UBE3A gene
Evidence from:
primary |
all sources
Related entities (4)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| CNV | associated_with | UBE3A | — | 1 |
| UBE3A | risk_factor_for | Angelman syndrome | — | 1 |
| UBE3A | targets | ARC | — | 1 |
| UBE3A | risk_factor_for | autism spectrum disorder | — | 1 |
Mentioned in (16)
Papers in which this entity is mentioned.
- Human 3D brain organoids: steering the demolecularization of brain and neurological diseases. (2023)
- PKA and Ube3a regulate SK2 channel trafficking to promote synaptic plasticity in hippocampus: Implications for Angelman Syndrome. (2020)
- DNA methylation and brain structure and function across the life course: A systematic review. (2020)
- Whole-exome sequencing of cervical carcinomas identifies activating ERBB2 and PIK3CA mutations as targets for combination therapy. (2019)
- Genome-wide DNA methylation profiling identifies convergent molecular signatures associated with idiopathic and syndromic autism in post-mortem human brain tissue. (2019)
- Hippocampal deficits in neurodevelopmental disorders. (2019)
- Ube3a reinstatement identifies distinct developmental windows in a murine Angelman syndrome model. (2015)
- Alcohol modulates expression of DNA methyltranferases and methyl CpG-/CpG domain-binding proteins in murine embryonic fibroblasts. (2013)
- Long-lasting alterations to DNA methylation and ncRNAs could underlie the effects of fetal alcohol exposure in mice. (2013)
- Aberrant expression of long noncoding RNAs in autistic brain. (2013)
- Whole-exome sequencing and homozygosity analysis implicate depolarization-regulated neuronal genes in autism. (2012)
- CNVs: harbingers of a rare variant revolution in psychiatric genetics. (2012)
- Role of ubiquitin-proteasome-mediated proteolysis in nervous system disease. (2011)
- Alcohol exposure alters DNA methylation profiles in mouse embryos at early neurulation. (2009)
- Large histone H3 lysine 9 dimethylated chromatin blocks distinguish differentiated from embryonic stem cells. (2009)
- Mice lacking the beta3 subunit of the GABAA receptor have the epilepsy phenotype and many of the behavioral characteristics of Angelman syndrome. (1998)
Merged raw entities (1)
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 |
|---|---|---|---|
| ube3a | gene | 16 | 96 |