Wagenblast, Elvin, Araújo, Joana, Gan, Olga I., Cutting, Sarah K., Murison, Alex, Krivdova, Gabriela, Azkanaz, Maria, McLeod, Jessica L., Smith, Sabrina A., Gratton, Blaise A., Marhon, Sajid A., Gabra, Martino, Medeiros, Jessie J. F., Manteghi, Sanaz, Chen, Jian, Chan-Seng-Yue, Michelle, Garcia-Prat, Laura, Salmena, Leonardo, De Carvalho, Daniel D., Abelson, Sagi, Abdelhaleem, Mohamed, Chong, Karen, Roifman, Maian, Shannon, Patrick, Wang, Jean C. Y., Hitzler, Johann K., Chitayat, David, Dick, John E., Lechman, Eric R. (2021) Mapping the cellular origin and early evolution of leukemia in Down syndrome. Science, 373 (6551) doi:10.1126/science.abf6202

See Also

These are possibly similar items as determined by title/reference text matching only.

	Wagenblast, Elvin, Azkanaz, Maria, Smith, Sabrina A., Shakib, Lorien, McLeod, Jessica L., Krivdova, Gabriela, Araújo, Joana, Shultz, Leonard D., Gan, Olga I., Dick, John E., Lechman, Eric R. (2019) Functional profiling of single CRISPR/Cas9-edited human long-term hematopoietic stem cells. Nature Communications, 10. doi:10.1038/s41467-019-12726-0
	Shlush, Liran I., Mitchell, Amanda, Heisler, Lawrence, Abelson, Sagi, Ng, Stanley W. K., Trotman-Grant, Aaron, Medeiros, Jessie J. F., Rao-Bhatia, Abilasha, Jaciw-Zurakowsky, Ivana, Marke, Rene, McLeod, Jessica L., Doedens, Monica, Bader, Gary, Voisin, Veronique, Xu, ChangJiang, McPherson, John D., Hudson, Thomas J., Wang, Jean C. Y., Minden, Mark D., Dick, John E. (2017) Tracing the origins of relapse in acute myeloid leukaemia to stem cells. Nature, 547 (7661). 104-108 doi:10.1038/nature22993
	Shlush, Liran I., Zandi, Sasan, Mitchell, Amanda, Chen, Weihsu Claire, Brandwein, Joseph M., Gupta, Vikas, Kennedy, James A., Schimmer, Aaron D., Schuh, Andre C., Yee, Karen W., McLeod, Jessica L., Doedens, Monica, Medeiros, Jessie J. F., Marke, Rene, Kim, Hyeoung Joon, Lee, Kwon, McPherson, John D., Hudson, Thomas J., Pan-Leukemia Gene Panel Consortium, The HALT, Brown, Andrew M. K., Yousif, Fouad, Trinh, Quang M., Stein, Lincoln D., Minden, Mark D., Wang, Jean C. Y., Dick, John E. (2014) Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia. Nature, 506 (7488). 328-333 doi:10.1038/nature13038
	Shlush, Liran I., Zandi, Sasan, Mitchell, Amanda, Chen, Weihsu Claire, Brandwein, Joseph M., Gupta, Vikas, Kennedy, James A., Schimmer, Aaron D., Schuh, Andre C., Yee, Karen W., McLeod, Jessica L., Doedens, Monica, Medeiros, Jessie J. F., Marke, Rene, Kim, Hyeoung Joon, Lee, Kwon, McPherson, John D., Hudson, Thomas J., Pan-Leukemia Gene Panel Consortium, The HALT, Brown, Andrew M. K., Yousif, Fouad, Trinh, Quang M., Stein, Lincoln D., Minden, Mark D., Wang, Jean C. Y., Dick, John E. (2014) Erratum: Corrigendum: Identification of pre-leukaemic haematopoietic stem cells in acute leukaemia. Nature, 508 (7496). 420 doi:10.1038/nature13190
	Mehdipour, Parinaz, Marhon, Sajid A., Ettayebi, Ilias, Chakravarthy, Ankur, Hosseini, Amir, Wang, Yadong, de Castro, Fabíola Attié, Yau, Helen Loo, Ishak, Charles, Abelson, Sagi, O’Brien, Catherine A., De Carvalho, Daniel D. (2021) Publisher Correction: Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency. Nature, 591 (7850). doi:10.1038/s41586-021-03329-1
	Mehdipour, Parinaz, Marhon, Sajid A., Ettayebi, Ilias, Chakravarthy, Ankur, Hosseini, Amir, Wang, Yadong, de Castro, Fabíola Attié, Loo Yau, Helen, Ishak, Charles, Abelson, Sagi, O’Brien, Catherine A., De Carvalho, Daniel D. (2020) Epigenetic therapy induces transcription of inverted SINEs and ADAR1 dependency. Nature, 588 (7836) 169-173 doi:10.1038/s41586-020-2844-1
	Nusinovich, Yevgeniya (2021) Down with leukemia. Science, 373 (6551) 175-177 doi:10.1126/science.373.6551.175-n
	Hughes, Joel J., Alkhunaizi, Ebba, Kruszka, Paul, Pyle, Louise C., Grange, Dorothy K., Berger, Seth I., Payne, Katelyn K., Masser-Frye, Diane, Hu, Tommy, Christie, Michelle R., Clegg, Nancy J., Everson, Joshua L., Martinez, Ariel F., Walsh, Laurence E., Bedoukian, Emma, Jones, Marilyn C., Harris, Catharine Jean, Riedhammer, Korbinian M., Choukair, Daniela, Fechner, Patricia Y., Rutter, Meilan M., Hufnagel, Sophia B., Roifman, Maian, Kletter, Gad B., Delot, Emmanuele, Vilain, Eric, Lipinski, Robert J., Vezina, Chad M., Muenke, Maximilian, Chitayat, David (2020) Loss-of-Function Variants in PPP1R12A: From Isolated Sex Reversal to Holoprosencephaly Spectrum and Urogenital Malformations. The American Journal of Human Genetics, 106 (1) 121-128 doi:10.1016/j.ajhg.2019.12.004
	Notta, F., Zandi, S., Takayama, N., Dobson, S., Gan, O. I., Wilson, G., Kaufmann, K. B., McLeod, J., Laurenti, E., Dunant, C. F., McPherson, J. D., Stein, L. D., Dror, Y., Dick, J. E. (2016) Distinct routes of lineage development reshape the human blood hierarchy across ontogeny. Science, 351 (6269). doi:10.1126/science.aab2116
	Smith, F. Donelson, Esseltine, Jessica L., Nygren, Patrick J., Veesler, David, Byrne, Dominic P., Vonderach, Matthias, Strashnov, Ilya, Eyers, Claire E., Eyers, Patrick A., Langeberg, Lorene K., Scott, John D. (2017) Local protein kinase A action proceeds through intact holoenzymes. Science, 356 (6344). 1288-1293 doi:10.1126/science.aaj1669
	Merico, Daniele, Roifman, Maian, Braunschweig, Ulrich, Yuen, Ryan K. C., Alexandrova, Roumiana, Bates, Andrea, Reid, Brenda, Nalpathamkalam, Thomas, Wang, Zhuozhi, Thiruvahindrapuram, Bhooma, Gray, Paul, Kakakios, Alyson, Peake, Jane, Hogarth, Stephanie, Manson, David, Buncic, Raymond, Pereira, Sergio L., Herbrick, Jo-Anne, Blencowe, Benjamin J., Roifman, Chaim M., Scherer, Stephen W. (2015) Compound heterozygous mutations in the noncoding RNU4ATAC cause Roifman Syndrome by disrupting minor intron splicing. Nature Communications, 6. doi:10.1038/ncomms9718