1,720,989 research outputs found

    Glutamicibacter creatinolyticus strain LGCM 259 chromosome, complete genome

    Full text link
    NCBI Reference Sequence: NZ_CP034412.1 The complete genome sequencing of G. creatinolyticus LGCM 259 was deposited with the National Center for Biotechnology Information (NCBI) under accession number CP034412; BioProject: PRJNA507728, BioSample: SAMN10502625, Assembly: GCF_006094275.1 and the same became NCBI RefSeq sequence NZ_CP034412.1. https://www.ncbi.nlm.nih.gov/nuccore/1679400616. LOCUS NZ_CP034412 3309128 bp DNA circular CON 08JUN2019 DEFINITION Glutamicibacter creatinolyticus strain LGCM 259 chromosome, complete genome. ACCESSION NZ_CP034412 VERSION NZ_CP034412.1 DBLINK BioProject: PRJNA224116 BioSample: SAMN10502625 Assembly: GCF_006094275.1 KEYWORDS RefSeq. SOURCE Glutamicibacter creatinolyticus ORGANISM Glutamicibacter creatinolyticus Bacteria; Actinobacteria; Micrococcales; Micrococcaceae; Glutamicibacter. REFERENCE 1 (bases 1 to 3309128) AUTHORS Santos,R.G., Silva,A.L., Seyffert,N., Castro,T.L.P., Attili,A.R., Rifici,C., Mazzullo,G., Brenig,B., Venanzi,F. and Azevedo,V. TITLE Complete Genome Sequence of Glutamicibacter creatinolyticus strain LGCM259,isolated from an abscess of a 12yearold mare in Italy JOURNAL Unpublished REFERENCE 2 (bases 1 to 3309128) AUTHORS Santos,R.G., Silva,A.L., Seyffert,N., Castro,T.L.P., Attili,A.R., Rifici,C., Mazzullo,G., Brenig,B., Venanzi,F. and Azevedo,V. TITLE Direct Submission JOURNAL Submitted (07DEC2018) General Biology, UFMG, Av Antonio Carlos 6627, Pampulha, Belo Horizonte, Minhas Gerais 31270901, Brazil COMMENT REFSEQ INFORMATION: The reference sequence was derived from CP034412. The annotation was added by the NCBI Prokaryotic Genome Annotation Pipeline (PGAP). Information about PGAP can be found here: https://www.ncbi.nlm.nih.gov/genome/annotation_prok/ Bacteria and source DNA available from GcLGCM259. ##GenomeAssemblyDataSTART## Assembly Date :: OCT2018 Assembly Method :: SPAdes v. 3.9.1 Assembly Name :: GcLGCM259 Genome Representation :: Full Expected Final Version :: Yes Genome Coverage :: 286.0x Sequencing Technology :: Illumina HiSeq ##GenomeAssemblyDataEND## ##GenomeAnnotationDataSTART## Annotation Provider :: NCBI RefSeq Annotation Date :: 06/07/2019 10:17:37 Annotation Pipeline :: NCBI Prokaryotic Genome Annotation Pipeline (PGAP) Annotation Method :: Bestplaced reference protein set; GeneMarkS2+ Annotation Software revision :: 4.8 Features Annotated :: Gene; CDS; rRNA; tRNA; ncRNA; repeat_region Genes (total) :: 3,035 CDSs (total) :: 2,962 Genes (coding) :: 2,882 CDSs (with protein) :: 2,882 Genes (RNA) :: 73 rRNAs :: 4, 4, 4 (5S, 16S, 23S) complete rRNAs :: 4, 4, 4 (5S, 16S, 23S) tRNAs :: 58 ncRNAs :: 3 Pseudo Genes (total) :: 80 CDSs (without protein) :: 80 Pseudo Genes (ambiguous residues) :: 0 of 80 Pseudo Genes (frameshifted) :: 31 of 80 Pseudo Genes (incomplete) :: 51 of 80 Pseudo Genes (internal stop) :: 6 of 80 GenBank Due to the large size of this record, sequence and annotated features are not shown. Use the "Customize view" panel to change the display##GenomeAnnotationDataEND## COMPLETENESS: full length. FEATURES Location/Qualifiers source 1..3309128 /organism="Glutamicibacter creatinolyticus" /mol_type="genomic DNA" /strain="LGCM 259" /isolation_source="abcess of a mare" /host="horse" /db_xref="taxon:162496" /country="Italy" /collection_date="2015" CONTIG join(CP034412.1:1..3309128) /

    Mast cells in canine mammary gland tumour: Number, distribution and EPOR positivity

    No full text
    Erythropoietin (EPO)-mediated mitogenic and anti-apoptotic effects involve all the cells expressing functional receptors for EPO (EPOR), as demonstrated by in vitro and in vivo studies. EPO shows pleiotropic effects and acts as an endogenous mediator of adaptive tissue response to metabolic stress protecting tissues from different injuries. Recently, the EPO/EPOR complex has been identified in several neoplastic cell lines and solid tumours. In this study, the authors investigated the mast cells (MCs) number, distribution and their immunoreactivity for EPOR in normal, dysplastic and neoplastic canine mammary gland. The results showed that MCs were more numerous in displastic glands compared with normal and neoplastic glands. As far as the EPOR immunoreactivity is concerned, we did not observe MCs reaction on cancer, in contrast with previously published data where epithelium of neoplastic gland showed an increase in EPOR expression along with the neoplastic progression. Overall, our results might be suggestive for MCs role in oncogenesis and offer new insight regarding to the expression of EPOR in mammary gland cancer in do

    Going Beyond Counting First Authors in Author Co-citation Analysis

    Full text link
    The present study examines one of the fundamental aspects of author co-citation analysis (ACA) - the way co-citation counts are defined. Co-citation counting provides the data on which all subsequent statistical analyses and mappings are based, and we compare ACA results based on two different types of co-citation counting - the traditional type that only counts the first one among a cited work's authors on the one hand and a non-traditional type that takes into account the first 5 authors of a cited work on the other hand. Results indicate that the picture produced through this non-traditional author co-citation counting contains more coherent author groups and is therefore considerably clearer. However, this picture represents fewer specialties in the research field being studied than that produced through the traditional first-author co-citation counting when the same number of top-ranked authors is selected and analyzed. Reasons for these effects are discussed
    corecore