Maurice Swanson - Publications

Molecular Genetics and Microbiology University of Florida, Gainesville, Gainesville, FL, United States 
Genetics, Molecular Biology, Neuroscience Biology

90 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 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  0.56
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  0.88
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  0.56
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  0.32
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  0.32
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  0.32
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  0.32
2018 Sznajder ŁJ, Thomas JD, Carrell EM, Reid T, McFarland KN, Cleary JD, Oliveira R, Nutter CA, Bhatt K, Sobczak K, Ashizawa T, Thornton CA, Ranum LPW, Swanson MS. Intron retention induced by microsatellite expansions as a disease biomarker. Proceedings of the National Academy of Sciences of the United States of America. PMID 29610297 DOI: 10.1073/pnas.1716617115  0.36
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  0.32
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  0.32
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  0.56
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  0.32
2015 Scotti MM, Swanson MS. RNA mis-splicing in disease. Nature Reviews. Genetics. PMID 26593421 DOI: 10.1038/nrg.2015.3  0.32
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  1
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  1
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  1
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  0.32
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2013 Xia G, Santostefano KE, Goodwin M, Liu J, Subramony SH, Swanson MS, Terada N, Ashizawa T. Generation of neural cells from DM1 induced pluripotent stem cells as cellular model for the study of central nervous system neuropathogenesis. Cellular Reprogramming. 15: 166-77. PMID 23550732 DOI: 10.1089/cell.2012.0086  0.32
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  1
2012 Warren SA, Briggs LE, Zeng H, Chuang J, Chang EI, Terada R, Li M, Swanson MS, Lecker SH, Willis MS, Spinale FG, Maupin-Furlowe J, McMullen JR, Moss RL, Kasahara H. Myosin light chain phosphorylation is critical for adaptation to cardiac stress. Circulation. 126: 2575-88. PMID 23095280 DOI: 10.1161/CIRCULATIONAHA.112.116202  1
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  1
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  1
2011 Swanson MS. Silence is not always golden Genetic Testing and Molecular Biomarkers. 15: 467. PMID 21762002 DOI: 10.1089/gtmb.2011.1521  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  0.88
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  1
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  1
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  1
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  1
2007 Swanson MS, Orr HT. Fragile X tremor/ataxia syndrome: blame the messenger! Neuron. 55: 535-7. PMID 17698005 DOI: 10.1016/j.neuron.2007.07.032  1
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  1
2007 Lueck JD, Mankodi A, Swanson MS, Thornton CA, Dirksen RT. Muscle chloride channel dysfunction in two mouse models of myotonic dystrophy. The Journal of General Physiology. 129: 79-94. PMID 17158949 DOI: 10.1085/jgp.200609635  1
2007 Swanson MS. Special issue on the muscular dystrophies: Molecular basis and therapeutic strategies Biochimica Et Biophysica Acta - Molecular Basis of Disease. 1772: 107. DOI: 10.1016/j.bbadis.2007.01.001  1
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  0.88
2006 O'Rourke JR, Swanson MS, Harfe BD. MicroRNAs in mammalian development and tumorigenesis Birth Defects Research Part C - Embryo Today: Reviews. 78: 172-179. PMID 16847882 DOI: 10.1002/bdrc.20071  1
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  0.36
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
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  1
2004 Cheng D, Yadav N, King RW, Swanson MS, Weinstein EJ, Bedford MT. Small molecule regulators of protein arginine methyltransferases. The Journal of Biological Chemistry. 279: 23892-9. PMID 15056663 DOI: 10.1074/jbc.M401853200  1
2004 Leppert J, Urbinati CR, Häfner S, Ohlenschläger O, Swanson MS, Görlach M, Ramachandran R. Identification of NH...N hydrogen bonds by magic angle spinning solid state NMR in a double-stranded RNA associated with myotonic dystrophy Nucleic Acids Research. 32: 1177-1183. PMID 14973225 DOI: 10.1093/nar/gkh288  1
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  0.36
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  1
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  1
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  1
2001 Hong B, Reeves P, Panning B, Swanson MS, Yang TP. Identification of an autoimmune serum containing antibodies against the Barr body. Proceedings of the National Academy of Sciences of the United States of America. 98: 8703-8. PMID 11438711 DOI: 10.1073/pnas.151259598  1
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  1
1999 Swanson MS, Dreyfuss G. Preparation of heterogeneous nuclear ribonucleoprotein complexes. Methods in Molecular Biology (Clifton, N.J.). 118: 299-308. PMID 10549532 DOI: 10.1385/1-59259-676-2:299  1
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  1
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  1
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  0.56
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  1
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  1
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  1
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  1
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  1
1990 Swanson MS. Heterogeneous nuclear ribonucleoprotein complexes Molecular Biology Reports. 14: 79-82. PMID 1972976 DOI: 10.1007/BF00360424  1
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  1
1989 Burd CG, Swanson MS, Görlach M, Dreyfuss G. Primary structures of the heterogeneous nuclear ribonucleoprotein A2, B1, and C2 proteins: a diversity of RNA binding proteins is generated by small peptide inserts. Proceedings of the National Academy of Sciences of the United States of America. 86: 9788-92. PMID 2557628 DOI: 10.1073/pnas.86.24.9788  1
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  1
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  1
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  1
1988 Weil SC, Rosner GL, Reid MS, Chisholm RL, Lemons RS, Swanson MS, Carrino JJ, Diaz MO, Le Beau MM. Translocation and rearrangement of myeloperoxidase gene in acute promyelocytic leukemia. Science (New York, N.Y.). 240: 790-2. PMID 2896388  1
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  1
1987 Weil SC, Rosner GL, Reid MS, Chisholm RL, Farber NM, Spitznagel JK, Swanson MS. cDNA cloning of human myeloperoxidase: Decrease in myeloperoxidase mRNA upon induction of HL-60 cells Proceedings of the National Academy of Sciences of the United States of America. 84: 2057-2061. PMID 3031662 DOI: 10.1073/pnas.84.7.2057  1
1987 Swanson MS, Roma SP, Dreyfuss G. hnRNPS and mRNPS Molecular Biology Reports. 12: 165-168. DOI: 10.1007/BF00356881  1
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  1
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  1
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  1
1983 Speck SH, Neu CA, Swanson MS, Margoliash E. Role of phospholipid in the low affinity reactions between cytochrome c and cytochrome oxidase Febs Letters. 164: 379-382. PMID 6317460 DOI: 10.1016/0014-5793(83)80321-4  1
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