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Asymmetric spindle positioning.
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Asymmetrically distributed C. elegans homologs of AGS3/PINS control spindle position in the early embryo.
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Astral microtubule asymmetry provides directional cues for spindle positioning in budding yeast.
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The forces that position a mitotic spindle asymmetrically are tethered until after the time of spindle assembly.
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Spindle positioning during the asymmetric first cell division of Caenorhabditis elegans embryos.
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Mechanisms of spindle positioning.
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Polarized branched Actin modulates cortical mechanics to produce unequal-size daughters during asymmetric division.
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Microtubule organizing centers regulate spindle positioning in mouse oocytes.
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RAB14 GTPase is essential for actin-based asymmetric division during mouse oocyte maturation.
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Splitting the cell, building the organism: Mechanisms of cell division in metazoan embryos.
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Evidence for dynein and astral microtubule-mediated cortical release and transport of Gαi/LGN/NuMA complex in mitotic cells.
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Germline-specific MATH-BTB substrate adaptor MAB1 regulates spindle length and nuclei identity in maize.
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Cell cycle-regulated cortical dynein/dynactin promotes symmetric cell division by differential pole motion in anaphase.
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Unequal first cleavage in the Tubifex egg: involvement of a monastral mitotic apparatus.
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Cortical localization of the Galpha protein GPA-16 requires RIC-8 function during C. elegans asymmetric cell division.
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The Bud14p-Glc7p complex functions as a cortical regulator of dynein in budding yeast.
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Molecular control of cell polarity and asymmetric cell division in Drosophila neuroblasts.
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The protein kinase Kin4 inhibits exit from mitosis in response to spindle position defects.
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Kin4 kinase delays mitotic exit in response to spindle alignment defects.
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C. elegans HAM-1 positions the cleavage plane and regulates apoptosis in asymmetric neuroblast divisions.
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