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Drug Screen Tugs at Common Thread for Repeat Disorders.
Reddy K, Cleary JD, Berglund JA. Reddy K, et al. Trends Pharmacol Sci. 2020 Feb;41(2):71-73. doi: 10.1016/j.tips.2019.12.004. Epub 2020 Jan 8. Trends Pharmacol Sci. 2020. PMID: 31926601
CCG•CGG interruptions in high-penetrance SCA8 families increase RAN translation and protein toxicity.
Perez BA, Shorrock HK, Banez-Coronel M, Zu T, Romano LE, Laboissonniere LA, Reid T, Ikeda Y, Reddy K, Gomez CM, Bird T, Ashizawa T, Schut LJ, Brusco A, Berglund JA, Hasholt LF, Nielsen JE, Subramony SH, Ranum LP. Perez BA, et al. Among authors: reddy k. EMBO Mol Med. 2021 Nov 8;13(11):e14095. doi: 10.15252/emmm.202114095. Epub 2021 Oct 11. EMBO Mol Med. 2021. PMID: 34632710 Free PMC article.
Disease-associated inosine misincorporation into RNA hinders translation.
Schroader JH, Jones LA, Meng R, Shorrock HK, Richardson JI, Shaughnessy SM, Lin Q, Begley TJ, Berglund JA, Fuchs G, Handley MT, Reddy K. Schroader JH, et al. Among authors: reddy k. Nucleic Acids Res. 2022 Sep 9;50(16):9306-9318. doi: 10.1093/nar/gkac709. Nucleic Acids Res. 2022. PMID: 35979951 Free PMC article.
ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy.
Handley MT, Reddy K, Wills J, Rosser E, Kamath A, Halachev M, Falkous G, Williams D, Cox P, Meynert A, Raymond ES, Morrison H, Brown S, Allan E, Aligianis I, Jackson AP, Ramsahoye BH, von Kriegsheim A, Taylor RW, Finch AJ, FitzPatrick DR. Handley MT, et al. Among authors: reddy k. PLoS Genet. 2019 Mar 11;15(3):e1007605. doi: 10.1371/journal.pgen.1007605. eCollection 2019 Mar. PLoS Genet. 2019. PMID: 30856165 Free PMC article.
3,882 results