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Biorxiv : the Preprint Server for Biology|May 22, 2023
Cryo-EM structures of both ends of the actin filament explain why the barbed end elongates faster than the pointed endSteven Z Chou, Thomas D PollardJournal of Molecular Biology|February 6, 2004
Identification of functionally important residues of Arp2/3 complex by analysis of homology models from diverse speciesChristopher C Beltzner, Thomas D PollardCell Structure and Function|October 1, 1996
The chemical mechanism of myosin-I: implications for actin-based motility and the evolution of the myosin family of motor proteinsT D Pollard, E M OstapMolecular Biology of the Cell|April 26, 2013
Separate roles of IQGAP Rng2p in forming and constricting the Schizosaccharomyces pombe cytokinetic contractile ringIrene R Tebbs, Thomas D PollardCell|February 26, 2003
Cellular motility driven by assembly and disassembly of actin filamentsThomas D Pollard, Gary G BorisyMuscle & Nerve|August 21, 2003
Neurophysiological changes in demyelinating and axonal forms of acute experimental autoimmune neuritis in the Lewis ratJude M Taylor, John D PollardJournal of Cell Science|November 15, 2002
Intracellular localization and dynamics of myosin-II and myosin-IC in live Acanthamoeba by transient transfection of EGFP fusion proteinsHyun-Hee Kong, Thomas D PollardThe Journal of Cell Biology|September 1, 1978
Evidence for actin filament-microtubule interaction mediated by microtubule-associated proteinsL M Griffith, T D PollardBiochemistry|December 18, 1984
Quantitative analysis of the effect of Acanthamoeba profilin on actin filament nucleation and elongationT D Pollard, J A CooperPageof 286