Onderzoeker
Warut Tulalamba
- Trefwoorden:Geneeskunde
Affiliaties
- Basis (bio)-medische wetenschappen (Departement)
Lid
Vanaf1 nov 2017 → 31 dec 2018 - Basis (bio)-medische wetenschappen (Departement)
Lid
Vanaf1 nov 2014 → 31 dec 2018 - Gentherapie & Regeneratieve Geneeskunde (Onderzoeksgroep)
Lid
Vanaf1 nov 2014 → 31 dec 2018
Publicaties
1 - 8 van 8
- Treatment of Infantile-Onset Pompe Disease in a Rat Model with Muscle-Directed AAV Gene Therapy(2024)
Auteurs: 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)
Auteurs: 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)
Auteurs: 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)
Auteurs: Warut Tulalamba, Jonas Weinmann, Hong Quang Pham, Jihad El Andari, Thierry VandenDriessche, Marinee K Chuah, Dirk Grimm
Pagina's: 170-179 - Validation of miR-20a as a Tumor Suppressor Gene in Liver Carcinoma Using Hepatocyte-Specific Hyperactive piggyBac Transposons(2020)
Auteurs: Jaitip Tipanee, Mario Di Matteo, Warut Tulalamba, Ermira Samara-Kuko, Jiri Keirsse, Jo A Van Ginderachter, Marinee K Chuah, Thierry VandenDriessche
Pagina's: 1309-1329 - Next-generation muscle-directed gene therapy by in silico vector design(2019)
Auteurs: Shilpita Sarcar, Warut Tulalamba, Melvin Rincon Acelas, Jaitip Tipanee, Hong Quang Pham, Hanneke Evens, Dimitri Boon, E. Samara-Kuko, Marleen Keyaerts, Mariana Loperfido, et al.
Pagina's: 492 - Efficient CRISPR/Cas9-mediated editing of trinucleotide repeat expansion in myotonic dystrophy patient-derived iPS and myogenic cells(2018)
Auteurs: Sumitava Dastidar, Simon Ardui, Kshitiz Singh, Debanjana Majumdar, Nisha Nair, Yanfang Fu, Deepak Reyon, Ermira Samara, Mattia FM Gerbil, Arnaud F. Klein, et al.
Pagina's: 8275-8298 - A Novel Platform for Immune Tolerance Induction in Hemophilia A Mice(2017)
Auteurs: 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.
Pagina's: 1815-1830