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Showing 1–18 of 18 results
Advanced filters: Author: Ralf Herwig Clear advanced filters
  • The temporal regulation of intracellular insulin signaling is not well studied. Here the authors conducted a time-resolved analysis of the global insulin-regulated phosphoproteome in human muscle cells, revealing synchronized signaling pathways for propagating information to insulin effector sites.

    • Michael Turewicz
    • Christine Skagen
    • Hadi Al-Hasani
    ResearchOpen Access
    Nature Communications
    Volume: 16, P: 1-19
  • This report from the 1000 Genomes Project describes the genomes of 1,092 individuals from 14 human populations, providing a resource for common and low-frequency variant analysis in individuals from diverse populations; hundreds of rare non-coding variants at conserved sites, such as motif-disrupting changes in transcription-factor-binding sites, can be found in each individual.

    • Gil A. McVean
    • David M. Altshuler (Co-Chair)
    • Gil A. McVean
    ResearchOpen Access
    Nature
    Volume: 491, P: 56-65
  • Results for the final phase of the 1000 Genomes Project are presented including whole-genome sequencing, targeted exome sequencing, and genotyping on high-density SNP arrays for 2,504 individuals across 26 populations, providing a global reference data set to support biomedical genetics.

    • Adam Auton
    • Gonçalo R. Abecasis
    • Gonçalo R. Abecasis
    ResearchOpen Access
    Nature
    Volume: 526, P: 68-74
  • STAT3 is an intracellular transducer of cytokine signals that cooperates with Ras in tumour formation and is often activated in lung cancer. Here the authors show that STAT3 acts as a tumour suppressor in a mouse model of Kras-driven lung adenocarcinoma.

    • Beatrice Grabner
    • Daniel Schramek
    • Emilio Casanova
    ResearchOpen Access
    Nature Communications
    Volume: 6, P: 1-14
  • The goal of the 1000 Genomes Project is to provide in-depth information on variation in human genome sequences. In the pilot phase reported here, different strategies for genome-wide sequencing, using high-throughput sequencing platforms, were developed and compared. The resulting data set includes more than 95% of the currently accessible variants found in any individual, and can be used to inform association and functional studies.

    • Richard M. Durbin
    • David Altshuler (Co-Chair)
    • Gil A. McVean
    ResearchOpen Access
    Nature
    Volume: 467, P: 1061-1073
  • The heterogeneity of colorectal cancer has important clinical and therapeutic implications. Here the authors analysed the responses of a large biobank of organoids and xenografts derived from colorectal patients to a panel of clinically relevant therapeutic agents to identify genes signatures associated with drug response.

    • Moritz Schütte
    • Thomas Risch
    • Marie-Laure Yaspo
    ResearchOpen Access
    Nature Communications
    Volume: 8, P: 1-19
  • Dysregulation of centrosome size and number is frequently associated with cancer. Fogeron et al. construct a protein-interaction network to identify proteins that are relevant for centrosome abnormalities in cancer, and show that deregulation of LGALS3BP affects centrosomal biogenesis.

    • Marie-Laure Fogeron
    • Hannah Müller
    • Bodo M.H. Lange
    Research
    Nature Communications
    Volume: 4, P: 1-14
  • 1000 Genomes imputation can increase the power of genome-wide association studies to detect genetic variants associated with human traits and diseases. Here, the authors develop a method to integrate and analyse low-coverage sequence data and SNP array data, and show that it improves imputation performance.

    • Olivier Delaneau
    • Jonathan Marchini
    • Leena Peltonenz
    Research
    Nature Communications
    Volume: 5, P: 1-9
  • This Registered Report presents the results of the Long-read RNA-Seq Genome Annotation Assessment Project, which is a community effort for benchmarking long-read methods for transcriptome analyses, including transcript isoform detection, quantification and de novo transcript detection.

    • Francisco J. Pardo-Palacios
    • Dingjie Wang
    • Angela N. Brooks
    ResearchOpen Access
    Nature Methods
    Volume: 21, P: 1349-1363
  • Using a network propagation approach with integrated multi-omic data, Selevsek et al. develop a reproducible workflow for identifying drug toxicity effects in cellular systems. This is demonstrated with the analysis of anthracycline cardiotoxicity in cardiac microtissues under the effect of multiple drugs.

    • Nathalie Selevsek
    • Florian Caiment
    • Jos Kleinjans
    ResearchOpen Access
    Communications Biology
    Volume: 3, P: 1-15
  • The IDG-DREAM Challenge carried out crowdsourced benchmarking of predictive algorithms for kinase inhibitor activities on unpublished data. This study provides a resource to compare emerging algorithms and prioritize new kinase activities to accelerate drug discovery and repurposing efforts.

    • Anna Cichońska
    • Balaguru Ravikumar
    • Tero Aittokallio
    ResearchOpen Access
    Nature Communications
    Volume: 12, P: 1-18
  • ConsensusPathDB combines molecular interaction data from multiple sources and provides a web interface to vizualize these data. This can be used to build interaction networks and to perform enrichment/over-representation analysis.

    • Ralf Herwig
    • Christopher Hardt
    • Atanas Kamburov
    Protocols
    Nature Protocols
    Volume: 11, P: 1889-1907