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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

Corridors for biodiversity among oil palms

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.1-835

Anti-Markovnikov hydroamination

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.2-834

Nectar—but not for parasites

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.3-834

Watching metal nanoparticle exsolution

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.4-835

Organelle fusion in fertility

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.5-835

VISTA is a pH-selective checkpoint

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.6-835

Predicting future terror attacks

Caroline Ash; Jesse Smith (eds.)

Palabras clave: Multidisciplinary.

Pp. 834.7-835

Structure of the RSC complex bound to the nucleosome

Youpi YeORCID; Hao WuORCID; Kangjing ChenORCID; Cedric R. Clapier; Naveen VermaORCID; Wenhao ZhangORCID; Haiteng DengORCID; Bradley R. Cairns; Ning Gao; Zhucheng ChenORCID

<jats:title>The architecture of the RSC complex</jats:title> <jats:p> RSC is a Snf2-family chromatin remodeler complex that controls the promoter architecture of most of the genes in yeast. Using single-particle cryo–electron microscopy, Ye <jats:italic>et al.</jats:italic> determined the structure of RSC bound to the nucleosome. The structure reveals the modular architecture of RSC, shows how RSC engages the nucleosome, and explains the remodeling directionality. RSC shows strong similarities to homologous human complexes that are frequently mutated in cancers, and this structure provides valuable information for understanding these systems. </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="6467" page="838" related-article-type="in-this-issue" vol="366" xlink:href="10.1126/science.aay0033">838</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 838-843

Activation of the ISR mediates the behavioral and neurophysiological abnormalities in Down syndrome

Ping Jun ZhuORCID; Sanjeev KhatiwadaORCID; Ya CuiORCID; Lucas C. Reineke; Sean W. DoolingORCID; Jean J. KimORCID; Wei Li; Peter WalterORCID; Mauro Costa-MattioliORCID

<jats:title>Tuning stress protects cognition</jats:title> <jats:p> Down syndrome (DS) is a chromosomal disorder that occurs when a person has an extra copy of chromosome 21. DS causes intellectual disabilities, among other health issues, but little is known about the mechanisms underlying the memory deficits in DS. Zhu <jats:italic>et al.</jats:italic> used a multidisciplinary approach to show that a defect in integrated stress response, a conserved pathway that controls protein homeostasis, can explain the cognitive and neuronal deficits in a mouse model of DS (see the Perspective by Halliday and Mallucci). These insights into the biological basis underlying DS could potentially help in the design of treatments for this condition. </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="6467" page="843" related-article-type="in-this-issue" vol="366" xlink:href="10.1126/science.aaw5185">843</jats:related-article> ; see also p. <jats:related-article xmlns:xlink="http://www.w3.org/1999/xlink" ext-link-type="doi" issue="6467" page="797" related-article-type="in-this-issue" vol="366" xlink:href="10.1126/science.aaz7128">797</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 843-849

Engineering bunched Pt-Ni alloy nanocages for efficient oxygen reduction in practical fuel cells

Xinlong TianORCID; Xiao ZhaoORCID; Ya-Qiong SuORCID; Lijuan Wang; Hongming WangORCID; Dai Dang; Bin Chi; Hongfang LiuORCID; Emiel J.M. HensenORCID; Xiong Wen (David) LouORCID; Bao Yu XiaORCID

<jats:title>Nanocage-chain fuel cell catalysts</jats:title> <jats:p> The expense and scarcity of platinum has driven efforts to improve oxygen-reduction catalysts in proton-exchange membrane fuel cells. Tian <jats:italic>et al.</jats:italic> synthesized chains of platinum-nickel alloy nanospheres connected by necking regions. These structures can be etched to form nanocages with platinum-rich surfaces that are highly active for oxygen reduction. In fuel cells running on air and hydrogen, these catalysts operated for at least 180 hours. </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="6467" page="850" related-article-type="in-this-issue" vol="366" xlink:href="10.1126/science.aaw7493">850</jats:related-article> </jats:p>

Palabras clave: Multidisciplinary.

Pp. 850-856