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Resuscitation|June 23, 2024
Analysis during chest compressions in out-of-hospital cardiac arrest patients, a cross/sectional study: The DEFI 2022 studyClément Derkenne, Benoit Frattini, Sarah Menetre, et al.
Nature Genetics|July 17, 2007
Osteoclast-poor human osteopetrosis due to mutations in the gene encoding RANKLCristina Sobacchi, Annalisa Frattini, Matteo M Guerrini, et al.
Iscience|April 18, 2024
Type I interferon regulation by USP18 is a key vulnerability in cancerVeronica Jové, Heather Wheeler, Chiachin Wilson Lee, et al.
Scientific Reports|May 27, 2021
The climatic and genetic heritage of Italian goat breeds with genomic SNP dataMatteo Cortellari, Mario Barbato, Andrea Talenti, et al.
The Lancet. Haematology|March 9, 2020
Enasidenib in patients with mutant IDH2 myelodysplastic syndromes: a phase 1 subgroup analysis of the multicentre, AG221-C-001 trialEytan M Stein, Amir T Fathi, Courtney D DiNardo, et al.
Nature Genetics|June 9, 2016
Clonal evolution of glioblastoma under therapyJiguang Wang, Emanuela Cazzato, Erik Ladewig, et al.
Proceedings of the National Academy of Sciences of the United States of America|January 30, 2026
Quantum benchmarking of high-fidelity noise-biased operations on a detuned Kerr-cat qubitBingcheng Qing, Ahmed Hajr, Ke Wang, et al.
American Journal of Human Genetics|July 9, 2008
Human osteoclast-poor osteopetrosis with hypogammaglobulinemia due to TNFRSF11A (RANK) mutationsMatteo M Guerrini, Cristina Sobacchi, Barbara Cassani, et al.
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