Endothelial progenitor cell-based therapy for hemophilia A. - Wikidata - awgldk - TriplyDB

Endothelial progenitor cell-based therapy for hemophilia A.

Endothelial progenitor cell-based therapy for hemophilia A.

http://www.wikidata.org/entity/Q37982239

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Advanced therapies for the treatment of hemophilia: future perspectives.An effective ex-vivo approach for inducing endothelial progenitor cells from umbilical cord blood CD34+ cells Evaluation of ex vivo produced endothelial progenitor cells for autologous transplantation in primates.

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Endothelial progenitor cell-based therapy for hemophilia A.

http://www.wikidata.org/entity/Q37982239

description

article científic

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article scientifique

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articolo scientifico

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artikel ilmiah

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name

Endothelial progenitor cell-based therapy for hemophilia A.

@en

Endothelial progenitor cell-based therapy for hemophilia A.

@nl

type

label

Endothelial progenitor cell-based therapy for hemophilia A.

@en

Endothelial progenitor cell-based therapy for hemophilia A.

@nl

prefLabel

Endothelial progenitor cell-based therapy for hemophilia A.

@en

Endothelial progenitor cell-based therapy for hemophilia A.

@nl

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S12185-012-1015-Z

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International Journal of Hematology

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Endothelial progenitor cell-based therapy for hemophilia A.

@en

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Hideto Matsui

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P2860

Origins of circulating endothelial cells and endothelial outgrowth from blood

LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1

Therapeutic factor VIII levels and negligible toxicity in mouse and dog models of hemophilia A following gene therapy with high-capacity adenoviral vectors.

Helper-dependent adenoviral vectors mediate therapeutic factor VIII expression for several months with minimal accompanying toxicity in a canine model of severe hemophilia A.

AAV-mediated factor IX gene transfer to skeletal muscle in patients with severe hemophilia B.

The hemophilias--from royal genes to gene therapy.

Gene therapy for hemophilia A: production of therapeutic levels of human factor VIII in vivo in mice.

Dangerous liaisons: the role of "danger" signals in the immune response to gene therapy.

Haemophilias A and B.

The World Federation of Hemophilia: 40 years of improving haemophilia care worldwide.

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s12185-012-1015-z

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119-124

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scholarly article

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10.1007/S12185-012-1015-Z

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2

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95

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2012-02-01T00:00:00Z

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22314304

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