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Daman Kumari

Showing results (1-10 of 36) with videos related to

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Human Molecular Genetics|September 17, 2010
The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndromeDaman Kumari, Karen Usdin
Human Molecular Genetics|July 6, 2016
Sustained expression of FMR1 mRNA from reactivated fragile X syndrome alleles after treatment with small molecules that prevent trimethylation of H3K27Daman Kumari, Karen Usdin
Brain Sciences|August 21, 2019
Towards Mechanism-Based Treatments for Fragile X SyndromeDaman Kumari, Inbal Gazy
Frontiers in Genetics|June 20, 2015
Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disordersKaren Usdin, Daman Kumari
The Journal of Biological Chemistry|October 30, 2008
Chromatin remodeling in the noncoding repeat expansion diseasesDaman Kumari, Karen Usdin
Clinical Epigenetics|March 15, 2012
Is Friedreich ataxia an epigenetic disorder?Daman Kumari, Karen Usdin
Human Molecular Genetics|July 25, 2014
Polycomb group complexes are recruited to reactivated FMR1 alleles in Fragile X syndrome in response to FMR1 transcriptionDaman Kumari, Karen Usdin
Expert Review of Molecular Diagnostics|February 19, 2020
Molecular analysis of <i>FMR1</i> alleles for fragile X syndrome diagnosis and patient stratificationDaman Kumari, Karen Usdin
Plos Genetics|March 29, 2008
SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndromeRea Biacsi, Daman Kumari, Karen Usdin
Brain Sciences|February 15, 2019
Pharmacological Reactivation of the Silenced <i>FMR1</i> Gene as a Targeted Therapeutic Approach for Fragile X SyndromeDaman Kumari, Inbal Gazy, Karen Usdin
Pageof 4

Showing results (1-10 of 36) with videos related to

Sort By:
Pageof 4
Human Molecular Genetics|September 17, 2010
The distribution of repressive histone modifications on silenced FMR1 alleles provides clues to the mechanism of gene silencing in fragile X syndromeDaman Kumari, Karen Usdin
Human Molecular Genetics|July 6, 2016
Sustained expression of FMR1 mRNA from reactivated fragile X syndrome alleles after treatment with small molecules that prevent trimethylation of H3K27Daman Kumari, Karen Usdin
Brain Sciences|August 21, 2019
Towards Mechanism-Based Treatments for Fragile X SyndromeDaman Kumari, Inbal Gazy
Frontiers in Genetics|June 20, 2015
Repeat-mediated epigenetic dysregulation of the FMR1 gene in the fragile X-related disordersKaren Usdin, Daman Kumari
The Journal of Biological Chemistry|October 30, 2008
Chromatin remodeling in the noncoding repeat expansion diseasesDaman Kumari, Karen Usdin
Clinical Epigenetics|March 15, 2012
Is Friedreich ataxia an epigenetic disorder?Daman Kumari, Karen Usdin
Human Molecular Genetics|July 25, 2014
Polycomb group complexes are recruited to reactivated FMR1 alleles in Fragile X syndrome in response to FMR1 transcriptionDaman Kumari, Karen Usdin
Expert Review of Molecular Diagnostics|February 19, 2020
Molecular analysis of <i>FMR1</i> alleles for fragile X syndrome diagnosis and patient stratificationDaman Kumari, Karen Usdin
Plos Genetics|March 29, 2008
SIRT1 inhibition alleviates gene silencing in Fragile X mental retardation syndromeRea Biacsi, Daman Kumari, Karen Usdin
Brain Sciences|February 15, 2019
Pharmacological Reactivation of the Silenced <i>FMR1</i> Gene as a Targeted Therapeutic Approach for Fragile X SyndromeDaman Kumari, Inbal Gazy, Karen Usdin
Pageof 4