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Institution

University of Zurich

EducationZurich, Switzerland
About: University of Zurich is a education organization based out in Zurich, Switzerland. It is known for research contribution in the topics: Population & Medicine. The organization has 50842 authors who have published 124042 publications receiving 5304521 citations. The organization is also known as: UZH & Uni Zurich.


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Journal ArticleDOI
Nasim Azani1, Marielle Babineau2, C. Donovan Bailey3, Hannah Banks4, Ariane R. Barbosa5, Rafael Barbosa Pinto6, James S. Boatwright7, Leonardo Maurici Borges8, Gillian K. Brown9, Anne Bruneau2, Elisa Silva Candido6, Domingos Cardoso10, Kuo-Fang Chung11, Ruth Clark4, Adilva de Souza Conceição, Michael D. Crisp12, Paloma Cubas13, Alfonso Delgado-Salinas14, Kyle G. Dexter, Jeff J. Doyle15, Jérôme Duminil16, Ashley N. Egan17, Manuel de la Estrella4, Marcus J. Falcao, Dmitry A. Filatov18, Ana Paula Fortuna-Perez19, Renee Hersilia Fortunato20, Edeline Gagnon2, Peter Gasson4, Juliana Gastaldello Rando21, Ana Maria Goulart de Azevedo Tozzi6, Bee F. Gunn12, David Harris22, Elspeth Haston22, Julie A. Hawkins23, Patrick S. Herendeen, Colin E. Hughes24, João Ricardo Vieira Iganci25, Firouzeh Javadi26, Sheku Alfred Kanu27, Shahrokh Kazempour-Osaloo28, Geoffrey C. Kite4, Bente B. Klitgaard4, Fabio J. Kochanovski6, Erik J. M. Koenen24, Lynsey Kovar3, Matt Lavin29, M. Marianne le Roux30, Gwilym P. Lewis4, Haroldo Cavalcante de Lima, Maria Cristina Lopez-Roberts5, Barbara A. Mackinder22, Vitor Hugo Maia31, Valéry Malécot32, Vidal de Freitas Mansano, Brigitte Marazzi, Sawai Mattapha23, Joseph T. Miller33, Chika Mitsuyuki26, Tania M. Moura34, Daniel J. Murphy4, Madhugiri Nageswara-Rao3, Bruno Nevado18, Danilo M. Neves4, Dario I. Ojeda16, R. Toby Pennington22, Darirn E. Prado35, Gerhard Prenner4, Luciano Paganucci de Queiroz5, Gustavo Ramos10, Fabiana L. Ranzato Filardi, Pétala Gomes Ribeiro5, María de Lourdes Rico-Arce4, Michael J. Sanderson36, Juliana Santos-Silva, Wallace M. B. São-Mateus37, Marcos J. S. Silva38, Marcelo F. Simon39, Carole Sinou2, Cristiane Snak5, Élvia R. de Souza, Janet I. Sprent40, Kelly P. Steele41, Julia E. Steier42, Royce Steeves2, Charles H. Stirton43, Shuichiro Tagane26, Benjamin M. Torke44, Hironori Toyama26, Daiane Trabuco da Cruz5, Mohammad Vatanparast17, Jan J. Wieringa45, Michael Wink46, Martin F. Wojciechowski42, Tetsukazu Yahara26, Ting-Shuang Yi47, Erin Zimmerman2 
01 Feb 2017-Taxon
TL;DR: The classification of the legume family proposed here addresses the long-known non-monophyly of the traditionally recognised subfamily Caesalpinioideae, by recognising six robustly supported monophyletic subfamilies and reflects the phylogenetic structure that is consistently resolved.
Abstract: The classification of the legume family proposed here addresses the long-known non-monophyly of the traditionally recognised subfamily Caesalpinioideae, by recognising six robustly supported monophyletic subfamilies. This new classification uses as its framework the most comprehensive phylogenetic analyses of legumes to date, based on plastid matK gene sequences, and including near-complete sampling of genera (698 of the currently recognised 765 genera) and ca. 20% (3696) of known species. The matK gene region has been the most widely sequenced across the legumes, and in most legume lineages, this gene region is sufficiently variable to yield well-supported clades. This analysis resolves the same major clades as in other phylogenies of whole plastid and nuclear gene sets (with much sparser taxon sampling). Our analysis improves upon previous studies that have used large phylogenies of the Leguminosae for addressing evolutionary questions, because it maximises generic sampling and provides a phylogenetic tree that is based on a fully curated set of sequences that are vouchered and taxonomically validated. The phylogenetic trees obtained and the underlying data are available to browse and download, facilitating subsequent analyses that require evolutionary trees. Here we propose a new community-endorsed classification of the family that reflects the phylogenetic structure that is consistently resolved and recognises six subfamilies in Leguminosae: a recircumscribed Caesalpinioideae DC., Cercidoideae Legume Phylogeny Working Group (stat. nov.), Detarioideae Burmeist., Dialioideae Legume Phylogeny Working Group (stat. nov.), Duparquetioideae Legume Phylogeny Working Group (stat. nov.), and Papilionoideae DC. The traditionally recognised subfamily Mimosoideae is a distinct clade nested within the recircumscribed Caesalpinioideae and is referred to informally as the mimosoid clade pending a forthcoming formal tribal and/or cladebased classification of the new Caesalpinioideae. We provide a key for subfamily identification, descriptions with diagnostic charactertistics for the subfamilies, figures illustrating their floral and fruit diversity, and lists of genera by subfamily. This new classification of Leguminosae represents a consensus view of the international legume systematics community; it invokes both compromise and practicality of use.

697 citations

Journal ArticleDOI
TL;DR: Comparing the results from conjoint and vignette experiments on which attributes of hypothetical immigrants generate support for naturalization with the outcomes of closely corresponding referendums in Switzerland, it is found that the effects estimated from the surveys match the effects of the same attributes in the behavioral benchmark remarkably well.
Abstract: Survey experiments, like vignette and conjoint analyses, are widely used in the social sciences to elicit stated preferences and study how humans make multidimensional choices. However, there is a paucity of research on the external validity of these methods that examines whether the determinants that explain hypothetical choices made by survey respondents match the determinants that explain what subjects actually do when making similar choices in real-world situations. This study compares results from conjoint and vignette analyses on which immigrant attributes generate support for naturalization with closely corresponding behavioral data from a natural experiment in Switzerland, where some municipalities used referendums to decide on the citizenship applications of foreign residents. Using a representative sample from the same population and the official descriptions of applicant characteristics that voters received before each referendum as a behavioral benchmark, we find that the effects of the applicant attributes estimated from the survey experiments perform remarkably well in recovering the effects of the same attributes in the behavioral benchmark. We also find important differences in the relative performances of the different designs. Overall, the paired conjoint design, where respondents evaluate two immigrants side by side, comes closest to the behavioral benchmark; on average, its estimates are within 2% percentage points of the effects in the behavioral benchmark.

696 citations

Journal ArticleDOI
TL;DR: This work has shown that nature has provided various safety mechanisms for the variety of novel pols identified in the last three years, including the lesion-replicating enzymes pol zeta, pol eta, pol iota, pol kappa, and Rev1, and a group of pols called pol theta that fulfill a variety of other tasks.
Abstract: ▪ Abstract Any living cell is faced with the fundamental task of keeping the genome intact in order to develop in an organized manner, to function in a complex environment, to divide at the right time, and to die when it is appropriate. To achieve this goal, an efficient machinery is required to maintain the genetic information encoded in DNA during cell division, DNA repair, DNA recombination, and the bypassing of damage in DNA. DNA polymerases (pols) α, β, γ, δ, and ϵ are the key enzymes required to maintain the integrity of the genome under all these circumstances. In the last few years the number of known pols, including terminal transferase and telomerase, has increased to at least 19. A particular pol might have more than one functional task in a cell and a particular DNA synthetic event may require more than one pol, which suggests that nature has provided various safety mechanisms. This multi-functional feature is especially valid for the variety of novel pols identified in the last three years. T...

696 citations

Journal ArticleDOI
TL;DR: Rindopepimut did not increase survival in patients with newly diagnosed glioblastoma, and combination approaches potentially including rindopEPimut might be required to show efficacy of immunotherapy in gliOBlastoma.
Abstract: Summary Background Rindopepimut (also known as CDX-110), a vaccine targeting the EGFR deletion mutation EGFRvIII, consists of an EGFRvIII-specific peptide conjugated to keyhole limpet haemocyanin. In the ACT IV study, we aimed to assess whether or not the addition of rindopepimut to standard chemotherapy is able to improve survival in patients with EGFRvIII-positive glioblastoma. Methods In this randomised, double-blind, phase 3 trial, we recruited patients aged 18 years and older with glioblastoma from 165 hospitals in 22 countries. Eligible patients had newly diagnosed glioblastoma confirmed to express EGFRvIII by central analysis, and had undergone maximal surgical resection and completion of standard chemoradiation without progression. Patients were stratified by European Organisation for Research and Treatment of Cancer recursive partitioning analysis class, MGMT promoter methylation, and geographical region, and randomly assigned (1:1) with a prespecified randomisation sequence (block size of four) to receive rindopepimut (500 μg admixed with 150 μg GM-CSF) or control (100 μg keyhole limpet haemocyanin) via monthly intradermal injection until progression or intolerance, concurrent with standard oral temozolomide (150–200 mg/m 2 for 5 of 28 days) for 6–12 cycles or longer. Patients, investigators, and the trial funder were masked to treatment allocation. The primary endpoint was overall survival in patients with minimal residual disease (MRD; enhancing tumour 2 post-chemoradiation by central review), analysed by modified intention to treat. This trial is registered with ClinicalTrials.gov, number NCT01480479. Findings Between April 12, 2012, and Dec 15, 2014, 745 patients were enrolled (405 with MRD, 338 with significant residual disease [SRD], and two unevaluable) and randomly assigned to rindopepimut and temozolomide (n=371) or control and temozolomide (n=374). The study was terminated for futility after a preplanned interim analysis. At final analysis, there was no significant difference in overall survival for patients with MRD: median overall survival was 20·1 months (95% CI 18·5–22·1) in the rindopepimut group versus 20·0 months (18·1–21·9) in the control group (HR 1·01, 95% CI 0·79–1·30; p=0·93). The most common grade 3–4 adverse events for all 369 treated patients in the rindopepimut group versus 372 treated patients in the control group were: thrombocytopenia (32 [9%] vs 23 [6%]), fatigue (six [2%] vs 19 [5%]), brain oedema (eight [2%] vs 11 [3%]), seizure (nine [2%] vs eight [2%]), and headache (six [2%] vs ten [3%]). Serious adverse events included seizure (18 [5%] vs 22 [6%]) and brain oedema (seven [2%] vs 12 [3%]). 16 deaths in the study were caused by adverse events (nine [4%] in the rindopepimut group and seven [3%] in the control group), of which one—a pulmonary embolism in a 64-year-old male patient after 11 months of treatment—was assessed as potentially related to rindopepimut. Interpretation Rindopepimut did not increase survival in patients with newly diagnosed glioblastoma. Combination approaches potentially including rindopepimut might be required to show efficacy of immunotherapy in glioblastoma. Funding Celldex Therapeutics, Inc.

695 citations

Journal ArticleDOI
25 Jun 2010-Science
TL;DR: A reversible germ-free colonization system in mice that is independent of diet or antibiotic manipulation is reported, and specific IgA induction occurred as a stepwise response to current bacterial exposure, such that the antibody repertoire matched the existing commensal content.
Abstract: The lower intestine of adult mammals is densely colonized with nonpathogenic (commensal) microbes. Gut bacteria induce protective immune responses, which ensure host-microbial mutualism. The continuous presence of commensal intestinal bacteria has made it difficult to study mucosal immune dynamics. Here, we report a reversible germ-free colonization system in mice that is independent of diet or antibiotic manipulation. A slow (more than 14 days) onset of a long-lived (half-life over 16 weeks), highly specific anticommensal immunoglobulin A (IgA) response in germ-free mice was observed. Ongoing commensal exposure in colonized mice rapidly abrogated this response. Sequential doses lacked a classical prime-boost effect seen in systemic vaccination, but specific IgA induction occurred as a stepwise response to current bacterial exposure, such that the antibody repertoire matched the existing commensal content.

694 citations


Authors

Showing all 51384 results

NameH-indexPapersCitations
Richard A. Flavell2311328205119
Peer Bork206697245427
Thomas C. Südhof191653118007
Stuart H. Orkin186715112182
Ruedi Aebersold182879141881
Tadamitsu Kishimoto1811067130860
Stanley B. Prusiner16874597528
Yang Yang1642704144071
Tomas Hökfelt158103395979
Dan R. Littman157426107164
Hans Lassmann15572479933
Matthias Egger152901184176
Lorenzo Bianchini1521516106970
Robert M. Strieter15161273040
Ashok Kumar1515654164086
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Performance
Metrics
No. of papers from the Institution in previous years
YearPapers
2023265
20221,039
20218,997
20208,398
20197,336
20186,832