Search | Result
| ID | 1578 |
|---|---|
| Class | Mammalia |
| Species | Homo sapiens |
| Tissue | Brain |
| Sample | Tissue |
| Disease type | Huntington Disease |
| Cell type | Neural cells |
| Cell type (subtype) | Neurons |
| Cell marker | STMN2, SYT1, SNAP25, RTN1, VSNL1, UCHL1, NRGN, NRGN, MAP1B, MAP1B, VAMP2, THY1, GPM6A, CCK, CHN1, CCK, GNAS, SYP, PCSK1N, MEF2C, BEX3, MEG3, BCYRN1, ATP1B1, CALM1, LINC00632, PPP3CA, BASP1, MIAT, YWHAH, BEX1, AHI1, BEX3, SNHG14, MAPK10 |
| 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 |
