4,855 research outputs found

    The canonical genus for Whitehead doubles of a family of alternating knots

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    For any given integer r1r \geq 1 and a quasitoric braid βr=(σrϵσr1ϵ...\beta_r=(\sigma_r^{-\epsilon} \sigma_{r-1}^{\epsilon}... σ1(1)rϵ)3 \sigma_{1}^{(-1)^{r}\epsilon})^3 with ϵ=±1\epsilon=\pm 1, we prove that the maximum degree in zz of the HOMFLYPT polynomial PW2(β^r)(v,z)P_{W_2(\hat\beta_r)}(v,z) of the doubled link W2(β^r)W_2(\hat\beta_r) of the closure β^r\hat\beta_r is equal to 6r16r-1. As an application, we give a family K3\mathcal K^3 of alternating knots, including (2,n)(2,n) torus knots, 2-bridge knots and alternating pretzel knots as its subfamilies, such that the minimal crossing number of any alternating knot in K3\mathcal K^3 coincides with the canonical genus of its Whitehead double. Consequently, we give a new family K3\mathcal K^3 of alternating knots for which Tripp's conjecture holds.Comment: 33 pages, 27 figure

    Roles of Primary Cilia in the Developing Brain

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    Essential to development, primary cilia are microtubule-based cellular organelles that protrude from the surface of cells. Acting as cellular antenna, primary cilia play central roles in transducing or regulating several signaling pathways, including Sonic hedgehog (Shh) and Wnt signaling. Defects in primary cilia contribute to a group of syndromic disorders known as “ciliopathies” and can adversely affect development of the brain and other essential organs, including the kidneys, eyes, and liver. The molecular mechanisms of how defective primary cilia contribute to neurological defects, however, remain poorly understood. In this mini review, we summarize recent advances in understanding of the interactions between primary cilia and signaling pathways essential to cellular homeostasis and brain development
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