Yüklüyor......
Overexpression of Lamin B Receptor Results in Impaired Skin Differentiation
Hutchinson-Gilford progeria syndrome (HGPS) is a rare segmental progeroid disorder commonly caused by a point mutation in the LMNA gene that results in the increased activation of an intra-exonic splice site and the production of a truncated lamin A protein, named progerin. In our previous work, ind...
Kaydedildi:
| Yayımlandı: | PLoS One |
|---|---|
| Asıl Yazarlar: | , , , |
| Materyal Türü: | Artigo |
| Dil: | Inglês |
| Baskı/Yayın Bilgisi: |
Public Library of Science
2015
|
| Konular: | |
| Online Erişim: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4459694/ https://ncbi.nlm.nih.gov/pubmed/26053873 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1371/journal.pone.0128917 |
| Etiketler: |
Etiketle
Etiket eklenmemiş, İlk siz ekleyin!
|