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MECP2 promoter methylation and X chromosome inactivation in autism.
Nagarajan RP, Patzel KA, Martin M, Yasui DH, Swanberg SE, Hertz-Picciotto I, Hansen RL, Van de Water J, Pessah IN, Jiang R, Robinson WP, LaSalle JM. Nagarajan RP, et al. Among authors: lasalle jm. Autism Res. 2008 Jun;1(3):169-78. doi: 10.1002/aur.24. Autism Res. 2008. PMID: 19132145 Free PMC article.
Wilson Disease: Epigenetic effects of choline supplementation on phenotype and clinical course in a mouse model.
Medici V, Kieffer DA, Shibata NM, Chima H, Kim K, Canovas A, Medrano JF, Islas-Trejo AD, Kharbanda KK, Olson K, Su RJ, Islam MS, Syed R, Keen CL, Miller AY, Rutledge JC, Halsted CH, LaSalle JM. Medici V, et al. Among authors: lasalle jm. Epigenetics. 2016 Nov;11(11):804-818. doi: 10.1080/15592294.2016.1231289. Epub 2016 Sep 9. Epigenetics. 2016. PMID: 27611852 Free PMC article.
Placental methylome analysis from a prospective autism study.
Schroeder DI, Schmidt RJ, Crary-Dooley FK, Walker CK, Ozonoff S, Tancredi DJ, Hertz-Picciotto I, LaSalle JM. Schroeder DI, et al. Among authors: lasalle jm. Mol Autism. 2016 Dec 15;7:51. doi: 10.1186/s13229-016-0114-8. eCollection 2016. Mol Autism. 2016. PMID: 28018572 Free PMC article.
156 results