Pluripotent stem cell based gene therapy for hematological diseases
- Author
- Stijn Vanhee (UGent) and Bart Vandekerckhove (UGent)
- Organization
- Keywords
- Gene therapy, Hematopoiesis, IPSC, hESC, Pluripotent stem cells, Tailored nucleases, Hematological diseases, Stem cells, SEVERE COMBINED IMMUNODEFICIENCY, HEMATOPOIETIC PROGENITOR CELLS, WISKOTT-ALDRICH SYNDROME, BLOOD MONONUCLEAR-CELLS, HUMAN CORD BLOOD, CD34(+) CELLS, DIFFERENTIATION CULTURES, HUMAN FIBROBLASTS, DEFINED FACTORS, STROMAL CELLS
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Citation
Please use this url to cite or link to this publication: http://hdl.handle.net/1854/LU-8506269
- MLA
- Vanhee, Stijn, and Bart Vandekerckhove. “Pluripotent Stem Cell Based Gene Therapy for Hematological Diseases.” CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, vol. 97, 2015, pp. 238–46, doi:10.1016/j.critrevonc.2015.08.022.
- APA
- Vanhee, S., & Vandekerckhove, B. (2015). Pluripotent stem cell based gene therapy for hematological diseases. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 97, 238–246. https://doi.org/10.1016/j.critrevonc.2015.08.022
- Chicago author-date
- Vanhee, Stijn, and Bart Vandekerckhove. 2015. “Pluripotent Stem Cell Based Gene Therapy for Hematological Diseases.” CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY 97: 238–46. https://doi.org/10.1016/j.critrevonc.2015.08.022.
- Chicago author-date (all authors)
- Vanhee, Stijn, and Bart Vandekerckhove. 2015. “Pluripotent Stem Cell Based Gene Therapy for Hematological Diseases.” CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY 97: 238–246. doi:10.1016/j.critrevonc.2015.08.022.
- Vancouver
- 1.Vanhee S, Vandekerckhove B. Pluripotent stem cell based gene therapy for hematological diseases. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY. 2015;97:238–46.
- IEEE
- [1]S. Vanhee and B. Vandekerckhove, “Pluripotent stem cell based gene therapy for hematological diseases,” CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, vol. 97, pp. 238–246, 2015.
@article{8506269, author = {{Vanhee, Stijn and Vandekerckhove, Bart}}, issn = {{1040-8428}}, journal = {{CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY}}, keywords = {{Gene therapy,Hematopoiesis,IPSC,hESC,Pluripotent stem cells,Tailored nucleases,Hematological diseases,Stem cells,SEVERE COMBINED IMMUNODEFICIENCY,HEMATOPOIETIC PROGENITOR CELLS,WISKOTT-ALDRICH SYNDROME,BLOOD MONONUCLEAR-CELLS,HUMAN CORD BLOOD,CD34(+) CELLS,DIFFERENTIATION CULTURES,HUMAN FIBROBLASTS,DEFINED FACTORS,STROMAL CELLS}}, language = {{eng}}, pages = {{238--246}}, title = {{Pluripotent stem cell based gene therapy for hematological diseases}}, url = {{http://doi.org/10.1016/j.critrevonc.2015.08.022}}, volume = {{97}}, year = {{2015}}, }
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