Researcher
Warut Tulalamba
- Keywords:Medicine
Affiliations
- Basic (bio-) Medical Sciences (Department)
Member
From1 Nov 2017 → 31 Dec 2018 - Basic (bio-) Medical Sciences (Department)
Member
From1 Nov 2014 → 31 Dec 2018 - Division of Gene Therapy & Regenerative Medicine (Research group)
Member
From1 Nov 2014 → 31 Dec 2018
Publications
1 - 8 of 8
- Treatment of Infantile-Onset Pompe Disease in a Rat Model with Muscle-Directed AAV Gene Therapy(2024)
Authors: Sergio Muñoz, Joan Bertolin, Veronica Jimenez, Maria Luisa Jaén, Miquel Garcia, Anna Pujol, Laia Vilà, Victor Sacristan, Elena Barbon, Giuseppe Ronzitti, et al.
- Semirational bioengineering of AAV vectors with increased potency and specificity for systemic gene therapy of muscle disorders(2022)
Authors: Jihad El Andari, Edith Renaud-Gabardos, Warut Tulalamba, Jonas Weinmann, Louise Mangin, Quang Hong Pham, Susanne Hille, Antonette Bennett, Esther Attebi, Emanuele Bourges, et al.
- Identification of a myotropic AAV by massively parallel in vivo evaluation of barcoded capsid variants(2020)
Authors: Jonas Weinmann, Sabrina Weis, Josefine Sippel, Warut Tulalamba, Anca Remes, Jihad El Andari, Anne-Kathrin Herrmann, Hong Quang Pham, Christopher Borowski, Susanne Hille, et al.
- Distinct transduction of muscle tissue in mice after systemic delivery of AAVpo1 vectors(2020)
Authors: Warut Tulalamba, Jonas Weinmann, Hong Quang Pham, Jihad El Andari, Thierry VandenDriessche, Marinee K Chuah, Dirk Grimm
Pages: 170-179 - Validation of miR-20a as a Tumor Suppressor Gene in Liver Carcinoma Using Hepatocyte-Specific Hyperactive piggyBac Transposons(2020)
Authors: Jaitip Tipanee, Mario Di Matteo, Warut Tulalamba, Ermira Samara-Kuko, Jiri Keirsse, Jo A Van Ginderachter, Marinee K Chuah, Thierry VandenDriessche
Pages: 1309-1329 - Next-generation muscle-directed gene therapy by in silico vector design(2019)
Authors: Shilpita Sarcar, Warut Tulalamba, Melvin Rincon Acelas, Jaitip Tipanee, Hong Quang Pham, Hanneke Evens, Dimitri Boon, E. Samara-Kuko, M Keyaerts, Mariana Loperfido, et al.
Pages: 492 - Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells(2018)
Authors: Sumitava Dastidar, Simon Ardui, Kshitiz Singh, Debanjana Majumdar, Nisha Nair, Yanfang Fu, Deepak Reyon, Ermira Samara, Mattia FM Gerbil, Arnaud F. Klein, et al.
Pages: 8275-8298 - A Novel Platform for Immune Tolerance Induction in Hemophilia A Mice(2017)
Authors: Simone Merlin, Elvira Stefania Cannizzo, Ester Borroni, Valentina Bruscaggin, Piercarla Schinco, Warut Tulalamba, Marinee K Chuah, Valder R Arruda, Thierry VandenDriessche, Maria Prat, et al.
Pages: 1815-1830