Bird A - Search Results

1

Reversibility of functional deficits in experimental models of Rett syndrome.

Cobb S, Guy J, Bird A. Cobb S, et al. Among authors: bird a. Biochem Soc Trans. 2010 Apr;38(2):498-506. doi: 10.1042/BST0380498. Biochem Soc Trans. 2010. PMID: 20298210 Review.

2

Morphological and functional reversal of phenotypes in a mouse model of Rett syndrome.

Robinson L, Guy J, McKay L, Brockett E, Spike RC, Selfridge J, De Sousa D, Merusi C, Riedel G, Bird A, Cobb SR. Robinson L, et al. Among authors: bird a. Brain. 2012 Sep;135(Pt 9):2699-710. doi: 10.1093/brain/aws096. Epub 2012 Apr 23. Brain. 2012. PMID: 22525157 Free PMC article.

3

Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes.

Ross PD, Guy J, Selfridge J, Kamal B, Bahey N, Tanner KE, Gillingwater TH, Jones RA, Loughrey CM, McCarroll CS, Bailey ME, Bird A, Cobb S. Ross PD, et al. Among authors: bird a. Hum Mol Genet. 2016 Oct 15;25(20):4389-4404. doi: 10.1093/hmg/ddw269. Hum Mol Genet. 2016. PMID: 28173151 Free PMC article.

4

Radically truncated MeCP2 rescues Rett syndrome-like neurological defects.

Tillotson R, Selfridge J, Koerner MV, Gadalla KKE, Guy J, De Sousa D, Hector RD, Cobb SR, Bird A. Tillotson R, et al. Among authors: bird a. Nature. 2017 Oct 19;550(7676):398-401. doi: 10.1038/nature24058. Epub 2017 Oct 11. Nature. 2017. PMID: 29019980 Free PMC article.

5

The role of MeCP2 in the brain.

Guy J, Cheval H, Selfridge J, Bird A. Guy J, et al. Among authors: bird a. Annu Rev Cell Dev Biol. 2011;27:631-52. doi: 10.1146/annurev-cellbio-092910-154121. Epub 2011 Jun 29. Annu Rev Cell Dev Biol. 2011. PMID: 21721946 Review.

6

Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows.

Cheval H, Guy J, Merusi C, De Sousa D, Selfridge J, Bird A. Cheval H, et al. Among authors: bird a. Hum Mol Genet. 2012 Sep 1;21(17):3806-14. doi: 10.1093/hmg/dds208. Epub 2012 May 31. Hum Mol Genet. 2012. PMID: 22653753 Free PMC article.

7

Rett syndrome mutations abolish the interaction of MeCP2 with the NCoR/SMRT co-repressor.

Lyst MJ, Ekiert R, Ebert DH, Merusi C, Nowak J, Selfridge J, Guy J, Kastan NR, Robinson ND, de Lima Alves F, Rappsilber J, Greenberg ME, Bird A. Lyst MJ, et al. Among authors: bird a. Nat Neurosci. 2013 Jul;16(7):898-902. doi: 10.1038/nn.3434. Epub 2013 Jun 16. Nat Neurosci. 2013. PMID: 23770565 Free PMC article.

8

The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome.

Brown K, Selfridge J, Lagger S, Connelly J, De Sousa D, Kerr A, Webb S, Guy J, Merusi C, Koerner MV, Bird A. Brown K, et al. Among authors: bird a. Hum Mol Genet. 2016 Feb 1;25(3):558-70. doi: 10.1093/hmg/ddv496. Epub 2015 Dec 8. Hum Mol Genet. 2016. PMID: 26647311 Free PMC article.

9

A mutation-led search for novel functional domains in MeCP2.

Guy J, Alexander-Howden B, FitzPatrick L, DeSousa D, Koerner MV, Selfridge J, Bird A. Guy J, et al. Among authors: bird a. Hum Mol Genet. 2018 Jul 15;27(14):2531-2545. doi: 10.1093/hmg/ddy159. Hum Mol Genet. 2018. PMID: 29718204 Free PMC article.

10

Affinity for DNA Contributes to NLS Independent Nuclear Localization of MeCP2.

Lyst MJ, Ekiert R, Guy J, Selfridge J, Koerner MV, Merusi C, De Sousa D, Bird A. Lyst MJ, et al. Among authors: bird a. Cell Rep. 2018 Aug 28;24(9):2213-2220. doi: 10.1016/j.celrep.2018.07.099. Cell Rep. 2018. PMID: 30157418 Free PMC article.

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