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BMC Evolutionary Biology|January 12, 2013
Consistent mutational paths predict eukaryotic thermostabilityVera van Noort, Bettina Bradatsch, Manimozhiyan Arumugam, et al.Science (New York, N.Y.)|November 3, 2012
Synchronizing nuclear import of ribosomal proteins with ribosome assemblyDieter Kressler, Gert Bange, Yutaka Ogawa, et al.Molecular Biology of the Cell|May 10, 2011
Signal sequence-independent SRP-SR complex formation at the membrane suggests an alternative targeting pathway within the SRP cycleDavid Braig, Miryana Mircheva, Ilie Sachelaru, et al.Nature|February 27, 2004
Structure of the signal recognition particle interacting with the elongation-arrested ribosomeMario Halic, Thomas Becker, Martin R Pool, et al.Nucleic Acids Research|December 30, 2022
Two modes of Cue2-mediated mRNA cleavage with distinct substrate recognition initiate no-go decayShota Tomomatsu, Atsuya Watanabe, Petr Tesina, et al.Elife|May 31, 2017
The force-sensing peptide VemP employs extreme compaction and secondary structure formation to induce ribosomal stallingTing Su, Jingdong Cheng, Daniel Sohmen, et al.Chemical Communications (Cambridge, England)|July 17, 2018
ALKBH5-induced demethylation of mono- and dimethylated adenosineTimm T Ensfelder, Matthias Q Kurz, Katharina Iwan, et al.Nature Microbiology|September 5, 2018
Structure of a hibernating 100S ribosome reveals an inactive conformation of the ribosomal protein S1Bertrand Beckert, Martin Turk, Andreas Czech, et al.Molecular Cell|August 2, 2002
90S pre-ribosomes include the 35S pre-rRNA, the U3 snoRNP, and 40S subunit processing factors but predominantly lack 60S synthesis factorsPaola Grandi, Vladimir Rybin, Jochen Bassler, et al.Cell Research|February 27, 2025
Structural insights into spliceosome fidelity: DHX35-GPATCH1- mediated rejection of aberrant splicing substratesYi Li, Paulina Fischer, Mengjiao Wang, et al.Pageof 33