(Q44546317)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

title

The Top3β way to untangle RNA (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

language of work or name

English

0 references

publication date

1 September 2013

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

volume

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

issue

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

page(s)

1163-1164

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

https://scigraph.springernature.com/pub.10.1038/nn.3506

8 March 2020

exact match

0 references

cites work

Natural RNA circles function as efficient microRNA sponges

1 reference

Circular RNAs are a large class of animal RNAs with regulatory potency

21 January 2018

1 reference

21 January 2018

1 reference

De novo gene mutations highlight patterns of genetic and neural complexity in schizophrenia.

21 January 2018

1 reference

De Novo Gene Disruptions in Children on the Autistic Spectrum

21 January 2018

1 reference

Geographic variation and sociodemographic characteristics of psychotic disorders in Finland.

21 January 2018

1 reference

Rare chromosomal deletions and duplications increase risk of schizophrenia

21 January 2018

1 reference

A copy number variation morbidity map of developmental delay

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

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

21 January 2018

1 reference

Characterization of dFMR1, a Drosophila melanogaster homolog of the fragile X mental retardation protein

21 January 2018

1 reference

Schizophrenia in the genetic isolate of Finland

21 January 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23982446

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Deletion of TOP3β, a component of FMRP-containing mRNPs, contributes to neurodevelopmental disorders

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23982446

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Top3β is an RNA topoisomerase that works with fragile X syndrome protein to promote synapse formation

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/23982446

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1038/NN.3506

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:23982446%20AND%20SRC:MED&resulttype=core&format=json

8 March 2020

1 reference