(Q34211875)

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

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1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

1 reference

based on heuristic

inferred from title

author name string

Joshua A Suhl

1

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Pankaj Chopra

2

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Bart R Anderson

3

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Gary J Bassell

4

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Stephen T Warren

5

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

publication date

29 May 2014

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

Human Molecular Genetics

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

23

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

20

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

5479-5491

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

A polygenic burden of rare disruptive mutations in schizophrenia

1 reference

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5 July 2018

De novo mutations in schizophrenia implicate synaptic networks

1 reference

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5 July 2018

A compendium of RNA-binding motifs for decoding gene regulation.

1 reference

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McGenus: a Monte Carlo algorithm to predict RNA secondary structures with pseudoknots

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

FMRP targets distinct mRNA sequence elements to regulate protein expression

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

De Novo Gene Disruptions in Children on the Autistic Spectrum

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Patterns and rates of exonic de novo mutations in autism spectrum disorders

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

De novo mutations revealed by whole-exome sequencing are strongly associated with autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Robust rank aggregation for gene list integration and meta-analysis

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Molecular Mechanisms of Fragile X Syndrome: A Twenty-Year Perspective

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

FMRP stalls ribosomal translocation on mRNAs linked to synaptic function and autism

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Structure-function studies of FMRP RGG peptide recognition of an RNA duplex-quadruplex junction

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Transcriptome-wide identification of RNA-binding protein and microRNA target sites by PAR-CLIP

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Incidence of fragile X syndrome by newborn screening for methylated FMR1 DNA.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Discrimination of common and unique RNA-binding activities among Fragile X mental retardation protein paralogs

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Predicting and understanding the stability of G-quadruplexes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Fragile X syndrome: loss of local mRNA regulation alters synaptic development and function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Fragile X mental retardation protein interactions with the microtubule associated protein 1B RNA

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Interactions of the G quartet forming semaphorin 3F RNA with the RGG box domain of the fragile X protein family

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Quadruplex DNA: sequence, topology and structure

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

QGRS Mapper: a web-based server for predicting G-quadruplexes in nucleotide sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Kissing complex RNAs mediate interaction between the Fragile-X mental retardation protein KH2 domain and brain polyribosomes

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

The fragile X mental retardation protein, FMRP, recognizes G-quartets

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

The fragile X mental retardation protein binds and regulates a novel class of mRNAs containing U rich target sequences

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Fragile X mental retardation protein targets G quartet mRNAs important for neuronal function

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Microarray identification of FMRP-associated brain mRNAs and altered mRNA translational profiles in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

The fragile X mental retardation protein binds specifically to its mRNA via a purine quartet motif

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

FMR1 Protein: Conserved RNP Family Domains and Selective RNA Binding

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Absence of expression of the FMR-1 gene in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

Identification of a gene (FMR-1) containing a CGG repeat coincident with a breakpoint cluster region exhibiting length variation in fragile X syndrome

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4168832

5 July 2018

RNA cargoes associating with FMRP reveal deficits in cellular functioning in Fmr1 null mice

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU272

21 January 2018

The fragile X mental retardation protein interacts with U-rich RNAs in a yeast three-hybrid system

1 reference

https://api.crossref.org/works/10.1093%2FHMG%2FDDU272

21 January 2018

A comparison of DNA and RNA quadruplex structures and stabilities

1 reference

https://pubmed.ncbi.nlm.nih.gov/24876161

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Quadruplex-based molecular beacons as tunable DNA probes

1 reference

https://pubmed.ncbi.nlm.nih.gov/24876161

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1093/HMG/DDU272

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PMC publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

31 July 2017

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