Young J - Search Results

1

Mice with truncated MeCP2 recapitulate many Rett syndrome features and display hyperacetylation of histone H3.

Shahbazian M, Young J, Yuva-Paylor L, Spencer C, Antalffy B, Noebels J, Armstrong D, Paylor R, Zoghbi H. Shahbazian M, et al. Among authors: young j. Neuron. 2002 Jul 18;35(2):243-54. doi: 10.1016/s0896-6273(02)00768-7. Neuron. 2002. PMID: 12160743 Free article.

2

X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndrome.

Young JI, Zoghbi HY. Young JI, et al. Am J Hum Genet. 2004 Mar;74(3):511-20. doi: 10.1086/382228. Epub 2004 Feb 17. Am J Hum Genet. 2004. PMID: 14973779 Free PMC article.

3

Regulation of RNA splicing by the methylation-dependent transcriptional repressor methyl-CpG binding protein 2.

Young JI, Hong EP, Castle JC, Crespo-Barreto J, Bowman AB, Rose MF, Kang D, Richman R, Johnson JM, Berget S, Zoghbi HY. Young JI, et al. Proc Natl Acad Sci U S A. 2005 Dec 6;102(49):17551-8. doi: 10.1073/pnas.0507856102. Epub 2005 Oct 26. Proc Natl Acad Sci U S A. 2005. PMID: 16251272 Free PMC article.

4

Cell-specific expression of wild-type MeCP2 in mouse models of Rett syndrome yields insight about pathogenesis.

Alvarez-Saavedra M, Sáez MA, Kang D, Zoghbi HY, Young JI. Alvarez-Saavedra M, et al. Hum Mol Genet. 2007 Oct 1;16(19):2315-25. doi: 10.1093/hmg/ddm185. Epub 2007 Jul 17. Hum Mol Genet. 2007. PMID: 17635839

5

Disruption of Mbd5 in mice causes neuronal functional deficits and neurobehavioral abnormalities consistent with 2q23.1 microdeletion syndrome.

Camarena V, Cao L, Abad C, Abrams A, Toledo Y, Araki K, Araki M, Walz K, Young JI. Camarena V, et al. EMBO Mol Med. 2014 Aug;6(8):1003-15. doi: 10.15252/emmm.201404044. EMBO Mol Med. 2014. PMID: 25001218 Free PMC article.

6

Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic mice.

Kerr B, Alvarez-Saavedra M, Sáez MA, Saona A, Young JI. Kerr B, et al. Hum Mol Genet. 2008 Jun 15;17(12):1707-17. doi: 10.1093/hmg/ddn061. Epub 2008 Mar 4. Hum Mol Genet. 2008. PMID: 18321865

7

Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndrome.

Kerr B, Silva PA, Walz K, Young JI. Kerr B, et al. PLoS One. 2010 Jul 12;5(7):e11534. doi: 10.1371/journal.pone.0011534. PLoS One. 2010. PMID: 20634955 Free PMC article.

8

Transcriptional consequences of MBD5 disruption in mouse brain and CRISPR-derived neurons.

Seabra CM, Aneichyk T, Erdin S, Tai DJC, De Esch CEF, Razaz P, An Y, Manavalan P, Ragavendran A, Stortchevoi A, Abad C, Young JI, Maciel P, Talkowski ME, Gusella JF. Seabra CM, et al. Among authors: young ji. Mol Autism. 2020 Jun 5;11(1):45. doi: 10.1186/s13229-020-00354-1. Mol Autism. 2020. PMID: 32503625 Free PMC article.

9

Transgenic complementation of MeCP2 deficiency: phenotypic rescue of Mecp2-null mice by isoform-specific transgenes.

Kerr B, Soto C J, Saez M, Abrams A, Walz K, Young JI. Kerr B, et al. Among authors: young ji. Eur J Hum Genet. 2012 Jan;20(1):69-76. doi: 10.1038/ejhg.2011.145. Epub 2011 Aug 10. Eur J Hum Genet. 2012. PMID: 21829232 Free PMC article.

10

The expanding role of MBD genes in autism: identification of a MECP2 duplication and novel alterations in MBD5, MBD6, and SETDB1.

Cukier HN, Lee JM, Ma D, Young JI, Mayo V, Butler BL, Ramsook SS, Rantus JA, Abrams AJ, Whitehead PL, Wright HH, Abramson RK, Haines JL, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Cukier HN, et al. Among authors: young ji. Autism Res. 2012 Dec;5(6):385-97. doi: 10.1002/aur.1251. Epub 2012 Oct 10. Autism Res. 2012. PMID: 23055267 Free PMC article.

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