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Science

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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

Meet the scientist painter who turns deadly viruses into beautiful works of art

Jon Cohen

Palabras clave: Multidisciplinary.

Pp. No disponible

White House eyes nuclear weapons expert to lead challenge to climate science

Scott Waldman

Palabras clave: Multidisciplinary.

Pp. No disponible

Top stories: Black hole’s first close-up, pseudoarchaeology, and hunting for human pheromones

Alex Fox

Palabras clave: Multidisciplinary.

Pp. No disponible

Boston University fires geologist found to have harassed women in Antarctica

Meredith Wadman

Palabras clave: Multidisciplinary.

Pp. No disponible

Ebola outbreak in Congo still not an international crisis, WHO decides

Jon Cohen

Palabras clave: Multidisciplinary.

Pp. No disponible

Renowned fellowships aren’t the only option

José E. Liquet y González

Palabras clave: Multidisciplinary.

Pp. No disponible

Ultrapotent chemogenetics for research and potential clinical applications

Christopher J. MagnusORCID; Peter H. LeeORCID; Jordi BonaventuraORCID; Roland ZemlaORCID; Juan L. GomezORCID; Melissa H. RamirezORCID; Xing HuORCID; Adriana GalvanORCID; Jayeeta Basu; Michael MichaelidesORCID; Scott M. SternsonORCID

<jats:title>Improved agonists for chemogenetics</jats:title> <jats:p> Targeting ligand-responsive receptors to specific groups of cells, a strategy known as chemogenetics, is a powerful tool in many neurological applications. There is increasing interest in extending these tools for human treatment. Magnus <jats:italic>et al.</jats:italic> designed chemogenetic ion channels that improve currently available systems and are activated by the clinically used antismoking drug varenicline. They engineered a ligand-binding domain less responsive to endogenous signals and identified agonists that function at nanomolar concentrations. The combination of drug and introduced channels transiently silenced neurons, with slow but effective washout, and induced behavioral changes in animal models after brain administration. </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" related-article-type="in-this-issue" xlink:href="10.1126/science.aav5282">eaav5282</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

Sustained rescue of prefrontal circuit dysfunction by antidepressant-induced spine formation

R. N. Moda-Sava; M. H. MurdockORCID; P. K. ParekhORCID; R. N. Fetcho; B. S. HuangORCID; T. N. HuynhORCID; J. WitztumORCID; D. C. Shaver; D. L. RosenthalORCID; E. J. AlwayORCID; K. LopezORCID; Y. MengORCID; L. Nellissen; L. GrosenickORCID; T. A. MilnerORCID; K. DeisserothORCID; H. BitoORCID; H. Kasai; C. ListonORCID

<jats:title>Why is ketamine an antidepressant?</jats:title> <jats:p> A better understanding of the mechanisms underlying the action of antidepressants is urgently needed. Moda-Sava <jats:italic>et al.</jats:italic> explored a possible mode of action for the drug ketamine, which has recently been shown to help patients recover from depression (see the Perspective by Beyeler). Ketamine rescued behavior in mice that was associated with depression-like phenotypes by selectively reversing stress-induced spine loss and restoring coordinated multicellular ensemble activity in prefrontal microcircuits. The initial induction of ketamine's antidepressant effect on mouse behavior occurred independently of effects on spine formation. Instead, synaptogenesis in the prefrontal region played a critical role in nourishing these effects over time. Interventions aimed at enhancing the survival of restored synapses may thus be useful for sustaining the behavioral effects of fast-acting antidepressants. </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" related-article-type="in-this-issue" xlink:href="10.1126/science.aat8078">eaat8078</jats:related-article> ; see also p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6436" page="129" related-article-type="in-this-issue" vol="364" xlink:href="10.1126/science.aax0719">129</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

Glycosidase and glycan polymorphism control hydrolytic release of immunogenic flagellin peptides

Pierre BuscaillORCID; Balakumaran ChandrasekarORCID; Nattapong SanguankiattichaiORCID; Jiorgos KourelisORCID; Farnusch Kaschani; Emma L. ThomasORCID; Kyoko MorimotoORCID; Markus KaiserORCID; Gail M. PrestonORCID; Yuki IchinoseORCID; Renier A. L. van der Hoorn

<jats:title>Glycosylation goes back and forth</jats:title> <jats:p> Plants produce receptors that recognize fragments of microbial flagellin, thus monitoring for infection by bacteria. Buscaill <jats:italic>et al.</jats:italic> studied how a flagellin fragment is made accessible for recognition by host glycosidases, which degrade the glycosylations shielding the peptide that triggers the immune response. The pathogen, in turn, evades detection by altering flagellin glycosylation and inhibiting the host glycosidase. This aspect of plant defense against infection plays out in the apoplast, the extracellular space within plant tissues. </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" related-article-type="in-this-issue" xlink:href="10.1126/science.aav0748">eaav0748</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible

The NASA Twins Study: A multidimensional analysis of a year-long human spaceflight

Francine E. Garrett-Bakelman; Manjula DarshiORCID; Stefan J. GreenORCID; Ruben C. Gur; Ling LinORCID; Brandon R. MaciasORCID; Miles J. McKennaORCID; Cem MeydanORCID; Tejaswini MishraORCID; Jad NasriniORCID; Brian D. PieningORCID; Lindsay F. RizzardiORCID; Kumar SharmaORCID; Jamila H. SiamwalaORCID; Lynn TaylorORCID; Martha Hotz VitaternaORCID; Maryam AfkarianORCID; Ebrahim AfshinnekooORCID; Sara AhadiORCID; Aditya AmbatiORCID; Maneesh AryaORCID; Daniela BezdanORCID; Colin M. CallahanORCID; Songjie ChenORCID; Augustine M. K. Choi; George E. ChlipalaORCID; Kévin ContrepoisORCID; Marisa CovingtonORCID; Brian E. Crucian; Immaculata De VivoORCID; David F. DingesORCID; Douglas J. EbertORCID; Jason I. Feinberg; Jorge A. GandaraORCID; Kerry A. GeorgeORCID; John GoutsiasORCID; George S. GrillsORCID; Alan R. HargensORCID; Martina HeerORCID; Ryan P. HillaryORCID; Andrew N. HoofnagleORCID; Vivian Y. H. Hook; Garrett JenkinsonORCID; Peng JiangORCID; Ali KeshavarzianORCID; Steven S. LaurieORCID; Brittany Lee-McMullenORCID; Sarah B. Lumpkins; Matthew MacKay; Mark G. Maienschein-ClineORCID; Ari M. MelnickORCID; Tyler M. MooreORCID; Kiichi Nakahira; Hemal H. PatelORCID; Robert Pietrzyk; Varsha RaoORCID; Rintaro Saito; Denis N. SalinsORCID; Jan M. SchillingORCID; Dorothy D. SearsORCID; Caroline K. SheridanORCID; Michael B. Stenger; Rakel TryggvadottirORCID; Alexander E. UrbanORCID; Tomas VaisarORCID; Benjamin Van EspenORCID; Jing Zhang; Michael G. Ziegler; Sara R. Zwart; John B. Charles; Craig E. KundrotORCID; Graham B. I. ScottORCID; Susan M. BaileyORCID; Mathias BasnerORCID; Andrew P. FeinbergORCID; Stuart M. C. LeeORCID; Christopher E. MasonORCID; Emmanuel MignotORCID; Brinda K. RanaORCID; Scott M. Smith; Michael P. Snyder; Fred W. TurekORCID

<jats:title>What to expect after a year in space</jats:title> <jats:p> Space is the final frontier for understanding how extreme environments affect human physiology. Following twin astronauts, one of which spent a year-long mission on the International Space Station, Garrett-Bakelman <jats:italic>et al.</jats:italic> examined molecular and physiological traits that may be affected by time in space (see the Perspective by Löbrich and Jeggo). Sequencing the components of whole blood revealed that the length of telomeres, which is important to maintain in dividing cells and may be related to human aging, changed substantially during space flight and again upon return to Earth. Coupled with changes in DNA methylation in immune cells and cardiovascular and cognitive effects, this study provides a basis to assess the hazards of long-term space habitation. </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" related-article-type="in-this-issue" xlink:href="10.1126/science.aau8650">eaau8650</jats:related-article> ; see also p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6436" page="127" related-article-type="in-this-issue" vol="364" xlink:href="10.1126/science.aaw7086">127</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible