Genome-wide identification of microRNA-related variants associated with risk of Alzheimer’s disease

por Ghanbari, Mohsen, Ikram, M. Arfan, de Looper, Hans W. J., Hofman, Albert, Erkeland, Stefan J., Franco, Oscar H., Dehghan, Abbas
Publicado 2016

S160: GATA2B HAPLOINSUFFICIENCY CAUSES ABERRANT TRANSCRIPTIONAL REGULATORY SIGNATURES IN HSPCS RESULTING IN MYELOID AND ERYTHROID DYSPLASIA IN ZEBRAFISH

por Zhang, Wei, Gioacchino, Emanuele, Koyunlar, Cansu, Zink, Joke, de Looper, Hans, Gussinklo, Kirsten J., Hoogenboezem, Remco, Bosch, Dennis, Bindels, Eric, Touw, Ivo P., de Pater, Emma
Publicado 2023

Gata2-regulated Gfi1b expression controls endothelial programming during endothelial-to-hematopoietic transition

por Koyunlar, Cansu, Gioacchino, Emanuele, Vadgama, Disha, de Looper, Hans, Zink, Joke, ter Borg, Mariette N. D., Hoogenboezem, Remco, Havermans, Marije, Sanders, Mathijs A., Bindels, Eric, Dzierzak, Elaine, Touw, Ivo P., de Pater, Emma
Publicado 2023

Truncated CSF3 receptors induce pro‐inflammatory responses in severe congenital neutropenia

por Olofsen, Patricia A., Bosch, Dennis A., de Looper, Hans W. J., van Strien, Paulina M. H., Hoogenboezem, Remco M., Roovers, Onno, van der Velden, Vincent H. J., Bindels, Eric M. J., De Pater, Emma M., Touw, Ivo P.
Publicado 2022

Malignant Transformation Involving CXXC4 Mutations Identified in a Leukemic Progression Model of Severe Congenital Neutropenia

por Olofsen, Patricia A., Fatrai, Szabolcs, van Strien, Paulina M.H., Obenauer, Julia C., de Looper, Hans W.J., Hoogenboezem, Remco M., Erpelinck-Verschueren, Claudia A.J., Vermeulen, Michael P.W.M., Roovers, Onno, Haferlach, Torsten, Jansen, Joop H., Ghazvini, Mehrnaz, Bindels, Eric M.J., Schneider, Rebekka K., de Pater, Emma M., Touw, Ivo P.
Publicado 2020