Livio Pellizzoni, Phd - Publications

Affiliations: 
Columbia University, New York, NY 
Area:
Neural Degeneration and Repair, Neurobiology of Disease, Synapses and Circuits, Stem Cell Biology, Cellular/Molecular/Developmental Neuroscience

47 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
2020 Osman EY, Van Alstyne M, Yen PF, Lotti F, Feng Z, Ling KK, Ko CP, Pellizzoni L, Lorson CL. Minor snRNA gene delivery improves the loss of proprioceptive synapses on SMA motor neurons. Jci Insight. PMID 32516136 DOI: 10.1172/jci.insight.130574  0.4
2019 Simon CM, Van Alstyne M, Lotti F, Bianchetti E, Tisdale S, Watterson DM, Mentis GZ, Pellizzoni L. Stasimon Contributes to the Loss of Sensory Synapses and Motor Neuron Death in a Mouse Model of Spinal Muscular Atrophy. Cell Reports. 29: 3885-3901.e5. PMID 31851921 DOI: 10.1016/j.celrep.2019.11.058  0.4
2019 Osman EY, Bolding MR, Villalón E, Kaifer KA, Lorson ZC, Tisdale S, Hao Y, Conant GC, Pires JC, Pellizzoni L, Lorson CL. Functional characterization of SMN evolution in mouse models of SMA. Scientific Reports. 9: 9472. PMID 31263170 DOI: 10.1038/s41598-019-45822-8  0.4
2018 Van Alstyne M, Lotti F, Dal Mas A, Area-Gomez E, Pellizzoni L. Stasimon/Tmem41b localizes to mitochondria-associated ER membranes and is essential for mouse embryonic development. Biochemical and Biophysical Research Communications. PMID 30352685 DOI: 10.1016/j.bbrc.2018.10.073  0.4
2018 Iyer CC, Corlett KM, Massoni-Laporte A, Duque SI, Madabusi N, Tisdale S, McGovern VL, Le TT, Zaworski PG, David Arnold W, Pellizzoni L, Burghes AHM. Mild SMN missense alleles are only functional in the presence of SMN2 in mammals. Human Molecular Genetics. PMID 29982416 DOI: 10.1093/hmg/ddy251  0.4
2016 Simon CM, Janas AM, Lotti F, Tapia JC, Pellizzoni L, Mentis GZ. A Stem Cell Model of the Motor Circuit Uncouples Motor Neuron Death from Hyperexcitability Induced by SMN Deficiency. Cell Reports. PMID 27452470 DOI: 10.1016/j.celrep.2016.06.087  0.4
2016 Zhao X, Feng Z, Ling KK, Mollin A, Sheedy J, Yeh S, Petruska J, Narasimhan J, Dakka A, Welch E, Karp G, Chen KS, Metzger F, Ratni H, Lotti F, ... ... Pellizzoni L, et al. Pharmacokinetics, Pharmacodynamics and Efficacy of a Small Molecule SMN2 Splicing Modifier in Mouse Models of Spinal Muscular Atrophy. Human Molecular Genetics. PMID 26931466 DOI: 10.1093/hmg/ddw062  0.4
2016 Butchbach ME, Lumpkin CJ, Harris AW, Saieva L, Edwards JD, Workman E, Simard LR, Pellizzoni L, Burghes AH. Protective effects of butyrate-based compounds on a mouse model for spinal muscular atrophy. Experimental Neurology. PMID 26892876 DOI: 10.1016/j.expneurol.2016.02.009  0.4
2015 Tisdale S, Pellizzoni L. Disease mechanisms and therapeutic approaches in spinal muscular atrophy. The Journal of Neuroscience : the Official Journal of the Society For Neuroscience. 35: 8691-700. PMID 26063904 DOI: 10.1523/JNEUROSCI.0417-15.2015  0.4
2015 Pellizzoni L. Skipping skin disease Human Mutation. 36: 1. DOI: 10.1002/humu.22650  0.4
2014 Li DK, Tisdale S, Lotti F, Pellizzoni L. SMN control of RNP assembly: from post-transcriptional gene regulation to motor neuron disease. Seminars in Cell & Developmental Biology. 32: 22-9. PMID 24769255 DOI: 10.1016/j.semcdb.2014.04.026  0.4
2013 Tisdale S, Lotti F, Saieva L, Van Meerbeke JP, Crawford TO, Sumner CJ, Mentis GZ, Pellizzoni L. SMN is essential for the biogenesis of U7 small nuclear ribonucleoprotein and 3'-end formation of histone mRNAs. Cell Reports. 5: 1187-95. PMID 24332368 DOI: 10.1016/j.celrep.2013.11.012  0.4
2013 Li DK, Tisdale S, Espinoza-Derout J, Saieva L, Lotti F, Pellizzoni L. A cell system for phenotypic screening of modifiers of SMN2 gene expression and function. Plos One. 8: e71965. PMID 23967270 DOI: 10.1371/journal.pone.0071965  0.4
2013 Van Meerbeke JP, Gibbs RM, Plasterer HL, Miao W, Feng Z, Lin MY, Rucki AA, Wee CD, Xia B, Sharma S, Jacques V, Li DK, Pellizzoni L, Rusche JR, Ko CP, et al. The DcpS inhibitor RG3039 improves motor function in SMA mice. Human Molecular Genetics. 22: 4074-83. PMID 23727836 DOI: 10.1093/hmg/ddt257  0.4
2012 Lotti F, Imlach WL, Saieva L, Beck ES, Hao le T, Li DK, Jiao W, Mentis GZ, Beattie CE, McCabe BD, Pellizzoni L. An SMN-dependent U12 splicing event essential for motor circuit function. Cell. 151: 440-54. PMID 23063131 DOI: 10.1016/j.cell.2012.09.012  0.4
2012 Imlach WL, Beck ES, Choi BJ, Lotti F, Pellizzoni L, McCabe BD. SMN is required for sensory-motor circuit function in Drosophila. Cell. 151: 427-39. PMID 23063130 DOI: 10.1016/j.cell.2012.09.011  0.4
2012 Ruggiu M, McGovern VL, Lotti F, Saieva L, Li DK, Kariya S, Monani UR, Burghes AH, Pellizzoni L. A role for SMN exon 7 splicing in the selective vulnerability of motor neurons in spinal muscular atrophy. Molecular and Cellular Biology. 32: 126-38. PMID 22037760 DOI: 10.1128/MCB.06077-11  0.4
2011 Lutz CM, Kariya S, Patruni S, Osborne MA, Liu D, Henderson CE, Li DK, Pellizzoni L, Rojas J, Valenzuela DM, Murphy AJ, Winberg ML, Monani UR. Postsymptomatic restoration of SMN rescues the disease phenotype in a mouse model of severe spinal muscular atrophy. The Journal of Clinical Investigation. 121: 3029-41. PMID 21785219 DOI: 10.1172/JCI57291  0.4
2010 Butchbach ME, Singh J, Thorsteinsdóttir M, Saieva L, Slominski E, Thurmond J, Andrésson T, Zhang J, Edwards JD, Simard LR, Pellizzoni L, Jarecki J, Burghes AH, Gurney ME. Effects of 2,4-diaminoquinazoline derivatives on SMN expression and phenotype in a mouse model for spinal muscular atrophy. Human Molecular Genetics. 19: 454-67. PMID 19897588 DOI: 10.1093/hmg/ddp510  0.4
2009 Workman E, Saieva L, Carrel TL, Crawford TO, Liu D, Lutz C, Beattie CE, Pellizzoni L, Burghes AH. A SMN missense mutation complements SMN2 restoring snRNPs and rescuing SMA mice. Human Molecular Genetics. 18: 2215-29. PMID 19329542 DOI: 10.1093/hmg/ddp157  0.4
2008 Walker MP, Rajendra TK, Saieva L, Fuentes JL, Pellizzoni L, Matera AG. SMN complex localizes to the sarcomeric Z-disc and is a proteolytic target of calpain. Human Molecular Genetics. 17: 3399-410. PMID 18689355 DOI: 10.1093/hmg/ddn234  0.4
2007 Gabanella F, Butchbach ME, Saieva L, Carissimi C, Burghes AH, Pellizzoni L. Ribonucleoprotein assembly defects correlate with spinal muscular atrophy severity and preferentially affect a subset of spliceosomal snRNPs. Plos One. 2: e921. PMID 17895963 DOI: 10.1371/journal.pone.0000921  0.4
2007 Pellizzoni L. Chaperoning ribonucleoprotein biogenesis in health and disease. Embo Reports. 8: 340-5. PMID 17401408 DOI: 10.1038/sj.embor.7400941  0.4
2007 Avila AM, Burnett BG, Taye AA, Gabanella F, Knight MA, Hartenstein P, Cizman Z, Di Prospero NA, Pellizzoni L, Fischbeck KH, Sumner CJ. Trichostatin A increases SMN expression and survival in a mouse model of spinal muscular atrophy. The Journal of Clinical Investigation. 117: 659-71. PMID 17318264 DOI: 10.1172/JCI29562  0.4
2006 Carissimi C, Saieva L, Gabanella F, Pellizzoni L. Gemin8 is required for the architecture and function of the survival motor neuron complex. The Journal of Biological Chemistry. 281: 37009-16. PMID 17023415 DOI: 10.1074/jbc.M607505200  0.4
2006 Carissimi C, Saieva L, Baccon J, Chiarella P, Maiolica A, Sawyer A, Rappsilber J, Pellizzoni L. Gemin8 is a novel component of the survival motor neuron complex and functions in small nuclear ribonucleoprotein assembly. The Journal of Biological Chemistry. 281: 8126-34. PMID 16434402 DOI: 10.1074/jbc.M512243200  0.4
2005 Gabanella F, Carissimi C, Usiello A, Pellizzoni L. The activity of the spinal muscular atrophy protein is regulated during development and cellular differentiation. Human Molecular Genetics. 14: 3629-42. PMID 16236758 DOI: 10.1093/hmg/ddi390  0.4
2005 Carissimi C, Baccon J, Straccia M, Chiarella P, Maiolica A, Sawyer A, Rappsilber J, Pellizzoni L. Unrip is a component of SMN complexes active in snRNP assembly. Febs Letters. 579: 2348-54. PMID 15848170 DOI: 10.1016/j.febslet.2005.03.034  0.4
2004 Yong J, Golembe TJ, Battle DJ, Pellizzoni L, Dreyfuss G. snRNAs contain specific SMN-binding domains that are essential for snRNP assembly. Molecular and Cellular Biology. 24: 2747-56. PMID 15024064 DOI: 10.1128/MCB.24.7.2747-2756.2004  0.4
2002 Pellizzoni L, Yong J, Dreyfuss G. Essential role for the SMN complex in the specificity of snRNP assembly. Science (New York, N.Y.). 298: 1775-9. PMID 12459587 DOI: 10.1126/science.1074962  0.4
2002 Massenet S, Pellizzoni L, Paushkin S, Mattaj IW, Dreyfuss G. The SMN complex is associated with snRNPs throughout their cytoplasmic assembly pathway. Molecular and Cellular Biology. 22: 6533-41. PMID 12192051 DOI: 10.1128/MCB.22.18.6533-6541.2002  0.4
2002 Baccon J, Pellizzoni L, Rappsilber J, Mann M, Dreyfuss G. Identification and characterization of Gemin7, a novel component of the survival of motor neuron complex. The Journal of Biological Chemistry. 277: 31957-62. PMID 12065586 DOI: 10.1074/jbc.M203478200  0.4
2002 Yong J, Pellizzoni L, Dreyfuss G. Sequence-specific interaction of U1 snRNA with the SMN complex. The Embo Journal. 21: 1188-96. PMID 11867547 DOI: 10.1093/emboj/21.5.1188  0.4
2002 Pellizzoni L, Baccon J, Rappsilber J, Mann M, Dreyfuss G. Purification of native survival of motor neurons complexes and identification of Gemin6 as a novel component. The Journal of Biological Chemistry. 277: 7540-5. PMID 11748230 DOI: 10.1074/jbc.M110141200  0.4
2001 Pellizzoni L, Baccon J, Charroux B, Dreyfuss G. The survival of motor neurons (SMN) protein interacts with the snoRNP proteins fibrillarin and GAR1. Current Biology : Cb. 11: 1079-88. PMID 11509230 DOI: 10.1016/S0960-9822(01)00316-5  0.4
2001 Pellizzoni L, Charroux B, Rappsilber J, Mann M, Dreyfuss G. A functional interaction between the survival motor neuron complex and RNA polymerase II. The Journal of Cell Biology. 152: 75-85. PMID 11149922 DOI: 10.1083/jcb.152.1.75  0.4
2000 Paushkin S, Charroux B, Abel L, Perkinson RA, Pellizzoni L, Dreyfuss G. The survival motor neuron protein of Schizosacharomyces pombe. Conservation of survival motor neuron interaction domains in divergent organisms. The Journal of Biological Chemistry. 275: 23841-6. PMID 10816558 DOI: 10.1074/jbc.M001441200  0.4
2000 Charroux B, Pellizzoni L, Perkinson RA, Yong J, Shevchenko A, Mann M, Dreyfuss G. Gemin4. A novel component of the SMN complex that is found in both gems and nucleoli. The Journal of Cell Biology. 148: 1177-86. PMID 10725331 DOI: 10.1083/jcb.148.6.1177  0.4
1999 Charroux B, Pellizzoni L, Perkinson RA, Shevchenko A, Mann M, Dreyfuss G. Gemin3: A novel DEAD box protein that interacts with SMN, the spinal muscular atrophy gene product, and is a component of gems. The Journal of Cell Biology. 147: 1181-94. PMID 10601333 DOI: 10.1083/jcb.147.6.1181  0.4
1999 Pellizzoni L, Charroux B, Dreyfuss G. SMN mutants of spinal muscular atrophy patients are defective in binding to snRNP proteins. Proceedings of the National Academy of Sciences of the United States of America. 96: 11167-72. PMID 10500148 DOI: 10.1073/pnas.96.20.11167  0.4
1998 Pellizzoni L, Kataoka N, Charroux B, Dreyfuss G. A novel function for SMN, the spinal muscular atrophy disease gene product, in pre-mRNA splicing. Cell. 95: 615-24. PMID 9845364  0.4
1998 Pellizzoni L, Lotti F, Rutjes SA, Pierandrei-Amaldi P. Involvement of the Xenopus laevis Ro60 autoantigen in the alternative interaction of La and CNBP proteins with the 5'UTR of l4 ribosomal protein mRNA Journal of Molecular Biology. 281: 593-608. PMID 9710533 DOI: 10.1006/jmbi.1998.1961  0.4
1997 Pellizzoni L, Lotti F, Maras B, Pierandrei-Amaldi P. Cellular nucleic acid binding protein binds a conserved region of the 5' UTR of Xenopus laevis ribosomal protein mRNAs Journal of Molecular Biology. 267: 264-275. PMID 9096224 DOI: 10.1006/jmbi.1996.0888  0.4
1996 Pellizzoni L, Cardinali B, Lin-Marq N, Mercanti D, Pierandrei-Amaldi P. A Xenopus laevis homologue of the La autoantigen binds the pyrimidine tract of the 5' UTR of ribosomal protein mRNAs in vitro: Implication of a protein factor in complex formation Journal of Molecular Biology. 259: 904-915. PMID 8683593 DOI: 10.1006/jmbi.1996.0368  0.4
1995 Amaldi F, Camacho-Vanegas O, Cardinall B, Cecconi F, Crosio C, Loreni F, Mariottini P, Pellizzoni L, Pierandrei-Amaldi P. Structure and expression of ribosomal protein genes in Xenopus laevis. Biochemistry and Cell Biology = Biochimie Et Biologie Cellulaire. 73: 969-77. PMID 8722012  0.4
1995 Pellizzoni L, Crosio C, Pierandrei-Amaldi P. Sequence of the cDNA and gene coding for ribosomal protein S 1 of Xenopus laevis Gene. 154: 145-151. PMID 7890156 DOI: 10.1016/0378-1119(94)00834-F  0.4
1994 Pellizzoni L, Crosio C, Campioni N, Loreni F, Pierandrei-Amaldi P. Different forms of U15 snoRNA are encoded in the introns of the ribosomal protein S1 gene of Xenopus laevis Nucleic Acids Research. 22: 4607-4613. PMID 7984408  0.4
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