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Pluripotent stem cell based gene therapy for hematological diseases

Stijn Vanhee (UGent) and Bart Vandekerckhove (UGent)
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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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Citation

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Chicago
Vanhee, Stijn, and Bart Vandekerckhove. 2015. “Pluripotent Stem Cell Based Gene Therapy for Hematological Diseases.” Critical Reviews in Oncology Hematology 97: 238–246.
APA
Vanhee, S., & Vandekerckhove, B. (2015). Pluripotent stem cell based gene therapy for hematological diseases. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY, 97, 238–246.
Vancouver
1.
Vanhee S, Vandekerckhove B. Pluripotent stem cell based gene therapy for hematological diseases. CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY. 2015;97:238–46.
MLA
Vanhee, Stijn, and Bart Vandekerckhove. “Pluripotent Stem Cell Based Gene Therapy for Hematological Diseases.” CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY 97 (2015): 238–246. Print.
@article{8506269,
  author       = {Vanhee, Stijn and Vandekerckhove, Bart},
  issn         = {1040-8428},
  journal      = {CRITICAL REVIEWS IN ONCOLOGY HEMATOLOGY},
  keyword      = {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://dx.doi.org/10.1016/j.critrevonc.2015.08.022},
  volume       = {97},
  year         = {2015},
}

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