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Page 1
Age-associated DNA methylation in pediatric populations.
Genome Res. 2012 Apr;22(4):623-32. doi: 10.1101/gr.125187.111. Epub 2012 Feb 1.
Genome Res. 2012.
PMID: 22300631
Free PMC article.
Fragile X syndrome due to a missense mutation.
Myrick LK, Nakamoto-Kinoshita M, Lindor NM, Kirmani S, Cheng X, Warren ST.
Myrick LK, et al.
Eur J Hum Genet. 2014 Oct;22(10):1185-9. doi: 10.1038/ejhg.2013.311. Epub 2014 Jan 22.
Eur J Hum Genet. 2014.
PMID: 24448548
Free PMC article.
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Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of Fmr1 Knock-Out Mice.
Deng PY, Carlin D, Oh YM, Myrick LK, Warren ST, Cavalli V, Klyachko VA.
Deng PY, et al. Among authors: myrick lk.
J Neurosci. 2019 Jan 2;39(1):28-43. doi: 10.1523/JNEUROSCI.1593-18.2018. Epub 2018 Nov 2.
J Neurosci. 2019.
PMID: 30389838
Free PMC article.
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Human FMRP contains an integral tandem Agenet (Tudor) and KH motif in the amino terminal domain.
Myrick LK, Hashimoto H, Cheng X, Warren ST.
Myrick LK, et al.
Hum Mol Genet. 2015 Mar 15;24(6):1733-40. doi: 10.1093/hmg/ddu586. Epub 2014 Nov 20.
Hum Mol Genet. 2015.
PMID: 25416280
Free PMC article.
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Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures.
Myrick LK, Deng PY, Hashimoto H, Oh YM, Cho Y, Poidevin MJ, Suhl JA, Visootsak J, Cavalli V, Jin P, Cheng X, Warren ST, Klyachko VA.
Myrick LK, et al.
Proc Natl Acad Sci U S A. 2015 Jan 27;112(4):949-56. doi: 10.1073/pnas.1423094112. Epub 2015 Jan 5.
Proc Natl Acad Sci U S A. 2015.
PMID: 25561520
Free PMC article.
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