Gene therapy for chronic granulomatous disease
Author:
Publisher
Informa Healthcare
Subject
Clinical Biochemistry,Drug Discovery,Pharmacology
Link
http://www.tandfonline.com/doi/pdf/10.1517/14712598.7.12.1799
Reference84 articles.
1. Current developments in the design of onco-retrovirus and lentivirus vector systems for hematopoietic cell gene therapy
2. Integration of murine leukemia virus DNA depends on mitosis.
3. Third-generation, self-inactivating gp91phoxlentivector corrects the oxidase defect in NOD/SCID mouse–repopulating peripheral blood–mobilized CD34+ cells from patients with X-linked chronic granulomatous disease
4. The Late Dividing Population of γ‐Retroviral Vector Transduced Human Mobilized Peripheral Blood Progenitor Cells Contributes Most to Gene‐Marked Cell Engraftment in Nonobese Diabetic/Severe Combined Immunodeficient Mice
5. Gene Therapy of Human Severe Combined Immunodeficiency (SCID)-X1 Disease
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1. The Evolution of Gene Therapy in the Treatment of Metabolic Liver Diseases;Genes;2020-08-10
2. Functional Restoration of gp91phox-Oxidase Activity by BAC Transgenesis and Gene Targeting in X-linked Chronic Granulomatous Disease iPSCs;Molecular Therapy;2016-04
3. P67-phox (NCF2) Lacking Exons 11 and 12 Is Functionally Active and Leads to an Extremely Late Diagnosis of Chronic Granulomatous Disease (CGD);PLoS ONE;2012-04-13
4. Retroviral and Lentiviral Vectors for the Induction of Immunological Tolerance;Scientifica;2012
5. TheSleeping Beautytransposon system for clinical applications;Expert Opinion on Biological Therapy;2011-12-19
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