Systemic gene delivery following intravenous administration of AAV9 to fetal and neonatal mice and late-gestation nonhuman primates-Reference-Cited by-同舟云学术

Systemic gene delivery following intravenous administration of AAV9 to fetal and neonatal mice and late-gestation nonhuman primates

Published:2015-09 Issue:9 Volume:29 Page:3876-3888
ISSN:0892-6638
Container-title:The FASEB Journal
language:en
Short-container-title:The FASEB Journal

Author:

Mattar Citra N.,Wong Andrew M. S.,Hoefer Klemens,Alonso-Ferrero Maria E.,Buckley Suzanne M. K.,Howe Steven J.,Cooper Jonathan D.,Waddington Simon N.,Chan Jerry K. Y.,Rahim Ahad A.

Publisher

Wiley

Subject

Genetics,Molecular Biology,Biochemistry,Biotechnology

Reference25 articles.

1. Therapeutic approaches to bone pathology in Gaucher disease: Past, present and future

2. Transfusion independence and HMGA2 activation after gene therapy of human β-thalassaemia

3. Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

4. Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy

5. Lentiviral Hematopoietic Stem Cell Gene Therapy Benefits Metachromatic Leukodystrophy

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