| Literature DB >> 27097230 |
Kitti Csályi1,2, Dávid Fazekas1,3, Tamás Kadlecsik1, Dénes Türei1,4,5, Leila Gul1, Balázs Horváth1, Dezső Módos1,6,7, Amanda Demeter1,8, Nóra Pápai1, Katalin Lenti6, Péter Csermely9, Tibor Vellai1, Tamás Korcsmáros1,3,8, Máté Varga1,10.
Abstract
Understanding living systems requires an in-depth knowledge of the signaling networks that drive cellular homeostasis, regulate intercellular communication, and contribute to cell fates during development. Several resources exist to provide high-throughput data sets or manually curated interaction information from human or invertebrate model organisms. We previously developed SignaLink, a uniformly curated, multi-layered signaling resource containing information for human and for the model organisms nematode Caenorhabditis elegans and fruit fly Drosophila melanogaster. Until now, the use of the SignaLink database for zebrafish pathway analysis was limited. To overcome this limitation, we created SignaFish ( http://signafish.org ), a fish-specific signaling resource, built using the concept of SignaLink. SignaFish contains more than 200 curation-based signaling interactions, 132 further interactions listed in other resources, and it also lists potential miRNA-based regulatory connections for seven major signaling pathways. From the SignaFish website, users can reach other web resources, such as ZFIN. SignaFish provides signaling or signaling-related interactions that can be examined for each gene or downloaded for each signaling pathway. We believe that the SignaFish resource will serve as a novel navigating point for experimental design and evaluation for the zebrafish community and for researchers focusing on nonmodel fish species, such as cyclids.Entities:
Keywords: database; miRNA; pathway; regulation; signaling network; zebrafish
Mesh:
Year: 2016 PMID: 27097230 DOI: 10.1089/zeb.2016.1277
Source DB: PubMed Journal: Zebrafish ISSN: 1545-8547 Impact factor: 1.985