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ARID1B gene

Known as: KIAA1235, AT Rich Interactive Domain 1B (SWI1-Like) Gene, ELD/OSA1 
This gene plays a role in both chromatin remodeling and transcriptional regulation.
National Institutes of Health

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ARID1B wt Allele
ARID3B geneAT-Rich Interactive Domain-Containing Protein 1BTranscriptional Regulationchromatin remodeling

Papers overview

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Review
2020
Review
2020
Striking phenotypic overlap between Nicolaides-Baraitser and Coffin-Siris syndromes in monozygotic twins with ARID1B intragenic deletion.
2019
2019
Corpus callosum metrics predict severity of visuospatial and neuromotor dysfuntions in ARID1B mutations with Coffin-Siris syndrome.
ARID1B mutations in Coffin-Siris syndrome are a cause of intellectual disability (0.5-1%), with various degrees of autism and… 
2018
2018
FGFR1 tyrosine kinase domain duplication in pilocytic astrocytoma with anaplasia
We report the case of a 27-yr-old male with visual field loss who had a 4.9-cm complex cystic mass in the right occipital lobe… 
2017
2017
A potentially functional variant of ARID1B interacts with physical activity in association with risk of hepatocellular carcinoma
The tumor suppressor role of AT-rich interactive domain containing protein 1B (ARID1B) has drawn much attention in area of cancer… 
Review
2017
Review
2017
Primary pulmonary malignant fibrous histiocytoma: case report and literature review.
Malignant fibrous histiocytoma (MFH) is an aggressive soft tissue sarcoma known to occur in various organs. Primary MFH arising… 
2016
2016
Coffin-Siris syndrome with café-au-lait spots, obesity and hyperinsulinism caused by a mutation in the ARID1B gene.
Coffin-Siris syndrome (CSS) (MIM 135900) is characterized by developmental delay, severe speech impairment, distinctive facial… 
2016
2016
Gonadal mosaicism in ARID1B gene causes intellectual disability and dysmorphic features in three siblings
The gene encoding the AT‐rich interaction domain‐containing protein 1B (ARID1B) has recently been shown to be one of the most… 
2016
2016
A novel familial autosomal dominant mutation in ARID1B causing neurodevelopmental delays, short stature, and dysmorphic features
Recent studies have identified mutations in the ARID1B gene responsible for neurodevelopmental delays, intellectual disability… 
2013
2013
MutComFocal: an integrative approach to identifying recurrent and focal genomic alterations in tumor samples
BackgroundMost tumors are the result of accumulated genomic alterations in somatic cells. The emerging spectrum of alterations in… 
2010
2010
Expression of New Red Cell–Related Genes in Erythroid Differentiation
Using a suppression subtractive hybridization method, we have previously identified genes differentially expressed in erythroid… 
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