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Joshua A Suhl

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

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Journal of Experimental Neuroscience|January 29, 2016
Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRPJoshua A Suhl, Stephen T Warren
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|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.
Nutrition and Cancer|September 16, 2008
The short chain fatty acid butyrate induces promoter demethylation and reactivation of RARbeta2 in colon cancer cellsColleen C Spurling, Joshua A Suhl, Nathalie Boucher, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed malesStephen C Collins, Steven M Bray, Joshua A Suhl, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 2015
A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuRJoshua A Suhl, Ravi S Muddashetty, Bart R Anderson, et al.
HGG Advances|January 22, 2025
Missense variants at the p.Arg225 residue in ARHGEF40 identified in individuals with multiple congenital anomalies and developmental delayMelanie P Napier, Erin Ryan, Adi Reich, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2015
Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizuresLeila K Myrick, Pan-Yue Deng, Hideharu Hashimoto, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Pageof 1

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

Sort By:
Pageof 1
Journal of Experimental Neuroscience|January 29, 2016
Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRPJoshua A Suhl, Stephen T Warren
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|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.
Nutrition and Cancer|September 16, 2008
The short chain fatty acid butyrate induces promoter demethylation and reactivation of RARbeta2 in colon cancer cellsColleen C Spurling, Joshua A Suhl, Nathalie Boucher, et al.
American Journal of Medical Genetics. Part A|August 28, 2010
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed malesStephen C Collins, Steven M Bray, Joshua A Suhl, et al.
Proceedings of the National Academy of Sciences of the United States of America|November 11, 2015
A 3' untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuRJoshua A Suhl, Ravi S Muddashetty, Bart R Anderson, et al.
HGG Advances|January 22, 2025
Missense variants at the p.Arg225 residue in ARHGEF40 identified in individuals with multiple congenital anomalies and developmental delayMelanie P Napier, Erin Ryan, Adi Reich, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 7, 2015
Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizuresLeila K Myrick, Pan-Yue Deng, Hideharu Hashimoto, et al.
Human Genome Variation|June 9, 2016
A catalog of hemizygous variation in 127 22q11 deletion patientsMatthew S Hestand, Beata A Nowakowska, Elfi Vergaelen, et al.
Pageof 1