Not logged in Share Save
Share Save
Share Save
Share Save
Cohesin haploinsufficiency is tolerated in Cbfb :: MYH11-driven murine acute myeloid leukemia Conneely, Shannon E.; Quezada, Alexis; Kurtz, Kristen J.; Zhang, Nenggang; de la Fuente, Josephine; Mercer, Nesa; Rogers, Jason H.; Aguilar, Rogelio; Medrano, Geraldo; Goodell, Margaret A.; Liu, Paul P.; Pati, Debananda; Rau, Rachel E. Share Save
CBFβ-SMMHC-driven leukemogenesis requires enhanced RUNX1-DNA binding affinity in mice Zhen, Tao; Cao, Yaqiang; Dou, Tongyi; Chen, Yun; Lopez, Guadalupe; Menezes, Ana catarina; Wu, Xufeng; Hammer, John A.; Cheng, Jun; Garrett, Lisa; Anderson, Stacie; Kirby, Martha; Wincovitch, Stephen; Sisay, Bayu; Elkahloun, Abdel G.; Wu, Di; Castilla, Lucio H.; Yang, Wei; Jiang, Jiansen; Zhao, Keji; Liu, P. Paul Share Save
Share Save
Genetic testing to identify hereditary predispositions to haematological malignancy is critical prior to allogenic haematopoietic cell transplant Kajdic, Amra; Deuitch, Natalie T.; Bresciani, Erica; Davis, Joie; Craft, Kathleen; Chong, Shawn; Liu, Yi; Young, David J.; Kanakry, Christopher G.; Cunningham, Lea; Liu, Paul Share Save
Single Cell Transcriptome Analysis of CD34+Cells from Patients with RUNX1-Fpdmm at Different Stages of Disease Progression Bresciani, Erica; Capaldo, Bian J.; Kajdic, Amra; Deuitch, Natalie T.; Craft, Kathleen; Chong, Shawn; Elkahloun, Abdel G.; Park, Morgan; Young, Alice; Young, David J.; Meerzaman, Daoud; Chen, Qingrong; Liu, Paul P. Share Save
Evaluation of Permanent Nipple-Areolar Complex Sensitivity Loss Following Reduction Mammaplasty Francalancia, Stephanie; Lou, Mary; McIntire, Damon; Sobti, Nikhil; Barrow, Brooke; Marquez-Garcia, Josue; Kwan, Daniel; Sullivan, Rachel; Liu, Paul; Breuing, Karl Share Save
Genomic landscape of patients with germline RUNX1 variants and familial platelet disorder with myeloid malignancy Yu, Kai; Deuitch, Natalie; Merguerian, Matthew; Cunningham, Lea; Davis, Joie; Bresciani, Erica; Diemer, Jamie; Andrews, Elizabeth; Young, Alice; Donovan, Frank; Sood, Raman; Craft, Kathleen; Chong, Shawn; Chandrasekharappa, Settara; Mullikin, Jim; Liu, Paul P. Share Save
Runx1-R188Q germ line mutation induces inflammation and predisposition to hematologic malignancies in mice Ahmad, Mohd Hafiz; Hegde, Mahesh; Wong, Waihay J.; Mohammadhosseini, Mona; Garrett, Lisa; Carrascoso, Anneliese; Issac, Neethu; Ebert, Benjamin; Silva, Jeffrey C.; Pihan, German; Zhu, Lihua J.; Wolfe, Scot A.; Agarwal, Anupriya; Liu, P. Paul; Castilla, Lucio H. Share Save
Somatic mutational landscape of hereditary hematopoietic malignancies caused by germline variants in RUNX1, GATA2, and DDX41 Homan, Claire C.; Drazer, Michael W.; Yu, Kai; Lawrence, David M.; Feng, Jinghua; Arriola-Martinez, Luis; Pozsgai, Matthew J.; Mcneely, Kelsey E.; Ha, Thuong; Venugopal, Parvathy; Arts, Peer; King-Smith, Sarah L.; Cheah, Jesse; Armstrong, Mark; Wang, Paul; Bodor, Csaba; Cantor, Alan B.; Cazzola, Mario; Degelman, Erin; Dinardo, Courtney D.; Duployez, Nicolas; Favier, Remi; Froehling, Stefan; Rio-Machin, Ana; Klco, Jeffery M.; Kraemer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil, V; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P.; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Kim, Erika; NISC Comparative Sequencing Program, Amy P.; Hsu, Amy P.; Holland, Steven M.; Phillips, Kerry; Poplawski, Nicola K.; Babic, Milena; Wei, Andrew H.; Forsyth, Cecily; Fan, Helen Mar; Lewis, Ian D.; Cooney, Julian; Susman, Rachel; Fox, Lucy C.; Blombery, Piers; Singhal, Deepak; Hiwase, Devendra; Phipson, Belinda; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Liu, Paul; Godley, Lucy A.; Brown, Anna L. Share Save
SOX9 is a key component of RUNX2-regulated transcriptional circuitry in osteosarcoma Kim, Young-Im; Tseng, Yu-Chou; Ayaz, Gamze; Wang, Shasha; Yan, Hualong; du Bois, Wendy; Yang, Howard; Zhen, Tao; Lee, Maxwell P. P.; Liu, Paul; Kaplan, Rosandra N.; Huang, Jing Share Save
Share Save
Share Save
Share Save
Redundant mechanisms driven independently by RUNX1 and GATA2 for hematopoietic development Bresciani, Erica; Carrington, Blake; Yu, Kai; Kim, Erika M.; Zhen, Tao; Guzman, Victoria Sanchez; Broadbridge, Elizabeth; Bishop, Kevin; Kirby, Martha; Harper, Ursula; Wincovitch, Stephen; Dell'Orso, Stefania; Sartorelli, Vittorio; Sood, Raman; Liu, Paul Share Save
Germline RUNX1 variation and predisposition to childhood acute lymphoblastic leukemia Li, Yizhen; Yang, Wentao; Devidas, Meenakshi; Winter, Stuart S.; Kesserwan, Chimene; Yang, Wenjian; Dunsmore, Kimberly P.; Smith, Colton; Qian, Maoxiang; Zhao, Xujie; Zhang, Ranran; Gastier-Foster, Julie M.; Raetz, Elizabeth A.; Carroll, William L.; Li, Chunliang; Liu, Paul P.; Rabin, Karen R.; Sanda, Takaomi; Mullighan, Charles G.; Nichols, Kim E.; Evans, William E.; Pui, Ching-Hon; Hunger, Stephen P.; Teachey, David T.; Relling, Mary, V; Loh, Mignon L.; Yang, Jun J. Share Save
The RUNX1 database (RUNX1db): establishment of an expert curated RUNX1 registry and genomics database as a public resource for familial platelet disorder with myeloid malignancy Homan, Claire C.; King-Smith, Sarah L.; Lawrence, David M.; Arts, Peer; Feng, Jinghua; Andrews, James; Armstrong, Mark; Ha, Thuong; Dobbins, Julia; Drazer, Michael W.; Yu, Kai; Bodor, Csaba; Cantor, Alan; Cazzola, Mario; Degelman, Erin; DiNardo, Courtney D.; Duployez, Nicolas; Favier, Remi; Frohling, Stefan; Fitzgibbon, Jude; Klco, Jeffery M.; Kramer, Alwin; Kurokawa, Mineo; Lee, Joanne; Malcovati, Luca; Morgan, Neil V.; Natsoulis, Georges; Owen, Carolyn; Patel, Keyur P.; Preudhomme, Claude; Raslova, Hana; Rienhoff, Hugh; Ripperger, Tim; Schulte, Rachael; Tawana, Kiran; Velloso, Elvira; Yan, Benedict; Liu, Paul; Godley, Lucy A.; Schreiber, Andreas W.; Hahn, Christopher N.; Scott, Hamish S.; Brown, Anna L. Share Save