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Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome

PloS one, 2016-10, Vol.11 (10), p.e0165499-e0165499

2016

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Identification of consensus binding sites clarifies FMRP binding determinants

Nucleic acids research, 2016-08, Vol.44 (14), p.6649-6659

2016

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Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences

Human molecular genetics, 2014-10, Vol.23 (20), p.5479-5491

2014

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Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures

Proceedings of the National Academy of Sciences - PNAS, 2015-01, Vol.112 (4), p.949-956

2015

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A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR

Proceedings of the National Academy of Sciences - PNAS, 2015-11, Vol.112 (47), p.E6553-E6561

2015

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Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males

American journal of medical genetics. Part A, 2010-10, Vol.152A (10), p.2512-2520

2010

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A catalog of hemizygous variation in 127 22q11 deletion patients

Human genome variation, 2016-01, Vol.3 (1), p.15065-15065, Article 15065

2016

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Short Chain Fatty Acid Butyrate Induces Promoter Demethylation and Reactivation of RARβ2 in Colon Cancer Cells

Nutrition and cancer, 2008-09, Vol.60 (5), p.692-702

2008

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Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP

Journal of experimental neuroscience, 2015-01, Vol.9s2, p.JEN.S25524

2015

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A 3′ untranslated region variant inFMR1eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR

Proceedings of the National Academy of Sciences - PNAS, 2015-11, Vol.112 (47), p.E6553-E6561

2015

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Independent role for presynaptic FMRP revealed by anFMR1missense mutation associated with intellectual disability and seizures

Proceedings of the National Academy of Sciences - PNAS, 2015-01, Vol.112 (4), p.949-956

2015

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The short chain fatty acid butyrate induces promoter demethylation and reactivation of RARbeta2 in colon cancer cells

Nutrition and cancer, 2008, Vol.60 (5), p.692-702

2008

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Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

Journal of medical genetics, 2013-02, Vol.50 (2), p.80-90

2013

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Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory

Hereditary cancer in clinical practice, 2018-01, Vol.16 (1), p.1-1, Article 1

2018

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PSPACE-completeness of Pulling Blocks to Reach a Goal

Journal of information processing (Tokyo), 2020, Vol.28, p.929-941

2020

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Mining the full information content of mitochondrial DNA

Suhl, Joshua Aaron

2008

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Radiation Therapy Post Prostatectomy Using Axumin Imaging for Target Definition

Medical Research Archives, 2021, Vol.9 (12)

2021

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Reactivation of FMR1 by CRISPR/Cas9-Mediated Deletion of the Expanded CGG-Repeat of the Fragile X Chromosome

Identification of consensus binding sites clarifies FMRP binding determinants

Analysis of FMRP mRNA target datasets reveals highly associated mRNAs mediated by G-quadruplex structures formed via clustered WGGA sequences

Independent role for presynaptic FMRP revealed by an FMR1 missense mutation associated with intellectual disability and seizures

A 3′ untranslated region variant in FMR1 eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR

Identification of novel FMR1 variants by massively parallel sequencing in developmentally delayed males

A catalog of hemizygous variation in 127 22q11 deletion patients

Short Chain Fatty Acid Butyrate Induces Promoter Demethylation and Reactivation of RARβ2 in Colon Cancer Cells

Single-Nucleotide Mutations in FMR1 Reveal Novel Functions and Regulatory Mechanisms of the Fragile X Syndrome Protein FMRP

A 3′ untranslated region variant inFMR1eliminates neuronal activity-dependent translation of FMRP by disrupting binding of the RNA-binding protein HuR

Independent role for presynaptic FMRP revealed by anFMR1missense mutation associated with intellectual disability and seizures

The short chain fatty acid butyrate induces promoter demethylation and reactivation of RARbeta2 in colon cancer cells

Hemizygous mutations in SNAP29 unmask autosomal recessive conditions and contribute to atypical findings in patients with 22q11.2DS

Evaluation of a 27-gene inherited cancer panel across 630 consecutive patients referred for testing in a clinical diagnostic laboratory

PSPACE-completeness of Pulling Blocks to Reach a Goal

Mining the full information content of mitochondrial DNA

Radiation Therapy Post Prostatectomy Using Axumin Imaging for Target Definition

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