A large research group led by Dr. Jeff Vierstra, a researcher at the Altius Institute for Biomedical Sciences in Seattle (USA), and Dr. Nikoletta Psatha, Assistant Professor in the Department…
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In a historic medical breakthrough, a child diagnosed with a rare genetic disorder was successfully treated with a personalized CRISPR gene-editing therapy by a group from the Children’s Hospital of…
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The U.S. Food and Drug Administration (FDA) has approved Abeona Therapeutics’ gene therapy, Zevaskyn (prademagene zamikeracel), for treating wounds in patients with recessive dystrophic epidermolysis bullosa (RDEB), a rare and…
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The very interesting event of the Hellenic Society of Gene Therapy and Regenerative Medicine (HSGTRM), supported by the Hellenic Pasteur Institute, has come to an end. At the welcoming Academy…
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Dear colleagues, On behalf of the Board of Directors of the Hellenic Society of Gene Therapy and Regenerative Medicine (HSGTRM), I have the pleasure to invite you to the…
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In a major medical breakthrough, India has successfully completed its first human gene therapy for severe hemophilia-A using a lentiviral vector, resulting in zero bleeding rates in patients. Hemophilia, a…
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The Board of Directors of the HSGTRM wishes you Merry Christmas and a Happy New Year 2025!