1-7 of 7
Authors: Adrian Bird
Journal Article
A mutation-led search for novel functional domains in MeCP2 Open Access
Human Molecular Genetics, Volume 27, Issue 14, 15 July 2018, Pages 2531–2545, https://doi.org/10.1093/hmg/ddy159
Published: 27 April 2018
Journal Article
Exclusive expression of MeCP2 in the nervous system distinguishes between brain and peripheral Rett syndrome-like phenotypes Open Access
Human Molecular Genetics, Volume 25, Issue 20, 15 October 2016, Pages 4389–4404, https://doi.org/10.1093/hmg/ddw269
Published: 09 August 2016
Journal Article
The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndrome Open Access
Human Molecular Genetics, Volume 25, Issue 3, 1 February 2016, Pages 558–570, https://doi.org/10.1093/hmg/ddv496
Published: 08 December 2015
Journal Article
Postnatal inactivation reveals enhanced requirement for MeCP2 at distinct age windows Get access
Human Molecular Genetics, Volume 21, Issue 17, 1 September 2012, Pages 3806–3814, https://doi.org/10.1093/hmg/dds208
Published: 31 May 2012
Journal Article
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndrome Get access
Human Molecular Genetics, Volume 14, Issue 15, 1 August 2005, Pages 2247–2256, https://doi.org/10.1093/hmg/ddi229
Published: 07 July 2005
Journal Article
DNA methylation and Rett syndrome Get access
Human Molecular Genetics, Volume 12, Issue suppl_2, 15 October 2003, Pages R221–R227, https://doi.org/10.1093/hmg/ddg286
Published: 15 October 2003
Journal Article
Mosaic methylation of the repeat unit of the human ribosomal RNA genes Get access
Human Molecular Genetics, Volume 6, Issue 3, March 1997, Pages 451–456, https://doi.org/10.1093/hmg/6.3.451
Published: 01 March 1997
