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https://stemcellsjournals.onlinelibrary.wiley.com/doi/full/10.1634/stemcells.2004-0138
First‐trimester fetal blood contains a readily expandable population of stem cells, human fetal mesenchymal stem cells (hfMSCs), which might be exploited for autologous intrauterine gene therapy. We investigated the self‐renewal and differentiation of hfMSCs after transduction with onco‐retroviral and lentiviral vectors.Author: Jerry Chan, Keelin O'Donoghue, Josu de la Fuente, Irene A. Roberts, Sailesh Kumar, Jennifer E. Morga...
http://onlinelibrary.wiley.com/doi/10.1634/stemcells.2004-0138/abstract
Jan 02, 2009 · First-trimester fetal blood contains a readily expandable population of stem cells, human fetal mesenchymal stem cells (hfMSCs), which might be exploited for autologous intrauterine gene therapy. We investigated the self-renewal and differentiation of hfMSCs after transduction with onco-retroviral and lentiviral vectors.
https://www.ncbi.nlm.nih.gov/pubmed/15625126
First-trimester fetal blood contains a readily expandable population of stem cells, human fetal mesenchymal stem cells (hfMSCs), which might be exploited for autologous intrauterine gene therapy. We investigated the self-renewal and differentiation of hfMSCs after transduction with onco-retroviral and lentiviral vectors.Author: Jerry Chan, Keelin O'Donoghue, Josu de la Fuente, Irene A. Roberts, Sailesh Kumar, Jennifer E. Morga...
https://www.researchgate.net/publication/8106090_Human_Fetal_Mesenchymal_Stem_Cells_as_Vehicles_for_Gene_Delivery
First-trimester fetal blood contains a readily expandable population of stem cells, human fetal mesenchymal stem cells (hfMSCs), which might be exploited for autologous intrauterine gene therapy.
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2699841/
May 15, 2009 · Human mesenchymal stem cells were transduced with a multiplicity of infection (MOI) of 10 virus particles for each cell and 4μg/ml of polybrene (Sigma Aldrich, Poole, UK). Human TRAIL expression was verified by ELISA (R&D Systems, Abingdon, UK) as …Author: Michael R. Loebinger, Ayad Eddaoudi, Derek Davies, Sam M. Janes
https://www.paediatrics.ox.ac.uk/publications/230516
First-trimester fetal blood contains a readily expandable population of stem cells, human fetal mesenchymal stem cells (hfMSCs), which might be exploited for autologous intrauterine gene therapy. We investigated the self-renewal and differentiation of hfMSCs after transduction with onco-retroviral and lentiviral vectors. After transduction with either a MoMuLV retrovirus or an HIV-1-based ...Author: Jerry Chan, Keelin O'Donoghue, Josu de la Fuente, Irene A. Roberts, Sailesh Kumar, Jennifer E. Morga...
https://www.academia.edu/14756702/Human_Fetal_Mesenchymal_Stem_Cells_as_Vehicles_for_Gene_Delivery
Human Fetal Mesenchymal Stem Cells as Vehicles for Gene Delivery
https://www.intechopen.com/books/gene-therapy-tools-and-potential-applications/mesenchymal-stem-cells-as-gene-delivery-vehicles
Mesenchymal stem cells (MSCs) possess a battery of unique properties which make them ideally suited not only for cellular therapies/regenerative medicine, but also as vehicles for gene delivery in a wide array of clinical settings.Author: Christopher Porada, Graça Almeida-Porada
https://www.academia.edu/9206648/Human_Fetal_Mesenchymal_Stem_Cells_as_Vehicles_for_Gene_Delivery
First-trimester fetal blood contains a readily expandable population of stem cells, human fetal mesenchymal stem cells (hfMSCs), which might be exploited for autologous intrauterine gene therapy. We investigated the self-renewal and differentiation
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