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RPL18 60S ribosomal protein L18-2

RPL18, ribosomal protein L18
Encodes cytoplasmic ribosomal protein L18. (from NCBI)
Top mentioned proteins: ACID, CAN, GAPDH, SET, fibrillin-1
Papers on RPL18
Dengue virus NS1 protein interacts with the ribosomal protein RPL18: this interaction is required for viral translation and replication in Huh-7 cells.
Del Angel et al., Mexico. In Virology, Oct 2015
The subcellular location and expression levels during infection of the ribosomal proteins RPS3a, RPL7, RPL18, RPL18a plus GAPDH were determined.
Translational control of the cytosolic stress response by mitochondrial ribosomal protein L18.
Qian et al., Ithaca, United States. In Nat Struct Mol Biol, May 2015
Here we report an unexpected role for mitochondrial ribosomal protein L18 (MRPL18) in the mammalian cytosolic stress response.
Selection of suitable reference genes for normalization of quantitative RT-PCR in peripheral blood samples of bottlenose dolphins (Tursiops truncatus).
Yang et al., Davis, United States. In Sci Rep, 2014
Seventy-five blood samples collected from 7 bottlenose dolphins were used to analyze 15 candidate HKGs (ACTB, B2M, GAPDH, HPRT1, LDHB, PGK1, RPL4, RPL8, RPL18, RPS9, RPS18, TFRC, YWHAZ, LDHA, SDHA).
Comprehensive analysis of the ubiquitinome during oncogene-induced senescence in human fibroblasts.
Zhang et al., Philadelphia, United States. In Cell Cycle, 2014
This includes several translation initiation factors (eIF2C2, eIF2B4, eIF3I, eIF3L, eIF4A1) and elongation factors (eEF1G, eEF1A) as well as 40S (RPS4X, RPS7, RPS11 and RPS20) and 60S ribosomal subunits (RPL10, RPL11, RPL18 and RPL35a).
Development of two molecular approaches for differentiation of clinically relevant yeast species closely related to Candida guilliermondii and Candida famata.
Yao et al., Shanghai, China. In J Clin Microbiol, 2014
The second method involves a multiplex PCR based on the intron size differences of RPL18, a gene coding for a protein component of the large (60S) ribosomal subunit, and species-specific amplification.
Identification and validation of reference genes for quantitative real-time PCR in Drosophila suzukii (Diptera: Drosophilidae).
Yu et al., Jinan, China. In Plos One, 2013
In this study, ten candidate reference genes (RPL18, RPS3, AK, EF-1β, TBP, NADH, HSP22, GAPDH, Actin, α-Tubulin), were evaluated for their suitability as normalization genes under different biotic (developmental stage, tissue and population), and abiotic (photoperiod, temperature) conditions.
Validation of reference genes for gene expression analysis in olive (Olea europaea) mesocarp tissue by quantitative real-time RT-PCR.
Johnson et al., Melbourne, Australia. In Bmc Res Notes, 2013
RESULTS: A total of eight candidate reference genes [glyceraldehyde 3-phosphate dehydrogenase (GAPDH), serine/threonine-protein phosphatase catalytic subunit (PP2A), elongation factor 1 alpha (EF1-alpha), polyubiquitin (OUB2), aquaporin tonoplast intrinsic protein (TIP2), tubulin alpha (TUBA), 60S ribosomal protein L18-3 (60S RBP L18-3) and polypyrimidine tract-binding protein homolog 3 (PTB)] were chosen based on their stability in olive tissues as well as in other plants.
Determination and validation of reference gene stability for qPCR analysis in polysaccharide hydrogel-based 3D chondrocytes and mesenchymal stem cell cultural models.
Wang et al., Singapore, Singapore. In Mol Biotechnol, 2013
On the other hand, HPRT, PPIA, and RPL18 were the stable reference genes for rabbit chondrocytes in alginate scaffold while TBP, RPL5, and RPL18 were selected for rabbit chondrocytes in agarose scaffold.
Isolation and analysis of mRNAs from specific cell types of plants by ribosome immunopurification.
Bailey-Serres et al., Bayreuth, Germany. In Methods Mol Biol, 2012
Here we present detailed methods for development of transgenics that express a FLAG-tagged version of ribosomal protein L18 (RPL18) under the direction of individual promoters with specific domains of expression, the immunopurification of ribosomes, and bioinformatic analyses of the resultant datasets obtained by microarray profiling.
Novel polysome messages and changes in translational activity appear after induction of adipogenesis in 3T3-L1 cells.
Baumgartner et al., Göttingen, Germany. In Bmc Mol Biol, 2011
Up-regulated genes comprise factors that are nucleic acid binding (eIF4B, HSF1, IRF6, MYC, POLR2a, RPL18, RPL27a, RPL6, RPL7a, RPS18, RPSa, TSC22d3), form part of ribosomes (RPL18, RPL27a, RPL6, RPL7a, RPS18, RPSa), act on the regulation of translation (eIF4B) or transcription (HSF1, IRF6, MYC, TSC22d3).
Identification and validation of reference genes for quantitative real-time polymerase chain reaction in Cimex lectularius.
Mittapalli et al., Wooster, United States. In J Med Entomol, 2011
Ribosomal protein (RPL18) exhibited the most stable gene expression across all the tissue and developmental-stage samples; a-tubulin revealed the least stability across all of the samples examined.
Biological significance of 5S rRNA import into human mitochondria: role of ribosomal protein MRP-L18.
Tarassov et al., Strasbourg, France. In Genes Dev, 2011
In this study, we describe an elegant molecular conveyor composed of a previously identified human 5S rRNA import factor, rhodanese, and mitochondrial ribosomal protein L18, thanks to which 5S rRNA molecules can be specifically withdrawn from the cytosolic pool and redirected to mitochondria, bypassing the classic nucleolar reimport pathway.
Identification of essential filovirion-associated host factors by serial proteomic analysis and RNAi screen.
Bavari et al., Frederick, United States. In Mol Cell Proteomics, 2010
HSPA5 and RPL18) significantly interfered with ebolavirus and marburgvirus infection, suggesting specific and relevant virion incorporation.
Tasco(®), a product of Ascophyllum nodosum, imparts thermal stress tolerance in Caenorhabditis elegans.
Prithiviraj et al., Truro, Canada. In Mar Drugs, 2010
Among them heat shock proteins, superoxide dismutase, glutathione peroxidase, aldehyde dehydrogenase, saposin-like proteins 20, myosin regulatory light chain 1, cytochrome c oxidase RAS-like, GTP-binding protein RHO A, OS were significantly up-regulated, while eukaryotic translation initiation factor 5A-1 OS, 60S ribosomal protein L18 OS, peroxiredoxin protein 2 were down regulated by TWE treatment.
Isolation of plant polysomal mRNA by differential centrifugation and ribosome immunopurification methods.
Bailey-Serres et al., Riverside, United States. In Methods Mol Biol, 2008
A modification of the conventional polysome isolation procedure is described for transgenic Arabidopsis thaliana that express an epitope-tagged version of ribosomal protein L18 (RPL18) that facilitates capture of ribosomes from crude cell extracts by a one-step immunoprecipitation method.
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