A Phase I Clinical Trial for a Lentiviral Gene Therapy Targeting the TCIRG1 Gene for Infantile Malignant Osteopetrosis (IMO)

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Rocket Pharmaceuticals is conducting a clinical trial using a gene therapy for infantile malignant osteopetrosis (IMO), a rare and life-threatening disorder that develops in infancy.  IMO is caused by defective bone cell…

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The role of WNT and BMP signaling pathways in iPSC to iTenocyte step-wise differentiation for tendon repair

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Research Objective Development-inspired differentiation will enable efficient and specific generation of tenocytes that can repair tendon injury, restore dysfunctional tissue, and prevent long term effects. Impact This study will eliminate…

Continue ReadingThe role of WNT and BMP signaling pathways in iPSC to iTenocyte step-wise differentiation for tendon repair