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Stephen T Warren

Showing results (31-40 of 99) with videos related to

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Human Molecular Genetics|December 10, 2019
Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypesIgor Albizua, Pankaj Chopra, Stephanie L Sherman, et al.
Plos One|February 12, 2014
Robust regression analysis of copy number variation data based on a univariate scoreGlen A Satten, Andrew S Allen, Morna Ikeda, et al.
Plos One|October 22, 2016
Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X ChromosomeNina Xie, He Gong, Joshua A Suhl, et al.
Nucleic Acids Research|July 6, 2016
Identification of consensus binding sites clarifies FMRP binding determinantsBart R Anderson, Pankaj Chopra, Joshua A Suhl, et al.
Human Molecular Genetics|October 23, 2003
Phosphorylation influences the translation state of FMRP-associated polyribosomesStephanie Ceman, William T O'Donnell, Matt Reed, et al.
Human Molecular Genetics|May 31, 2014
Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequencesJoshua A Suhl, Pankaj Chopra, Bart R Anderson, et al.
Neurobiology of Disease|September 25, 2002
Gene expression profiles in a transgenic animal model of fragile X syndromeVelia D'Agata, Stephen T Warren, Weiqin Zhao, et al.
BMC Medical Genetics|January 30, 2013
Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locusReid S Alisch, Tao Wang, Pankaj Chopra, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 21, 2007
Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptorsMika Nakamoto, Vijayalaxmi Nalavadi, Michael P Epstein, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literatureBradford Coffee, Morna Ikeda, Dejan B Budimirovic, et al.
Pageof 10

Showing results (31-40 of 99) with videos related to

Sort By:
Pageof 10
Human Molecular Genetics|December 10, 2019
Analysis of the genomic expression profile in trisomy 18: insight into possible genes involved in the associated phenotypesIgor Albizua, Pankaj Chopra, Stephanie L Sherman, et al.
Plos One|February 12, 2014
Robust regression analysis of copy number variation data based on a univariate scoreGlen A Satten, Andrew S Allen, Morna Ikeda, et al.
Plos One|October 22, 2016
Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X ChromosomeNina Xie, He Gong, Joshua A Suhl, et al.
Nucleic Acids Research|July 6, 2016
Identification of consensus binding sites clarifies FMRP binding determinantsBart R Anderson, Pankaj Chopra, Joshua A Suhl, et al.
Human Molecular Genetics|October 23, 2003
Phosphorylation influences the translation state of FMRP-associated polyribosomesStephanie Ceman, William T O'Donnell, Matt Reed, et al.
Human Molecular Genetics|May 31, 2014
Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequencesJoshua A Suhl, Pankaj Chopra, Bart R Anderson, et al.
Neurobiology of Disease|September 25, 2002
Gene expression profiles in a transgenic animal model of fragile X syndromeVelia D'Agata, Stephen T Warren, Weiqin Zhao, et al.
BMC Medical Genetics|January 30, 2013
Genome-wide analysis validates aberrant methylation in fragile X syndrome is specific to the FMR1 locusReid S Alisch, Tao Wang, Pankaj Chopra, et al.
Proceedings of the National Academy of Sciences of the United States of America|September 21, 2007
Fragile X mental retardation protein deficiency leads to excessive mGluR5-dependent internalization of AMPA receptorsMika Nakamoto, Vijayalaxmi Nalavadi, Michael P Epstein, et al.
American Journal of Medical Genetics. Part A|April 17, 2008
Mosaic FMR1 deletion causes fragile X syndrome and can lead to molecular misdiagnosis: a case report and review of the literatureBradford Coffee, Morna Ikeda, Dejan B Budimirovic, et al.
Pageof 10