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Adrian Bird

Showing results (61-70 of 84) with videos related to

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Epigenetics & Chromatin|November 28, 2013
Identical sets of methylated and nonmethylated genes in Ciona intestinalis sperm and muscle cellsMiho M Suzuki, Akiko Yoshinari, Madoka Obara, et al.
Epigenetics & Chromatin|August 30, 2014
DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distributionCongdi Song, Yana Feodorova, Jacky Guy, et al.
Human Molecular Genetics|December 10, 2015
The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndromeKyla Brown, Jim Selfridge, Sabine Lagger, et al.
Nature|October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defectsRebekah Tillotson, Jim Selfridge, Martha V Koerner, et al.
Brain : a Journal of Neurology|April 25, 2012
Morphological and functional reversal of phenotypes in a mouse model of Rett syndromeLianne Robinson, Jacky Guy, Leanne McKay, et al.
Science (New York, N.Y.)|July 20, 2002
Enhanced CpG mutability and tumorigenesis in MBD4-deficient miceCatherine B Millar, Jacky Guy, Owen J Sansom, et al.
Human Molecular Genetics|July 9, 2005
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndromeUlrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.
Genes & Development|November 23, 2018
Toxicity of overexpressed MeCP2 is independent of HDAC3 activityMartha V Koerner, Laura FitzPatrick, Jim Selfridge, et al.
Nature Communications|April 17, 2026
MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylationJames A Watson, Beatrice K Alexander-Howden, Theo S Hall, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2013
Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndromeSaurabh K Garg, Daniel T Lioy, Hélène Cheval, et al.
Pageof 9

Showing results (61-70 of 84) with videos related to

Sort By:
Pageof 9
Epigenetics & Chromatin|November 28, 2013
Identical sets of methylated and nonmethylated genes in Ciona intestinalis sperm and muscle cellsMiho M Suzuki, Akiko Yoshinari, Madoka Obara, et al.
Epigenetics & Chromatin|August 30, 2014
DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distributionCongdi Song, Yana Feodorova, Jacky Guy, et al.
Human Molecular Genetics|December 10, 2015
The molecular basis of variable phenotypic severity among common missense mutations causing Rett syndromeKyla Brown, Jim Selfridge, Sabine Lagger, et al.
Nature|October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defectsRebekah Tillotson, Jim Selfridge, Martha V Koerner, et al.
Brain : a Journal of Neurology|April 25, 2012
Morphological and functional reversal of phenotypes in a mouse model of Rett syndromeLianne Robinson, Jacky Guy, Leanne McKay, et al.
Science (New York, N.Y.)|July 20, 2002
Enhanced CpG mutability and tumorigenesis in MBD4-deficient miceCatherine B Millar, Jacky Guy, Owen J Sansom, et al.
Human Molecular Genetics|July 9, 2005
Up-regulation of glucocorticoid-regulated genes in a mouse model of Rett syndromeUlrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.
Genes & Development|November 23, 2018
Toxicity of overexpressed MeCP2 is independent of HDAC3 activityMartha V Koerner, Laura FitzPatrick, Jim Selfridge, et al.
Nature Communications|April 17, 2026
MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylationJames A Watson, Beatrice K Alexander-Howden, Theo S Hall, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|August 23, 2013
Systemic delivery of MeCP2 rescues behavioral and cellular deficits in female mouse models of Rett syndromeSaurabh K Garg, Daniel T Lioy, Hélène Cheval, et al.
Pageof 9