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Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder
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scholarly article
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PubMed
title
Orchestration of neurodevelopmental programs by RBFOX1: implications for autism spectrum disorder
(English)
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stated in
PubMed
main subject
autism spectrum disorder
0 references
autism
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author name string
Brent R. Bill
series ordinal
1
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Crossref
Jennifer K. Lowe
series ordinal
2
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Crossref
Christina T. DyBuncio
series ordinal
3
1 reference
stated in
Crossref
Brent L. Fogel
series ordinal
4
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stated in
Crossref
language of work or name
English
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stated in
PubMed
publication date
2013
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stated in
PubMed
published in
International Review of Neurobiology
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stated in
PubMed
volume
113
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stated in
PubMed
page(s)
251-67
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PubMed
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Rbfox-regulated alternative splicing is critical for zebrafish cardiac and skeletal muscle functions
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Meta-analysis of genome-wide association studies in five cohorts reveals common variants in RBFOX1, a regulator of tissue-specific splicing, associated with refractive error
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Copy number variants in German patients with schizophrenia
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Intragenic deletion of RBFOX1 associated with neurodevelopmental/neuropsychiatric disorders and possibly other clinical presentations
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ATAXIN-2 activates PERIOD translation to sustain circadian rhythms in Drosophila.
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Single nucleotide polymorphism array analysis of microsatellite-stable, diploid/near-diploid colorectal carcinomas without the CpG island methylator phenotype
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RBFOX1 regulates both splicing and transcriptional networks in human neuronal development.
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Microduplications disrupting the MYT1L gene (2p25.3) are associated with schizophrenia
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Homeodomain protein otp and activity-dependent splicing modulate neuronal adaptation to stress
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Germline mosaic transmission of a novel duplication of PXDN and MYT1L to two male half-siblings with autism
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Copy number variants for schizophrenia and related psychotic disorders in Oceanic Palau: risk and transmission in extended pedigrees
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Genomic sequencing of colorectal adenocarcinomas identifies a recurrent VTI1A-TCF7L2 fusion
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28 September 2017
The splicing regulator Rbfox1 (A2BP1) controls neuronal excitation in the mammalian brain
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28 September 2017
Evaluation of A2BP1 as an obesity gene
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28 September 2017
Contributions of the environment and environmentally vulnerable physiology to autism spectrum disorders
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28 September 2017
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28 September 2017
Autoregulation of Fox protein expression to produce dominant negative splicing factors
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28 September 2017
An inducible change in Fox-1/A2BP1 splicing modulates the alternative splicing of downstream neuronal target exons
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28 September 2017
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28 September 2017
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28 September 2017
Genetic advances in autism: heterogeneity and convergence on shared pathways
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28 September 2017
Convergent functional genomics of genome-wide association data for bipolar disorder: comprehensive identification of candidate genes, pathways and mechanisms.
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28 September 2017
Recurrent CNVs disrupt three candidate genes in schizophrenia patients
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28 September 2017
Defining the regulatory network of the tissue-specific splicing factors Fox-1 and Fox-2.
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28 September 2017
Central CRH system in depression and anxiety--evidence from clinical studies with CRH1 receptor antagonists
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28 September 2017
Variations in the progranulin gene affect global gene expression in frontotemporal lobar degeneration
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28 September 2017
Alternative splicing events identified in human embryonic stem cells and neural progenitors
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28 September 2017
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28 September 2017
Discovery and analysis of evolutionarily conserved intronic splicing regulatory elements
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28 September 2017
A vertebrate RNA-binding protein Fox-1 regulates tissue-specific splicing via the pentanucleotide GCAUG.
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28 September 2017
Identification of a candidate primary sex determination locus, fox-1, on the X chromosome of Caenorhabditis elegans
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28 September 2017
COXPRESdb: a database to compare gene coexpression in seven model animals
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31 May 2018
Repression of prespliceosome complex formation at two distinct steps by Fox-1/Fox-2 proteins
1 reference
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PubMed Central
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31 May 2018
Rare exonic deletions of the RBFOX1 gene increase risk of idiopathic generalized epilepsy
1 reference
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PubMed Central
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28 November 2018
MYT1L is a candidate gene for intellectual disability in patients with 2p25.3 (2pter) deletions.
1 reference
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PubMed Central
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28 November 2018
Interaction between Ataxin-2 Binding Protein 1 and Cubitus-interruptus during wing development in Drosophila
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28 November 2018
Cytogenetic and molecular characterization of A2BP1/FOX1 as a candidate gene for autism.
1 reference
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28 November 2018
Identification of a novel target of D/V signaling in Drosophila wing disc: Wg-independent function of the organizer.
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28 November 2018
The de novo chromosome 16 translocations of two patients with abnormal phenotypes (mental retardation and epilepsy) disrupt the A2BP1 gene.
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28 November 2018
Rare inherited A2BP1 deletion in a proband with autism and developmental hemiparesis
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https://pubmed.ncbi.nlm.nih.gov/24290388
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based on heuristic
inferred from PubMed ID database lookup
Molecular Evolution of Recombination Hotspots and Highly Recombining Pseudoautosomal Regions in Hominoids
1 reference
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PubMed
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https://pubmed.ncbi.nlm.nih.gov/24290388
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12 December 2020
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inferred from PubMed ID database lookup
Clinically relevant single gene or intragenic deletions encompassing critical neurodevelopmental genes in patients with developmental delay, mental retardation, and/or autism spectrum disorders
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24290388
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identification of rare copy number variants in high burden schizophrenia families
1 reference
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PubMed
reference URL
https://pubmed.ncbi.nlm.nih.gov/24290388
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1016/B978-0-12-418700-9.00008-3
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1843170
OpenCitations bibliographic resource ID
1843170
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1843170
PMCID
4318517
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1843170
PubMed ID
24290388
1 reference
stated in
Consolidated OpenCitations Corpus – April 2017
OpenCitations bibliographic resource ID
1843170
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