Cargando…
In silico analysis of alpha1-antitrypsin variants: The effects of a novel mutation
Alpha1-antitrypsin (AAT) is a highly polymorphic protein with more than 120 variants that are classified as normal (normal protein secretion), deficient (reduced circulating AAT level caused by defective secretion) or null (no protein secretion). Alpha1-antitrypsin deficiency, one of the most common...
Autores principales: | Denden, Sabri, Leban, Nadia, Hayek, Donia, Knani, Jalel, Chibani, Jemni Ben, Khelil, Amel Haj |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Sociedade Brasileira de Genética
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3036143/ https://www.ncbi.nlm.nih.gov/pubmed/21637569 http://dx.doi.org/10.1590/S1415-47572010005000089 |
Ejemplares similares
-
Alpha-1 antitrypsin gene polymorphism in Chronic Obstructive Pulmonary Disease (COPD)
por: Denden, Sabri, et al.
Publicado: (2010) -
Screening for Alpha 1 antitrypsin deficiency in Tunisian subjects with obstructive lung disease: a feasibility report
por: Denden, Sabri, et al.
Publicado: (2009) -
Combined Analysis of EPHX1, GSTP1, GSTM1 and GSTT1 Gene Polymorphisms in Relation to Chronic Obstructive Pulmonary Disease Risk and Lung Function Impairment
por: Lakhdar, Ramzi, et al.
Publicado: (2011) -
Polymorphism of C3 complement in association with myocardial infarction in a sample of central Tunisia
por: Leban, Nadia, et al.
Publicado: (2013) -
Polymorphism of alpha-1-antitrypsin in hematological malignancies
por: Topic, Aleksandra, et al.
Publicado: (2009)