 
                Lv41
780 积分 2021-07-26 加入
 In vivo HSC Gene Therapy Using BaEVRLess-Pseudotyped Alpha-Retroviral and Lentiviral Vectors
                                            6小时前
                                            已完结
In vivo HSC Gene Therapy Using BaEVRLess-Pseudotyped Alpha-Retroviral and Lentiviral Vectors
                                            6小时前
                                            已完结
                                         Novel strategies to expand and engineer hematopoietic stem cells
                                            18天前
                                            已完结
Novel strategies to expand and engineer hematopoietic stem cells
                                            18天前
                                            已完结
                                         Stereo-cell: Spatial enhanced-resolution single-cell sequencing with high-density DNA nanoball-patterned arrays
                                            2个月前
                                            已完结
Stereo-cell: Spatial enhanced-resolution single-cell sequencing with high-density DNA nanoball-patterned arrays
                                            2个月前
                                            已完结
                                         Chemical reprogramming of human blood cells to pluripotent stem cells
                                            2个月前
                                            已完结
Chemical reprogramming of human blood cells to pluripotent stem cells
                                            2个月前
                                            已完结
                                         Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212): a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trial
                                            3个月前
                                            已完结
Betibeglogene autotemcel gene therapy in patients with transfusion-dependent, severe genotype β-thalassaemia (HGB-212): a non-randomised, multicentre, single-arm, open-label, single-dose, phase 3 trial
                                            3个月前
                                            已完结
                                         In vivo HSC Gene Therapy Using BaEVRLess-Pseudotyped Alpha-Retroviral and Lentiviral Vectors
                                            3个月前
                                            已关闭
In vivo HSC Gene Therapy Using BaEVRLess-Pseudotyped Alpha-Retroviral and Lentiviral Vectors
                                            3个月前
                                            已关闭
                                         An integrated network analysis approach to identify potential key genes, transcription factors, and microRNAs regulating human hematopoietic stem cell aging
                                            3个月前
                                            已完结
An integrated network analysis approach to identify potential key genes, transcription factors, and microRNAs regulating human hematopoietic stem cell aging
                                            3个月前
                                            已完结
                                         Distinct Mechanisms Underlying the Ex Vivo Expansion of Human Cord Blood Stem Cells with Different Strategies Currently Used for Allogeneic Transplantation
                                            3个月前
                                            已关闭
Distinct Mechanisms Underlying the Ex Vivo Expansion of Human Cord Blood Stem Cells with Different Strategies Currently Used for Allogeneic Transplantation
                                            3个月前
                                            已关闭
                                         Ex Vivo Expansion of Adult Hematopoietic Stem and Progenitor Cells with Valproic Acid
                                            4个月前
                                            已完结
Ex Vivo Expansion of Adult Hematopoietic Stem and Progenitor Cells with Valproic Acid
                                            4个月前
                                            已完结
                                         Reducing the transcriptional read‐through rate of a lentiviral vector for β‐thalassemia gene therapy
                                            4个月前
                                            已完结
Reducing the transcriptional read‐through rate of a lentiviral vector for β‐thalassemia gene therapy
                                            4个月前
                                            已完结