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Science (New York, N.Y.)|December 17, 2013
Genome-scale CRISPR-Cas9 knockout screening in human cellsOphir Shalem, Neville E Sanjana, Ella Hartenian, et al.Plos One|May 3, 2014
Loss of function of TET2 cooperates with constitutively active KIT in murine and human models of mastocytosisSerena De Vita, Rebekka K Schneider, Michael Garcia, et al.Nature|January 19, 2008
Identification of RPS14 as a 5q- syndrome gene by RNA interference screenBenjamin L Ebert, Jennifer Pretz, Jocelyn Bosco, et al.EMBO Molecular Medicine|March 8, 2017
Deletion of ribosomal protein genes is a common vulnerability in human cancer, especially in concert with TP53 mutationsRam Ajore, David Raiser, Marie McConkey, et al.British Journal of Haematology|April 1, 2022
Evolution of severe (transfusion-dependent) anaemia in myelodysplastic syndromes with 5q deletion is characterized by a macrophage-associated failure of the eythropoietic nicheGuntram Buesche, Huesniye Teoman, Rebekka K Schneider, et al.The Journal of Clinical Investigation|September 7, 2016
Functionally identifiable apoptosis-insensitive subpopulations determine chemoresistance in acute myeloid leukemiaPatrick D Bhola, Brenton G Mar, R Coleman Lindsley, et al.Blood|March 4, 2010
The Apc(min) mouse has altered hematopoietic stem cell function and provides a model for MPD/MDSSteven W Lane, Stephen M Sykes, Fatima Al-Shahrour, et al.Blood|November 12, 2010
Haploinsufficiency for ribosomal protein genes causes selective activation of p53 in human erythroid progenitor cellsShilpee Dutt, Anupama Narla, Katherine Lin, et al.Proceedings of the National Academy of Sciences of the United States of America|October 4, 2005
Gene set enrichment analysis: a knowledge-based approach for interpreting genome-wide expression profilesAravind Subramanian, Pablo Tamayo, Vamsi K Mootha, et al.Science (New York, N.Y.)|October 15, 2011
Correction of sickle cell disease in adult mice by interference with fetal hemoglobin silencingJian Xu, Cong Peng, Vijay G Sankaran, et al.Pageof 35