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Human Mutation
|
July 30, 2008
Microarray-based mutation detection in the dystrophin gene
Madhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 4, 2018
Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of <i>Fmr1</i> Knock-Out Mice
Pan-Yue Deng, Dan Carlin, Young Mi Oh, et al.
Journal of Neuroscience Research
|
November 19, 2016
Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders
Timothy P Rutkowski, Jason P Schroeder, Georgette M Gafford, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 13, 2010
Excess phosphoinositide 3-kinase subunit synthesis and activity as a novel therapeutic target in fragile X syndrome
Christina Gross, Mika Nakamoto, Xiaodi Yao, et al.
American Journal of Medical Genetics. Part A
|
August 28, 2010
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males
Stephen C Collins, Steven M Bray, Joshua A Suhl, et al.
Genome Research
|
February 4, 2012
Age-associated DNA methylation in pediatric populations
Reid S Alisch, Benjamin G Barwick, Pankaj Chopra, et al.
Molecular Cell
|
June 11, 2011
Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling
Ravi S Muddashetty, Vijayalaxmi C Nalavadi, Christina Gross, 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 HuR
Joshua A Suhl, Ravi S Muddashetty, Bart R Anderson, et al.
Nature Neuroscience
|
November 13, 2007
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration
Meyer J Friedman, Anjali G Shah, Zhi-Hui Fang, et al.
Neuron
|
August 19, 2007
Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome
Peng Jin, Ranhui Duan, Abrar Qurashi, et al.
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of 10
Search research articles
Search
Showing results (51-60 of 99) with videos related to
Sort By:
Page
of 10
Human Mutation
|
July 30, 2008
Microarray-based mutation detection in the dystrophin gene
Madhuri R Hegde, Ephrem L H Chin, Jennifer G Mulle, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
November 4, 2018
Voltage-Independent SK-Channel Dysfunction Causes Neuronal Hyperexcitability in the Hippocampus of <i>Fmr1</i> Knock-Out Mice
Pan-Yue Deng, Dan Carlin, Young Mi Oh, et al.
Journal of Neuroscience Research
|
November 19, 2016
Unraveling the genetic architecture of copy number variants associated with schizophrenia and other neuropsychiatric disorders
Timothy P Rutkowski, Jason P Schroeder, Georgette M Gafford, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience
|
August 13, 2010
Excess phosphoinositide 3-kinase subunit synthesis and activity as a novel therapeutic target in fragile X syndrome
Christina Gross, Mika Nakamoto, Xiaodi Yao, et al.
American Journal of Medical Genetics. Part A
|
August 28, 2010
Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males
Stephen C Collins, Steven M Bray, Joshua A Suhl, et al.
Genome Research
|
February 4, 2012
Age-associated DNA methylation in pediatric populations
Reid S Alisch, Benjamin G Barwick, Pankaj Chopra, et al.
Molecular Cell
|
June 11, 2011
Reversible inhibition of PSD-95 mRNA translation by miR-125a, FMRP phosphorylation, and mGluR signaling
Ravi S Muddashetty, Vijayalaxmi C Nalavadi, Christina Gross, 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 HuR
Joshua A Suhl, Ravi S Muddashetty, Bart R Anderson, et al.
Nature Neuroscience
|
November 13, 2007
Polyglutamine domain modulates the TBP-TFIIB interaction: implications for its normal function and neurodegeneration
Meyer J Friedman, Anjali G Shah, Zhi-Hui Fang, et al.
Neuron
|
August 19, 2007
Pur alpha binds to rCGG repeats and modulates repeat-mediated neurodegeneration in a Drosophila model of fragile X tremor/ataxia syndrome
Peng Jin, Ranhui Duan, Abrar Qurashi, et al.
Page
of 10