Isoforms of the TAL1 transcription factor have different roles in hematopoiesis and cell growth
Sharma, Aveksha, Mistriel-Zerbib, Shani, Najar, Rauf Ahmad, Engal, Eden, Bentata, Mercedes, Taqatqa, Nadeen, Dahan, Sara, Cohen, Klil, Jaffe-Herman, Shiri, Geminder, Ophir, Baker, Mai, Nevo, Yuval, Plaschkes, Inbar, Kay, Gillian, Drier, Yotam, Berger, Michael, Salton, Maayan
Published in PLoS biology (28.06.2023)
Published in PLoS biology (28.06.2023)
Get full text
Journal Article
The spectrum of pre-mRNA splicing in autism
Engal, Eden, Zhang, Zhenwei, Geminder, Ophir, Jaffe-Herman, Shiri, Kay, Gillian, Ben-Hur, Asa, Salton, Maayan
Published in Wiley interdisciplinary reviews. RNA (01.03.2024)
Published in Wiley interdisciplinary reviews. RNA (01.03.2024)
Get more information
Journal Article
Bi-allelic loss-of-function variants in WBP4, encoding a spliceosome protein, result in a variable neurodevelopmental syndrome
Engal, Eden, Oja, Kaisa Teele, Maroofian, Reza, Geminder, Ophir, Le, Thuy-Linh, Marzin, Pauline, Guimier, Anne, Mor, Evyatar, Zvi, Naama, Elefant, Naama, Zaki, Maha S., Gleeson, Joseph G., Muru, Kai, Pajusalu, Sander, Wojcik, Monica H., Pachat, Divya, Elmaksoud, Marwa Abd, Chan Jeong, Won, Lee, Hane, Bauer, Peter, Zifarelli, Giovanni, Houlden, Henry, Daana, Muhannad, Elpeleg, Orly, Amiel, Jeanne, Lyonnet, Stanislas, Gordon, Christopher T., Harel, Tamar, Õunap, Katrin, Salton, Maayan, Mor-Shaked, Hagar
Published in American journal of human genetics (07.12.2023)
Published in American journal of human genetics (07.12.2023)
Get full text
Journal Article
DNMT3B splicing dysregulation mediated by SMCHD1 loss contributes to DUX4 overexpression and FSHD pathogenesis
Engal, Eden, Sharma, Aveksha, Aviel, Uria, Taqatqa, Nadeen, Juster, Sarah, Jaffe-Herman, Shiri, Bentata, Mercedes, Geminder, Ophir, Gershon, Adi, Lewis, Reyut, Kay, Gillian, Hecht, Merav, Epsztejn-Litman, Silvina, Gotkine, Marc, Mouly, Vincent, Eiges, Rachel, Salton, Maayan, Drier, Yotam
Published in Science advances (31.05.2024)
Published in Science advances (31.05.2024)
Get full text
Journal Article
Biallelic loss of function variants in WBP4 , encoding a spliceosome protein, result in a variable neurodevelopmental delay syndrome
Engal, Eden, Oja, Kaisa Teele, Maroofian, Reza, Geminder, Ophir, Le, Thuy-Linh, Mor, Evyatar, Tzvi, Naama, Elefant, Naama, Zaki, Maha S, Gleeson, Joseph G, Muru, Kai, Pajusalu, Sander, Wojcik, Monica H, Pachat, Divya, Elmaksoud, Marwa Abd, Jeong, Won Chan, Lee, Hane, Bauer, Peter, Zifarelli, Giovanni, Houlden, Henry, Elpeleg, Orly, Gordon, Chris, Harel, Tamar, Õunap, Katrin, Salton, Maayan, Mor-Shaked, Hagar
Published in medRxiv : the preprint server for health sciences (27.06.2023)
Get more information
Published in medRxiv : the preprint server for health sciences (27.06.2023)
Journal Article
Hematopoiesis and cell growth are differentially regulated by TAL1 isoforms
Sharma, Aveksha, Mistriel-Zerbib, Shani, Rauf Ahmad Najar, Eden Engal, Bentata, Mercedes, Taqatqa, Nadeen, Dahan, Sara, Cohen, Klil, Jaffe-Herman, Shiri, Ophir Geminder, Baker, Mai, Nevo, Yuval, Inbar Plaschkes, Kay, Gillian, Drier, Yotam, Berger, Michael, Salton, Maayan
Published in bioRxiv (26.12.2022)
Published in bioRxiv (26.12.2022)
Get full text
Paper