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Träfflista för sökning "(L773:0036 8075 OR L773:1095 9203) lar1:(liu) srt2:(2015-2019)"

Sökning: (L773:0036 8075 OR L773:1095 9203) lar1:(liu) > (2015-2019)

  • Resultat 1-9 av 9
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1.
  • Anderson, Christopher P., et al. (författare)
  • Electrical and optical control of single spins integrated in scalable semiconductor devices
  • 2019
  • Ingår i: Science. - : AMER ASSOC ADVANCEMENT SCIENCE. - 0036-8075 .- 1095-9203. ; 366:6470, s. 1225-
  • Tidskriftsartikel (refereegranskat)abstract
    • Spin defects in silicon carbide have the advantage of exceptional electron spin coherence combined with a near-infrared spin-photon interface, all in a material amenable to modern semiconductor fabrication. Leveraging these advantages, we integrated highly coherent single neutral divacancy spins in commercially available p-i-n structures and fabricated diodes to modulate the local electrical environment of the defects. These devices enable deterministic charge-state control and broad Stark-shift tuning exceeding 850 gigahertz. We show that charge depletion results in a narrowing of the optical linewidths by more than 50-fold, approaching the lifetime limit. These results demonstrate a method for mitigating the ubiquitous problem of spectral diffusion in solid-state emitters by engineering the electrical environment while using classical semiconductor devices to control scalable, spin-based quantum systems.
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2.
  • Barbier, Estelle, et al. (författare)
  • A molecular mechanism for choosing alcohol over an alternative reward
  • 2018
  • Ingår i: Science. - : American Association for the Advancement of Science (AAAS). - 0036-8075 .- 1095-9203. ; 360:6395
  • Tidskriftsartikel (refereegranskat)abstract
    • Alcohol addiction leads to increased choice of alcohol over healthy rewards. We established an exclusive choice procedure in which similar to 15% of outbred rats chose alcohol over a high-value reward. These animals displayed addiction-like traits, including high motivation to obtain alcohol and pursuit of this drug despite adverse consequences. Expression of the g-aminobutyric acid (GABA) transporter GAT-3 was selectively decreased within the amygdala of alcohol-choosing rats, whereas a knockdown of this transcript reversed choice preference of rats that originally chose a sweet solution over alcohol. GAT-3 expression was selectively decreased in the central amygdala of alcohol-dependent people compared to those who died of unrelated causes. Impaired GABA clearance within the amygdala contributes to alcohol addiction, appears to translate between species, and may offer targets for new pharmacotherapies for treating this disorder.
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3.
  • Berggren, Magnus, 1968-, et al. (författare)
  • How conducting polymer electrodes operate
  • 2019
  • Ingår i: Science. - Washington, DC, United States : American Association for the Advancement of Science (A A A S). - 0036-8075 .- 1095-9203. ; 364:6437, s. 233-234
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)abstract
    • n/a
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4.
  • Gallardo, Rodrigo, et al. (författare)
  • De novo design of a biologically active amyloid
  • 2016
  • Ingår i: Science. - : AMER ASSOC ADVANCEMENT SCIENCE. - 0036-8075 .- 1095-9203. ; 354:6313, s. 720-
  • Tidskriftsartikel (refereegranskat)abstract
    • Most human proteins possess amyloidogenic segments, but only about 30 are associated with amyloid-associated pathologies, and it remains unclear what determines amyloid toxicity. We designed vascin, a synthetic amyloid peptide, based on an amyloidogenic fragment of vascular endothelial growth factor receptor 2 (VEGFR2), a protein that is not associated to amyloidosis. Vascin recapitulates key biophysical and biochemical characteristics of natural amyloids, penetrates cells, and seeds the aggregation of VEGFR2 through direct interaction. We found that amyloid toxicity is observed only in cells that both express VEGFR2 and are dependent on VEGFR2 activity for survival. Thus, amyloid toxicity here appears to be both protein-specific and conditional-determined by VEGFR2 loss of function in a biological context in which target protein function is essential.
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5.
  • Hemmungs Wirtén, Eva (författare)
  • The making and remaking of Marie Curie
  • 2017
  • Ingår i: Science. - : AMER ASSOC ADVANCEMENT SCIENCE. - 0036-8075 .- 1095-9203. ; 358:6363, s. 599-600
  • Recension (övrigt vetenskapligt/konstnärligt)abstract
    • n/a
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6.
  • Hiruma, Yoshitaka, et al. (författare)
  • Competition between MPS1 and microtubules at kinetochores regulates spindle checkpoint signaling
  • 2015
  • Ingår i: Science. - Washington, DC, United States : American Association for the Advancement of Science (A A A S). - 0036-8075 .- 1095-9203. ; 348:6240, s. 1264-1267
  • Tidskriftsartikel (refereegranskat)abstract
    • Cell division progresses to anaphase only after all chromosomes are connected to spindle microtubules through kinetochores and the spindle assembly checkpoint (SAC) is satisfied. We show that the amino-terminal localization module of the SAC protein kinase MPS1 (monopolar spindle 1) directly interacts with the HEC1 (highly expressed in cancer 1) calponin homology domain in the NDC80 (nuclear division cycle 80) kinetochore complex in vitro, in a phosphorylation-dependent manner. Microtubule polymers disrupted this interaction. In cells, MPS1 binding to kinetochores or to ectopic NDC80 complexes was prevented by end-on microtubule attachment, independent of known kinetochore protein-removal mechanisms. Competition for kinetochore binding between SAC proteins and microtubules provides a direct and perhaps evolutionarily conserved way to detect a properly organized spindle ready for cell division.
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7.
  • Mjösberg, Jenny, et al. (författare)
  • Lung inflammation originating in the gut
  • 2018
  • Ingår i: Science (New York, N.Y.). - : American Association for the Advancement of Science (AAAS). - 1095-9203 .- 0036-8075. ; 359:6371, s. 36-37
  • Tidskriftsartikel (refereegranskat)abstract
    • Parasite infection in the intestine can lead to inflammatory immune cells in the lung
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8.
  • Schwarze, Martin, et al. (författare)
  • Band structure engineering in organic semiconductors
  • 2016
  • Ingår i: Science. - : AMER ASSOC ADVANCEMENT SCIENCE. - 0036-8075 .- 1095-9203. ; 352:6292, s. 1446-1449
  • Tidskriftsartikel (refereegranskat)abstract
    • A key breakthrough in modern electronics was the introduction of band structure engineering, the design of almost arbitrary electronic potential structures by alloying different semiconductors to continuously tune the band gap and band-edge energies. Implementation of this approach in organic semiconductors has been hindered by strong localization of the electronic states in these materials. We show that the influence of so far largely ignored long-range Coulomb interactions provides a workaround. Photoelectron spectroscopy confirms that the ionization energies of crystalline organic semiconductors can be continuously tuned over a wide range by blending them with their halogenated derivatives. Correspondingly, the photovoltaic gap and open-circuit voltage of organic solar cells can be continuously tuned by the blending ratio of these donors.
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9.
  • Uhlén, Mathias, et al. (författare)
  • A genome-wide transcriptomic analysis of protein-coding genes in human blood cells
  • 2019
  • Ingår i: Science. - : American Association for the Advancement of Science. - 0036-8075 .- 1095-9203. ; 366:6472, s. 1471-
  • Tidskriftsartikel (refereegranskat)abstract
    • Blood is the predominant source for molecular analyses in humans, both in clinical and research settings. It is the target for many therapeutic strategies, emphasizing the need for comprehensive molecular maps of the cells constituting human blood. In this study, we performed a genome-wide transcriptomic analysis of protein-coding genes in sorted blood immune cell populations to characterize the expression levels of each individual gene across the blood cell types. All data are presented in an interactive, open-access Blood Atlas as part of the Human Protein Atlas and are integrated with expression profiles across all major tissues to provide spatial classification of all protein-coding genes. This allows for a genome-wide exploration of the expression profiles across human immune cell populations and all major human tissues and organs.
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  • Resultat 1-9 av 9
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