amyotrophic lateral sclerosis phenotype
Evidence from:
primary |
all sources
No related entities found.
Mentioned in (11)
Papers in which this entity is mentioned.
- Large-scale exome analyses reveal new rare variant contributions in amyotrophic lateral sclerosis. (2026)
- RNA splicing dysregulation and the hallmarks of cancer. (2023)
- mutations, genetic mosaicism and human disease. (2022)
- SPOTlight: seeded NMF regression to deconvolute spatial transcriptomics spots with single-cell transcriptomes. (2021)
- HSP70 and HSP90 in neurodegenerative diseases. (2020)
- New insights into the generation and role of de novo mutations in health and disease. (2016)
- Ewing sarcoma protein: a key player in human cancer. (2013)
- Genic intolerance to functional variation and the interpretation of personal genomes. (2013)
- Common inversion polymorphism at 17q21.31 affects expression of multiple genes in tissue-specific manner. (2012)
- Long pre-mRNA depletion and RNA missplicing contribute to neuronal vulnerability from loss of TDP-43. (2011)
- Integrative analysis of the melanoma transcriptome. (2010)
Merged raw entities (4)
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 |
|---|---|---|---|
| amyotrophic lateral sclerosis | phenotype | 41 | 57 |
| motor neuron disease | phenotype | 3 | 3 |
| familial als | phenotype | 1 | 1 |
| lou gehrig’s disease | phenotype | — | — |