Recombinant human complement component C2 produced in a human cell line restores the classical complement pathway activity in-vitro: an alternative treatment for C2 deficiency diseases

BACKGROUND: Complement C2 deficiency is the most common genetically determined complete complement deficiency and is associated with a number of diseases. Most prominent are the associations with recurrent serious infections in young children and the development of systemic lupus erythematosus (SLE)...

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Detalles Bibliográficos
Autores principales: Martini, Paolo GV, Cook, Lynette C, Alderucci, Scott, Norton, Angela W, Lundberg, Dianna M, Fish, Susan M, Langsetmo, Knut, Jönsson, Göran, Lood, Christian, Gullstrand, Birgitta, Zaleski, Kate J, Savioli, Nancy, Lottherand, Jason, Bedard, Charles, Gill, John, Concino, Michael F, Heartlein, Michael W, Truedsson, Lennart, Powell, Jan L, Tzianabos, Arthur O
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2931460/
https://www.ncbi.nlm.nih.gov/pubmed/20727163
http://dx.doi.org/10.1186/1471-2172-11-43

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2931460/
https://www.ncbi.nlm.nih.gov/pubmed/20727163
http://dx.doi.org/10.1186/1471-2172-11-43

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