Francisco Baralle - Publications

University of Oxford, Oxford, United Kingdom 

211 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
2015 Skoko N, Baralle M, Baralle FE. Absence of TDP-43 is difficult to digest. The Embo Journal. PMID 26702101 DOI: 10.15252/embj.201593603  0.88
2015 Cragnaz L, Klima R, De Conti L, Romano G, Feiguin F, Buratti E, Baralle M, Baralle FE. An age-related reduction of brain TBPH/TDP-43 levels precedes the onset of locomotion defects in a Drosophila ALS model. Neuroscience. PMID 26518462 DOI: 10.1016/j.neuroscience.2015.10.037  0.88
2015 Colombrita C, Onesto E, Buratti E, de la Grange P, Gumina V, Baralle FE, Silani V, Ratti A. From transcriptomic to protein level changes in TDP-43 and FUS loss-of-function cell models. Biochimica Et Biophysica Acta. 1849: 1398-1410. PMID 26514432 DOI: 10.1016/j.bbagrm.2015.10.015  0.88
2015 Romano G, Appocher C, Scorzeto M, Klima R, Baralle FE, Megighian A, Feiguin F. Glial TDP-43 regulates axon wrapping, GluRIIA clustering and fly motility by autonomous and non-autonomous mechanisms. Human Molecular Genetics. 24: 6134-45. PMID 26276811 DOI: 10.1093/hmg/ddv330  0.88
2015 Mompeán M, Hervás R, Xu Y, Tran TH, Guarnaccia C, Buratti E, Baralle F, Tong L, Carrión-Vázquez M, McDermott AE, Laurents DV. Structural Evidence of Amyloid Fibril Formation in the Putative Aggregation Domain of TDP-43. The Journal of Physical Chemistry Letters. 6: 2608-15. PMID 26266742 DOI: 10.1021/Acs.Jpclett.5B00918  0.88
2015 Romano V, Quadri Z, Baralle FE, Buratti E. The structural integrity of TDP-43 N-terminus is required for efficient aggregate entrapment and consequent loss of protein function. Prion. 9: 1-9. PMID 25635624 DOI: 10.1080/19336896.2015.1011885  0.88
2015 Budini M, Romano V, Quadri Z, Buratti E, Baralle FE. TDP-43 loss of cellular function through aggregation requires additional structural determinants beyond its C-terminal Q/N prion-like domain. Human Molecular Genetics. 24: 9-20. PMID 25122661 DOI: 10.1093/hmg/ddu415  0.88
2014 Romano G, Klima R, Buratti E, Verstreken P, Baralle FE, Feiguin F. Chronological requirements of TDP-43 function in synaptic organization and locomotive control. Neurobiology of Disease. 71: 95-109. PMID 25088713 DOI: 10.1016/j.nbd.2014.07.007  0.88
2014 Cragnaz L, Klima R, Skoko N, Budini M, Feiguin F, Baralle FE. Aggregate formation prevents dTDP-43 neurotoxicity in the Drosophila melanogaster eye. Neurobiology of Disease. 71: 74-80. PMID 25088712 DOI: 10.1016/j.nbd.2014.07.009  0.88
2014 Budini M, Baralle FE, Buratti E. Targeting TDP-43 in neurodegenerative diseases. Expert Opinion On Therapeutic Targets. 18: 617-32. PMID 24649927 DOI: 10.1517/14728222.2014.896905  0.88
2014 Grodecká L, Lockerová P, Rav?uková B, Buratti E, Baralle FE, Dušek L, Freiberger T. Exon first nucleotide mutations in splicing: evaluation of in silico prediction tools. Plos One. 9: e89570. PMID 24586880 DOI: 10.1371/journal.pone.0089570  0.88
2014 Langellotti S, Romano M, Guarnaccia C, Granata V, Orrù S, Zagari A, Baralle FE, Salvatore F. A novel anti-aldolase C antibody specifically interacts with residues 85-102 of the protein. Mabs. 6: 708-17. PMID 24525694 DOI: 10.4161/mabs.28191  0.88
2014 Romano M, Buratti E, Romano G, Klima R, Del Bel Belluz L, Stuani C, Baralle F, Feiguin F. Evolutionarily conserved heterogeneous nuclear ribonucleoprotein (hnRNP) A/B proteins functionally interact with human and Drosophila TAR DNA-binding protein 43 (TDP-43). The Journal of Biological Chemistry. 289: 7121-30. PMID 24492607 DOI: 10.1074/Jbc.M114.548859  0.88
2014 Mompeán M, Buratti E, Guarnaccia C, Brito RM, Chakrabartty A, Baralle FE, Laurents DV. "Structural characterization of the minimal segment of TDP-43 competent for aggregation". Archives of Biochemistry and Biophysics. 545: 53-62. PMID 24440310 DOI: 10.1016/J.Abb.2014.01.007  0.88
2014 Bembich S, Herzog JS, De Conti L, Stuani C, Avendaño-Vázquez SE, Buratti E, Baralle M, Baralle FE. Predominance of spliceosomal complex formation over polyadenylation site selection in TDP-43 autoregulation. Nucleic Acids Research. 42: 3362-71. PMID 24369426 DOI: 10.1093/nar/gkt1343  0.88
2014 Dardis A, Zanin I, Zampieri S, Stuani C, Pianta A, Romanello M, Baralle FE, Bembi B, Buratti E. Functional characterization of the common c.-32-13T>G mutation of GAA gene: identification of potential therapeutic agents. Nucleic Acids Research. 42: 1291-302. PMID 24150945 DOI: 10.1093/nar/gkt987  0.88
2013 Baralle M, Buratti E, Baralle FE. The role of TDP-43 in the pathogenesis of ALS and FTLD. Biochemical Society Transactions. 41: 1536-40. PMID 24256250 DOI: 10.1042/BST20130186  0.88
2013 Lukavsky PJ, Daujotyte D, Tollervey JR, Ule J, Stuani C, Buratti E, Baralle FE, Damberger FF, Allain FH. Molecular basis of UG-rich RNA recognition by the human splicing factor TDP-43. Nature Structural & Molecular Biology. 20: 1443-9. PMID 24240615 DOI: 10.1038/Nsmb.2698  0.88
2013 Baralle FE, Buratti E. RNA and splicing regulation in neurodegeneration. Molecular and Cellular Neurosciences. 56: 404-5. PMID 24090657 DOI: 10.1016/j.mcn.2013.09.001  0.88
2013 Bonomi S, di Matteo A, Buratti E, Cabianca DS, Baralle FE, Ghigna C, Biamonti G. HnRNP A1 controls a splicing regulatory circuit promoting mesenchymal-to-epithelial transition. Nucleic Acids Research. 41: 8665-79. PMID 23863836 DOI: 10.1093/nar/gkt579  0.88
2013 Bhardwaj A, Myers MP, Buratti E, Baralle FE. Characterizing TDP-43 interaction with its RNA targets. Nucleic Acids Research. 41: 5062-74. PMID 23519609 DOI: 10.1093/nar/gkt189  0.88
2013 Buratti E, Romano M, Baralle FE. TDP-43 high throughput screening analyses in neurodegeneration: advantages and pitfalls. Molecular and Cellular Neurosciences. 56: 465-74. PMID 23500590 DOI: 10.1016/j.mcn.2013.03.001  0.88
2013 Buratti E, Baralle M, Baralle FE. From single splicing events to thousands: the ambiguous step forward in splicing research. Briefings in Functional Genomics. 12: 3-12. PMID 23165350 DOI: 10.1093/bfgp/els048  0.88
2012 Avendaño-Vázquez SE, Dhir A, Bembich S, Buratti E, Proudfoot N, Baralle FE. Autoregulation of TDP-43 mRNA levels involves interplay between transcription, splicing, and alternative polyA site selection. Genes & Development. 26: 1679-84. PMID 22855830 DOI: 10.1101/gad.194829.112  0.88
2012 Becker K, Braune M, Benderska N, Buratti E, Baralle F, Villmann C, Stamm S, Eulenburg V, Becker CM. A retroelement modifies pre-mRNA splicing: the murine Glrb(spa) allele is a splicing signal polymorphism amplified by long interspersed nuclear element insertion. The Journal of Biological Chemistry. 287: 31185-94. PMID 22782896 DOI: 10.1074/Jbc.M112.375691  0.88
2012 Buratti E, Baralle FE. TDP-43: gumming up neurons through protein-protein and protein-RNA interactions. Trends in Biochemical Sciences. 37: 237-47. PMID 22534659 DOI: 10.1016/j.tibs.2012.03.003  0.88
2012 Zubovi? L, Baralle M, Baralle FE. Mutually exclusive splicing regulates the Nav 1.6 sodium channel function through a combinatorial mechanism that involves three distinct splicing regulatory elements and their ligands. Nucleic Acids Research. 40: 6255-69. PMID 22434879 DOI: 10.1093/nar/gks249  0.88
2012 Colombrita C, Onesto E, Megiorni F, Pizzuti A, Baralle FE, Buratti E, Silani V, Ratti A. TDP-43 and FUS RNA-binding proteins bind distinct sets of cytoplasmic messenger RNAs and differently regulate their post-transcriptional fate in motoneuron-like cells. The Journal of Biological Chemistry. 287: 15635-47. PMID 22427648 DOI: 10.1074/jbc.M111.333450  0.88
2012 Budini M, Romano V, Avendaño-Vázquez SE, Bembich S, Buratti E, Baralle FE. Role of selected mutations in the Q/N rich region of TDP-43 in EGFP-12xQ/N-induced aggregate formation. Brain Research. 1462: 139-50. PMID 22406069 DOI: 10.1016/j.brainres.2012.02.031  0.88
2012 Budini M, Buratti E, Stuani C, Guarnaccia C, Romano V, De Conti L, Baralle FE. Cellular model of TAR DNA-binding protein 43 (TDP-43) aggregation based on its C-terminal Gln/Asn-rich region. The Journal of Biological Chemistry. 287: 7512-25. PMID 22235134 DOI: 10.1074/jbc.M111.288720  0.88
2012 Curlin M, Kapuralin K, Muro AF, Baralle FE, Chowdhury K, Gajovi? S. Stam2 expression pattern during embryo development. Gene Expression Patterns : Gep. 12: 68-76. PMID 22143071 DOI: 10.1016/j.gep.2011.11.005  0.88
2012 Buratti E, Baralle FE. Splicing and Disease Alternative Pre-Mrna Splicing: Theory and Protocols. 119-128. DOI: 10.1002/9783527636778.ch10  0.88
2012 Buratti E, Romano M, Baralle FE. Splicing in the RNA World Alternative Pre-Mrna Splicing: Theory and Protocols. 1-12. DOI: 10.1002/9783527636778.ch1  0.88
2011 Baralle FE, Buratti E. TDP-43: Overview of the series. The Febs Journal. 278: 3529. PMID 21810175 DOI: 10.1111/j.1742-4658.2011.08278.x  0.88
2011 Buratti E, Baralle FE. TDP-43: new aspects of autoregulation mechanisms in RNA binding proteins and their connection with human disease. The Febs Journal. 278: 3530-8. PMID 21777388 DOI: 10.1111/j.1742-4658.2011.08257.x  0.88
2011 Zago P, Buratti E, Stuani C, Baralle FE. Evolutionary connections between coding and splicing regulatory regions in the fibronectin EDA exon. Journal of Molecular Biology. 411: 1-15. PMID 21663748 DOI: 10.1016/j.jmb.2011.05.031  0.88
2011 Godena VK, Romano G, Romano M, Appocher C, Klima R, Buratti E, Baralle FE, Feiguin F. TDP-43 regulates Drosophila neuromuscular junctions growth by modulating Futsch/MAP1B levels and synaptic microtubules organization. Plos One. 6: e17808. PMID 21412434 DOI: 10.1371/journal.pone.0017808  0.88
2011 Budini M, Baralle FE, Buratti E. Regulation of gene expression by TDP-43 and FUS/TLS in frontotemporal lobar degeneration. Current Alzheimer Research. 8: 237-45. PMID 21222602 DOI: 10.2174/156720511795563719  0.88
2011 Ayala YM, De Conti L, Avendaño-Vázquez SE, Dhir A, Romano M, D'Ambrogio A, Tollervey J, Ule J, Baralle M, Buratti E, Baralle FE. TDP-43 regulates its mRNA levels through a negative feedback loop. The Embo Journal. 30: 277-88. PMID 21131904 DOI: 10.1038/Emboj.2010.310  0.88
2010 Valacca C, Bonomi S, Buratti E, Pedrotti S, Baralle FE, Sette C, Ghigna C, Biamonti G. Sam68 regulates EMT through alternative splicing-activated nonsense-mediated mRNA decay of the SF2/ASF proto-oncogene. The Journal of Cell Biology. 191: 87-99. PMID 20876280 DOI: 10.1083/jcb.201001073  0.88
2010 Buratti E, Baralle FE. Neurons don't appreciate FUSsing in the cytoplasm. The Embo Journal. 29: 2769-71. PMID 20717146 DOI: 10.1038/emboj.2010.163  0.88
2010 Buratti E, Baralle FE. The multiple roles of TDP-43 in pre-mRNA processing and gene expression regulation. Rna Biology. 7: 420-9. PMID 20639693 DOI: 10.4161/rna.7.4.12205  0.88
2010 Buratti E, De Conti L, Stuani C, Romano M, Baralle M, Baralle F. Nuclear factor TDP-43 can affect selected microRNA levels. The Febs Journal. 277: 2268-81. PMID 20423455 DOI: 10.1111/J.1742-4658.2010.07643.X  0.88
2010 Dhir A, Buratti E, van Santen MA, Lührmann R, Baralle FE. The intronic splicing code: multiple factors involved in ATM pseudoexon definition. The Embo Journal. 29: 749-60. PMID 20094034 DOI: 10.1038/emboj.2009.397  0.88
2010 Haque A, Buratti E, Baralle FE. Functional properties and evolutionary splicing constraints on a composite exonic regulatory element of splicing in CFTR exon 12. Nucleic Acids Research. 38: 647-59. PMID 19910374 DOI: 10.1093/nar/gkp1040  0.88
2010 Sorarú G, Orsetti V, Buratti E, Baralle F, Cima V, Volpe M, D'ascenzo C, Palmieri A, Koutsikos K, Pegoraro E, Angelini C. TDP-43 in skeletal muscle of patients affected with amyotrophic lateral sclerosis. Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group On Motor Neuron Diseases. 11: 240-3. PMID 19306141 DOI: 10.3109/17482960902810890  0.88
2009 Buratti E, Baralle FE. The molecular links between TDP-43 dysfunction and neurodegeneration. Advances in Genetics. 66: 1-34. PMID 19737636 DOI: 10.1016/S0065-2660(09)66001-6  0.88
2009 Baralle FE. Italy leads the way in supporting African biotechnology. Nature. 460: 1079. PMID 19713913 DOI: 10.1038/4601079a  0.88
2009 D'Ambrogio A, Buratti E, Stuani C, Guarnaccia C, Romano M, Ayala YM, Baralle FE. Functional mapping of the interaction between TDP-43 and hnRNP A2 in vivo. Nucleic Acids Research. 37: 4116-26. PMID 19429692 DOI: 10.1093/Nar/Gkp342  0.88
2009 Zhang YJ, Xu YF, Cook C, Gendron TF, Roettges P, Link CD, Lin WL, Tong J, Castanedes-Casey M, Ash P, Gass J, Rangachari V, Buratti E, Baralle F, Golde TE, et al. Aberrant cleavage of TDP-43 enhances aggregation and cellular toxicity. Proceedings of the National Academy of Sciences of the United States of America. 106: 7607-12. PMID 19383787 DOI: 10.1073/Pnas.0900688106  0.88
2009 Feiguin F, Godena VK, Romano G, D'Ambrogio A, Klima R, Baralle FE. Depletion of TDP-43 affects Drosophila motoneurons terminal synapsis and locomotive behavior. Febs Letters. 583: 1586-92. PMID 19379745 DOI: 10.1016/j.febslet.2009.04.019  0.88
2009 Corrado L, Ratti A, Gellera C, Buratti E, Castellotti B, Carlomagno Y, Ticozzi N, Mazzini L, Testa L, Taroni F, Baralle FE, Silani V, D'Alfonso S. High frequency of TARDBP gene mutations in Italian patients with amyotrophic lateral sclerosis. Human Mutation. 30: 688-94. PMID 19224587 DOI: 10.1002/humu.20950  0.88
2009 Marcucci R, Romano M, Feiguin F, O'Connell MA, Baralle FE. Dissecting the splicing mechanism of the Drosophila editing enzyme; dADAR. Nucleic Acids Research. 37: 1663-71. PMID 19153139 DOI: 10.1093/nar/gkn1080  0.88
2009 Nonaka T, Arai T, Buratti E, Baralle FE, Akiyama H, Hasegawa M. Phosphorylated and ubiquitinated TDP-43 pathological inclusions in ALS and FTLD-U are recapitulated in SH-SY5Y cells. Febs Letters. 583: 394-400. PMID 19111550 DOI: 10.1016/j.febslet.2008.12.031  0.88
2009 Pagani F, Baralle FE. Analysis of Human Splicing Defects Using Hybrid Minigenes Molecular Diagnostics: Second Edition. 155-169. DOI: 10.1016/B978-0-12-374537-8.00011-0  0.88
2008 Ayala YM, Zago P, D'Ambrogio A, Xu YF, Petrucelli L, Buratti E, Baralle FE. Structural determinants of the cellular localization and shuttling of TDP-43. Journal of Cell Science. 121: 3778-85. PMID 18957508 DOI: 10.1242/Jcs.038950  0.88
2008 White ES, Baralle FE, Muro AF. New insights into form and function of fibronectin splice variants. The Journal of Pathology. 216: 1-14. PMID 18680111 DOI: 10.1002/path.2388  0.88
2008 Inukai Y, Nonaka T, Arai T, Yoshida M, Hashizume Y, Beach TG, Buratti E, Baralle FE, Akiyama H, Hisanaga S, Hasegawa M. Abnormal phosphorylation of Ser409/410 of TDP-43 in FTLD-U and ALS. Febs Letters. 582: 2899-904. PMID 18656473 DOI: 10.1016/j.febslet.2008.07.027  0.88
2008 Baralle M, Baralle FE. Genetics and molecular biology: variations in alternative spliced pre-mRNA-protein isoforms and their role in disease. Current Opinion in Lipidology. 19: 429-30. PMID 18607191 DOI: 10.1097/MOL.0b013e328306f0b8  0.88
2008 Hasegawa M, Arai T, Nonaka T, Kametani F, Yoshida M, Hashizume Y, Beach TG, Buratti E, Baralle F, Morita M, Nakano I, Oda T, Tsuchiya K, Akiyama H. Phosphorylated TDP-43 in frontotemporal lobar degeneration and amyotrophic lateral sclerosis. Annals of Neurology. 64: 60-70. PMID 18546284 DOI: 10.1002/Ana.21425  0.88
2008 Skoko N, Baralle M, Buratti E, Baralle FE. The pathological splicing mutation c.6792C>G in NF1 exon 37 causes a change of tenancy between antagonistic splicing factors. Febs Letters. 582: 2231-6. PMID 18503770 DOI: 10.1016/j.febslet.2008.05.018  0.88
2008 Sreedharan J, Blair IP, Tripathi VB, Hu X, Vance C, Rogelj B, Ackerley S, Durnall JC, Williams KL, Buratti E, Baralle F, de Belleroche J, Mitchell JD, Leigh PN, Al-Chalabi A, et al. TDP-43 mutations in familial and sporadic amyotrophic lateral sclerosis. Science (New York, N.Y.). 319: 1668-72. PMID 18309045 DOI: 10.1126/Science.1154584  0.88
2008 Ayala YM, Misteli T, Baralle FE. TDP-43 regulates retinoblastoma protein phosphorylation through the repression of cyclin-dependent kinase 6 expression. Proceedings of the National Academy of Sciences of the United States of America. 105: 3785-9. PMID 18305152 DOI: 10.1073/Pnas.0800546105  0.88
2008 Romano M, Bacalini MG, Verschoor EJ, Crovella S, Baralle FE. Origin and evolution of the c.844_845ins68/c.833T>C mutations within the cystathionine beta-synthase gene in great apes. Febs Letters. 582: 423-6. PMID 18201569 DOI: 10.1016/j.febslet.2007.12.038  0.88
2008 Muro AF, Moretti FA, Moore BB, Yan M, Atrasz RG, Wilke CA, Flaherty KR, Martinez FJ, Tsui JL, Sheppard D, Baralle FE, Toews GB, White ES. An essential role for fibronectin extra type III domain A in pulmonary fibrosis. American Journal of Respiratory and Critical Care Medicine. 177: 638-45. PMID 18096707 DOI: 10.1164/Rccm.200708-1291Oc  0.88
2008 Chauhan AK, Kisucka J, Cozzi MR, Walsh MT, Moretti FA, Battiston M, Mazzucato M, De Marco L, Baralle FE, Wagner DD, Muro AF. Prothrombotic effects of fibronectin isoforms containing the EDA domain. Arteriosclerosis, Thrombosis, and Vascular Biology. 28: 296-301. PMID 17991876 DOI: 10.1161/Atvbaha.107.149146  0.88
2008 Buratti E, Baralle FE. Multiple roles of TDP-43 in gene expression, splicing regulation, and human disease. Frontiers in Bioscience : a Journal and Virtual Library. 13: 867-78. PMID 17981595 DOI: 10.2741/2727  0.88
2008 Babaev VR, Porro F, Linton MF, Fazio S, Baralle FE, Muro AF. Absence of regulated splicing of fibronectin EDA exon reduces atherosclerosis in mice. Atherosclerosis. 197: 534-40. PMID 17897651 DOI: 10.1016/J.Atherosclerosis.2007.08.015  0.88
2007 Zhang YJ, Xu YF, Dickey CA, Buratti E, Baralle F, Bailey R, Pickering-Brown S, Dickson D, Petrucelli L. Progranulin mediates caspase-dependent cleavage of TAR DNA binding protein-43. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 27: 10530-4. PMID 17898224 DOI: 10.1523/Jneurosci.3421-07.2007  0.88
2007 Giraud M, Taubert R, Vandiedonck C, Ke X, Lévi-Strauss M, Pagani F, Baralle FE, Eymard B, Tranchant C, Gajdos P, Vincent A, Willcox N, Beeson D, Kyewski B, Garchon HJ. An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus. Nature. 448: 934-7. PMID 17687331 DOI: 10.1038/nature06066  0.88
2007 Moretti FA, Chauhan AK, Iaconcig A, Porro F, Baralle FE, Muro AF. A major fraction of fibronectin present in the extracellular matrix of tissues is plasma-derived. The Journal of Biological Chemistry. 282: 28057-62. PMID 17644525 DOI: 10.1074/jbc.M611315200  0.88
2007 Buratti E, Dhir A, Lewandowska MA, Baralle FE. RNA structure is a key regulatory element in pathological ATM and CFTR pseudoexon inclusion events. Nucleic Acids Research. 35: 4369-83. PMID 17580311 DOI: 10.1093/nar/gkm447  0.88
2007 Buratti E, Stuani C, De Prato G, Baralle FE. SR protein-mediated inhibition of CFTR exon 9 inclusion: molecular characterization of the intronic splicing silencer. Nucleic Acids Research. 35: 4359-68. PMID 17576688 DOI: 10.1093/nar/gkm444  0.88
2007 Baralle M, Baralle FE. Genetics and molecular biology: micro RNAs are welcome to the lipid field. Current Opinion in Lipidology. 18: 375-7. PMID 17495611 DOI: 10.1097/MOL.0b013e32813aee6e  0.88
2007 Raponi M, Baralle FE, Pagani F. Reduced splicing efficiency induced by synonymous substitutions may generate a substrate for natural selection of new splicing isoforms: the case of CFTR exon 12. Nucleic Acids Research. 35: 606-13. PMID 17172597 DOI: 10.1093/nar/gkl1087  0.88
2007 Marcucci R, Baralle FE, Romano M. Complex splicing control of the human Thrombopoietin gene by intronic G runs. Nucleic Acids Research. 35: 132-42. PMID 17158158 DOI: 10.1093/nar/gkl965  0.88
2006 Baralle M, Skoko N, Knezevich A, De Conti L, Motti D, Bhuvanagiri M, Baralle D, Buratti E, Baralle FE. NF1 mRNA biogenesis: effect of the genomic milieu in splicing regulation of the NF1 exon 37 region. Febs Letters. 580: 4449-56. PMID 16870183 DOI: 10.1016/j.febslet.2006.07.018  0.88
2006 Buratti E, Baralle M, Baralle FE. Defective splicing, disease and therapy: searching for master checkpoints in exon definition. Nucleic Acids Research. 34: 3494-510. PMID 16855287 DOI: 10.1093/nar/gkl498  0.88
2006 Baralle M, Baralle FE. Genetics and molecular biology: single nucleotide polymorphism associations and their functional significance. Current Opinion in Lipidology. 17: 360-2. PMID 16680040 DOI: 10.1097/01.mol.0000226127.40500.0c  0.88
2006 Ayala YM, Pagani F, Baralle FE. TDP43 depletion rescues aberrant CFTR exon 9 skipping. Febs Letters. 580: 1339-44. PMID 16458894 DOI: 10.1016/J.Febslet.2006.01.052  0.88
2006 Costessi L, Devescovi G, Baralle FE, Muro AF. Brain-specific promoter and polyadenylation sites of the beta-adducin pre-mRNA generate an unusually long 3'-UTR. Nucleic Acids Research. 34: 243-53. PMID 16414955 DOI: 10.1093/nar/gkj425  0.88
2005 Mercado PA, Ayala YM, Romano M, Buratti E, Baralle FE. Depletion of TDP 43 overrides the need for exonic and intronic splicing enhancers in the human apoA-II gene. Nucleic Acids Research. 33: 6000-10. PMID 16254078 DOI: 10.1093/Nar/Gki897  0.88
2005 Buratti E, Brindisi A, Giombi M, Tisminetzky S, Ayala YM, Baralle FE. TDP-43 binds heterogeneous nuclear ribonucleoprotein A/B through its C-terminal tail: an important region for the inhibition of cystic fibrosis transmembrane conductance regulator exon 9 splicing. The Journal of Biological Chemistry. 280: 37572-84. PMID 16157593 DOI: 10.1074/Jbc.M505557200  0.88
2005 Fededa JP, Petrillo E, Gelfand MS, Neverov AD, Kadener S, Nogués G, Pelisch F, Baralle FE, Muro AF, Kornblihtt AR. A polar mechanism coordinates different regions of alternative splicing within a single gene. Molecular Cell. 19: 393-404. PMID 16061185 DOI: 10.1016/j.molcel.2005.06.035  0.88
2005 Lewandowska MA, Stuani C, Parvizpur A, Baralle FE, Pagani F. Functional studies on the ATM intronic splicing processing element. Nucleic Acids Research. 33: 4007-15. PMID 16030351 DOI: 10.1093/nar/gki710  0.88
2005 Zanetti M, Barazzoni R, Stebel M, Roder E, Biolo G, Baralle FE, Cattin L, Guarnieri G. Dysregulation of the endothelial nitric oxide synthase-soluble guanylate cyclase pathway is normalized by insulin in the aorta of diabetic rat. Atherosclerosis. 181: 69-73. PMID 15939056 DOI: 10.1016/j.atherosclerosis.2005.01.011  0.88
2005 Chauhan AK, Moretti FA, Iaconcig A, Baralle FE, Muro AF. Impaired motor coordination in mice lacking the EDA exon of the fibronectin gene. Behavioural Brain Research. 161: 31-8. PMID 15904707 DOI: 10.1016/j.bbr.2005.02.020  0.88
2005 Baralle M, Baralle FE. Genetics and molecular biology. Current Opinion in Lipidology. 16: 385-7. PMID 15891399  0.88
2005 Pagani F, Raponi M, Baralle FE. Synonymous mutations in CFTR exon 12 affect splicing and are not neutral in evolution. Proceedings of the National Academy of Sciences of the United States of America. 102: 6368-72. PMID 15840711 DOI: 10.1073/pnas.0502288102  0.88
2005 Ayala YM, Pantano S, D'Ambrogio A, Buratti E, Brindisi A, Marchetti C, Romano M, Baralle FE. Human, Drosophila, and C.elegans TDP43: nucleic acid binding properties and splicing regulatory function. Journal of Molecular Biology. 348: 575-88. PMID 15826655 DOI: 10.1016/J.Jmb.2005.02.038  0.88
2005 Buratti E, Baralle FE. Another step forward for SELEXive splicing. Trends in Molecular Medicine. 11: 5-9. PMID 15649816 DOI: 10.1016/j.molmed.2004.11.007  0.88
2004 Buratti E, Baralle FE. Influence of RNA secondary structure on the pre-mRNA splicing process. Molecular and Cellular Biology. 24: 10505-14. PMID 15572659 DOI: 10.1128/MCB.24.24.10505-10514.2004  0.88
2004 Marchetti C, Patriarca P, Solero GP, Baralle FE, Romano M. Genetic studies on myeloperoxidase deficiency in Italy. Japanese Journal of Infectious Diseases. 57: S10-2. PMID 15507752  0.88
2004 Porro F, Costessi L, Marro ML, Baralle FE, Muro AF. The erythrocyte skeletons of beta-adducin deficient mice have altered levels of tropomyosin, tropomodulin and EcapZ. Febs Letters. 576: 36-40. PMID 15474006 DOI: 10.1016/j.febslet.2004.08.057  0.88
2004 Zhang L, Vincent GM, Baralle M, Baralle FE, Anson BD, Benson DW, Whiting B, Timothy KW, Carlquist J, January CT, Keating MT, Splawski I. An intronic mutation causes long QT syndrome. Journal of the American College of Cardiology. 44: 1283-91. PMID 15364333 DOI: 10.1016/J.Jacc.2004.06.045  0.88
2004 Buratti E, Baralle M, De Conti L, Baralle D, Romano M, Ayala YM, Baralle FE. hnRNP H binding at the 5' splice site correlates with the pathological effect of two intronic mutations in the NF-1 and TSHbeta genes. Nucleic Acids Research. 32: 4224-36. PMID 15299088 DOI: 10.1093/Nar/Gkh752  0.88
2004 Probst MC, Thumann H, Aslanidis C, Langmann T, Buechler C, Patsch W, Baralle FE, Dallinga-Thie GM, Geisel J, Keller C, Menys VC, Schmitz G. Screening for functional sequence variations and mutations in ABCA1. Atherosclerosis. 175: 269-79. PMID 15262183 DOI: 10.1016/j.atherosclerosis.2004.02.019  0.88
2004 Arrisi-Mercado P, Romano M, Muro AF, Baralle FE. An exonic splicing enhancer offsets the atypical GU-rich 3' splice site of human apolipoprotein A-II exon 3. The Journal of Biological Chemistry. 279: 39331-9. PMID 15247216 DOI: 10.1074/jbc.M405566200  0.88
2004 Baralle M, Baralle FE. Vascular gene therapy: getting to know the players, avoiding the pitfalls. Current Opinion in Lipidology. 15: 479-81. PMID 15243223 DOI: 10.1097/  0.88
2004 Buratti E, Brindisi A, Pagani F, Baralle FE. Nuclear factor TDP-43 binds to the polymorphic TG repeats in CFTR intron 8 and causes skipping of exon 9: a functional link with disease penetrance. American Journal of Human Genetics. 74: 1322-5. PMID 15195661 DOI: 10.1086/420978  0.88
2004 Pagani F, Baralle FE. Genomic variants in exons and introns: identifying the splicing spoilers. Nature Reviews. Genetics. 5: 389-96. PMID 15168696 DOI: 10.1038/nrg1327  0.88
2004 Marchetti C, Patriarca P, Solero GP, Baralle FE, Romano M. Genetic characterization of myeloperoxidase deficiency in Italy. Human Mutation. 23: 496-505. PMID 15108282 DOI: 10.1002/humu.20027  0.88
2004 Zuccato E, Buratti E, Stuani C, Baralle FE, Pagani F. An intronic polypyrimidine-rich element downstream of the donor site modulates cystic fibrosis transmembrane conductance regulator exon 9 alternative splicing. The Journal of Biological Chemistry. 279: 16980-8. PMID 14966131 DOI: 10.1074/jbc.M313439200  0.88
2004 Buratti E, Muro AF, Giombi M, Gherbassi D, Iaconcig A, Baralle FE. RNA folding affects the recruitment of SR proteins by mouse and human polypurinic enhancer elements in the fibronectin EDA exon. Molecular and Cellular Biology. 24: 1387-400. PMID 14729981 DOI: 10.1128/MCB.24.3.1387-1400.2004  0.88
2004 Chauhan AK, Iaconcig A, Baralle FE, Muro AF. Alternative splicing of fibronectin: a mouse model demonstrates the identity of in vitro and in vivo systems and the processing autonomy of regulated exons in adult mice. Gene. 324: 55-63. PMID 14693371 DOI: 10.1016/j.gene.2003.09.026  0.88
2003 Muro AF, Chauhan AK, Gajovic S, Iaconcig A, Porro F, Stanta G, Baralle FE. Regulated splicing of the fibronectin EDA exon is essential for proper skin wound healing and normal lifespan. The Journal of Cell Biology. 162: 149-60. PMID 12847088 DOI: 10.1083/jcb.200212079  0.88
2003 Buratti E, Baralle FE, Pagani F. Can a 'patch' in a skipped exon make the pre-mRNA splicing machine run better? Trends in Molecular Medicine. 9: 229-32; discussion 2. PMID 12829008 DOI: 10.1016/S1471-4914(03)00072-8  0.88
2003 Pagani F, Buratti E, Stuani C, Baralle FE. Missense, nonsense, and neutral mutations define juxtaposed regulatory elements of splicing in cystic fibrosis transmembrane regulator exon 9. The Journal of Biological Chemistry. 278: 26580-8. PMID 12732620 DOI: 10.1074/jbc.M212813200  0.88
2003 Pagani F, Stuani C, Tzetis M, Kanavakis E, Efthymiadou A, Doudounakis S, Casals T, Baralle FE. New type of disease causing mutations: The example of the composite exonic regulatory elements of splicing in CFTR exon 12 Human Molecular Genetics. 12: 1111-1120. PMID 12719375 DOI: 10.1093/hmg/ddg131  0.88
2003 Baralle M, Baralle D, De Conti L, Mattocks C, Whittaker J, Knezevich A, Ffrench-Constant C, Baralle FE. Identification of a mutation that perturbs NF1 agene splicing using genomic DNA samples and a minigene assay. Journal of Medical Genetics. 40: 220-2. PMID 12624144  0.88
2003 Portal D, Espinosa JM, Lobo GS, Kadener S, Pereira CA, De La Mata M, Tang Z, Lin RJ, Kornblihtt AR, Baralle FE, Flawiá MM, Torres HN. An early ancestor in the evolution of splicing: a Trypanosoma cruzi serine-arginine-rich protein (TcSR) is functional in cis-splicing. Molecular and Biochemical Parasitology. 127: 37-46. PMID 12615334 DOI: 10.1016/S0166-6851(02)00301-8  0.88
2003 Pagani F, Stuani C, Zuccato E, Kornblihtt AR, Baralle FE. Promoter architecture modulates CFTR exon 9 skipping. The Journal of Biological Chemistry. 278: 1511-7. PMID 12421814 DOI: 10.1074/jbc.M209676200  0.88
2002 Toto L, Parodi MB, Baralle F, Casari G, Ravalico G, Romano M. Genetic heterogeneity in Malattia Laventinese Clinical Genetics. 62: 399-403. PMID 12431256 DOI: 10.1034/J.1399-0004.2002.620508.X  0.88
2002 Paganil F, Burattil E, Stuani C, Bendix R, Dörk T, Baralle FE. A new type of mutation causes a splicing defect in ATM Nature Genetics. 30: 426-429. PMID 11889466 DOI: 10.1038/ng858  0.88
2002 Masri MA, Abdel Seed NM, Fahal AH, Romano M, Baralle F, El Hassan AM, Ibrahim ME. Minor role for BRCA2 (exon11) and p53 (exon 5-9) among Sudanese breast cancer patients Breast Cancer Research and Treatment. 71: 145-147. PMID 11883440 DOI: 10.1023/A:1013807830329  0.88
2002 Romano M, Marcucci R, Buratti E, Ayala YM, Sebastio G, Baralle FE. Regulation of 3′ splice site selection in the 844ins68 polymorphism of the cystathionine β-synthase gene Journal of Biological Chemistry. 277: 43821-43829. DOI: 10.1074/jbc.M208107200  0.88
2002 Baralle FE, Zakin MM. Apolipoprotein E and A-IV diagnostic and functional aspects | Aspectos diagnósticos y funcionales de las Apolipoproteínas Ey A-IV Acta Bioquimica Clinica Latinoamericana. 36: 495-503.  0.88
2001 Odreman-Macchioli F, Baralle FE, Buratti E. Mutational Analysis of the Different Bulge Regions of Hepatitis C Virus Domain II and Their Influence on Internal Ribosome Entry Site Translational Ability Journal of Biological Chemistry. 276: 41648-41655. PMID 11498532 DOI: 10.1074/jbc.M104128200  0.88
2001 Buratti E, Baralle FE. Characterization and Functional Implications of the RNA Binding Properties of Nuclear Factor TDP-43, a Novel Splicing Regulator of CFTR Exon 9 Journal of Biological Chemistry. 276: 36337-36343. PMID 11470789 DOI: 10.1074/jbc.M104236200  0.88
2001 Fló J, Tisminetzky S, Baralle F. Codelivery of DNA coding for the soluble form of CD86 results in the down-regulation of the immune response to DNA vaccines Cellular Immunology. 209: 120-131. PMID 11446744 DOI: 10.1006/Cimm.2001.1784  0.88
2001 Buratti E, Dörk T, Zuccato E, Pagani F, Romano M, Baralle FE. Nuclear factor TDP-43 and SR proteins promote in vitro and in vivo CFTR exon 9 skipping Embo Journal. 20: 1774-1784. PMID 11285240 DOI: 10.1093/emboj/20.7.1774  0.88
2001 Fló J, Tisminetzky S, Baralle F. Oral transgene vaccination mediated by attenuated Salmonellae is an effective method to prevent Herpes simplex virus-2 induced disease in mice Vaccine. 19: 1772-1782. PMID 11166903 DOI: 10.1016/S0264-410X(00)00375-3  0.88
2001 Romano M, Marcucci R, Baralle FE. Splicing of constitutive upstream introns is essential for the recognition of intra-exonic suboptimal splice sites in the thrombopoietin gene Nucleic Acids Research. 29: 886-894. PMID 11160920  0.88
2000 Marro ML, Scremin OU, Jordan MC, Huynh L, Porro F, Roos KP, Gajoví S, Baralle FE, Muro AF. Hypertension in β-adducin-deficient mice Hypertension. 36: 449-453. PMID 10988280  0.88
2000 Romano M, Danek GM, Baralle FE, Mazzotti R, Filocamo M. Functional characterization of the novel mutation IVS 8 (-11delC) (-14T>A) in the intron 8 of the glucocerebrosidase gene of two Italian siblings with Gaucher disease type I Blood Cells, Molecules, and Diseases. 26: 171-176. PMID 10950936 DOI: 10.1006/bcmd.2000.0293  0.88
2000 Fló J, Tisminetzky S, Baralle F. Modulation of the immune response to DNA vaccine by co-delivery of costimulatory molecules Immunology. 100: 259-267. PMID 10886404 DOI: 10.1046/J.1365-2567.2000.00041.X  0.88
2000 Fló J, Beatriz Perez A, Tisminetzky S, Baralle F. Superiority of intramuscular route and full length glycoprotein D for DNA vaccination against herpes simplex 2. Enhancement of protection by the co-delivery of the GM-CSF gene Vaccine. 18: 3242-3253. PMID 10869769 DOI: 10.1016/S0264-410X(00)00132-8  0.88
2000 Romano M, Baralle FE, Patriarca P. Expression and characterization of recombinant human eosinophil peroxidase. Impact of the R286H substitution on the biosynthesis and activity of the enzyme European Journal of Biochemistry. 267: 3704-3711. PMID 10848988 DOI: 10.1046/j.1432-1327.2000.01403.x  0.88
2000 Muro AF, Marro ML, Gajović S, Porro F, Luzzatto L, Baralle FE. Mild spherocytic hereditary elliptocytosis and altered levels of α- and γ-adducins in β-adducin-deficient mice Blood. 95: 3978-3985. PMID 10845937  0.88
2000 Stanta G, Crocè LS, Bonin S, Tisminetzky SG, Baralle FE, Tiribelli C. Cohort effect of HCV infection in liver cirrhosis assessed by a 25 year study Journal of Clinical Virology. 17: 51-56. PMID 10814939 DOI: 10.1016/S1386-6532(00)00072-X  0.88
2000 Pagani F, Buratti E, Stuani C, Romano M, Zuccato E, Niksic M, Giglio L, Faraguna D, Baralle FE. Splicing factors induce cystic fibrosis transmembrane regulator exon 9 skipping through a nonevolutionary conserved intronic element Journal of Biological Chemistry. 275: 21041-21047. PMID 10766763 DOI: 10.1074/jbc.M910165199  0.88
2000 Odreman-Macchioli FE, Tisminetzky SG, Zotti M, Baralle FE, Buratti E. Influence of correct secondary and tertiary RNA folding on the binding of cellular factors to the HCV IRES Nucleic Acids Research. 28: 875-885. PMID 10648778  0.88
2000 Cleveland SM, Buratti E, Jones TD, North P, Baralle F, McLain L, McInerney T, Durrani Z, Dimmock NJ. Immunogenic and antigenic dominance of a nonneutralizing epitope over a highly conserved neutralizing epitope in the gp41 envelope glycoprotein of human immunodeficiency virus type 1: its deletion leads to a strong neutralizing response. Virology. 266: 66-78. PMID 10612661 DOI: 10.1006/Viro.1999.0041  0.88
1999 Vergnes L, Baroukh N, Léhy T, Moizo L, Bado A, Baralle M, Baralle FE, Zakin MM, Ochoa A. Human apolipoprotein A-IV reduces gastric acid secretion and diminishes ulcer formation in transgenic mice Febs Letters. 460: 178-181. PMID 10571083 DOI: 10.1016/S0014-5793(99)01332-0  0.88
1999 Niksic M, Romano M, Buratti E, Pagani F, Baralle FE. Functional analysis of cis-acting elements regulating the alternative splicing of human CFTR exon 9 Human Molecular Genetics. 8: 2339-2349. PMID 10556281  0.88
1999 Stanta G, Bonin S, Niccolini B, Raccanelli A, Baralle F. Catalytic subunit of telomerase expression is related to RNA component expression. Febs Letters. 460: 285-8. PMID 10544251 DOI: 10.1016/S0014-5793(99)01357-5  0.88
1999 Cramer P, Cáceres JF, Cazalla D, Kadener S, Muro AF, Baralle FE, Kornblihtt AR. Coupling of transcription with alternative splicing: RNA pol II promoters modulate SF2/ASF and 9G8 effects on an exonic splicing enhancer. Molecular Cell. 4: 251-8. PMID 10488340 DOI: 10.1016/S1097-2765(00)80372-X  0.88
1999 Pesce CG, Nogués G, Alonso CR, Baralle FE, Kornblihtt AR. Interaction between the (-170) CRE and the (-150) CCAAT box is necessaryfor efficient activation of the fibronectin gene promoter by cAMP and ATF-2. Febs Letters. 457: 445-51. PMID 10471826 DOI: 10.1016/S0014-5793(99)01091-1  0.88
1999 Ramasamy R, Yasawardena S, Kanagaratnam R, Buratti E, Baralle FE, Ramasamy MS. Antibodies to a merozoite surface protein promote multiple invasion of red blood cells by malaria parasites Parasite Immunology. 21: 397-407. PMID 10417674 DOI: 10.1046/j.1365-3024.1999.00239.x  0.88
1999 Muro AF, Caputi M, Pariyarath R, Pagani F, Buratti E, Baralle FE. Regulation of fibronectin EDA exon alternative splicing: Possible role of RNA secondary structure for enhancer display Molecular and Cellular Biology. 19: 2657-2671. PMID 10082532  0.88
1999 Baralle M, Vergnes L, Muro AF, Zakin MM, Baralle FE, Ochoa A. Regulation of the human apolipoprotein AIV gene expression in transgenic mice Febs Letters. 445: 45-52. PMID 10069372 DOI: 10.1016/S0014-5793(99)00096-4  0.88
1999 Ramasamy R, Yasawardena SG, Kanagaratnam R, Buratti E, Baralle FE, Ramasamy MS. Mammalian cell expression of malaria merozoite surface proteins and experimental DNA and RNA immunisation Biochimica Et Biophysica Acta - Molecular Basis of Disease. 1453: 1-13. PMID 9989240 DOI: 10.1016/S0925-4439(98)00056-8  0.88
1998 Buratti E, McLain L, Tisminetzky S, Cleveland SM, Dimmock NJ, Baralle FE. The neutralizing antibody response against a conserved region of human immunodeficiency virus type 1 gp41 (amino acid residues 731-752) is uniquely directed against a conformational epitope Journal of General Virology. 79: 2709-2716. PMID 9820146  0.88
1998 Muro AF, Iaconcig A, Baralle FE. Regulation of the fibronectin EDA exon alternative splicing. Cooperative role of the exonic enhancer element and the 5' splicing site Febs Letters. 437: 137-141. PMID 9804187 DOI: 10.1016/S0014-5793(98)01201-0  0.88
1998 Urtreger A, Porro F, Puricelli L, Werbajh S, Baralle FE, Bal de Kier Joffé E, Kornblihtt AR, Muro AF. Expression of RGD minus fibronectin that does not form extracellular matrix fibrils is sufficient to decrease tumor metastasis. International Journal of Cancer. Journal International Du Cancer. 78: 233-41. PMID 9754657 DOI: 10.1002/(SICI)1097-0215(19981005)78:2<233::AID-IJC18>3.0.CO;2-B  0.88
1998 Pagani F, Pariyarath R, Garcia R, Stuani C, Burlina AB, Ruotolo G, Rabusin M, Baralle FE. New lysosomal acid lipase gene mutants explain the phenotype of Wolman disease and cholesteryl ester storage disease Journal of Lipid Research. 39: 1382-1388. PMID 9684740  0.88
1998 Buratti E, Tisminetzky S, Zotti M, Baralle FE. Functional analysis of the interaction between HCV 5'UTR and putative subunits of eukaryotic translation initiation factor elF3 Nucleic Acids Research. 26: 3179-3187. PMID 9628916 DOI: 10.1093/nar/26.13.3179  0.88
1998 Buratti E, Baralle FE, Tisminetzky SG. Localization of the different hepatitis C virus core gene products expressed in COS-1 cells Cellular and Molecular Biology (Noisy-Le-Grand, France). 44: 505-512. PMID 9620447  0.88
1998 Pirisi M, Toniutto P, Fabris C, Lombardelli T, Falleti E, Tisminetzky SG, Baralle F, Bartoli E. Factors associated with serum HCV RNA positivity in anti-HCV antibody positive intravenous drug users Journal of Clinical Epidemiology. 51: 423-427. PMID 9619970 DOI: 10.1016/S0895-4356(97)00305-3  0.88
1998 Danek GM, Valenti M, Baralle FE, Romano M. The A/G polymorphism in the - 78 position of the apolipoprotein A-I promoter does not have a direct effect on transcriptional efficiency Biochimica Et Biophysica Acta - Gene Structure and Expression. 1398: 67-74. PMID 9602064 DOI: 10.1016/S0167-4781(98)00029-3  0.88
1998 Toniutto P, Pirisi M, Fabris C, Bardus P, Soardo G, Vitulli D, Tisminetzky SG, Pacco P, Gasparini V, Baralle F, Bartoli E. High prevalence of infection with hepatitis G virus in patients with hepatic and extrahepatic malignancies Journal of Hepatology. 28: 550-555. PMID 9566822 DOI: 10.1016/S0168-8278(98)80277-8  0.88
1998 Tonizzo M, Fisicartr M, Cattin L, Danek GM, Fonda M, Valenti M, Casagrande S, Petrucco A, Bovenzi M, Baralle F. Influence of polymorphism of angiotensinconverting enzyme and apolipoprotein e genes on carotid wall thickness in asymptomatic adults Italian Journal of Neurological Sciences. 19: S58.  0.88
1997 Chen Y, Garcia R, Baralle FE. HIV-1 env glycoprotein gp120 and gp160 expressed in vaccinia virus system and their antigenicity analysis Zhongguo Yi Xue Ke Xue Yuan Xue Bao. Acta Academiae Medicinae Sinicae. 19: 120-126. PMID 10453506  0.88
1997 Romano M, Dri P, Dadalt L, Patriarca P, Baralle FE. Biochemical and molecular characterization of hereditary myeloperoxidase deficiency Blood. 90: 4126-4134. PMID 9354683  0.88
1997 Pagani F, Pariyarath R, Stuani C, Garcia R, Baralle FE. Cysteine residues in human lysosomal acid lipase are involved in selective cholesteryl esterase activity Biochemical Journal. 326: 265-269. PMID 9337878  0.88
1997 Cramer P, Pesce CG, Baralle FE, Kornblihtt AR. Functional association between promoter structure and transcript alternative splicing. Proceedings of the National Academy of Sciences of the United States of America. 94: 11456-60. PMID 9326631 DOI: 10.1073/pnas.94.21.11456  0.88
1997 Buratti E, Gerotto M, Pontisso P, Alberti A, Tisminetzky SG, Baralle FE. In vivo translational efficiency of different hepatitis C virus 5'-UTRs Febs Letters. 411: 275-280. PMID 9271220 DOI: 10.1016/S0014-5793(97)00715-1  0.88
1997 Pirisi M, Fabris C, Toniutto P, Falleti E, Tisminetzky SG, Gerotto M, Soardo G, Vitulli D, Del Forno M, Baralle F, Bartoli E. Endogenous interferon-α concentration and outcome of interferon treatment in patients with chronic hepatitis C Digestive Diseases and Sciences. 42: 767-771. PMID 9125646 DOI: 10.1023/A:1018808012823  0.88
1997 Buratti E, Di Michele M, Song P, Monti-Bragadin C, Scodeller EA, Baralle FE, Tisminetzky SG. Improved reactivity of hepatitis C virus core protein epitopes in a conformational antigen-presenting system Clinical and Diagnostic Laboratory Immunology. 4: 117-121. PMID 9067642  0.88
1997 Buratti E, Tisminetzky SG, D'Agaro P, Baralle FE. A neutralizing monoclonal antibody previously mapped exclusively on human immunodeficiency virus type 1 gp41 recognizes an epitope in p17 sharing the core sequence IEEE Journal of Virology. 71: 2457-2462. PMID 9032383  0.88
1997 Schiappacassi M, Buratti E, D'Agaro P, Ciani L, Scodeller ES, Tisminetzky SG, Baralle FE. V3 loop core region serotyping of HIV-1 infected patients using the FHV epitope presenting system Journal of Virological Methods. 63: 121-127. PMID 9015282 DOI: 10.1016/S0166-0934(96)02120-9  0.88
1997 Cattin L, Fisicaro M, Tonizzo M, Valenti M, Danek GM, Fonda M, Da Col PG, Casagrande S, Pincetti E, Bovenzi M, Baralle F. Polymorphism of the apolipoprotein E gene and early carotid atherosclerosis defined by ultrasonography in asymptomatic adults Arteriosclerosis, Thrombosis, and Vascular Biology. 17: 91-94. PMID 9012642 DOI: 10.1161/01.Atv.17.1.91  0.88
1997 Gajović S, Muro AF, Baralle FE. Appearance of vaginal duplication in outbred CD1 mice Veterinarski Arhiv. 67: 145-150.  0.88
1996 Pariyarath R, Pagani F, Stuani C, Garcia R, Baralle FE. L273S missense substitution in human lysosomal acid lipase creates a new N-glycosylation site Febs Letters. 397: 79-82. PMID 8941718 DOI: 10.1016/S0014-5793(96)01134-9  0.88
1996 Pagani F, Garcia R, Pariyarath R, Stuani C, Gridelli B, Paone G, Baralle FE. Expression of lysosomal acid lipase mutants detected in three patients with cholesteryl ester storage disease Human Molecular Genetics. 5: 1611-1617. PMID 8894696  0.88
1996 Buratti E, Tisminetzky SG, Scodeller ES, Baralle FE. Conformational display of two neutralizing epitopes of HIV-1 gp41 on the Flock House virus capsid protein Journal of Immunological Methods. 197: 7-18. PMID 8890890 DOI: 10.1016/0022-1759(96)00097-X  0.88
1996 Toniutto P, Pirisi M, Tisminetzky SG, Fabris C, Chinellato E, Gerotto M, Falleti E, Ferroni P, Lombardelli T, Bartoli E, Baralle F. Discordant results from hepatitis C virus genotyping by procedures based on amplification of different genomic regions Journal of Clinical Microbiology. 34: 2382-2385. PMID 8880484 DOI: 10.1128/Jcm.34.10.2382-2385.1996  0.88
1996 Pontisso P, Gerotto M, Ruvoletto MG, Fattovich G, Chemello L, Tisminetzky S, Baralle F, Alberti A. Hepatitis C genotypes in patients with dual hepatitis B and C virus infection Journal of Medical Virology. 48: 157-160. PMID 8835349 DOI: 10.1002/(SICI)1096-9071(199602)48:2<157::AID-JMV7>3.0.CO;2-8  0.88
1996 Zentilin L, Tafuro S, Grassi G, Garcia R, Ventura A, Baralle F, Falaschi A, Giacca M. Functional reconstitution of oxidase activity in X-linked chronic granulomatous disease by retrovirus-mediated gene transfer Experimental Cell Research. 225: 257-267. PMID 8660913 DOI: 10.1006/Excr.1996.0175  0.88
1995 Tisminetzky S, Gerotto M, Pontisso P, Chemello L, Prescott LE, Rose KA, Baralle F, Simmonds P, Alberti A. Comparison of genotyping and serotyping methods for the identification of hepatitis C virus types Journal of Virological Methods. 55: 303-307. PMID 8609196 DOI: 10.1016/0166-0934(95)00067-X  0.88
1995 Scodeller EA, Tisminetzky SG, Porro F, Schiappacassi M, De Rossi A, Chiecco-Bianchi L, Baralle FE. A new epitope presenting system displays a HIV-1 V3 loop sequence and induces neutralizing antibodies Vaccine. 13: 1233-1239. PMID 8578809 DOI: 10.1016/0264-410X(95)00058-9  0.88
1995 Tisminetzky S, Devescovi G, Tripodi G, Muro A, Bianchi G, Colombi M, Moro L, Barlati S, Tuteja R, Baralle FE. Genomic organisation and chromosomal localisation of the gene encoding human beta adducin Gene. 167: 313-316. PMID 8566798 DOI: 10.1016/0378-1119(95)00591-9  0.88
1995 Tripodi G, Casari G, Tisminetzky S, Bianchi G, Devescovi G, Muro A, Tuteja R, Baralle FE. Characterisation and chromosomal localisation of the rat α- and β-adducin-encoding genes Gene. 166: 307-311. PMID 8543181 DOI: 10.1016/0378-1119(95)00590-0  0.88
1995 Caputi M, Melo CA, Baralle FE. Regulation of fibronectin expression in rat regenerating liver Nucleic Acids Research. 23: 238-243. PMID 7862527 DOI: 10.1093/nar/23.2.238  0.88
1995 Caputi M, Baralle FE, Melo CA. Analysis of the linkage between fibronectin alternative spliced sites during ageing in rat tissues Bba - Gene Structure and Expression. 1263: 53-59. PMID 7632733 DOI: 10.1016/0167-4781(95)00067-Q  0.88
1995 Garcia ES, Gonzalez MS, de Azambuja P, Baralle FE, Fraidenraich D, Torres HN, Flawiá MM. Induction of Trypanosoma cruzi metacyclogenesis in the gut of the hematophagous insect vector, Rhodnius prolixus, by hemoglobin and peptides carrying alpha D-globin sequences. Experimental Parasitology. 81: 255-61. PMID 7498422 DOI: 10.1006/expr.1995.1116  0.88
1994 Bianchi G, Tripodi G, Casari G, Salardi S, Barber BR, Garcia R, Leoni P, Torielli L, Cusi D, Ferrandi M. Two point mutations within the adducin genes are involved in blood pressure variation. Proceedings of the National Academy of Sciences of the United States of America. 91: 3999-4003. PMID 8171025  0.88
1994 Caputi M, Casari G, Guenzi S, Tagliabue R, Sidoli A, Melo CA, Baralle FE. A novel bipartite splicing enhancer modulates the differential processing of the human fibronectin EDA exon Nucleic Acids Research. 22: 1018-1022. PMID 8152907 DOI: 10.1093/nar/22.6.1018  0.88
1994 Tuteja R, Tuteja N, Lilliu F, Bembi B, Galanello R, Cao A, Baralle FE. Y418C: a novel mutation in exon 9 of the glucocerebrosidase gene of a patient with Gaucher disease creates a new Bgl I site Human Genetics. 94: 314-315. PMID 8076951 DOI: 10.1007/BF00208292  0.88
1994 Bembi B, Agosti E, Zanatta M, Carrozzi M, Gornati R, Berra B, Baralle F. Enzyme replacement treatment in type 1 and type 3 Gaucher's disease The Lancet. 344: 1679-1682. PMID 7996964 DOI: 10.1016/S0140-6736(94)90462-6  0.88
1994 Romano M, Patriarca P, Melo C, Baralle FE, Dri P. Hereditary eosinophil peroxidase deficiency: Immunochemical and spectroscopic studies and evidence for a compound heterozygosity of the defect Proceedings of the National Academy of Sciences of the United States of America. 91: 12496-12500. PMID 7809065 DOI: 10.1073/pnas.91.26.12496  0.88
1994 Tisminetzky SG, Scodeller EA, Evangelisti P, Chen Y, Schiappacassi M, Porro F, Bizik F, Zacchi T, Lunazzi G, Miertus S, Baralle FE. Immunoreactivity of chimeric proteins carrying the HIV-1 epitope IGPGRAF Correlation between predicted conformation and antigenicity Febs Letters. 353: 1-4. PMID 7523192 DOI: 10.1016/0014-5793(94)00972-4  0.88
1993 Fraidenraich D, Peña C, Isola EL, Lammel EM, Coso O, Añel AD, Pongor S, Baralle F, Torres HN, Flawia MM. Stimulation of Trypanosoma cruzi adenylyl cyclase by an alpha D-globin fragment from Triatoma hindgut: effect on differentiation of epimastigote to trypomastigote forms. Proceedings of the National Academy of Sciences of the United States of America. 90: 10140-4. PMID 8234267 DOI: 10.1073/Pnas.90.21.10140  0.88
1993 Tuteja R, Bembi B, Agosti E, Baralle FE. 1448C mutation linked to the Pv1 · 1- genotype in Italian patients with Gaucher disease Human Molecular Genetics. 2: 781-784. PMID 8102572  0.88
1993 Sidoli A, Tamborini E, Giuntini I, Levi S, Volonte G, Paini C, De Lalla C, Siccardi AG, Baralle FE, Galliani S, Arosio P. Cloning, expression, and immunological characterization of recombinant Lolium perenne allergen Lol p II Journal of Biological Chemistry. 268: 21819-21825. PMID 7691817  0.88
1993 Melo CA, Serra C, Stoyanova V, Aguzzoli C, Faraguna D, Tamanini A, Berton G, Cabrini G, Baralle FE. Alternative splicing of a previously unidentified CFTR exon introduces an in-frame stop codon 5' of the R region Febs Letters. 329: 159-162. PMID 7689062 DOI: 10.1016/0014-5793(93)80214-F  0.88
1993 Fraidenraich D, Peña C, Isola EL, Lammel EM, Coso O, Añel AD, Baralle F, Torres HN, Flawia MM. An alpha D-globin fragment from Triatoma infestans hindgut stimulates Trypanosoma cruzi adenylyl cyclase and promotes metacyclogenesis. Biological Research. 26: 279-83. PMID 7670540  0.88
1989 Shoulders CC, Ball MJ, Baralle FE. Variation in the apo AI/CIII/AIV gene complex: its association with hyperlipidemia. Atherosclerosis. 80: 111-8. PMID 2514696 DOI: 10.1016/0021-9150(89)90018-X  0.44
1989 Lucero MA, Sanchez D, Ochoa AR, Brunel F, Cohen GN, Baralle FE, Zakin MM. Interaction of DNA-binding proteins with the tissue-specific human apolipoprotein-AII enhancer. Nucleic Acids Research. 17: 2283-300. PMID 2495523 DOI: 10.1093/Nar/17.6.2283  0.88
1987 Shelley CS, Baralle FE. Deletion analysis of a unique 3' splice site indicates that alternating guanine and thymine residues represent an efficient splicing signal. Nucleic Acids Research. 15: 3787-99. PMID 3108860 DOI: 10.1093/nar/15.9.3787  0.88
1987 Shelley CS, Baralle FE. Dual tissue-specific expression of apo-AII is directed by an upstream enhancer. Nucleic Acids Research. 15: 3801-21. PMID 3035501 DOI: 10.1093/nar/15.9.3801  0.88
1987 Korneluk RG, Macleod HL, Leblond SC, Monteith NL, Baralle FE, Hunter AGW. Avall RFLP at the human apolipoprotein CII (APO CII) gene locus Nucleic Acids Research. 15: 6769. PMID 2888095 DOI: 10.1093/Nar/15.16.6769  0.88
1986 Colombi M, Barlati S, Kornblihtt A, Baralle FE, Vaheri A. A family of fibronectin mRNAs in human normal and transformed cells Bba - Gene Structure and Expression. 868: 207-214. PMID 3790566 DOI: 10.1016/0167-4781(86)90056-4  0.88
1986 Owens RJ, Kornblihtt AR, Baralle FE. Fibronectin, the generation of multiple polypeptides from a single gene. Oxford Surveys On Eukaryotic Genes. 3: 141-60. PMID 3334363  0.88
1986 Colombi M, Barlati S, Kornblihtt AR, Baralle FE, Vaheri A. Analysis of fibronectin mRNAs in human normal and transformed cells Cell Biology International Reports. 10: 201. DOI: 10.1016/S0309-1651(86)80055-8  0.88
1985 Shelley CS, Sharpe CR, Baralle FE, Shoulders CC. Comparison of the human apolipoprotein genes. Apo AII presents a unique functional intron-exon junction. Journal of Molecular Biology. 186: 43-51. PMID 3935800 DOI: 10.1016/0022-2836(85)90255-4  0.88
1985 Park I, Schaeffer E, Sidoli A, Baralle FE, Cohen GN, Zakin MM. Organization of the human transferrin gene: direct evidence that it originated by gene duplication. Proceedings of the National Academy of Sciences of the United States of America. 82: 3149-53. PMID 3858812 DOI: 10.1073/Pnas.82.10.3149  0.88
1985 Kornblihtt AR, Umezawa K, Vibe-Pedersen K, Baralle FE. Primary structure of human fibronectin: differential splicing may generate at least 10 polypeptides from a single gene. The Embo Journal. 4: 1755-9. PMID 2992939 DOI: 10.1002/J.1460-2075.1985.Tb03847.X  0.88
1985 Umezawa K, Kornblihtt AR, Baralle FE. Isolation and characterization of cDNA clones for human liver fibronectin. Febs Letters. 186: 31-4. PMID 2989004 DOI: 10.1016/0014-5793(85)81333-8  0.88
1984 Kornblihtt AR, Vibe-Pedersen K, Baralle FE. Human fibronectin: cell specific alternative mRNA splicing generates polypeptide chains differing in the number of internal repeats. Nucleic Acids Research. 12: 5853-68. PMID 6462919 DOI: 10.1093/Nar/12.14.5853  0.88
1984 Sharpe CR, Sidoli A, Shelley CS, Lucero MA, Shoulders CC, Baralle FE. Human apolipoproteins AI, AII, CII and CIII. cDNA sequences and mRNA abundance. Nucleic Acids Research. 12: 3917-32. PMID 6328445 DOI: 10.1093/NAR/12.9.3917  0.44
1984 Kornblihtt AR, Vibe-Pedersen K, Baralle FE. Human fibronectin: molecular cloning evidence for two mRNA species differing by an internal segment coding for a structural domain. The Embo Journal. 3: 221-6. PMID 6200322 DOI: 10.1002/J.1460-2075.1984.Tb01787.X  0.88
1984 Vibe-Pedersen K, Kornblihtt AR, Baralle FE. Expression of a human alpha-globin/fibronectin gene hybrid generates two mRNAs by alternative splicing. The Embo Journal. 3: 2511-6. PMID 6096127 DOI: 10.1002/J.1460-2075.1984.Tb02165.X  0.88
1984 Kornblihtt AR, Vibe-pedersen K, Baralle FE. Human fibronectin: Cell specific alternative mRNA splicing generates polypeptide chains dfffering in the number of internal repeats Nucleic Acids Research. 12: 5853-5868. DOI: 10.1093/nar/12.14.5853  0.88
1983 Shoulders CC, Kornblihtt AR, Munro BS, Baralle FE. Gene structure of human apolipoprotein A1. Nucleic Acids Research. 11: 2827-37. PMID 6406984 DOI: 10.1093/Nar/11.9.2827  0.88
1983 Kornblihtt AR, Vibe-Pedersen K, Baralle FE. Isolation and characterization of cDNA clones for human and bovine fibronectins. Proceedings of the National Academy of Sciences of the United States of America. 80: 3218-22. PMID 6304699 DOI: 10.1073/Pnas.80.11.3218  0.88
1983 Shoulders CC, Kornblihtt AR, Munro BS, Baralle FE. Gene structure of human apolipoprotein Al Nucleic Acids Research. 11: 2827-2837. DOI: 10.1093/nar/11.9.2827  0.88
1980 Baralle FE, Proudfoot NJ, Clegg JB. The structural analysis of the human epsilon-globin gene and its product Annals of the New York Academy of Sciences. 344: 76-82. PMID 6930885 DOI: 10.1111/j.1749-6632.1980.tb33651.x  0.88
1980 Baralle FE, Shoulders CC, Proudfoot NJ. The primary structure of the human ε-globin gene Cell. 21: 621-626. PMID 6254663 DOI: 10.1016/0092-8674(80)90425-0  0.88
1980 Baralle FE, Shoulders CC, Goodbourn S, Jeffreys A, Proudfoot NJ. The 5′ flanking region of human ε-globin gene Nucleic Acids Research. 8: 4393-4404. PMID 6253916 DOI: 10.1093/Nar/8.19.4393  0.88
1979 Proudfoot NJ, Baralle FE. Molecular cloning of human ε-globin gene Proceedings of the National Academy of Sciences of the United States of America. 76: 5435-5439. PMID 160554 DOI: 10.1073/PNAS.76.11.5435  0.88
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