Safety of Adeno-associated virus-based vector-mediated gene therapy—impact of vector dose von Maurya, Shubham, Sarangi, Pratiksha, Jayandharan, Giridhara R.

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Intraarticular Delivery of AAV5-Mir-125a-5p Regulates Key Molecular Mediators of Hemophilic Arthropathy von SenthilKumar, Mohan Kumar B, Sarangi, Pratiksha, Amit, Sonal, Senguttuvan, Senthil, Kumar, Narendra, Jayandharan, Giridhara R.

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AAV mediated genome engineering with a bypass coagulation factor alleviates the bleeding phenotype in a murine model of hemophilia B von Sarangi, Pratiksha, Kumar, Narendra, Sambasivan, Ramkumar, Ramalingam, Sivaprakash, Amit, Sonal, Chandra, Dinesh, Jayandharan, Giridhara R.

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AAV mediated repression of Neat1 lncRNA combined with F8 gene augmentation mitigates pathological mediators of joint disease in haemophilia von Sarangi, Pratiksha, Senthilkumar, Mohankumar B., Amit, Sonal, Kumar, Narendra, Jayandharan, Giridhara R.

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Targeted delivery of miR125a-5p and human Factor VIII attenuates molecular mediators of hemophilic arthropathy von Senthilkumar, Mohankumar B., Sarangi, Pratiksha, Amit, Sonal, Senguttuvan, Senthilnathan, Kumar, Narendra, Jayandharan, Giridhara R.

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Potential role of long non‐coding RNA H19 and Neat1 in haemophilic arthropathy von Sarangi, Pratiksha, Senthilkumar, Mohankumar B., Kumar, Narendra, Senguttuvan, Senthilnathan, Vasudevan, Madavan, Jayandharan, Giridhara R.

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Gene therapy for female infertility: A farfetched dream or reality? von Pathak, Subhajit, Sarangi, Pratiksha, Jayandharan, Giridhara R.

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AN OPTIMIZED AAV VECTOR FOR GENE THERAPY OF MUSCULAR DYSTROPHY von SARANGI, Pratiksha, SINGH, Vijayata, SRINIVASAN, Navaneeth, RAO, Jayandharan Giridhara, VARGHESE, Anila

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