Wordt geladen...
Alexander Disease-Associated Glial Fibrillary Acidic Protein Mutations in Mice Induce Rosenthal Fiber Formation and a White Matter Stress Response
Mutations in the gene for the astrocyte specific intermediate filament, glial fibrillary acidic protein (GFAP), cause the rare leukodystrophy Alexander disease (AxD). To study the pathology of this primary astrocyte defect, we have generated knock-in mice with missense mutations homologous to those...
Bewaard in:
| Gepubliceerd in: | J Neurosci |
|---|---|
| Hoofdauteurs: | , , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Society for Neuroscience
2006
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6674663/ https://ncbi.nlm.nih.gov/pubmed/17065456 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1523/JNEUROSCI.3260-06.2006 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|