Lataa...

The role of gigaxonin in the degradation of the glial-specific intermediate filament protein GFAP

Alexander disease (AxD) is a primary genetic disorder of astrocytes caused by dominant mutations in the gene encoding the intermediate filament (IF) protein GFAP. This disease is characterized by excessive accumulation of GFAP, known as Rosenthal fibers, within astrocytes. Abnormal GFAP aggregation...

Täydet tiedot

Tallennettuna:
Bibliografiset tiedot
Julkaisussa:Mol Biol Cell
Päätekijät: Lin, Ni-Hsuan, Huang, Yu-Shan, Opal, Puneet, Goldman, Robert D., Messing, Albee, Perng, Ming-Der
Aineistotyyppi: Artigo
Kieli:Inglês
Julkaistu: The American Society for Cell Biology 2016
Aiheet:
Linkit:https://ncbi.nlm.nih.gov/pmc/articles/PMC5156539/
https://ncbi.nlm.nih.gov/pubmed/27798231
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1091/mbc.E16-06-0362
Tagit: Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!