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Spatially coordinated heterochromatinization of long synaptic genes in fragile X syndrome.
Malachowski T, Chandradoss KR, Boya R, Zhou L, Cook AL, Su C, Pham K, Haws SA, Kim JH, Ryu HS, Ge C, Luppino JM, Nguyen SC, Titus KR, Gong W, Wallace O, Joyce EF, Wu H, Rojas LA, Phillips-Cremins JE. Malachowski T, et al. Among authors: wallace o. Cell. 2023 Dec 21;186(26):5840-5858.e36. doi: 10.1016/j.cell.2023.11.019. Cell. 2023. PMID: 38134876 Free article.
Fragile X Syndrome Patient-Derived Neurons Developing in the Mouse Brain Show FMR1-Dependent Phenotypes.
Krzisch MA, Wu H, Yuan B, Whitfield TW, Liu XS, Fu D, Garrett-Engele CM, Khalil AS, Lungjangwa T, Shih J, Chang AN, Warren S, Cacace A, Andrykovich KR, Rietjens RGJ, Wallace O, Sur M, Jain B, Jaenisch R. Krzisch MA, et al. Among authors: wallace o. Biol Psychiatry. 2023 Jan 1;93(1):71-81. doi: 10.1016/j.biopsych.2022.08.020. Epub 2022 Aug 28. Biol Psychiatry. 2023. PMID: 36372569
Surface-reacted calcium carbonate microparticles as templates for lactoferrin encapsulation.
Kiryukhin MV, Lim SH, Lau HH, Antipina M, Khin YW, Chia CY, Harris P, Weeks M, Berry C, Hurford D, Wallace O, Broadhurst M, Ridgway CJ, Schoelkopf J. Kiryukhin MV, et al. Among authors: wallace o. J Colloid Interface Sci. 2021 Jul 15;594:362-371. doi: 10.1016/j.jcis.2021.03.059. Epub 2021 Mar 17. J Colloid Interface Sci. 2021. PMID: 33774393
p38α Regulates Expression of DUX4 in a Model of Facioscapulohumeral Muscular Dystrophy.
Rojas LA, Valentine E, Accorsi A, Maglio J, Shen N, Robertson A, Kazmirski S, Rahl P, Tawil R, Cadavid D, Thompson LA, Ronco L, Chang AN, Cacace AM, Wallace O. Rojas LA, et al. Among authors: wallace o. J Pharmacol Exp Ther. 2020 Sep;374(3):489-498. doi: 10.1124/jpet.119.264689. Epub 2020 Jun 23. J Pharmacol Exp Ther. 2020. PMID: 32576599
46 results