Sharpening the Molecular Scissors: Advances in Gene-Editing Technology

por Broeders, Mike, Herrero-Hernandez, Pablo, Ernst, Martijn P.T., van der Ploeg, Ans T., Pijnappel, W.W.M. Pim
Publicado 2019

Ready for Repair? Gene Editing Enters the Clinic for the Treatment of Human Disease

por Ernst, Martijn P.T., Broeders, Mike, Herrero-Hernandez, Pablo, Oussoren, Esmee, van der Ploeg, Ans T., Pijnappel, W.W.M. Pim
Publicado 2020

Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies

por Decker, Melanie, Lammens, Tim, Ferster, Alina, Erlacher, Miriam, Yoshimi, Ayami, Niemeyer, Charlotte M., Ernst, Martijn P. T., Raaijmakers, Marc H. G. P., Duployez, Nicolas, Flaum, Andreas, Steinemann, Doris, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim
Publicado 2021

Correction to: Functional classification of RUNX1 variants in familial platelet disorder with associated myeloid malignancies

por Decker, Melanie, Lammens, Tim, Ferster, Alina, Erlacher, Miriam, Yoshimi, Ayami, Niemeyer, Charlotte M., Ernst, Martijn P. T., Raaijmakers, Marc H. G. P., Duployez, Nicolas, Flaum, Andreas, Steinemann, Doris, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim
Publicado 2022

Hematopoietic Cell Autonomous Disruption of Hematopoiesis in a Germline Loss-of-function Mouse Model of RUNX1-FPD

por Ernst, Martijn P. T., Pronk, Eline, van Dijk, Claire, van Strien, Paulina M. H., van Tienhoven, Tim V. D., Wevers, Michiel J. W., Sanders, Mathijs A., Bindels, Eric M. J., Speck, Nancy A., Raaijmakers, Marc H. G. P.
Publicado 2023

Validation and clinical application of transactivation assays for RUNX1 variant classification

por Decker, Melanie, Agarwal, Anupriya, Benneche, Andreas, Churpek, Jane, Duployez, Nicolas, Duvall, Adam, Ernst, Martijn P. T., Förster, Alisa, Høberg-Vetti, Hildegunn, Hofmann, Inga, Nash, Michelle, Raaijmakers, Marc H. G. P., Tvedt, Tor H. A., Vlachos, Adrianna, Schlegelberger, Brigitte, Illig, Thomas, Ripperger, Tim
Publicado 2022