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Juan I Young

Showing results (1-10 of 96) with videos related to

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Rare Diseases (Austin, Tex.)|March 5, 2016
The methyl binding domain containing protein MBD5 is a transcriptional regulator responsible for 2q23.1 deletion syndromeKatherina Walz, Juan I Young
American Journal of Human Genetics|February 20, 2004
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndromeJuan I Young, Huda Y Zoghbi
Annual Review of Nutrition|May 15, 2015
Regulation of the Epigenome by Vitamin CJuan I Young, Stephan Züchner, Gaofeng Wang
The Journal of Biological Chemistry|April 1, 2003
Telomerase expression in normal human fibroblasts stabilizes DNA 5-methylcytosine transferase IJuan I Young, John M Sedivy, James R Smith
Plos One|July 17, 2010
Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndromeBredford Kerr, Pamela A Silva, Katherina Walz, et al.
The Journal of Biological Chemistry|April 4, 2013
Ascorbate induces ten-eleven translocation (Tet) methylcytosine dioxygenase-mediated generation of 5-hydroxymethylcytosineEmily A Minor, Brenda L Court, Juan I Young, et al.
Frontiers in Cell and Developmental Biology|May 31, 2021
DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and PalateJuan I Young, Susan Slifer, Jacqueline T Hecht, et al.
Antioxidants & Redox Signaling|July 8, 2017
The NAD<sup>+</sup>-Dependent Family of Sirtuins in Cerebral Ischemia and PreconditioningNathalie Khoury, Kevin B Koronowski, Juan I Young, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|July 23, 2013
Ischemic preconditioning alters the epigenetic profile of the brain from ischemic intolerance to ischemic toleranceJohn W Thompson, Kunjan R Dave, Juan I Young, et al.
Human Molecular Genetics|March 7, 2008
Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic miceBredford Kerr, Matías Alvarez-Saavedra, Mauricio A Sáez, et al.
Pageof 10

Showing results (1-10 of 96) with videos related to

Sort By:
Pageof 10
Rare Diseases (Austin, Tex.)|March 5, 2016
The methyl binding domain containing protein MBD5 is a transcriptional regulator responsible for 2q23.1 deletion syndromeKatherina Walz, Juan I Young
American Journal of Human Genetics|February 20, 2004
X-chromosome inactivation patterns are unbalanced and affect the phenotypic outcome in a mouse model of rett syndromeJuan I Young, Huda Y Zoghbi
Annual Review of Nutrition|May 15, 2015
Regulation of the Epigenome by Vitamin CJuan I Young, Stephan Züchner, Gaofeng Wang
The Journal of Biological Chemistry|April 1, 2003
Telomerase expression in normal human fibroblasts stabilizes DNA 5-methylcytosine transferase IJuan I Young, John M Sedivy, James R Smith
Plos One|July 17, 2010
Unconventional transcriptional response to environmental enrichment in a mouse model of Rett syndromeBredford Kerr, Pamela A Silva, Katherina Walz, et al.
The Journal of Biological Chemistry|April 4, 2013
Ascorbate induces ten-eleven translocation (Tet) methylcytosine dioxygenase-mediated generation of 5-hydroxymethylcytosineEmily A Minor, Brenda L Court, Juan I Young, et al.
Frontiers in Cell and Developmental Biology|May 31, 2021
DNA Methylation Variation Is Identified in Monozygotic Twins Discordant for Non-syndromic Cleft Lip and PalateJuan I Young, Susan Slifer, Jacqueline T Hecht, et al.
Antioxidants & Redox Signaling|July 8, 2017
The NAD<sup>+</sup>-Dependent Family of Sirtuins in Cerebral Ischemia and PreconditioningNathalie Khoury, Kevin B Koronowski, Juan I Young, et al.
Neurotherapeutics : the Journal of the American Society for Experimental Neurotherapeutics|July 23, 2013
Ischemic preconditioning alters the epigenetic profile of the brain from ischemic intolerance to ischemic toleranceJohn W Thompson, Kunjan R Dave, Juan I Young, et al.
Human Molecular Genetics|March 7, 2008
Defective body-weight regulation, motor control and abnormal social interactions in Mecp2 hypomorphic miceBredford Kerr, Matías Alvarez-Saavedra, Mauricio A Sáez, et al.
Pageof 10