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Epigenetics & Chromatin
|
November 28, 2013
Identical sets of methylated and nonmethylated genes in Ciona intestinalis sperm and muscle cells
Miho M Suzuki, Akiko Yoshinari, Madoka Obara, et al.
Epigenetics & Chromatin
|
August 30, 2014
DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution
Congdi 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 syndrome
Kyla Brown, Jim Selfridge, Sabine Lagger, et al.
Nature
|
October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects
Rebekah 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 syndrome
Lianne Robinson, Jacky Guy, Leanne McKay, et al.
Science (New York, N.Y.)
|
July 20, 2002
Enhanced CpG mutability and tumorigenesis in MBD4-deficient mice
Catherine 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 syndrome
Ulrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.
Genes & Development
|
November 23, 2018
Toxicity of overexpressed MeCP2 is independent of HDAC3 activity
Martha V Koerner, Laura FitzPatrick, Jim Selfridge, et al.
Nature Communications
|
April 17, 2026
MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylation
James 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 syndrome
Saurabh K Garg, Daniel T Lioy, Hélène Cheval, et al.
Page
of 9
Search research articles
Search
Showing results (61-70 of 84) with videos related to
Sort By:
Page
of 9
Epigenetics & Chromatin
|
November 28, 2013
Identical sets of methylated and nonmethylated genes in Ciona intestinalis sperm and muscle cells
Miho M Suzuki, Akiko Yoshinari, Madoka Obara, et al.
Epigenetics & Chromatin
|
August 30, 2014
DNA methylation reader MECP2: cell type- and differentiation stage-specific protein distribution
Congdi 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 syndrome
Kyla Brown, Jim Selfridge, Sabine Lagger, et al.
Nature
|
October 12, 2017
Radically truncated MeCP2 rescues Rett syndrome-like neurological defects
Rebekah 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 syndrome
Lianne Robinson, Jacky Guy, Leanne McKay, et al.
Science (New York, N.Y.)
|
July 20, 2002
Enhanced CpG mutability and tumorigenesis in MBD4-deficient mice
Catherine 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 syndrome
Ulrike A Nuber, Skirmantas Kriaucionis, Tim C Roloff, et al.
Genes & Development
|
November 23, 2018
Toxicity of overexpressed MeCP2 is independent of HDAC3 activity
Martha V Koerner, Laura FitzPatrick, Jim Selfridge, et al.
Nature Communications
|
April 17, 2026
MeCP2 requires interactions with nucleosome linker DNA to read chromatin DNA methylation
James 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 syndrome
Saurabh K Garg, Daniel T Lioy, Hélène Cheval, et al.
Page
of 9