerve-independence of limb regeneration in larval Xenopus laevis is correlated to the level of fgf-2 mRNA expression in limb tissues. Developmental Biology. 231: 436-46. PMID 11237471 DOI: 10.1006/dbio.2001.0161  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
1996 Hsu T, Bagni C, Sutherland JD, Kafatos FC. The transcriptional factor CF2 is a mediator of EGF-R-activated dorsoventral patterning in Drosophila oogenesis. Genes & Development. 10: 1411-21. PMID 8647437  0.96
1994 Girard JP, Bagni C, Caizergues-Ferrer M, Amalric F, Lapeyre B. Identification of a segment of the small nucleolar ribonucleoprotein-associated protein GAR1 that is sufficient for nucleolar accumulation. The Journal of Biological Chemistry. 269: 18499-506. PMID 8034598  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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  0.96
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