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Science

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Palabras clave – provistas por la editorial

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Disponibilidad
Institución detectada Período Navegá Descargá Solicitá
No detectada desde mar. 1997 / hasta dic. 2023 Science Journals

Información

Tipo de recurso:

revistas

ISSN impreso

0036-8075

ISSN electrónico

1095-9203

Editor responsable

American Association for the Advancement of Science (AAAS)

País de edición

Estados Unidos

Fecha de publicación

Cobertura temática

Tabla de contenidos

Editors' Choice

Stella M. Hurtley; Catherine Griffin; Gemma Alderton; Marc S. Lavine; Melissa McCartney; Seth Scanlon; Phil Szuromi

Palabras clave: Multidisciplinary.

Pp. 367-368

The yin and yang of TDP-43 reduction

Stella M. Hurtley

Palabras clave: Multidisciplinary.

Pp. 367.1-367

Support is needed to leave the lab

Melissa McCartney

Palabras clave: Multidisciplinary.

Pp. 367.2-368

Diagnostic tumor methylation profiles

Catherine Griffin

Palabras clave: Multidisciplinary.

Pp. 367.3-368

Tumors in green turtles

Gemma Alderton

Palabras clave: Multidisciplinary.

Pp. 367.4-368

Getting random with thermal noise

Marc S. Lavine

Palabras clave: Multidisciplinary.

Pp. 367.5-368

DNA methylation makes for tired T cells

Seth Scanlon

Palabras clave: Multidisciplinary.

Pp. 367.6-368

Smoothing graphene by encapsulation

Phil Szuromi

Palabras clave: Multidisciplinary.

Pp. 367.7-368

Second-scale nuclear spin coherence time of ultracold 23 Na 40 K molecules

Jee Woo ParkORCID; Zoe Z. YanORCID; Huanqian LohORCID; Sebastian A. WillORCID; Martin W. ZwierleinORCID

<jats:title>Extending the coherence time of molecules</jats:title> <jats:p> Quantum properties of atoms and molecules can be exploited for precision measurements or quantum information processing. The complex state structure of molecules can be exploited, but it is hard to preserve the coherence between pairs of those states in applications. Park <jats:italic>et al.</jats:italic> created fermionic molecules of NaK in the rovibrational ground state that maintained coherence between their nuclear spin states on a time scale of 1 second. This long coherence time makes dipolar ultracold molecules a valuable quantum resource. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6349" page="372" related-article-type="in-this-issue" vol="357" xlink:href="10.1126/science.aal5066">372</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 372-375

Spectral narrowing of x-ray pulses for precision spectroscopy with nuclear resonances

K. P. HeegORCID; A. KaldunORCID; C. StrohmORCID; P. ReiserORCID; C. OttORCID; R. Subramanian; D. LentrodtORCID; J. HaberORCID; H.-C. WilleORCID; S. Goerttler; R. RüfferORCID; C. H. Keitel; R. RöhlsbergerORCID; T. PfeiferORCID; J. EversORCID

<jats:title>Spectral narrowing of x-rays</jats:title> <jats:p> Modern photon factories typically provide x-ray pulses that are orders of magnitude broader in frequency space than the corresponding atomic or nuclear resonances to be probed. For many spectroscopic applications, however, narrower x-ray light sources are desired. By using precise mechanical displacements of a reference absorber to simulate the effect of an x-ray control field, Heeg <jats:italic>et al.</jats:italic> show that they can spectrally narrow input x-ray pulses. The conversion of off-resonant photons into resonant ones results in increased pulse brilliance at the desired resonant frequency, thereby providing a sharp x-ray probe for precision spectroscopy. </jats:p> <jats:p> <jats:italic>Science</jats:italic> , this issue p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6349" page="375" related-article-type="in-this-issue" vol="357" xlink:href="10.1126/science.aan3512">375</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 375-378