Yasui DH - Search Results

1

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. Adhikari A, et al. Among authors: yasui dh. Neurobiol Learn Mem. 2019 Nov;165:106874. doi: 10.1016/j.nlm.2018.05.011. Epub 2018 May 23. Neurobiol Learn Mem. 2019. PMID: 29800646 Free PMC article. Review.

2

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. Thatcher KN, et al. Among authors: yasui dh. Hum Mol Genet. 2005 Mar 15;14(6):785-97. doi: 10.1093/hmg/ddi073. Epub 2005 Feb 2. Hum Mol Genet. 2005. PMID: 15689352

3

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. Peddada S, et al. Among authors: yasui dh. Hum Mol Genet. 2006 Jun 15;15(12):2003-14. doi: 10.1093/hmg/ddl124. Epub 2006 May 8. Hum Mol Genet. 2006. PMID: 16682435 Free PMC article.

4

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. Hogart A, et al. Among authors: yasui dh. Hum Mol Genet. 2007 Mar 15;16(6):691-703. doi: 10.1093/hmg/ddm014. Epub 2007 Mar 5. Hum Mol Genet. 2007. PMID: 17339270 Free PMC article.

5

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. Yasui DH, et al. Proc Natl Acad Sci U S A. 2007 Dec 4;104(49):19416-21. doi: 10.1073/pnas.0707442104. Epub 2007 Nov 27. Proc Natl Acad Sci U S A. 2007. PMID: 18042715 Free PMC article.

6

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

Swanberg SE, Nagarajan RP, Peddada S, Yasui DH, LaSalle JM. Swanberg SE, et al. Among authors: yasui dh. Hum Mol Genet. 2009 Feb 1;18(3):525-34. doi: 10.1093/hmg/ddn380. Epub 2008 Nov 10. Hum Mol Genet. 2009. PMID: 19000991 Free PMC article.

7

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: yasui dh. Autism Res. 2008 Jun;1(3):169-78. doi: 10.1002/aur.24. Autism Res. 2008. PMID: 19132145 Free PMC article.

8

Evolving role of MeCP2 in Rett syndrome and autism.

LaSalle JM, Yasui DH. LaSalle JM, et al. Among authors: yasui dh. Epigenomics. 2009 Oct;1(1):119-30. doi: 10.2217/epi.09.13. Epigenomics. 2009. PMID: 20473347 Free PMC article. Review.

9

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. Singleton MK, et al. Among authors: yasui dh. Neurobiol Dis. 2011 Jul;43(1):190-200. doi: 10.1016/j.nbd.2011.03.011. Epub 2011 Mar 21. Neurobiol Dis. 2011. PMID: 21420494 Free PMC article.

10

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. Meguro-Horike M, et al. Among authors: yasui dh. Hum Mol Genet. 2011 Oct 1;20(19):3798-810. doi: 10.1093/hmg/ddr298. Epub 2011 Jul 1. Hum Mol Genet. 2011. PMID: 21725066 Free PMC article.

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

43 results

Search Page