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Skeletal muscle thermogenesis enables aquatic life in the smallest marine mammal 期刊论文
Science, 2021
作者:  Traver Wright;  Randall W. Davis;  Heidi C. Pearson;  Michael Murray;  Melinda Sheffield-Moore
收藏  |  浏览/下载:19/0  |  提交时间:2021/07/27
Beijing’s Crackdown on Human Rights and the Rule of Law in Hong Kong 科技报告
来源:National Bureau of Asian Research. 出版年: 2021
作者:  Michael C. Davis
收藏  |  浏览/下载:6/0  |  提交时间:2021/05/07
Barcoded viral tracing of single-cell interactions in central nervous system inflammation 期刊论文
Science, 2021
作者:  Iain C. Clark;  Cristina Gutiérrez-Vázquez;  Michael A. Wheeler;  Zhaorong Li;  Veit Rothhammer;  Mathias Linnerbauer;  Liliana M. Sanmarco;  Lydia Guo;  Manon Blain;  Stephanie E. J. Zandee;  Chun-Cheih Chao;  Katelyn V. Batterman;  Marius Schwabenland;  Peter Lotfy;  Amalia Tejeda-Velarde;  Patrick Hewson;  Carolina Manganeli Polonio;  Michael W. Shultis;  Yasmin Salem;  Emily C. Tjon;  Pedro H. Fonseca-Castro;  Davis M. Borucki;  Kalil Alves de Lima;  Agustin Plasencia;  Adam R. Abate;  Douglas L. Rosene;  Kevin J. Hodgetts;  Marco Prinz;  Jack P. Antel;  Alexandre Prat;  Francisco J. Quintana
收藏  |  浏览/下载:14/0  |  提交时间:2021/04/29
A ubiquitous tire rubber–derived chemical induces acute mortality in coho salmon 期刊论文
Science, 2021
作者:  Zhenyu Tian;  Haoqi Zhao;  Katherine T. Peter;  Melissa Gonzalez;  Jill Wetzel;  Christopher Wu;  Ximin Hu;  Jasmine Prat;  Emma Mudrock;  Rachel Hettinger;  Allan E. Cortina;  Rajshree Ghosh Biswas;  Flávio Vinicius Crizóstomo Kock;  Ronald Soong;  Amy Jenne;  Bowen Du;  Fan Hou;  Huan He;  Rachel Lundeen;  Alicia Gilbreath;  Rebecca Sutton;  Nathaniel L. Scholz;  Jay W. Davis;  Michael C. Dodd;  Andre Simpson;  Jenifer K. McIntyre;  Edward P. Kolodziej
收藏  |  浏览/下载:11/0  |  提交时间:2021/01/15
Distemper, extinction, and vaccination of the Amur tiger 期刊论文
Proceedings of the National Academy of Sciences, 2020
作者:  Martin Gilbert;  Nadezhda Sulikhan;  Olga Uphyrkina;  Mikhail Goncharuk;  Linda Kerley;  Enrique Hernandez Castro;  Richard Reeve;  Tracie Seimon;  Denise McAloose;  Ivan V. Seryodkin;  Sergey V. Naidenko;  Christopher A. Davis;  Gavin S. Wilkie;  Sreenu B. Vattipally;  Walt E. Adamson;  Chris Hinds;  Emma C. Thomson;  Brian J. Willett;  Margaret J. Hosie;  Nicola Logan;  Michael McDonald;  Robert J. Ossiboff;  Elena I. Shevtsova;  Stepan Belyakin;  Anna A. Yurlova;  Steven A. Osofsky;  Dale G. Miquelle;  Louise Matthews;  Sarah Cleaveland
收藏  |  浏览/下载:10/0  |  提交时间:2020/11/30
Ecological insights from three decades of animal movement tracking across a changing Arctic 期刊论文
Science, 2020
作者:  Sarah C. Davidson;  Gil Bohrer;  Eliezer Gurarie;  Scott LaPoint;  Peter J. Mahoney;  Natalie T. Boelman;  Jan U. H. Eitel;  Laura R. Prugh;  Lee A. Vierling;  Jyoti Jennewein;  Emma Grier;  Ophélie Couriot;  Allicia P. Kelly;  Arjan J. H. Meddens;  Ruth Y. Oliver;  Roland Kays;  Martin Wikelski;  Tomas Aarvak;  Joshua T. Ackerman;  José A. Alves;  Erin Bayne;  Bryan Bedrosian;  Jerrold L. Belant;  Andrew M. Berdahl;  Alicia M. Berlin;  Dominique Berteaux;  Joël Bêty;  Dmitrijs Boiko;  Travis L. Booms;  Bridget L. Borg;  Stan Boutin;  W. Sean Boyd;  Kane Brides;  Stephen Brown;  Victor N. Bulyuk;  Kurt K. Burnham;  David Cabot;  Michael Casazza;  Katherine Christie;  Erica H. Craig;  Shanti E. Davis;  Tracy Davison;  Dominic Demma;  Christopher R. DeSorbo;  Andrew Dixon;  Robert Domenech;  Götz Eichhorn;  Kyle Elliott;  Joseph R. Evenson;  Klaus-Michael Exo;  Steven H. Ferguson;  Wolfgang Fiedler;  Aaron Fisk;  Jérôme Fort;  Alastair Franke;  Mark R. Fuller;  Stefan Garthe;  Gilles Gauthier;  Grant Gilchrist;  Petr Glazov;  Carrie E. Gray;  David Grémillet;  Larry Griffin;  Michael T. Hallworth;  Autumn-Lynn Harrison;  Holly L. Hennin;  J. Mark Hipfner;  James Hodson;  James A. Johnson;  Kyle Joly;  Kimberly Jones;  Todd E. Katzner;  Jeff W. Kidd;  Elly C. Knight;  Michael N. Kochert;  Andrea Kölzsch;  Helmut Kruckenberg;  Benjamin J. Lagassé;  Sandra Lai;  Jean-François Lamarre;  Richard B. Lanctot;  Nicholas C. Larter;  A. David M. Latham;  Christopher J. Latty;  James P. Lawler;  Don-Jean Léandri-Breton;  Hansoo Lee;  Stephen B. Lewis;  Oliver P. Love;  Jesper Madsen;  Mark Maftei;  Mark L. Mallory;  Buck Mangipane;  Mikhail Y. Markovets;  Peter P. Marra;  Rebecca McGuire;  Carol L. McIntyre;  Emily A. McKinnon;  Tricia A. Miller;  Sander Moonen;  Tong Mu;  Gerhard J. D. M. Müskens;  Janet Ng;  Kerry L. Nicholson;  Ingar Jostein Øien;  Cory Overton;  Patricia A. Owen;  Allison Patterson;  Aevar Petersen;  Ivan Pokrovsky;  Luke L. Powell;  Rui Prieto;  Petra Quillfeldt;  Jennie Rausch;  Kelsey Russell;  Sarah T. Saalfeld;  Hans Schekkerman;  Joel A. Schmutz;  Philipp Schwemmer;  Dale R. Seip;  Adam Shreading;  Mónica A. Silva;  Brian W. Smith;  Fletcher Smith;  Jeff P. Smith;  Katherine R. S. Snell;  Aleksandr Sokolov;  Vasiliy Sokolov;  Diana V Solovyeva;  Mathew S. Sorum;  Grigori Tertitski;  J. F. Therrien;  Kasper Thorup;  T. Lee Tibbitts;  Ingrid Tulp;  Brian D. Uher-Koch;  Rob S. A. van Bemmelen;  Steven Van Wilgenburg;  Andrew L. Von Duyke;  Jesse L. Watson;  Bryan D. Watts;  Judy A. Williams;  Matthew T. Wilson;  James R. Wright;  Michael A. Yates;  David J. Yurkowski;  Ramūnas Žydelis;  Mark Hebblewhite
收藏  |  浏览/下载:19/0  |  提交时间:2020/11/09
Transcriptomic signatures across human tissues identify functional rare genetic variation 期刊论文
Science, 2020
作者:  Nicole M. Ferraro;  Benjamin J. Strober;  Jonah Einson;  Nathan S. Abell;  Francois Aguet;  Alvaro N. Barbeira;  Margot Brandt;  Maja Bucan;  Stephane E. Castel;  Joe R. Davis;  Emily Greenwald;  Gaelen T. Hess;  Austin T. Hilliard;  Rachel L. Kember;  Bence Kotis;  YoSon Park;  Gina Peloso;  Shweta Ramdas;  Alexandra J. Scott;  Craig Smail;  Emily K. Tsang;  Seyedeh M. Zekavat;  Marcello Ziosi;  Aradhana;  TOPMed Lipids Working Group;  Kristin G. Ardlie;  Themistocles L. Assimes;  Michael C. Bassik;  Christopher D. Brown;  Adolfo Correa;  Ira Hall;  Hae Kyung Im;  Xin Li;  Pradeep Natarajan;  GTEx Consortium;  Tuuli Lappalainen;  Pejman Mohammadi;  Stephen B. Montgomery;  Alexis Battle
收藏  |  浏览/下载:12/0  |  提交时间:2020/09/14
Clonally expanded CD8 T cells patrol the cerebrospinal fluid in Alzheimer's disease 期刊论文
NATURE, 2020, 577 (7790) : 399-+
作者:  Gate, David;  Saligrama, Naresha;  Leventhal, Olivia;  Yang, Andrew C.;  Unger, Michael S.;  Middeldorp, Jinte;  Chen, Kelly;  Lehallier, Benoit;  Channappa, Divya;  De Los Santos, Mark B.;  McBride, Alisha;  Pluvinage, John;  Elahi, Fanny;  Tam, Grace Kyin-Ye;  Kim, Yongha;  Greicius, Michael;  Wagner, Anthony D.;  Aigner, Ludwig;  Galasko, Douglas R.;  Davis, Mark M.;  Wyss-Coray, Tony
收藏  |  浏览/下载:6/0  |  提交时间:2020/07/03

Alzheimer'  s disease is an incurable neurodegenerative disorder in which neuroinflammation has a critical function(1). However, little is known about the contribution of the adaptive immune response in Alzheimer'  s disease(2). Here, using integrated analyses of multiple cohorts, we identify peripheral and central adaptive immune changes in Alzheimer'  s disease. First, we performed mass cytometry of peripheral blood mononuclear cells and discovered an immune signature of Alzheimer'  s disease that consists of increased numbers of CD8(+) T effector memory CD45RA(+) (T-EMRA) cells. In a second cohort, we found that CD8(+) T-EMRA cells were negatively associated with cognition. Furthermore, single-cell RNA sequencing revealed that T cell receptor (TCR) signalling was enhanced in these cells. Notably, by using several strategies of single-cell TCR sequencing in a third cohort, we discovered clonally expanded CD8(+) T-EMRA cells in the cerebrospinal fluid of patients with Alzheimer'  s disease. Finally, we used machine learning, cloning and peptide screens to demonstrate the specificity of clonally expanded TCRs in the cerebrospinal fluid of patients with Alzheimer'  s disease to two separate Epstein-Barr virus antigens. These results reveal an adaptive immune response in the blood and cerebrospinal fluid in Alzheimer'  s disease and provide evidence of clonal, antigen-experienced T cells patrolling the intrathecal space of brains affected by age-related neurodegeneration.


  
Structure of the M2 muscarinic receptor-beta-arrestin complex in a lipid nanodisc 期刊论文
NATURE, 2020, 579 (7798) : 297-+
作者:  Gate, David;  Saligrama, Naresha;  Leventhal, Olivia;  Yang, Andrew C.;  Unger, Michael S.;  Middeldorp, Jinte;  Chen, Kelly;  Lehallier, Benoit;  Channappa, Divya;  De Los Santos, Mark B.;  McBride, Alisha;  Pluvinage, John;  Elahi, Fanny;  Tam, Grace Kyin-Ye;  Kim, Yongha;  Greicius, Michael;  Wagner, Anthony D.;  Aigner, Ludwig;  Galasko, Douglas R.;  Davis, Mark M.;  Wyss-Coray, Tony
收藏  |  浏览/下载:29/0  |  提交时间:2020/07/03

After activation by an agonist, G-protein-coupled receptors (GPCRs) recruit beta-arrestin, which desensitizes heterotrimeric G-protein signalling and promotes receptor endocytosis(1). Additionally, beta-arrestin directly regulates many cell signalling pathways that can induce cellular responses distinct from that of G proteins(2). In contrast to G proteins, for which there are many high-resolution structures in complex with GPCRs, the molecular mechanisms underlying the interaction of beta-arrestin with GPCRs are much less understood. Here we present a cryo-electron microscopy structure of beta-arrestin 1 (beta arr1) in complex with M2 muscarinic receptor (M2R) reconstituted in lipid nanodiscs. The M2R-beta arr1 complex displays a multimodal network of flexible interactions, including binding of the N domain of beta arr1 to phosphorylated receptor residues and insertion of the finger loop of beta arr1 into the M2R seven-transmembrane bundle, which adopts a conformation similar to that in the M2R-heterotrimeric G(o) protein complex(3). Moreover, the cryo-electron microscopy map reveals that the C-edge of beta arr1 engages the lipid bilayer. Through atomistic simulations and biophysical, biochemical and cellular assays, we show that the C-edge is critical for stable complex formation, beta arr1 recruitment, receptor internalization, and desensitization of G-protein activation. Taken together, these data suggest that the cooperative interactions of beta-arrestin with both the receptor and the phospholipid bilayer contribute to its functional versatility.


  
Quantum crystal structure in the 250-kelvin superconducting lanthanum hydride 期刊论文
NATURE, 2020, 578 (7793) : 66-+
作者:  Gate, David;  Saligrama, Naresha;  Leventhal, Olivia;  Yang, Andrew C.;  Unger, Michael S.;  Middeldorp, Jinte;  Chen, Kelly;  Lehallier, Benoit;  Channappa, Divya;  De Los Santos, Mark B.;  McBride, Alisha;  Pluvinage, John;  Elahi, Fanny;  Tam, Grace Kyin-Ye;  Kim, Yongha;  Greicius, Michael;  Wagner, Anthony D.;  Aigner, Ludwig;  Galasko, Douglas R.;  Davis, Mark M.;  Wyss-Coray, Tony
收藏  |  浏览/下载:20/0  |  提交时间:2020/07/03

The discovery of superconductivity at 200 kelvin in the hydrogen sulfide system at high pressures(1) demonstrated the potential of hydrogen-rich materials as high-temperature superconductors. Recent theoretical predictions of rare-earth hydrides with hydrogen cages(2,3) and the subsequent synthesis of LaH10 with a superconducting critical temperature (T-c) of 250 kelvin(4,5) have placed these materials on the verge of achieving the long-standing goal of room-temperature superconductivity. Electrical and X-ray diffraction measurements have revealed a weakly pressure-dependent T-c for LaH10 between 137 and 218 gigapascals in a structure that has a face-centred cubic arrangement of lanthanum atoms(5). Here we show that quantum atomic fluctuations stabilize a highly symmetrical Fm (3) over barm crystal structure over this pressure range. The structure is consistent with experimental findings and has a very large electron-phonon coupling constant of 3.5. Although ab initio classical calculations predict that this Fm (3) over barm structure undergoes distortion at pressures below 230 gigapascals(2,3,) yielding a complex energy landscape, the inclusion of quantum effects suggests that it is the true ground-state structure. The agreement between the calculated and experimental Tc values further indicates that this phase is responsible for the superconductivity observed at 250 kelvin. The relevance of quantum fluctuations calls into question many of the crystal structure predictions that have been made for hydrides within a classical approach and that currently guide the experimental quest for room-temperature superconductivity(6-8). Furthermore, we find that quantum effects are crucial for the stabilization of solids with high electron-phonon coupling constants that could otherwise be destabilized by the large electron-phonon interaction(9), thus reducing the pressures required for their synthesis.