生物發育新知特論一 Jui-Chou Hsu

This is a course to discuss the latest advance in the field of cell and developmental biology using mice, Xenopus, Drosophila, and C elegans as model organisms.

(1) Epithelial junctions maintain tissue architecture by directing planar spindle orientation. Nature. 500, 359, 2013.
(2) Oskar Is Targeted for Degradation by the Sequential Action of Par-1, GSK-3, and the SCF-Slimb Ubiquitin Ligase. Developmental Cell 26, 303, 2013.
(3) Microtubule Polarity Predicts Direction of Egg Chamber Rotation in Drosophila. Current Biology 23, 1472, 2013.
(4) Vesicles modulate an actin network for asymmetric spindle positioning. NATURE CELL BIOLOG. 15, 937, 2013.
(5) Apical domain polarization localizes actin_myosin activity to drive ratchet-like apical constriction. NATURE CELL BIOLOG. 15, 926, 2013.
(6) Oscillation and Polarity of E-Cadherin Asymmetries Control Actomyosin Flow Patterns during Morphogenesis. Developmental Cell 26, 162, 2013.
(7) Chase-and-run between adjacent cell populations promotes directional collective migration. NATURE CELL BIOLOG. 15, 763, 2013.
(8) Coordinated waves of actomyosin flow and apical cell constriction immediately after wounding. J. Cell Biol. 202, 365, 2013.
(9) In vitro contraction of cytokinetic ring depends on myosin II but not on actin dynamics. NATURE CELL BIOLOG. 15,853, 2013.
(10) Dynamic microtubules produce an asymmetric E-cadherin–Bazooka complex to maintain segment boundaries. J. Cell Biol. 201, 887, 2013.
(11) PTEN Controls Junction Lengthening and Stability during Cell Rearrangement in Epithelial Tissue. Developmental Cell 25, 1, 2013.
(12) Binding to F-actin guides cadherin cluster assembly, stability, and movement. J. Cell Biol. 201, 131, 2013.