Onderzoeker
Marinee Chuah
- Disciplines:Cardiale en vasculaire geneeskunde, Moleculaire en celbiologie
Affiliaties
- Centrum voor Moleculaire en Vasculaire Biologie (Afdeling)
Lid
Vanaf1 okt 2000 → Heden
Projecten
1 - 2 of 2
- Ontwikkeling van stamcel-gentherapie voor Duchenne musculaire dystrofie.Vanaf27 sep 2010 → 16 jun 2016Financiering: FWO mandaten
- Rol van microRNA regulatie in de controle van hepatocarcinogenese: in vivo validatie, moleculaire mechanismen en therapeutische implicaties.Vanaf1 jan 2010 → 31 dec 2015Financiering: FWO Onderzoeksproject (incl. WEAVE projecten)
Publicaties
21 - 30 van 108
- Transposons Expressing Full-Length Human Dystrophin Enable Genetic Correction of Dystrophic Mesoangioblasts and iPS-Derived Mesoangioblast-Like Cells(2016)
Auteurs: Mariana Loperfido, Susan Jarmin, Sumitava Dastidar, Mario di Matteo, Ilaria Perini, Marc Moore, Nisha Nair, Ermira Samara-Kuko, Takis Athanasopoulos, Francesco Saverio Tedesco, et al.
Pagina's: S249 - S249 - Gene therapy for cardiovascular disease: advances in vector development, targeting, and delivery for clinical translation(2015)
Auteurs: Thierry Vandendriessche, Marinee Chuah
Pagina's: 4 - 20 - Therapeutic Approaches for Dominant Muscle Diseases: Highlight on Myotonic Dystrophy(2015)
Auteurs: Marinee Chuah
Pagina's: 329 - 337 - Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells(2015)
Auteurs: Thierry Vandendriessche, Marinee Chuah
Pagina's: 941 - 958 - Hitting the target without pulling the trigger(2015)
Auteurs: Thierry Vandendriessche, Marinee Chuah
Pagina's: 4 - 6 - Moving Forward Toward a Cure for Hemophilia B(2015)
Auteurs: Thierry Vandendriessche, Marinee Chuah
Pagina's: 809 - 811 - Hyperactive PiggyBac Transposons for Sustained and Robust Liver-targeted Gene Therapy (vol 22, pg 1614, 2014)(2015)
Auteurs: Mario di Matteo, Emira Samara-Kuko, Natalie J Ward, Simon N Waddingon, John H Mcvey, Marinee Chuah, Thierry Vandendriessche
Pagina's: 1671 - 1671 - Editorial: Stem Cell-Based and Gene Therapy for Hereditary Muscle Disorders.(2015)
Auteurs: Marinee Chuah
Pagina's: 327 - 328 - Stem Cell-Based and Gene Therapy for Hereditary Muscle Disorders(2015)
Auteurs: Marinee Chuah
Pagina's: 327 - 328 - Efficient derivation and inducible differentiation of expandable skeletal myogenic cells from human ES and patient-specific iPS cells (vol 10, pg 941, 2015)(2015)
Auteurs: Sara M Maffioletti, Mattia FM Gerli, Martina Ragazzi, Sumitava Dastidar, Sara Benedetti, Mariana Loperfido, Thierry Vandendriessche, Marinee Chuah, Francesco Saverio Tedesco
Pagina's: 1457 - 1457
Patenten
1 - 1 van 1