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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

Researchers need better access to US Census data

Cory McCartan; Tyler Simko; Kosuke Imai

Palabras clave: Multidisciplinary.

Pp. 902-903

Understanding our own order

Sacha Vignieri

Palabras clave: Multidisciplinary.

Pp. 904-905

In Science Journals

Michael Funk (eds.)

<jats:p> Highlights from the <jats:italic>Science</jats:italic> family of journals </jats:p>

Palabras clave: Multidisciplinary.

Pp. 931-933

In Other Journals

Caroline Ash; Jesse Smith (eds.)

<jats:p>Editors’ selections from the current scientific literature</jats:p>

Palabras clave: Multidisciplinary.

Pp. 932-933

A functional group–guided approach to aptamers for small molecules

Kyungae YangORCID; Noelle M. MitchellORCID; Saswata BanerjeeORCID; Zhenzhuang Cheng; Steven Taylor; Aleksandra M. KosticORCID; Isabel WongORCID; Sairaj SajjathORCID; Yameng ZhangORCID; Jacob StevensORCID; Sumit MohanORCID; Donald W. LandryORCID; Tilla S. WorgallORCID; Anne M. AndrewsORCID; Milan N. StojanovicORCID

<jats:p>Aptameric receptors are important biosensor components, yet our ability to identify them depends on the target structures. We analyzed the contributions of individual functional groups on small molecules to binding within 27 target-aptamer pairs, identifying potential hindrances to receptor isolation—for example, negative cooperativity between sterically hindered functional groups. To increase the probability of aptamer isolation for important targets, such as leucine and voriconazole, for which multiple previous selection attempts failed, we designed tailored strategies focused on overcoming individual structural barriers to successful selections. This approach enables us to move beyond standardized protocols into functional group–guided searches, relying on sequences common to receptors for targets and their analogs to serve as anchors in regions of vast oligonucleotide spaces wherein useful reagents are likely to be found.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 942-948

Body-based units of measure in cultural evolution

Roope O. KaaronenORCID; Mikael A. ManninenORCID; Jussi T. EronenORCID

<jats:p>Measurement systems are important drivers of cultural and technological evolution. However, the evolution of measurement is still insufficiently understood. Many early standardized measurement systems evolved from body-based units of measure, such as the cubit and fathom, but researchers have rarely studied how or why body-based measurement has been used. We documented body-based units of measure in 186 cultures, illustrating how body-based measurement is an activity common to cultures around the world. Here, we describe the cultural and technological domains these units are used in. We argue that body-based units have had, and may still have, advantages over standardized systems, such as in the design of ergonomic technologies. This helps explain the persistence of body-based measurement centuries after the first standardized measurement systems emerged.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 948-954

Miniature magneto-mechanical resonators for wireless tracking and sensing

Bernhard GleichORCID; Ingo SchmaleORCID; Tim Nielsen; Jürgen RahmerORCID

<jats:p>Sensor miniaturization enables applications such as minimally invasive medical procedures or patient monitoring by providing process feedback in situ. Ideally, miniature sensors should be wireless, inexpensive, and allow for remote detection over sufficient distance by an affordable detection system. We analyze the signal strength of wireless sensors theoretically and derive a simple design of high-signal resonant magneto-mechanical sensors featuring volumes below 1 cubic millimeter. As examples, we demonstrate real-time tracking of position and attitude of a flying bee, navigation of a biopsy needle, tracking of a free-flowing marker, and sensing of pressure and temperature, all in unshielded environments. The achieved sensor size, measurement accuracy, and workspace of ~25 centimeters show the potential for a low-cost wireless tracking and sensing platform for medical and nonmedical applications.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 966-971

Rhythmic cilia changes support SCN neuron coherence in circadian clock

Hai-Qing TuORCID; Sen LiORCID; Yu-Ling XuORCID; Yu-Cheng ZhangORCID; Pei-Yao LiORCID; Li-Yun Liang; Guang-Ping Song; Xiao-Xiao Jian; Min Wu; Zeng-Qing Song; Ting-Ting LiORCID; Huai-Bin Hu; Jin-Feng Yuan; Xiao-Lin Shen; Jia-Ning Li; Qiu-Ying HanORCID; Kai Wang; Tao Zhang; Tao ZhouORCID; Ai-Ling Li; Xue-Min ZhangORCID; Hui-Yan LiORCID

<jats:p>The suprachiasmatic nucleus (SCN) drives circadian clock coherence through intercellular coupling, which is resistant to environmental perturbations. We report that primary cilia are required for intercellular coupling among SCN neurons to maintain the robustness of the internal clock in mice. Cilia in neuromedin S–producing (NMS) neurons exhibit pronounced circadian rhythmicity in abundance and length. Genetic ablation of ciliogenesis in NMS neurons enabled a rapid phase shift of the internal clock under jet-lag conditions. The circadian rhythms of individual neurons in cilia-deficient SCN slices lost their coherence after external perturbations. Rhythmic cilia changes drive oscillations of Sonic Hedgehog (Shh) signaling and clock gene expression. Inactivation of Shh signaling in NMS neurons phenocopied the effects of cilia ablation. Thus, cilia-Shh signaling in the SCN aids intercellular coupling.</jats:p>

Palabras clave: Multidisciplinary.

Pp. 972-979

One job wasn’t enough

Greta Faccio

Palabras clave: Multidisciplinary.

Pp. 982-982

A microbiota-modulated checkpoint directs immunosuppressive intestinal T cells into cancers

Marine FidelleORCID; Conrad RauberORCID; Carolina Alves Costa SilvaORCID; Ai-Ling TianORCID; Imran Lahmar; Anne-Laure Mallard de La Varende; Liwei Zhao; Cassandra Thelemaque; Isabelle Lebhar; Meriem Messaoudene; Eugenie Pizzato; Roxanne BirebentORCID; Maxime Descartes Mbogning FonkouORCID; Silvia ZoppiORCID; Anna Reni; Cécile Dalban; Marion LeducORCID; Gladys FerrereORCID; Sylvère Durand; Pierre Ly; Aymeric SilvinORCID; Kevin MulderORCID; Charles-Antoine DutertreORCID; Florent GinhouxORCID; Satoru YonekuraORCID; Maria Paula RobertiORCID; Maryam Tidjani-AlouORCID; Safae Terrisse; Jianzhou ChenORCID; Oliver KeppORCID; Angela SchippersORCID; Norbert Wagner; Javier Suárez-GosálvezORCID; Sebastian KoboldORCID; Jean-Eudes FahrnerORCID; Corentin Richard; Jacques BosqORCID; Leonardo Lordello; Giacomo Vitali; Nathalie GalleronORCID; Benoît QuinquisORCID; Emmanuelle Le ChatelierORCID; Lucas BlanchardORCID; Jean-Philippe GirardORCID; Anne JarryORCID; Nadine GervoisORCID; Emmanuelle GodefroyORCID; Nathalie LabarrièreORCID; Ronald Koschny; Romain DaillèreORCID; Benjamin BesseORCID; Caroline TruntzerORCID; François Ghiringhelli; Nicolas Coatnoan; Vanessa Mhanna; David KlatzmannORCID; Damien Drubay; Laurence AlbigesORCID; Andrew Maltez ThomasORCID; Nicola SegataORCID; François-Xavier DanlosORCID; Aurélien MarabelleORCID; Bertrand Routy; Lisa DerosaORCID; Guido KroemerORCID; Laurence ZitvogelORCID

<jats:p> Antibiotics (ABX) compromise the efficacy of programmed cell death protein 1 (PD-1) blockade in cancer patients, but the mechanisms underlying their immunosuppressive effects remain unknown. By inducing the down-regulation of mucosal addressin cell adhesion molecule 1 (MAdCAM-1) in the ileum, post-ABX gut recolonization by <jats:italic>Enterocloster</jats:italic> species drove the emigration of enterotropic α4β7 <jats:sup>+</jats:sup> CD4 <jats:sup>+</jats:sup> regulatory T 17 cells into the tumor. These deleterious ABX effects were mimicked by oral gavage of <jats:italic>Enterocloster</jats:italic> species, by genetic deficiency, or by antibody-mediated neutralization of MAdCAM-1 and its receptor, α4β7 integrin. By contrast, fecal microbiota transplantation or interleukin-17A neutralization prevented ABX-induced immunosuppression. In independent lung, kidney, and bladder cancer patient cohorts, low serum levels of soluble MAdCAM-1 had a negative prognostic impact. Thus, the MAdCAM-1–α4β7 axis constitutes an actionable gut immune checkpoint in cancer immunosurveillance. </jats:p>

Palabras clave: Multidisciplinary.

Pp. No disponible