Cell and gene therapy for Hemophilia A: development of a transplantation strategy in the liver of...

Employer
Università degli Studi del Piemonte Orientale
Location
Italy
Posted
September 14 2017
Discipline
Life Sciences, Biology
Position Type
Full Time
Organization Type
Academia

Characterization and analysis of BOECs derived from hemophilic patients and correction by lentiviral vectors to be used for the expression of FVIII for Hemophilia A cell and gene therapy. A pre-clinical study in immunocompromised hemophilic mice after xenotransplantation of human cells.



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