| Year |
Citation |
Score |
| 2023 |
Lumpkin CJ, Harris AW, Connell AJ, Kirk RW, Whiting JA, Saieva L, Pellizzoni L, Burghes AHM, Butchbach MER. Evaluation of the orally bioavailable 4-phenylbutyrate-tethered trichostatin A analogue AR42 in models of spinal muscular atrophy. Scientific Reports. 13: 10374. PMID 37365234 DOI: 10.1038/s41598-023-37496-0 |
0.371 |
|
| 2022 |
Tisdale S, Van Alstyne M, Simon CM, Mentis GZ, Pellizzoni L. SMN controls neuromuscular junction integrity through U7 snRNP. Cell Reports. 40: 111393. PMID 36130491 DOI: 10.1016/j.celrep.2022.111393 |
0.379 |
|
| 2022 |
Chen L, Roake CM, Maccallini P, Bavasso F, Dehghannasiri R, Santonicola P, Mendoza-Ferreira N, Scatolini L, Rizzuti L, Esposito A, Gallotta I, Francia S, Cacchione S, Galati A, Palumbo V, ... ... Pellizzoni L, et al. TGS1 impacts snRNA 3'-end processing, ameliorates survival motor neuron-dependent neurological phenotypes in vivo and prevents neurodegeneration. Nucleic Acids Research. PMID 35947650 DOI: 10.1093/nar/gkac659 |
0.49 |
|
| 2022 |
Carlini MJ, Triplett MK, Pellizzoni L. Neuromuscular denervation and deafferentation but not motor neuron death are disease features in the Smn2B/- mouse model of SMA. Plos One. 17: e0267990. PMID 35913953 DOI: 10.1371/journal.pone.0267990 |
0.525 |
|
| 2021 |
Van Alstyne M, Tattoli I, Delestrée N, Recinos Y, Workman E, Shihabuddin LS, Zhang C, Mentis GZ, Pellizzoni L. Gain of toxic function by long-term AAV9-mediated SMN overexpression in the sensorimotor circuit. Nature Neuroscience. PMID 33795885 DOI: 10.1038/s41593-021-00827-3 |
0.5 |
|
| 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 |
0.625 |
|
| 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 |
0.604 |
|
| 2019 |
Briese M, Haberman N, Sibley CR, Faraway R, Elser AS, Chakrabarti AM, Wang Z, König J, Perera D, Wickramasinghe VO, Venkitaraman AR, Luscombe NM, Saieva L, Pellizzoni L, Smith CWJ, et al. A systems view of spliceosomal assembly and branchpoints with iCLIP. Nature Structural & Molecular Biology. PMID 31570875 DOI: 10.1038/S41594-019-0300-4 |
0.329 |
|
| 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 |
0.56 |
|
| 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 |
0.513 |
|
| 2018 |
Van Alstyne M, Simon CM, Sardi SP, Shihabuddin LS, Mentis GZ, Pellizzoni L. Dysregulation of Mdm2 and Mdm4 alternative splicing underlies motor neuron death in spinal muscular atrophy. Genes & Development. PMID 30012555 DOI: 10.1101/Gad.316059.118 |
0.6 |
|
| 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 |
0.475 |
|
| 2017 |
Simon CM, Dai Y, Van Alstyne M, Koutsioumpa C, Pagiazitis JG, Chalif JI, Wang X, Rabinowitz JE, Henderson CE, Pellizzoni L, Mentis GZ. Converging Mechanisms of p53 Activation Drive Motor Neuron Degeneration in Spinal Muscular Atrophy. Cell Reports. 21: 3767-3780. PMID 29281826 DOI: 10.1016/J.Celrep.2017.12.003 |
0.575 |
|
| 2016 |
Van Alstyne M, Pellizzoni L. Advances in modeling and treating spinal muscular atrophy. Current Opinion in Neurology. PMID 27472505 DOI: 10.1097/Wco.0000000000000368 |
0.575 |
|
| 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 |
0.564 |
|
| 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 |
0.541 |
|
| 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 |
0.552 |
|
| 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 |
0.614 |
|
| 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 |
0.707 |
|
| 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 |
0.488 |
|
| 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 |
0.632 |
|
| 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 |
0.704 |
|
| 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 |
0.713 |
|
| 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 |
0.566 |
|
| 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 |
0.711 |
|
| 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 |
0.697 |
|
| 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 |
0.562 |
|
| 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 |
0.563 |
|
| 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 |
0.523 |
|
| 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 |
0.551 |
|
| 2007 |
Pellizzoni L. Chaperoning ribonucleoprotein biogenesis in health and disease. Embo Reports. 8: 340-5. PMID 17401408 DOI: 10.1038/sj.embor.7400941 |
0.545 |
|
| 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 |
0.494 |
|
| 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 |
0.537 |
|
| 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 |
0.555 |
|
| 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 |
0.561 |
|
| 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 |
0.51 |
|
| 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 |
0.408 |
|
| 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 |
0.519 |
|
| 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 |
0.467 |
|
| 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 |
0.545 |
|
| 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 |
0.452 |
|
| 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 |
0.576 |
|
| 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 |
0.607 |
|
| 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 |
0.477 |
|
| 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 |
0.618 |
|
| 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 |
0.553 |
|
| 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 |
0.611 |
|
| 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 |
0.578 |
|
| 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 DOI: 10.1016/S0092-8674(00)81632-3 |
0.596 |
|
| 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 |
0.377 |
|
| 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 |
0.353 |
|
| 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 |
0.319 |
|
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