Correcting the aberrant Fanconi anemia transcriptional program by gene therapy

por Dror, Yigal
Publicado 2023

ERCC6L2‐associated inherited bone marrow failure syndrome

por Shabanova, Iren, Cohen, Elisa, Cada, Michaela, Vincent, Ajoy, Cohn, Ronald D., Dror, Yigal
Publicado 2018

The Use of Induced Pluripotent Stem Cells to Study the Effects of Adenosine Deaminase Deficiency on Human Neutrophil Development

por Tsui, Michael, Min, Weixian, Ng, Stephanie, Dobbs, Kerry, Notarangelo, Luigi D., Dror, Yigal, Grunebaum, Eyal
Publicado 2021

Reanalysing genomic data by normalized coverage values uncovers CNVs in bone marrow failure gene panels

por Lauhasurayotin, Supanun, Cuvelier, Geoff D., Klaassen, Robert J., Fernandez, Conrad V., Pastore, Yves D., Abish, Sharon, Rayar, Meera, Steele, MacGregor, Jardine, Lawrence, Breakey, Vicky R., Brossard, Josee, Sinha, Roona, Silva, Mariana, Goodyear, Lisa, Lipton, Jeffrey H., Michon, Bruno, Corriveau-Bourque, Catherine, Sung, Lillian, Shabanova, Iren, Li, Hongbing, Zlateska, Bozana, Dhanraj, Santhosh, Cada, Michaela, Scherer, Stephen W., Dror, Yigal
Publicado 2019

The clinical impact of copy number variants in inherited bone marrow failure syndromes

por Waespe, Nicolas, Dhanraj, Santhosh, Wahala, Manju, Tsangaris, Elena, Enbar, Tom, Zlateska, Bozana, Li, Hongbing, Klaassen, Robert J., Fernandez, Conrad V., Cuvelier, Geoff D. E., Wu, John K., Pastore, Yves D., Silva, Mariana, Lipton, Jeffrey H., Brossard, Joseé, Michon, Bruno, Abish, Sharon, Steele, MacGregor, Sinha, Roona, Belletrutti, Mark J., Breakey, Vicky R., Jardine, Lawrence, Goodyear, Lisa, Kofler, Liat, Cada, Michaela, Sung, Lillian, Shago, Mary, Scherer, Stephen W., Dror, Yigal
Publicado 2017