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Blood|June 21, 2019
Germline mutations in the transcription factor IKZF5 cause thrombocytopeniaClaire Lentaigne, Daniel Greene, Suthesh Sivapalaratnam, et al.Science (New York, N.Y.)|July 20, 2021
Accurate prediction of protein structures and interactions using a three-track neural networkMinkyung Baek, Frank DiMaio, Ivan Anishchenko, et al.Structure (London, England : 1993)|June 23, 2015
Outcome of the First wwPDB Hybrid/Integrative Methods Task Force WorkshopAndrej Sali, Helen M Berman, Torsten Schwede, et al.Nature Genetics|October 3, 2006
Mutations in FRMD7, a newly identified member of the FERM family, cause X-linked idiopathic congenital nystagmusPatrick Tarpey, Shery Thomas, Nagini Sarvananthan, et al.Structure (London, England : 1993)|April 7, 2016
Outcome of the First wwPDB/CCDC/D3R Ligand Validation WorkshopPaul D Adams, Kathleen Aertgeerts, Cary Bauer, et al.Science (New York, N.Y.)|September 27, 2014
Transcriptional diversity during lineage commitment of human blood progenitorsLu Chen, Myrto Kostadima, Joost H A Martens, et al.Research Square|February 12, 2024
Outcomes of the EMDataResource Cryo-EM Ligand Modeling ChallengeCatherine L Lawson, Andriy Kryshtafovych, Grigore D Pintilie, et al.Nature Methods|June 25, 2024
Outcomes of the EMDataResource cryo-EM Ligand Modeling ChallengeCatherine L Lawson, Andriy Kryshtafovych, Grigore D Pintilie, et al.Acta Crystallographica. Section D, Structural Biology|June 1, 2023
The CCP4 suite: integrative software for macromolecular crystallographyJon Agirre, Mihaela Atanasova, Haroldas Bagdonas, et al.Pageof 17