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Items: 32


Placental DNA methylation levels at CYP2E1 and IRS2 are associated with child outcome in a prospective autism study.

Zhu Y, Mordaunt CE, Yasui DH, Marathe R, Coulson RL, Dunaway KW, Jianu JM, Walker CK, Ozonoff S, Hertz-Picciotto I, Schmidt RJ, LaSalle JM.

Hum Mol Genet. 2019 Apr 22. pii: ddz084. doi: 10.1093/hmg/ddz084. [Epub ahead of print]


MeCP2 isoform e1 mutant mice recapitulate motor and metabolic phenotypes of Rett syndrome.

Vogel Ciernia A, Yasui DH, Pride MC, Durbin-Johnson B, Noronha AB, Chang A, Knotts TA, Rutkowsky JR, Ramsey JJ, Crawley JN, LaSalle JM.

Hum Mol Genet. 2018 Dec 1;27(23):4077-4093. doi: 10.1093/hmg/ddy301.


Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuN.

Coulson RL, Powell WT, Yasui DH, Dileep G, Resnick J, LaSalle JM.

Hum Mol Genet. 2018 Dec 1;27(23):4051-4060. doi: 10.1093/hmg/ddy296.


Cognitive deficits in the Snord116 deletion mouse model for Prader-Willi syndrome.

Adhikari A, Copping NA, Onaga B, Pride MC, Coulson RL, Yang M, Yasui DH, LaSalle JM, Silverman JL.

Neurobiol Learn Mem. 2018 May 23. pii: S1074-7427(18)30119-9. doi: 10.1016/j.nlm.2018.05.011. [Epub ahead of print] Review.


Snord116-dependent diurnal rhythm of DNA methylation in mouse cortex.

Coulson RL, Yasui DH, Dunaway KW, Laufer BI, Vogel Ciernia A, Zhu Y, Mordaunt CE, Totah TS, LaSalle JM.

Nat Commun. 2018 Apr 24;9(1):1616. doi: 10.1038/s41467-018-03676-0.


Experience-dependent neuroplasticity of the developing hypothalamus: integrative epigenomic approaches.

Vogel Ciernia A, Laufer BI, Dunaway KW, Mordaunt CE, Coulson RL, Totah TS, Stolzenberg DS, Frahm JC, Singh-Taylor A, Baram TZ, LaSalle JM, Yasui DH.

Epigenetics. 2018;13(3):318-330. doi: 10.1080/15592294.2018.1451720. Epub 2018 May 10.


Early motor phenotype detection in a female mouse model of Rett syndrome is improved by cross-fostering.

Vogel Ciernia A, Pride MC, Durbin-Johnson B, Noronha A, Chang A, Yasui DH, Crawley JN, LaSalle JM.

Hum Mol Genet. 2017 May 15;26(10):1839-1854. doi: 10.1093/hmg/ddx087.


Cumulative Impact of Polychlorinated Biphenyl and Large Chromosomal Duplications on DNA Methylation, Chromatin, and Expression of Autism Candidate Genes.

Dunaway KW, Islam MS, Coulson RL, Lopez SJ, Vogel Ciernia A, Chu RG, Yasui DH, Pessah IN, Lott P, Mordaunt C, Meguro-Horike M, Horike SI, Korf I, LaSalle JM.

Cell Rep. 2016 Dec 13;17(11):3035-3048. doi: 10.1016/j.celrep.2016.11.058.


Loss of MeCP2 in the rat models regression, impaired sociability and transcriptional deficits of Rett syndrome.

Veeraragavan S, Wan YW, Connolly DR, Hamilton SM, Ward CS, Soriano S, Pitcher MR, McGraw CM, Huang SG, Green JR, Yuva LA, Liang AJ, Neul JL, Yasui DH, LaSalle JM, Liu Z, Paylor R, Samaco RC.

Hum Mol Genet. 2016 Aug 1;25(15):3284-3302. doi: 10.1093/hmg/ddw178. Epub 2016 Jun 30.


Sequence features accurately predict genome-wide MeCP2 binding in vivo.

Rube HT, Lee W, Hejna M, Chen H, Yasui DH, Hess JF, LaSalle JM, Song JS, Gong Q.

Nat Commun. 2016 Mar 24;7:11025. doi: 10.1038/ncomms11025.


MeCP2 regulates activity-dependent transcriptional responses in olfactory sensory neurons.

Lee W, Yun JM, Woods R, Dunaway K, Yasui DH, Lasalle JM, Gong Q.

Hum Mol Genet. 2014 Dec 1;23(23):6366-74. doi: 10.1093/hmg/ddu358. Epub 2014 Jul 9.


Mice with an isoform-ablating Mecp2 exon 1 mutation recapitulate the neurologic deficits of Rett syndrome.

Yasui DH, Gonzales ML, Aflatooni JO, Crary FK, Hu DJ, Gavino BJ, Golub MS, Vincent JB, Carolyn Schanen N, Olson CO, Rastegar M, Lasalle JM.

Hum Mol Genet. 2014 May 1;23(9):2447-58. doi: 10.1093/hmg/ddt640. Epub 2013 Dec 18. Erratum in: Hum Mol Genet. 2014 Dec 15;23(24):6695.


R-loop formation at Snord116 mediates topotecan inhibition of Ube3a-antisense and allele-specific chromatin decondensation.

Powell WT, Coulson RL, Gonzales ML, Crary FK, Wong SS, Adams S, Ach RA, Tsang P, Yamada NA, Yasui DH, Ch├ędin F, LaSalle JM.

Proc Natl Acad Sci U S A. 2013 Aug 20;110(34):13938-43. doi: 10.1073/pnas.1305426110. Epub 2013 Aug 5.


A Prader-Willi locus lncRNA cloud modulates diurnal genes and energy expenditure.

Powell WT, Coulson RL, Crary FK, Wong SS, Ach RA, Tsang P, Alice Yamada N, Yasui DH, Lasalle JM.

Hum Mol Genet. 2013 Nov 1;22(21):4318-28. doi: 10.1093/hmg/ddt281. Epub 2013 Jun 13.


Epigenetic layers and players underlying neurodevelopment.

LaSalle JM, Powell WT, Yasui DH.

Trends Neurosci. 2013 Aug;36(8):460-70. doi: 10.1016/j.tins.2013.05.001. Epub 2013 May 31. Review.


MeCP2 modulates gene expression pathways in astrocytes.

Yasui DH, Xu H, Dunaway KW, Lasalle JM, Jin LW, Maezawa I.

Mol Autism. 2013 Jan 25;4(1):3. doi: 10.1186/2040-2392-4-3.


Long-lived epigenetic interactions between perinatal PBDE exposure and Mecp2308 mutation.

Woods R, Vallero RO, Golub MS, Suarez JK, Ta TA, Yasui DH, Chi LH, Kostyniak PJ, Pessah IN, Berman RF, LaSalle JM.

Hum Mol Genet. 2012 Jun 1;21(11):2399-411. doi: 10.1093/hmg/dds046. Epub 2012 Feb 15.


15q11.2-13.3 chromatin analysis reveals epigenetic regulation of CHRNA7 with deficiencies in Rett and autism brain.

Yasui DH, Scoles HA, Horike S, Meguro-Horike M, Dunaway KW, Schroeder DI, Lasalle JM.

Hum Mol Genet. 2011 Nov 15;20(22):4311-23. doi: 10.1093/hmg/ddr357. Epub 2011 Aug 12.


Neuron-specific impairment of inter-chromosomal pairing and transcription in a novel model of human 15q-duplication syndrome.

Meguro-Horike M, Yasui DH, Powell W, Schroeder DI, Oshimura M, Lasalle JM, Horike S.

Hum Mol Genet. 2011 Oct 1;20(19):3798-810. doi: 10.1093/hmg/ddr298. Epub 2011 Jul 1.


Investigation of modifier genes within copy number variations in Rett syndrome.

Artuso R, Papa FT, Grillo E, Mucciolo M, Yasui DH, Dunaway KW, Disciglio V, Mencarelli MA, Pollazzon M, Zappella M, Hayek G, Mari F, Renieri A, Lasalle JM, Ariani F.

J Hum Genet. 2011 Jul;56(7):508-15. doi: 10.1038/jhg.2011.50. Epub 2011 May 19. Erratum in: J Hum Genet. 2012 May;57(5):342-4.


MeCP2 is required for global heterochromatic and nucleolar changes during activity-dependent neuronal maturation.

Singleton MK, Gonzales ML, Leung KN, Yasui DH, Schroeder DI, Dunaway K, LaSalle JM.

Neurobiol Dis. 2011 Jul;43(1):190-200. doi: 10.1016/j.nbd.2011.03.011. Epub 2011 Mar 21.


Evolving role of MeCP2 in Rett syndrome and autism.

LaSalle JM, Yasui DH.

Epigenomics. 2009 Oct;1(1):119-30. doi: 10.2217/epi.09.13. Review.


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.

Autism Res. 2008 Jun;1(3):169-78. doi: 10.1002/aur.24.


Epigenetics in the nervous system.

Jiang Y, Langley B, Lubin FD, Renthal W, Wood MA, Yasui DH, Kumar A, Nestler EJ, Akbarian S, Beckel-Mitchener AC.

J Neurosci. 2008 Nov 12;28(46):11753-9. doi: 10.1523/JNEUROSCI.3797-08.2008. Review.


Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autism.

Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM.

Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10.


Integrated epigenomic analyses of neuronal MeCP2 reveal a role for long-range interaction with active genes.

Yasui DH, Peddada S, Bieda MC, Vallero RO, Hogart A, Nagarajan RP, Thatcher KN, Farnham PJ, Lasalle JM.

Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19416-21. Epub 2007 Nov 27.


15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disorders.

Hogart A, Nagarajan RP, Patzel KA, Yasui DH, Lasalle JM.

Hum Mol Genet. 2007 Mar 15;16(6):691-703. Epub 2007 Mar 5.


Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndrome.

Peddada S, Yasui DH, LaSalle JM.

Hum Mol Genet. 2006 Jun 15;15(12):2003-14. Epub 2006 May 8.


Protein composition of the intranuclear inclusions of FXTAS.

Iwahashi CK, Yasui DH, An HJ, Greco CM, Tassone F, Nannen K, Babineau B, Lebrilla CB, Hagerman RJ, Hagerman PJ.

Brain. 2006 Jan;129(Pt 1):256-71. Epub 2005 Oct 24.


Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samples.

Thatcher KN, Peddada S, Yasui DH, Lasalle JM.

Hum Mol Genet. 2005 Mar 15;14(6):785-97. Epub 2005 Feb 2.


The MAR-binding protein SATB1 orchestrates temporal and spatial expression of multiple genes during T-cell development.

Alvarez JD, Yasui DH, Niida H, Joh T, Loh DY, Kohwi-Shigematsu T.

Genes Dev. 2000 Mar 1;14(5):521-35.


Transcriptional repression of the IL-2 gene in Th cells by ZEB.

Yasui DH, Genetta T, Kadesch T, Williams TM, Swain SL, Tsui LV, Huber BT.

J Immunol. 1998 May 1;160(9):4433-40.

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