Search alternatives:
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
2 step » _ step (Expand Search), a step (Expand Search)
step decrease » sizes decrease (Expand Search), teer decrease (Expand Search), we decrease (Expand Search)
nn decrease » _ decrease (Expand Search), gy decreased (Expand Search), b1 decreased (Expand Search)
a decrease » _ decrease (Expand Search), _ decreased (Expand Search), _ decreases (Expand Search)
2 step » _ step (Expand Search), a step (Expand Search)
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6661
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6662
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6663
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6664
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6665
Identification of +TIPs required for MT plus-end targeting of dynein-dynactin in the <i>C</i>. <i>elegans</i> early embryo.
Published 2017“…<b>(C)</b> Cortical confocal section in one-cell embryos co-expressing GFP::p50<sup>DNC-2</sup> and EBP-2::mKate2, showing that depletion of dynein intermediate chain<sup>DYCI-1</sup> or LIS-1 decreases dynactin levels at MT plus ends. …”
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6666
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6667
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6668
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6669
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6670
Image_1_Eph-ephrin Signaling Affects Eye Lens Fiber Cell Intracellular Voltage and Membrane Conductance.TIF
Published 2021“…Immunostaining revealed changes in connexin 50 (Cx50) subcellular localization in EphA2<sup>–/–</sup> peripheral lens fibers and alteration in aquaporin 0 (Aqp0) staining patterns in ephrin-A5<sup>–/–</sup> and EphA2<sup>–/–</sup> inner mature fiber cells. …”
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6671
Disorder–Order Structural Transformation in Electron-Poor Sr<sub>3</sub>Au<sub>8</sub>Sn<sub>3</sub> Driven by Chemical Bonding Optimization
Published 2013“…Single-crystal X-ray diffraction analyses revealed that Sr<sub>3</sub>Au<sub>8</sub>Sn<sub>3</sub> has a La<sub>3</sub>Al<sub>11</sub>-type <i>Immm</i> structure (<i>a</i> = 4.6767(8) Å, <i>b</i> = 9.646(2) Å, <i>c</i> = 14.170(2) Å, <i>Z</i> = 2) if annealed at 550 °C and above but a Ca<sub>3</sub>Au<sub>8</sub>Ge<sub>3</sub>-type structure (<i>Pnnm</i>, <i>a</i> = 9.6082(8) Å, <i>b</i> = 14.171(1) Å, <i>c</i> = 4.6719(4) Å, <i>Z</i> = 2) if annealed at 400 °C. …”
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6672
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6673
Saturation Kinetics in Phenolic O–H Bond Oxidation by a Mononuclear Mn(III)–OH Complex Derived from Dioxygen
Published 2014“…The mononuclear hydroxomanganese(III) complex, [Mn<sup>III</sup>(OH)(dpaq)]<sup>+</sup>, which is supported by the amide-containing N<sub>5</sub> ligand dpaq (dpaq = 2-[bis(pyridin-2-ylmethyl)]amino-<i>N</i>-quinolin-8-yl-acetamidate) was generated by treatment of the manganese(II) species, [Mn<sup>II</sup>(dpaq)](OTf), with dioxygen in acetonitrile solution at 25 °C. …”
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6674
Saturation Kinetics in Phenolic O–H Bond Oxidation by a Mononuclear Mn(III)–OH Complex Derived from Dioxygen
Published 2014“…The mononuclear hydroxomanganese(III) complex, [Mn<sup>III</sup>(OH)(dpaq)]<sup>+</sup>, which is supported by the amide-containing N<sub>5</sub> ligand dpaq (dpaq = 2-[bis(pyridin-2-ylmethyl)]amino-<i>N</i>-quinolin-8-yl-acetamidate) was generated by treatment of the manganese(II) species, [Mn<sup>II</sup>(dpaq)](OTf), with dioxygen in acetonitrile solution at 25 °C. …”
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6675
Engineering of p150<sup>DNC-1</sup> mutants for functional characterization of dynactin's MT binding activity.
Published 2017“…<p><b>(A)</b> Cartoon of the dynactin complex and its interaction with MTs and end-binding protein (EB). …”
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6676
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6677
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6678
The C-terminal tyrosine of α-tubulin is required for centration/rotation of the nucleus-centrosome complex but not for MT tip tracking of dynactin.
Published 2017“…<b>(I)</b> <i>(left)</i> Cortical confocal section of a control and <i>tba-1/2(YA/YA)</i> one-cell embryo in metaphase expressing GFP::p50<sup>DNC-2</sup>. …”
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6679
Morphological schematic diagram of <i>A</i>. <i>Adenophora</i>.
Published 2024“…The phytochemical variability of the extracts was also studied. The LC<sub>50</sub> value of the <i>A</i>. <i>adenophora</i> extract against <i>L</i>. …”
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6680