BAF drug
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Related entities (24)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| BAF | risk_factor_for | amyotrophic lateral sclerosis | — | 1 |
| BAF | risk_factor_for | autism | — | 1 |
| BAF | associated_with | brain | — | 1 |
| BAF | interacts_with | BRG1 | — | 1 |
| BAF | associated_with | CNV | — | 1 |
| BAF | risk_factor_for | cognitive disorders | — | 1 |
| BAF | regulates | H3K27me3 | — | 1 |
| BAF | associated_with | intellectual disability | — | 1 |
| BAF | risk_factor_for | intellectual disability | — | 1 |
| BAF | regulates | LTP | — | 1 |
| BAF | risk_factor_for | microcephaly | — | 1 |
| BAF | associated_with | neurodegenerative disease | — | 1 |
| BAF | regulates | neurogenesis | — | 1 |
| BAF | interacts_with | Pax6 | — | 1 |
| BAF | interacts_with | PRC2 | — | 1 |
| BAF | associated_with | psychiatric disorders | — | 1 |
| BAF | risk_factor_for | schizophrenia | — | 1 |
| BAF | interacts_with | SMARCA2 | — | 1 |
| BAF | regulates | SOX11 | — | 1 |
| BAF | interacts_with | β-catenin | — | 1 |
| Bcl11b | interacts_with | BAF | — | 1 |
| Pax6 | interacts_with | BAF | — | 1 |
| Rest | interacts_with | BAF | — | 1 |
| STAT3 | interacts_with | BAF | — | 1 |
Mentioned in (22)
Papers in which this entity is mentioned.
- Integrated Genomic Analysis Identifies Driver Genes and Cisplatin-Resistant Progenitor Phenotype in Pediatric Liver Cancer. (2021)
- A practical guide to cancer subclonal reconstruction from DNA sequencing. (2021)
- Simultaneous single cell measurements of intranuclear proteins and gene expression (2021)
- Ploidy- and Purity-Adjusted Allele-Specific DNA Analysis Using CLONETv2. (2019)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Allele-Specific HLA Loss and Immune Escape in Lung Cancer Evolution. (2017)
- Cancer-Specific Retargeting of BAF Complexes by a Prion-like Domain. (2017)
- The impact of structural variation on human gene expression. (2017)
- FACETS: allele-specific copy number and clonal heterogeneity analysis tool for high-throughput DNA sequencing. (2016)
- Post-translational modifications of histones that influence nucleosome dynamics. (2015)
- Hidden Markov Model-Based CNV Detection Algorithms for Illumina Genotyping Microarrays. (2014)
- The role of BAF (mSWI/SNF) complexes in mammalian neural development. (2014)
- Rare genomic structural variants in complex disease: lessons from the replication of associations with obesity. (2013)
- Emerging landscape of oncogenic signatures across human cancers. (2013)
- Control-FREEC: a tool for assessing copy number and allelic content using next-generation sequencing data. (2012)
- Detectable clonal mosaicism from birth to old age and its relationship to cancer. (2012)
- Regulation of chromatin by histone modifications. (2011)
- Epigenetics and psychoneuroimmunology: mechanisms and models. (2011)
- Allele-specific copy number analysis of tumors. (2010)
- Genomic copy number determination in cancer cells from single nucleotide polymorphism microarrays based on quantitative genotyping corrected for aneuploidy. (2009)
- Distinct function of 2 chromatin remodeling complexes that share a common subunit, Williams syndrome transcription factor (WSTF). (2009)
- PennCNV: an integrated hidden Markov model designed for high-resolution copy number variation detection in whole-genome SNP genotyping data. (2007)
Merged raw entities (6)
All extracted name/type variants the normalize job merged into this entity. Use this to spot wrong merges, or aliases that should be split off.
| Raw name | Type | Papers | Mentions |
|---|---|---|---|
| baf | drug | 10 | 18 |
| b allele frequency | drug | 5 | 6 |
| swi/snf | drug | 5 | 10 |
| baf complex | drug | 4 | 20 |
| b-allele frequency | drug | 1 | 1 |
| brg1-associated factor | drug | — | — |