| Year |
Citation |
Score |
| 2023 |
Wang Y, Traugot CM, Bubenik JL, Li T, Sheng P, Hiers NM, Fernandez P, Li L, Bian J, Swanson MS, Xie M. N-methyladenosine in 7SK small nuclear RNA underlies RNA polymerase II transcription regulation. Molecular Cell. PMID 37820733 DOI: 10.1016/j.molcel.2023.09.020 |
0.491 |
|
| 2023 |
Sznajder L, Khan M, Tadross M, Ciesiołka A, Nutter C, Taylor K, Pearson C, Sobczak K, Lewis M, Swanson M, Yuen R. Autistic traits in myotonic dystrophy type 1 due to MBNL inhibition and RNA mis-splicing. Research Square. PMID 37645891 DOI: 10.21203/rs.3.rs-3221704/v1 |
0.396 |
|
| 2023 |
Nutter CA, Kidd BM, Carter HA, Hamel JI, Mackie PM, Kumbkarni N, Davenport ML, Tuyn DM, Gopinath A, Creigh PD, Sznajder ŁJ, Wang ET, Ranum LPW, Khoshbouei H, Day JW, ... ... Swanson MS, et al. Choroid plexus mis-splicing and altered cerebrospinal fluid composition in myotonic dystrophy type 1. Brain : a Journal of Neurology. PMID 37143315 DOI: 10.1093/brain/awad148 |
0.497 |
|
| 2022 |
Spruce T, Plass M, Gohr A, Ray D, Martínez de Lagrán M, Rot G, Nóvoa A, Burguera D, Permanyer J, Miret M, Zheng H, Swanson MS, Morris Q, Mallo M, Dierssen M, et al. The X-linked splicing regulator MBNL3 has been co-opted to restrict placental growth in eutherians. Plos Biology. 20: e3001615. PMID 35476669 DOI: 10.1371/journal.pbio.3001615 |
0.443 |
|
| 2022 |
Franck S, Couvreu De Deckersberg E, Bubenik JL, Markouli C, Barbé L, Allemeersch J, Hilven P, Duqué G, Swanson MS, Gheldof A, Spits C, Sermon KD. Myotonic dystrophy type 1 embryonic stem cells show decreased myogenic potential, increased CpG methylation at the DMPK locus and RNA mis-splicing. Biology Open. 11. PMID 35019138 DOI: 10.1242/bio.058978 |
0.35 |
|
| 2021 |
Leary S, Gaudieri S, Parker MD, Chopra A, James I, Pakala S, Alves E, John M, Lindsey BB, Keeley AJ, Rowland-Jones SL, Swanson MS, Ostrov DA, Bubenik JL, Das S, et al. Generation of a novel SARS-CoV-2 sub-genomic RNA due to the R203K/G204R variant in nucleocapsid. Biorxiv : the Preprint Server For Biology. PMID 33880475 DOI: 10.1101/2020.04.10.029454 |
0.384 |
|
| 2020 |
Bubenik JL, Hale M, McConnell O, Wang E, Swanson MS, Spitale R, Berglund JA. RNA structure probing to characterize RNA-protein interactions on a low abundance pre-mRNA in living cells. Rna (New York, N.Y.). PMID 33310817 DOI: 10.1261/rna.077263.120 |
0.436 |
|
| 2020 |
Batra R, Nelles DA, Roth DM, Krach F, Nutter CA, Tadokoro T, Thomas JD, Sznajder ŁJ, Blue SM, Gutierrez HL, Liu P, Aigner S, Platoshyn O, Miyanohara A, Marsala M, ... Swanson MS, et al. The sustained expression of Cas9 targeting toxic RNAs reverses disease phenotypes in mouse models of myotonic dystrophy type 1. Nature Biomedical Engineering. PMID 32929188 DOI: 10.1038/S41551-020-00607-7 |
0.561 |
|
| 2020 |
Sznajder ŁJ, Scotti MM, Shin J, Taylor K, Ivankovic F, Nutter CA, Aslam FN, Subramony SH, Ranum LPW, Swanson MS. Loss of MBNL1 induces RNA misprocessing in the thymus and peripheral blood. Nature Communications. 11: 2022. PMID 32332745 DOI: 10.1038/s41467-020-15962-x |
0.834 |
|
| 2020 |
Li M, Zhuang Y, Batra R, Thomas JD, Li M, Nutter CA, Scotti MM, Carter HA, Wang ZJ, Huang XS, Pu CQ, Swanson MS, Xie W. HNRNPA1-induced spliceopathy in a transgenic mouse model of myotonic dystrophy. Proceedings of the National Academy of Sciences of the United States of America. PMID 32086392 DOI: 10.1073/pnas.1907297117 |
0.575 |
|
| 2019 |
Nutter CA, Bubenik JL, Oliveira R, Ivankovic F, Sznajder ŁJ, Kidd BM, Pinto BS, Otero BA, Carter HA, Vitriol EA, Wang ET, Swanson MS. Cell-type-specific dysregulation of RNA alternative splicing in short tandem repeat mouse knockin models of myotonic dystrophy. Genes & Development. PMID 31624084 DOI: 10.1101/Gad.328963.119 |
0.466 |
|
| 2019 |
Sznajder ŁJ, Swanson MS. Short Tandem Repeat Expansions and RNA-Mediated Pathogenesis in Myotonic Dystrophy. International Journal of Molecular Sciences. 20. PMID 31323950 DOI: 10.3390/ijms20133365 |
0.565 |
|
| 2018 |
Taylor K, Sznajder LJ, Cywoniuk P, Thomas JD, Swanson MS, Sobczak K. MBNL splicing activity depends on RNA binding site structural context. Nucleic Acids Research. PMID 29955876 DOI: 10.1093/nar/gky565 |
0.51 |
|
| 2018 |
Thomas JD, Oliveira R, Sznajder ŁJ, Swanson MS. Myotonic Dystrophy and Developmental Regulation of RNA Processing. Comprehensive Physiology. 8: 509-553. PMID 29687899 DOI: 10.1002/cphy.c170002 |
0.602 |
|
| 2018 |
Iradi MCG, Triplett JC, Thomas JD, Davila R, Crown AM, Brown H, Lewis J, Swanson MS, Xu G, Rodriguez-Lebron E, Borchelt DR. Characterization of gene regulation and protein interaction networks for Matrin 3 encoding mutations linked to amyotrophic lateral sclerosis and myopathy. Scientific Reports. 8: 4049. PMID 29511296 DOI: 10.1038/S41598-018-21371-4 |
0.357 |
|
| 2017 |
Li J, Tseng CS, Federico A, Ivankovic F, Huang YS, Ciccodicola A, Swanson MS, Yu P. SFMetaDB: a comprehensive annotation of mouse RNA splicing factor RNA-Seq datasets. Database : the Journal of Biological Databases and Curation. 2017. PMID 29220461 DOI: 10.1093/Database/Bax071 |
0.516 |
|
| 2017 |
Pinto BS, Saxena T, Oliveira R, Méndez-Gómez HR, Cleary JD, Denes LT, McConnell O, Arboleda J, Xia G, Swanson MS, Wang ET. Impeding Transcription of Expanded Microsatellite Repeats by Deactivated Cas9. Molecular Cell. PMID 29056323 DOI: 10.1016/J.Molcel.2017.09.033 |
0.526 |
|
| 2017 |
Zu T, Cleary JD, Liu Y, Bañez-Coronel M, Bubenik JL, Ayhan F, Ashizawa T, Xia G, Clark HB, Yachnis AT, Swanson MS, Ranum LPW. RAN Translation Regulated by Muscleblind Proteins in Myotonic Dystrophy Type 2. Neuron. 95: 1292-1305.e5. PMID 28910618 DOI: 10.1016/J.Neuron.2017.08.039 |
0.572 |
|
| 2017 |
Batra R, Nelles DA, Pirie E, Blue SM, Marina RJ, Wang H, Chaim IA, Thomas JD, Zhang N, Nguyen V, Aigner S, Markmiller S, Xia G, Corbett KD, Swanson MS, et al. Elimination of Toxic Microsatellite Repeat Expansion RNA by RNA-Targeting Cas9. Cell. PMID 28803727 DOI: 10.1016/J.Cell.2017.07.010 |
0.536 |
|
| 2017 |
Thomas JD, Sznajder ŁJ, Bardhi O, Aslam FN, Anastasiadis ZP, Scotti MM, Nishino I, Nakamori M, Wang ET, Swanson MS. Disrupted prenatal RNA processing and myogenesis in congenital myotonic dystrophy. Genes & Development. PMID 28698297 DOI: 10.1101/Gad.300590.117 |
0.6 |
|
| 2017 |
Sicot G, Servais L, Dinca DM, Leroy A, Prigogine C, Medja F, Braz SO, Huguet-Lachon A, Chhuon C, Nicole A, Gueriba N, Oliveira R, Dan B, Furling D, Swanson MS, et al. Downregulation of the Glial GLT1 Glutamate Transporter and Purkinje Cell Dysfunction in a Mouse Model of Myotonic Dystrophy. Cell Reports. 19: 2718-2729. PMID 28658620 DOI: 10.1016/J.Celrep.2017.06.006 |
0.357 |
|
| 2016 |
Freyermuth F, Rau F, Kokunai Y, Linke T, Sellier C, Nakamori M, Kino Y, Arandel L, Jollet A, Thibault C, Philipps M, Vicaire S, Jost B, Udd B, Day JW, ... ... Swanson MS, et al. Splicing misregulation of SCN5A contributes to cardiac-conduction delay and heart arrhythmia in myotonic dystrophy. Nature Communications. 7: 11067. PMID 27063795 DOI: 10.1038/Ncomms11067 |
0.353 |
|
| 2016 |
Taliaferro JM, Vidaki M, Oliveira R, Olson S, Zhan L, Saxena T, Wang ET, Graveley BR, Gertler FB, Swanson MS, Burge CB. Distal Alternative Last Exons Localize mRNAs to Neural Projections. Molecular Cell. PMID 26907613 DOI: 10.1016/J.Molcel.2016.01.020 |
0.326 |
|
| 2015 |
Davis J, Salomonis N, Ghearing N, Lin SC, Kwong JQ, Mohan A, Swanson MS, Molkentin JD. MBNL1-mediated regulation of differentiation RNAs promotes myofibroblast transformation and the fibrotic response. Nature Communications. 6: 10084. PMID 26670661 DOI: 10.1038/Ncomms10084 |
0.344 |
|
| 2015 |
Scotti MM, Swanson MS. RNA mis-splicing in disease. Nature Reviews. Genetics. PMID 26593421 DOI: 10.1038/nrg.2015.3 |
0.516 |
|
| 2015 |
Goodwin M, Mohan A, Batra R, Lee KY, Charizanis K, Gómez FJ, Eddarkaoui S, Sergeant N, Buée L, Kimura T, Clark HB, Dalton J, Takamura K, Weyn-Vanhentenryck SM, Zhang C, ... ... Swanson MS, et al. MBNL Sequestration by Toxic RNAs and RNA Misprocessing in the Myotonic Dystrophy Brain. Cell Reports. PMID 26257173 DOI: 10.1016/J.Celrep.2015.07.029 |
0.848 |
|
| 2015 |
Rau F, Lainé J, Ramanoudjame L, Ferry A, Arandel L, Delalande O, Jollet A, Dingli F, Lee KY, Peccate C, Lorain S, Kabashi E, Athanasopoulos T, Koo T, Loew D, ... Swanson MS, et al. Abnormal splicing switch of DMD's penultimate exon compromises muscle fibre maintenance in myotonic dystrophy. Nature Communications. 6: 7205. PMID 26018658 DOI: 10.1038/ncomms8205 |
0.462 |
|
| 2015 |
Batra R, Manchanda M, Swanson MS. Global insights into alternative polyadenylation regulation Rna Biology. 12: 597-602. PMID 25892335 DOI: 10.1080/15476286.2015.1040974 |
0.484 |
|
| 2015 |
Xia G, Gao Y, Jin S, Subramony SH, Terada N, Ranum LP, Swanson MS, Ashizawa T. Genome modification leads to phenotype reversal in human myotonic dystrophy type 1 induced pluripotent stem cell-derived neural stem cells. Stem Cells (Dayton, Ohio). 33: 1829-38. PMID 25702800 DOI: 10.1002/Stem.1970 |
0.315 |
|
| 2015 |
Swanson MS. Rectifying RNA splicing errors in hereditary neurodegenerative disease Proceedings of the National Academy of Sciences of the United States of America. 112: 2637-2638. PMID 25691745 DOI: 10.1073/pnas.1500976112 |
0.447 |
|
| 2014 |
Batra R, Charizanis K, Manchanda M, Mohan A, Li M, Finn DJ, Goodwin M, Zhang C, Sobczak K, Thornton CA, Swanson MS. Loss of MBNL leads to disruption of developmentally regulated alternative polyadenylation in RNA-mediated disease. Molecular Cell. 56: 311-22. PMID 25263597 DOI: 10.1016/J.Molcel.2014.08.027 |
0.858 |
|
| 2014 |
Goodwin M, Swanson MS. RNA-binding protein misregulation in microsatellite expansion disorders. Advances in Experimental Medicine and Biology. 825: 353-88. PMID 25201111 DOI: 10.1007/978-1-4939-1221-6_10 |
0.564 |
|
| 2014 |
Mohan A, Goodwin M, Swanson MS. RNA-protein interactions in unstable microsatellite diseases. Brain Research. 1584: 3-14. PMID 24709120 DOI: 10.1016/j.brainres.2014.03.039 |
0.568 |
|
| 2013 |
Lee KY, Li M, Manchanda M, Batra R, Charizanis K, Mohan A, Warren SA, Chamberlain CM, Finn D, Hong H, Ashraf H, Kasahara H, Ranum LP, Swanson MS. Compound loss of muscleblind-like function in myotonic dystrophy. Embo Molecular Medicine. 5: 1887-900. PMID 24293317 DOI: 10.1002/Emmm.201303275 |
0.841 |
|
| 2013 |
Nakamori M, Sobczak K, Puwanant A, Welle S, Eichinger K, Pandya S, Dekdebrun J, Heatwole CR, McDermott MP, Chen T, Cline M, Tawil R, Osborne RJ, Wheeler TM, Swanson MS, et al. Splicing biomarkers of disease severity in myotonic dystrophy. Annals of Neurology. 74: 862-72. PMID 23929620 DOI: 10.1002/Ana.23992 |
0.414 |
|
| 2013 |
Zhang C, Lee KY, Swanson MS, Darnell RB. Prediction of clustered RNA-binding protein motif sites in the mammalian genome. Nucleic Acids Research. 41: 6793-807. PMID 23685613 DOI: 10.1093/Nar/Gkt421 |
0.321 |
|
| 2013 |
Poulos MG, Batra R, Li M, Yuan Y, Zhang C, Darnell RB, Swanson MS. Progressive impairment of muscle regeneration in muscleblind-like 3 isoform knockout mice. Human Molecular Genetics. 22: 3547-58. PMID 23660517 DOI: 10.1093/Hmg/Ddt209 |
0.786 |
|
| 2013 |
Hernández-Hernández O, Guiraud-Dogan C, Sicot G, Huguet A, Luilier S, Steidl E, Saenger S, Marciniak E, Obriot H, Chevarin C, Nicole A, Revillod L, Charizanis K, Lee KY, Suzuki Y, ... ... Swanson MS, et al. Myotonic dystrophy CTG expansion affects synaptic vesicle proteins, neurotransmission and mouse behaviour. Brain : a Journal of Neurology. 136: 957-70. PMID 23404338 DOI: 10.1093/Brain/Aws367 |
0.799 |
|
| 2013 |
Sakai N, Sato M, Charizanis K, Lee K, Swanson M, Nishino S. Sleep phenotype characterization of peripheral and central mouse models of myotonic dystrophy Sleep Medicine. 14: e220-e221. DOI: 10.1016/J.Sleep.2013.11.528 |
0.741 |
|
| 2012 |
Charizanis K, Lee KY, Batra R, Goodwin M, Zhang C, Yuan Y, Shiue L, Cline M, Scotti MM, Xia G, Kumar A, Ashizawa T, Clark HB, Kimura T, Takahashi MP, ... ... Swanson MS, et al. Muscleblind-like 2-mediated alternative splicing in the developing brain and dysregulation in myotonic dystrophy. Neuron. 75: 437-50. PMID 22884328 DOI: 10.1016/J.Neuron.2012.05.029 |
0.824 |
|
| 2012 |
Suenaga K, Lee KY, Nakamori M, Tatsumi Y, Takahashi MP, Fujimura H, Jinnai K, Yoshikawa H, Du H, Ares M, Swanson MS, Kimura T. Muscleblind-like 1 knockout mice reveal novel splicing defects in the myotonic dystrophy brain. Plos One. 7: e33218. PMID 22427994 DOI: 10.1371/Journal.Pone.0033218 |
0.398 |
|
| 2011 |
Swanson MS. Silence is not always golden Genetic Testing and Molecular Biomarkers. 15: 467. PMID 21762002 DOI: 10.1089/gtmb.2011.1521 |
0.334 |
|
| 2011 |
Zu T, Gibbens B, Doty NS, Gomes-Pereira M, Huguet A, Stone MD, Margolis J, Peterson M, Markowski TW, Ingram MA, Nan Z, Forster C, Low WC, Schoser B, Somia NV, ... ... Swanson MS, et al. Non-ATG-initiated translation directed by microsatellite expansions. Proceedings of the National Academy of Sciences of the United States of America. 108: 260-5. PMID 21173221 DOI: 10.1073/Pnas.1013343108 |
0.434 |
|
| 2011 |
Poulos MG, Batra R, Charizanis K, Swanson MS. Developments in RNA splicing and disease. Cold Spring Harbor Perspectives in Biology. 3: a000778. PMID 21084389 DOI: 10.1101/Cshperspect.A000778 |
0.826 |
|
| 2010 |
Ranum LP, Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner T, Swanson MS. Double the trouble: bidirectional expression of the SCA8 CAG/CTG expansion mutation - evidence for RNA and protein gain of function effects. Rinshō Shinkeigaku = Clinical Neurology. 50: 982-3. PMID 21921535 DOI: JST.JSTAGE/clinicalneurol/50.982 |
0.437 |
|
| 2010 |
Batra R, Charizanis K, Swanson MS. Partners in crime: Bidirectional transcription in unstable microsatellite disease Human Molecular Genetics. 19. PMID 20368264 DOI: 10.1093/Hmg/Ddq132 |
0.827 |
|
| 2010 |
Du H, Cline MS, Osborne RJ, Tuttle DL, Clark TA, Donohue JP, Hall MP, Shiue L, Swanson MS, Thornton CA, Ares M. Aberrant alternative splicing and extracellular matrix gene expression in mouse models of myotonic dystrophy. Nature Structural & Molecular Biology. 17: 187-93. PMID 20098426 DOI: 10.1038/Nsmb.1720 |
0.588 |
|
| 2009 |
Daughters RS, Tuttle DL, Gao W, Ikeda Y, Moseley ML, Ebner TJ, Swanson MS, Ranum LP. RNA gain-of-function in spinocerebellar ataxia type 8. Plos Genetics. 5: e1000600. PMID 19680539 DOI: 10.1371/journal.pgen.1000600 |
0.586 |
|
| 2009 |
Shin J, Charizanis K, Swanson MS. Pathogenic RNAs in microsatellite expansion disease Neuroscience Letters. 466: 99-102. PMID 19647781 DOI: 10.1016/J.Neulet.2009.07.079 |
0.797 |
|
| 2009 |
Osborne RJ, Lin X, Welle S, Sobczak K, O'Rourke JR, Swanson MS, Thornton CA. Transcriptional and post-transcriptional impact of toxic RNA in myotonic dystrophy. Human Molecular Genetics. 18: 1471-81. PMID 19223393 DOI: 10.1093/Hmg/Ddp058 |
0.857 |
|
| 2009 |
O'Rourke JR, Swanson MS. Mechanisms of RNA-mediated disease Journal of Biological Chemistry. 284: 7419-7423. PMID 18957432 DOI: 10.1074/Jbc.R800025200 |
0.839 |
|
| 2007 |
Wheeler TM, Lueck JD, Swanson MS, Dirksen RT, Thornton CA. Correction of ClC-1 splicing eliminates chloride channelopathy and myotonia in mouse models of myotonic dystrophy. The Journal of Clinical Investigation. 117: 3952-7. PMID 18008009 DOI: 10.1172/Jci33355 |
0.367 |
|
| 2007 |
O'Rourke JR, Georges SA, Seay HR, Tapscott SJ, McManus MT, Goldhamer DJ, Swanson MS, Harfe BD. Essential role for Dicer during skeletal muscle development. Developmental Biology. 311: 359-68. PMID 17936265 DOI: 10.1016/J.Ydbio.2007.08.032 |
0.782 |
|
| 2007 |
Yuan Y, Compton SA, Sobczak K, Stenberg MG, Thornton CA, Griffith JD, Swanson MS. Muscleblind-like 1 interacts with RNA hairpins in splicing target and pathogenic RNAs. Nucleic Acids Research. 35: 5474-86. PMID 17702765 DOI: 10.1093/Nar/Gkm601 |
0.509 |
|
| 2007 |
Vicente M, Monferrer L, Poulos MG, Houseley J, Monckton DG, O'dell KM, Swanson MS, Artero RD. Muscleblind isoforms are functionally distinct and regulate alpha-actinin splicing. Differentiation; Research in Biological Diversity. 75: 427-40. PMID 17309604 DOI: 10.1111/J.1432-0436.2006.00156.X |
0.782 |
|
| 2006 |
Kanadia RN, Shin J, Yuan Y, Beattie SG, Wheeler TM, Thornton CA, Swanson MS. Reversal of RNA missplicing and myotonia after muscleblind overexpression in a mouse poly(CUG) model for myotonic dystrophy. Proceedings of the National Academy of Sciences of the United States of America. 103: 11748-53. PMID 16864772 DOI: 10.1073/Pnas.0604970103 |
0.832 |
|
| 2006 |
Lin X, Miller JW, Mankodi A, Kanadia RN, Yuan Y, Moxley RT, Swanson MS, Thornton CA. Failure of MBNL1-dependent post-natal splicing transitions in myotonic dystrophy. Human Molecular Genetics. 15: 2087-97. PMID 16717059 DOI: 10.1093/Hmg/Ddl132 |
0.782 |
|
| 2006 |
Thornton CA, Swanson MS, Cooper TA. The RNA-mediated disease process in myotonic dystrophy Genetic Instabilities and Neurological Diseases, Second Edition. 37-54. DOI: 10.1016/B978-012369462-1/50004-1 |
0.527 |
|
| 2005 |
Mankodi A, Lin X, Blaxall BC, Swanson MS, Thornton CA. Nuclear RNA foci in the heart in myotonic dystrophy. Circulation Research. 97: 1152-5. PMID 16254211 DOI: 10.1161/01.RES.0000193598.89753.e3 |
0.562 |
|
| 2005 |
Ho TH, Savkur RS, Poulos MG, Mancini MA, Swanson MS, Cooper TA. Colocalization of muscleblind with RNA foci is separable from mis-regulation of alternative splicing in myotonic dystrophy. Journal of Cell Science. 118: 2923-33. PMID 15961406 DOI: 10.1242/Jcs.02404 |
0.823 |
|
| 2005 |
Dheur S, Nykamp KR, Viphakone N, Swanson MS, Minvielle-Sebastia L. Yeast mRNA poly(A) tail length control can be reconstituted in vitro in the absence of Pab1p-dependent poly(A) nuclease activity Journal of Biological Chemistry. 280: 24532-24538. PMID 15894541 DOI: 10.1074/Jbc.M504720200 |
0.729 |
|
| 2005 |
Ladd AN, Stenberg MG, Swanson MS, Cooper TA. Dynamic balance between activation and repression regulates pre-mRNA alternative splicing during heart development Developmental Dynamics. 233: 783-793. PMID 15830352 DOI: 10.1002/Dvdy.20382 |
0.3 |
|
| 2004 |
Jun KY, Xia Y, Han X, Zhang H, Timchenko L, Swanson MS, Gao X. (1)H, (15)N and (13)C chemical shift assignments of RNA repeats binding protein -- CUGBP1ab. Journal of Biomolecular Nmr. 30: 371-2. PMID 15756469 DOI: 10.1007/S10858-005-2598-Y |
0.341 |
|
| 2004 |
Jiang H, Mankodi A, Swanson MS, Moxley RT, Thornton CA. Myotonic dystrophy type 1 is associated with nuclear foci of mutant RNA, sequestration of muscleblind proteins and deregulated alternative splicing in neurons. Human Molecular Genetics. 13: 3079-88. PMID 15496431 DOI: 10.1093/hmg/ddh327 |
0.519 |
|
| 2004 |
Ho TH, Charlet-B N, Poulos MG, Singh G, Swanson MS, Cooper TA. Muscleblind proteins regulate alternative splicing. The Embo Journal. 23: 3103-12. PMID 15257297 DOI: 10.1038/Sj.Emboj.7600300 |
0.764 |
|
| 2004 |
Nykamp KR, Swanson MS. Toxic RNA in the nucleus: unstable microsatellite expression in neuromuscular disease Progress in Molecular and Subcellular Biology. 35: 57-77. PMID 15113079 DOI: 10.1007/978-3-540-74266-1_3 |
0.789 |
|
| 2003 |
Mankodi A, Teng-Umnuay P, Krym M, Henderson D, Swanson M, Thornton CA. Ribonuclear inclusions in skeletal muscle in myotonic dystrophy types 1 and 2. Annals of Neurology. 54: 760-8. PMID 14681885 DOI: 10.1002/Ana.10763 |
0.649 |
|
| 2003 |
Kanadia RN, Johnstone KA, Mankodi A, Lungu C, Thornton CA, Esson D, Timmers AM, Hauswirth WW, Swanson MS. A muscleblind knockout model for myotonic dystrophy. Science (New York, N.Y.). 302: 1978-80. PMID 14671308 DOI: 10.1126/Science.1088583 |
0.837 |
|
| 2003 |
Kanadia RN, Urbinati CR, Crusselle VJ, Luo D, Lee YJ, Harrison JK, Oh SP, Swanson MS. Developmental expression of mouse muscleblind genes Mbnl1, Mbnl2 and Mbnl3. Gene Expression Patterns : Gep. 3: 459-62. PMID 12915312 DOI: 10.1016/S1567-133X(03)00064-4 |
0.795 |
|
| 2002 |
Hector RE, Nykamp KR, Dheur S, Anderson JT, Non PJ, Urbinati CR, Wilson SM, Minvielle-Sebastia L, Swanson MS. Dual requirement for yeast hnRNP Nab2p in mRNA poly(A) tail length control and nuclear export. The Embo Journal. 21: 1800-10. PMID 11927564 DOI: 10.1093/Emboj/21.7.1800 |
0.801 |
|
| 2001 |
Mankodi A, Urbinati CR, Yuan QP, Moxley RT, Sansone V, Krym M, Henderson D, Schalling M, Swanson MS, Thornton CA. Muscleblind localizes to nuclear foci of aberrant RNA in myotonic dystrophy types 1 and 2. Human Molecular Genetics. 10: 2165-70. PMID 11590133 DOI: 10.1093/hmg/10.19.2165 |
0.473 |
|
| 2000 |
Miller JW, Urbinati CR, Teng-Umnuay P, Stenberg MG, Byrne BJ, Thornton CA, Swanson MS. Recruitment of human muscleblind proteins to (CUG)(n) expansions associated with myotonic dystrophy. The Embo Journal. 19: 4439-48. PMID 10970838 DOI: 10.1093/Emboj/19.17.4439 |
0.558 |
|
| 2000 |
Gallouzi IE, Brennan CM, Stenberg MG, Swanson MS, Eversole A, Maizels N, Steitz JA. HuR binding to cytoplasmic mRNA is perturbed by heat shock. Proceedings of the National Academy of Sciences of the United States of America. 97: 3073-8. PMID 10737787 DOI: 10.1073/Pnas.97.7.3073 |
0.446 |
|
| 2000 |
Conrad NK, Wilson SM, Steinmetz EJ, Brow DA, Swanson MS, Corden JL. A NRD1-NAB3 COMPLEX ASSOCIATED WITH YEAST RNA POLYMERASE II Biochemical Society Transactions. 28: A442-A442. DOI: 10.1042/Bst028A442B |
0.388 |
|
| 1999 |
Michalowski S, Miller JW, Urbinati CR, Paliouras M, Swanson MS, Griffith J. Visualization of double-stranded RNAs from the myotonic dystrophy protein kinase gene and interactions with CUG-binding protein Nucleic Acids Research. 27: 3534-3542. PMID 10446244 DOI: 10.1093/Nar/27.17.3534 |
0.516 |
|
| 1999 |
Krecic AM, Swanson MS. hnRNP complexes: Composition, structure, and function Current Opinion in Cell Biology. 11: 363-371. PMID 10395553 DOI: 10.1016/S0955-0674(99)80051-9 |
0.496 |
|
| 1998 |
Minvielle-Sebastia L, Beyer K, Krecic AM, Hector RE, Swanson MS, Keller W. Control of cleavage site selection during mRNA 3' end formation by a yeast hnRNP. The Embo Journal. 17: 7454-68. PMID 9857200 DOI: 10.1093/emboj/17.24.7454 |
0.69 |
|
| 1997 |
Roberts R, Timchenko NA, Miller JW, Reddy S, Caskey CT, Swanson MS, Timchenko LT. Altered phosphorylation and intracellular distribution of a (CUG)n triplet repeat RNA-binding protein in patients with myotonic dystrophy and in myotonin protein kinase knockout mice. Proceedings of the National Academy of Sciences of the United States of America. 94: 13221-6. PMID 9371827 DOI: 10.1073/pnas.94.24.13221 |
0.327 |
|
| 1996 |
Timchenko LT, Miller JW, Timchenko NA, DeVore DR, Datar KV, Lin L, Roberts R, Caskey CT, Swanson MS. Identification of a (CUG)n triplet repeat RNA-binding protein and its expression in myotonic dystrophy. Nucleic Acids Research. 24: 4407-14. PMID 8948631 DOI: 10.1093/nar/24.22.4407 |
0.44 |
|
| 1994 |
Wilson SM, Datar KV, Paddy MR, Swedlow JR, Swanson MS. Characterization of nuclear polyadenylated RNA-binding proteins in Saccharomyces cerevisiae Journal of Cell Biology. 127: 1173-1184. PMID 7962083 DOI: 10.1083/jcb.127.5.1173 |
0.492 |
|
| 1993 |
Anderson JT, Wilson SM, Datar KV, Swanson MS. NAB2: A yeast nuclear polyadenylated RNA-binding protein essential for cell viability Molecular and Cellular Biology. 13: 2730-2741. PMID 8474438 DOI: 10.1128/MCB.13.5.2730 |
0.525 |
|
| 1993 |
Datar KV, Dreyfuss G, Swanson MS. The human hnRNP M proteins: identification of a methionine/arginine-rich repeat motif in ribonucleoproteins. Nucleic Acids Research. 21: 439-46. PMID 8441656 DOI: 10.1093/Nar/21.3.439 |
0.386 |
|
| 1993 |
Anderson JT, Paddy MR, Swanson MS. PUB1 is a major nuclear and cytoplasmic polyadenylated RNA-binding protein in Saccharomyces cerevisiae Molecular and Cellular Biology. 13: 6102-6113. PMID 8413212 DOI: 10.1128/MCB.13.10.6102 |
0.478 |
|
| 1989 |
Piñol-Roma S, Swanson MS, Gall JG, Dreyfuss G. A novel heterogeneous nuclear RNP protein with a unique distribution on nascent transcripts. The Journal of Cell Biology. 109: 2575-87. PMID 2687284 DOI: 10.1083/Jcb.109.6.2575 |
0.311 |
|
| 1989 |
Bandziulis RJ, Swanson MS, Dreyfuss G. RNA-binding proteins as developmental regulators. Genes & Development. 3: 431-7. PMID 2470643 DOI: 10.1101/Gad.3.4.431 |
0.424 |
|
| 1988 |
Swanson MS, Dreyfuss G. Classification and purification of proteins of heterogeneous nuclear ribonucleoprotein particles by RNA-binding specificities. Molecular and Cellular Biology. 8: 2237-41. PMID 3386636 DOI: 10.1128/Mcb.8.5.2237 |
0.308 |
|
| 1988 |
Dreyfuss G, Swanson MS, Piñol-Roma S. Heterogeneous nuclear ribonucleoprotein particles and the pathway of mRNA formation. Trends in Biochemical Sciences. 13: 86-91. PMID 3072706 DOI: 10.1016/0968-0004(88)90046-1 |
0.328 |
|
| 1988 |
Swanson MS, Dreyfuss G. RNA binding specificity of hnRNP proteins: a subset bind to the 3′ end of introns. The Embo Journal. 7: 3519-3529. DOI: 10.1002/j.1460-2075.1988.tb03228.x |
0.385 |
|
| 1987 |
Swanson MS, Nakagawa TY, LeVan K, Dreyfuss G. Primary structure of human nuclear ribonucleoprotein particle C proteins: Conservation of sequence and domain structures in heterogeneous nuclear RNA, mRNA, and pre-rRNA-binding proteins Molecular and Cellular Biology. 7: 1731-1739. PMID 3110598 DOI: 10.1128/Mcb.7.5.1731 |
0.402 |
|
| 1986 |
Adam SA, Nakagawa T, Swanson MS, Woodruff TK, Dreyfuss G. mRNA polyadenylate-binding protein: gene isolation and sequencing and identification of a ribonucleoprotein consensus sequence Molecular and Cellular Biology. 6: 2932-2943. PMID 3537727 DOI: 10.1128/mcb.6.8.2932-2943.1986 |
0.356 |
|
| 1986 |
Nakagawa TY, Swanson MS, Wold BJ, Dreyfuss G. Molecular cloning of cDNA for the nuclear ribonucleoprotein particle C proteins: a conserved gene family. Proceedings of the National Academy of Sciences of the United States of America. 83: 2007-11. PMID 3457372 DOI: 10.1073/Pnas.83.7.2007 |
0.319 |
|
| 1985 |
Swanson MS, Zieminn SM, Miller DD, Garber EA, Margoliash E. Developmental expression of nuclear genes that encode mitochondrial proteins: Insect cytochromes c Proceedings of the National Academy of Sciences of the United States of America. 82: 1964-1968. PMID 2984675 DOI: 10.1073/pnas.82.7.1964 |
0.34 |
|
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