John Cleary - Publications

Affiliations: 
2000-2010 Molecular Genetics University of Toronto, Toronto, ON, Canada 

21 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
2024 Shorrock HK, Aliyeva A, Frias JA, DeMeo VA, Lennon CD, DeMeo CC, Mascorro AK, Shaughnessy S, Mazdiyasni H, Cleary JD, Reddy K, Vangaveti S, Shin DS, Berglund JA. CAG repeat-selective compounds reduce abundance of expanded CAG RNAs in patient cell and murine models of SCAs. Biorxiv : the Preprint Server For Biology. PMID 39211226 DOI: 10.1101/2024.08.17.608349  0.728
2024 Louis JM, Frias JA, Schroader JH, Jones LA, Davey EE, Lennon CD, Chacko J, Cleary JD, Berglund JA, Reddy K. Expression levels of core spliceosomal proteins modulate the MBNL-mediated spliceopathy in DM1. Human Molecular Genetics. PMID 39180495 DOI: 10.1093/hmg/ddae125  0.718
2023 Shorrock HK, Lennon CD, Aliyeva A, Davey EE, DeMeo CC, Pritchard CE, Planco L, Velez JM, Mascorro-Huamancaja A, Shin DS, Cleary JD, Berglund JA. Widespread alternative splicing dysregulation occurs presymptomatically in CAG expansion spinocerebellar ataxias. Brain : a Journal of Neurology. PMID 37776516 DOI: 10.1093/brain/awad329  0.341
2023 Mishra SK, Hicks SM, Frias JA, Vangaveti S, Nakamori M, Cleary JD, Reddy K, Berglund JA. Quercetin selectively reduces expanded repeat RNA levels in models of myotonic dystrophy. Biorxiv : the Preprint Server For Biology. PMID 36778282 DOI: 10.1101/2023.02.02.526846  0.719
2022 Jenquin JR, O'Brien AP, Poukalov K, Lu Y, Frias JA, Shorrock HK, Richardson JI, Mazdiyasni H, Yang H, Huigens RW, Boykin D, Ranum LPW, Cleary JD, Wang ET, Berglund JA. Molecular characterization of myotonic dystrophy fibroblast cell lines for use in small molecule screening. Iscience. 25: 104198. PMID 35479399 DOI: 10.1016/j.isci.2022.104198  0.311
2020 Reddy K, Cleary JD, Berglund JA. Drug Screen Tugs at Common Thread for Repeat Disorders. Trends in Pharmacological Sciences. PMID 31926601 DOI: 10.1016/J.Tips.2019.12.004  0.676
2019 Reddy K, Jenquin JR, McConnell OL, Cleary JD, Richardson JI, Pinto BS, Haerle MC, Delgado E, Planco L, Nakamori M, Wang ET, Berglund JA. A CTG repeat-selective chemical screen identifies microtubule inhibitors as selective modulators of toxic CUG RNA levels. Proceedings of the National Academy of Sciences of the United States of America. PMID 31570586 DOI: 10.1073/Pnas.1901893116  0.72
2019 Reddy K, Jenquin JR, Cleary JD, Berglund JA. Mitigating RNA Toxicity in Myotonic Dystrophy using Small Molecules. International Journal of Molecular Sciences. 20. PMID 31426500 DOI: 10.3390/Ijms20164017  0.703
2018 Wang Y, Hao L, Wang H, Santostefano K, Thapa A, Cleary J, Li H, Guo X, Terada N, Ashizawa T, Xia G. Therapeutic Genome Editing for Myotonic Dystrophy Type 1 Using CRISPR/Cas9. Molecular Therapy : the Journal of the American Society of Gene Therapy. PMID 30274788 DOI: 10.1016/J.Ymthe.2018.09.003  0.31
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  0.325
2014 Cleary JD, Ranum LP. Repeat associated non-ATG (RAN) translation: new starts in microsatellite expansion disorders. Current Opinion in Genetics & Development. 26: 6-15. PMID 24852074 DOI: 10.1016/j.gde.2014.03.002  0.331
2013 Cleary JD, Ranum LP. Repeat-associated non-ATG (RAN) translation in neurological disease. Human Molecular Genetics. 22: R45-51. PMID 23918658 DOI: 10.1093/hmg/ddt371  0.319
2010 Cleary JD, Tomé S, López Castel A, Panigrahi GB, Foiry L, Hagerman KA, Sroka H, Chitayat D, Gourdon G, Pearson CE. Tissue- and age-specific DNA replication patterns at the CTG/CAG-expanded human myotonic dystrophy type 1 locus. Nature Structural & Molecular Biology. 17: 1079-87. PMID 20711191 DOI: 10.1038/Nsmb.1876  0.717
2010 López Castel A, Cleary JD, Pearson CE. Repeat instability as the basis for human diseases and as a potential target for therapy. Nature Reviews. Molecular Cell Biology. 11: 165-70. PMID 20177394 DOI: 10.1038/Nrm2854  0.622
2008 Libby RT, Hagerman KA, Pineda VV, Lau R, Cho DH, Baccam SL, Axford MM, Cleary JD, Moore JM, Sopher BL, Tapscott SJ, Filippova GN, Pearson CE, La Spada AR. CTCF cis-regulates trinucleotide repeat instability in an epigenetic manner: a novel basis for mutational hot spot determination. Plos Genetics. 4: e1000257. PMID 19008940 DOI: 10.1371/Journal.Pgen.1000257  0.643
2005 Pearson CE, Nichol Edamura K, Cleary JD. Repeat instability: mechanisms of dynamic mutations. Nature Reviews. Genetics. 6: 729-42. PMID 16205713 DOI: 10.1038/Nrg1689  0.622
2005 Cleary JD, Pearson CE. Replication fork dynamics and dynamic mutations: the fork-shift model of repeat instability. Trends in Genetics : Tig. 21: 272-80. PMID 15851063 DOI: 10.1016/J.Tig.2005.03.008  0.614
2003 Cleary JD, Pearson CE. The contribution of cis-elements to disease-associated repeat instability: clinical and experimental evidence. Cytogenetic and Genome Research. 100: 25-55. PMID 14526163 DOI: 10.1159/000072837  0.614
2002 Pearson CE, Tam M, Wang YH, Montgomery SE, Dar AC, Cleary JD, Nichol K. Slipped-strand DNAs formed by long (CAG)*(CTG) repeats: slipped-out repeats and slip-out junctions. Nucleic Acids Research. 30: 4534-47. PMID 12384601 DOI: 10.1093/Nar/Gkf572  0.57
2002 Cleary JD, Nichol K, Wang YH, Pearson CE. Evidence of cis-acting factors in replication-mediated trinucleotide repeat instability in primate cells. Nature Genetics. 31: 37-46. PMID 11967533 DOI: 10.1038/Ng870  0.616
2002 Panigrahi GB, Cleary JD, Pearson CE. In vitro (CTG)*(CAG) expansions and deletions by human cell extracts. The Journal of Biological Chemistry. 277: 13926-34. PMID 11832482 DOI: 10.1074/Jbc.M109761200  0.628
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