Samia Martin
Genethon (France)(FR)
Publications by Year
Research Areas
Virus-based gene therapy research, CRISPR and Genetic Engineering, Muscle Physiology and Disorders, CAR-T cell therapy research, RNA Interference and Gene Delivery
Most-Cited Works
- → A conserved mechanism of retrovirus restriction in mammals(2000)244 cited
- → Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy(2017)230 cited
- → Gene Therapy Prolongs Survival and Restores Function in Murine and Canine Models of Myotubular Myopathy(2014)168 cited
- → Liver-directed lentiviral gene therapy in a dog model of hemophilia B(2015)153 cited
- → Humoral and Cellular Capsid-Specific Immune Responses to Adeno-Associated Virus Type 1 in Randomized Healthy Donors(2012)80 cited
- → Safety and Efficacy of AAV-Mediated Calpain 3 Gene Transfer in a Mouse Model of Limb-Girdle Muscular Dystrophy Type 2A(2005)75 cited
- → Vectofusin-1, a New Viral Entry Enhancer, Strongly Promotes Lentiviral Transduction of Human Hematopoietic Stem Cells(2013)67 cited
- → A translationally optimized AAV-UGT1A1 vector drives safe and long-lasting correction of Crigler-Najjar syndrome(2016)60 cited
- → Preclinical Development of an AAV8-hUGT1A1 Vector for the Treatment of Crigler-Najjar Syndrome(2018)59 cited
- → Correction of the Exon 2 Duplication in DMD Myoblasts by a Single CRISPR/Cas9 System(2017)54 cited