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Almeida-Porada, M Graca

One or more keywords matched the following items that are connected to Almeida-Porada, M Graca

Item Type	Name
Academic Article	Phenotypic correction of hemophilia A in sheep by postnatal intraperitoneal transplantation of FVIII-expressing MSC.
Academic Article	Development and characterization of recombinant ovine coagulation factor VIII.
Academic Article	Clinical and molecular characterization of a re-established line of sheep exhibiting hemophilia A.
Concept	Hemophilia A
Concept	Hemophilia B
Academic Article	Gene therapy: the promise of a permanent cure.
Academic Article	Hemophilia A: an ideal disease to correct in utero.
Academic Article	Treatment of Hemophilia A in Utero and Postnatally using Sheep as a Model for Cell and Gene Delivery.
Grant	Postnatal Cell-Based Therapies for Hemophilia A
Grant	In Utero Stem Cell Transplantation for Hemophilia A
Grant	Prenatal Cell and Gene Therapy for Hemophilia A
Grant	cGMP Manufacture Of FVIII-Expressing Placental Cells For Hemophilia A
Academic Article	Effects of Shear Stress on Production of FVIII and vWF in a Cell-Based Therapeutic for Hemophilia A.
Academic Article	Defining the Optimal FVIII Transgene for Placental Cell-Based Gene Therapy to Treat Hemophilia A.
Academic Article	Investigating Optimal Autologous Cellular Platforms for Prenatal or Perinatal Factor VIII Delivery to Treat Hemophilia A.
Academic Article	Acceptability of prenatal diagnosis and prenatal treatment of haemophilia using cell and gene therapies within US haemophilia community.
Academic Article	Comparison of different gene addition strategies to modify placental derived-mesenchymal stromal cells to produce FVIII.
Academic Article	Autologous bone marrow-derived MSCs engineered to express oFVIII-FLAG engraft in adult sheep and produce an effective increase in plasma FVIII levels.
Academic Article	A new "FIX" for hemophilia B gene therapy.
Academic Article	Mechanistic Insights into Factor VIII Immune Tolerance Induction via Prenatal Cell Therapy in Hemophilia A.
Grant	Defining the therapeutic efficacy, tolerogenic potential, and genotoxicity of liver-targeted AAV gene therapy for hemophilia A

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Hemophilia B