Erdj3 Has an Essential Role for Z Variant Alpha‐1‐Antitrypsin Degradation

Alpha‐1‐antitrypsin deficiency (AATD) is an inherited disease characterized by emphysema and liver disease. AATD is most often caused by a single amino acid substitution at amino acid 342 in the mature protein, resulting in the Z mutation of the alpha‐1‐antitrypsin gene (ZAAT). This substitution is...

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Detalles Bibliográficos
Autores principales: Khodayari, Nazli, Marek, George, Lu, Yuanqing, Krotova, Karina, Wang, Rejean Liqun, Brantly, Mark
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2017
Materias:
Articles
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575529/
https://www.ncbi.nlm.nih.gov/pubmed/28419579
http://dx.doi.org/10.1002/jcb.26069

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5575529/
https://www.ncbi.nlm.nih.gov/pubmed/28419579
http://dx.doi.org/10.1002/jcb.26069

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