Lataa...
Introduction of a human-specific deletion in mouse Cmah increases disease severity in the mdx model of Duchenne muscular dystrophy
The evolution of humans included introduction of an inactivating deletion in the CMAH gene, which eliminated biosynthesis of N-glycolylneuraminic acid from all human cells. Here we show that this human-specific sialylation change contributes to the marked discrepancy in phenotype between the mdx mou...
Tallennettuna:
| Päätekijät: | , , , , , , , |
|---|---|
| Aineistotyyppi: | Artigo |
| Kieli: | Inglês |
| Julkaistu: |
2010
|
| Aiheet: | |
| Linkit: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2950110/ https://ncbi.nlm.nih.gov/pubmed/20668298 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1126/scitranslmed.3000692 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|