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Pluripotent stem cell based gene therapy for hematological diseases

Stijn Vanhee (UGent) and Bart Vandekerckhove (UGent)
(2015) CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY. 97. p.238-246
Author
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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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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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