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Dag H Yasui

Showing results (1-10 of 44) with videos related to

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Frontiers in Genetics|May 10, 2021
The Molecular Functions of MeCP2 in Rett Syndrome PathologyOsman Sharifi, Dag H Yasui
Frontiers in Genetics|September 20, 2021
Editorial: Epigenetic Mechanisms and Their Involvement in Rare DiseasesMojgan Rastegar, Dag H Yasui
Epigenomics|May 18, 2010
Evolving role of MeCP2 in Rett syndrome and autismJanine M LaSalle, Dag H Yasui
Human Molecular Genetics|May 10, 2006
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndromeSailaja Peddada, Dag H Yasui, Janine M LaSalle
Trends in Neurosciences|June 5, 2013
Epigenetic layers and players underlying neurodevelopmentJanine M LaSalle, Weston T Powell, Dag H Yasui
Human Molecular Genetics|February 4, 2005
Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samplesKaren N Thatcher, Sailaja Peddada, Dag H Yasui, et al.
Epigenomics|October 3, 2025
MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndromeJessica L Huang, Osman Sharifi, Dag H Yasui, et al.
Human Molecular Genetics|March 7, 2007
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disordersAmber Hogart, Raman P Nagarajan, Katherine A Patzel, et al.
Human Molecular Genetics|November 13, 2008
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autismSusan E Swanberg, Raman P Nagarajan, Sailaja Peddada, et al.
Human Molecular Genetics|August 21, 2018
Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuNRochelle L Coulson, Weston T Powell, Dag H Yasui, et al.
Pageof 5

Showing results (1-10 of 44) with videos related to

Sort By:
Pageof 5
Frontiers in Genetics|May 10, 2021
The Molecular Functions of MeCP2 in Rett Syndrome PathologyOsman Sharifi, Dag H Yasui
Frontiers in Genetics|September 20, 2021
Editorial: Epigenetic Mechanisms and Their Involvement in Rare DiseasesMojgan Rastegar, Dag H Yasui
Epigenomics|May 18, 2010
Evolving role of MeCP2 in Rett syndrome and autismJanine M LaSalle, Dag H Yasui
Human Molecular Genetics|May 10, 2006
Inhibitors of differentiation (ID1, ID2, ID3 and ID4) genes are neuronal targets of MeCP2 that are elevated in Rett syndromeSailaja Peddada, Dag H Yasui, Janine M LaSalle
Trends in Neurosciences|June 5, 2013
Epigenetic layers and players underlying neurodevelopmentJanine M LaSalle, Weston T Powell, Dag H Yasui
Human Molecular Genetics|February 4, 2005
Homologous pairing of 15q11-13 imprinted domains in brain is developmentally regulated but deficient in Rett and autism samplesKaren N Thatcher, Sailaja Peddada, Dag H Yasui, et al.
Epigenomics|October 3, 2025
MeCP2 at the crossroads of hypoxia, oxidative stress, and gene regulation in Rett syndromeJessica L Huang, Osman Sharifi, Dag H Yasui, et al.
Human Molecular Genetics|March 7, 2007
15q11-13 GABAA receptor genes are normally biallelically expressed in brain yet are subject to epigenetic dysregulation in autism-spectrum disordersAmber Hogart, Raman P Nagarajan, Katherine A Patzel, et al.
Human Molecular Genetics|November 13, 2008
Reciprocal co-regulation of EGR2 and MECP2 is disrupted in Rett syndrome and autismSusan E Swanberg, Raman P Nagarajan, Sailaja Peddada, et al.
Human Molecular Genetics|August 21, 2018
Prader-Willi locus Snord116 RNA processing requires an active endogenous allele and neuron-specific splicing by Rbfox3/NeuNRochelle L Coulson, Weston T Powell, Dag H Yasui, et al.
Pageof 5