Search | Result
ID | 1582 |
---|---|
Class | Mammalia |
Species | Homo sapiens |
Tissue | Brain |
Sample | Tissue |
Disease type | Huntington Disease |
Cell type | Oligodendrocytes |
Cell type (subtype) | Oligodendrocytes |
Cell marker | PLP1, MBP, MBP, MOBP, MOBP, MAG, CLDN11, TF, SCD, CNP, QDPR, TMEM144, CLDND1, CNTN2, LINC00844, TMEM120, CRYAB, TTLL7, APLP1, SLC44A1, GPM6B, SOX2-OT, PCDH9, PIP4K2A, LAMP2, AMER2, DOCK5, MAP7, PTMA, ABCA2, MIR219A2, HAPLN2, SLC12A2, MID1IP1, EVI2A, CA2 |
Frequency | |
PubMed ID | 32070434 |
Journal | Acta Neuropathol Commun |
SCI IF | 6.27 |
Evidence | For example, if one pre-cluster was characterized by oligodendrocytic (MBP, TMEM120, MOBP) as well as neuronal (CCK, MAP1B, BEX3, NRGN) or microglial (HLA-B, IBA1, C1QB) genes, / Table S2 |
Title | Single-nucleus RNA-seq identifies Huntington disease astrocyte states |
Authors | Osama Al-Dalahmah et al. |
Date | 2020.2 |
Data available | NA |