hypomyelination phenotype
Evidence from:
primary |
all sources
Related entities (3)
| Subject | Relation | Object | p-value | Evidence |
|---|---|---|---|---|
| fatty acids | risk_factor_for | hypomyelination | — | 1 |
| sphingolipids | risk_factor_for | hypomyelination | — | 1 |
| total cholesterol | associated_with | hypomyelination | — | 1 |
Mentioned in (13)
Papers in which this entity is mentioned.
- Chronic oligodendrocyte injury in central nervous system pathologies. (2022)
- Decreased microglial Wnt/β-catenin signalling drives microglial pro-inflammatory activation in the developing brain. (2019)
- Imaging structural and functional brain development in early childhood. (2018)
- Genetic studies of alcohol dependence in the context of the addiction cycle. (2017)
- Genome-wide association analysis identifies common variants influencing infant brain volumes. (2017)
- Integrative genomics of microglia implicates DLG4 (PSD95) in the white matter development of preterm infants. (2017)
- The Placenta as a Mediator of Stress Effects on Neurodevelopmental Reprogramming. (2016)
- Epigenomic profiling of preterm infants reveals DNA methylation differences at sites associated with neural function. (2016)
- Iron deficiency in infancy is associated with altered neural correlates of recognition memory at 10 years. (2012)
- Neuregulin 1 in neural development, synaptic plasticity and schizophrenia. (2008)
- Maternal immune activation alters fetal brain development through interleukin-6. (2007)
- Spatial genetic patterning of the embryonic neuroepithelium generates GABAergic interneuron diversity in the adult cortex. (2007)
- Biochemical and morphometric analyses show that myelination in the insulin-like growth factor 1 null brain is proportionate to its neuronal composition. (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 |
|---|---|---|---|
| hypomyelination | phenotype | 13 | 19 |