Use my Search Websuite to scan PubMed, PMCentral, Journal Hosts and Journal Archives, FullText.
Kick-your-searchterm to multiple Engines kick-your-query now !>
A dictionary by aggregated review articles of nephrology, medicine and the life sciences
Your one-stop-run pathway from word to the immediate pdf of peer-reviewed on-topic knowledge.

suck abstract from ncbi


10.1371/journal.pone.0154134

http://scihub22266oqcxt.onion/10.1371/journal.pone.0154134
suck pdf from google scholar
C4839687!4839687 !27101102
unlimited free pdf from europmc27101102
    free
PDF from PMC    free
html from PMC    free

Warning: file_get_contents(https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&id=27101102 &cmd=llinks): Failed to open stream: HTTP request failed! HTTP/1.1 429 Too Many Requests in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 215

suck abstract from ncbi

pmid27101102
      PLoS+One 2016 ; 11 (4 ): e0154134
Nephropedia Template TP

gab.com Text

Twit Text FOAVip

Twit Text #

English Wikipedia


  • Guanine-Rich Sequences Are a Dominant Feature of Exosomal microRNAs across the Mammalian Species and Cell Types #MMPMID27101102
  • Momose F ; Seo N ; Akahori Y ; Sawada S ; Harada N ; Ogura T ; Akiyoshi K ; Shiku H
  • PLoS One 2016[]; 11 (4 ): e0154134 PMID27101102 show ga
  • Exosome is an extracellular vesicle released from multivesicular endosomes and contains micro (mi) RNAs and functional proteins derived from the donor cells. Exosomal miRNAs act as an effector during communication with appropriate recipient cells, this can aid in the utilization of the exosomes in a drug delivery system for various disorders including malignancies. Differences in the miRNA distribution pattern between exosomes and donor cells indicate the active translocation of miRNAs into the exosome cargos in a miRNA sequence-dependent manner, although the molecular mechanism is little known. In this study, we statistically analyzed the miRNA microarray data and revealed that the guanine (G)-rich sequence is a dominant feature of exosome-dominant miRNAs, across the mammalian species-specificity and the cell types. Our results provide important information regarding the potential use of exosome cargos to develop miRNA-based drugs for the treatment of human diseases.
  • |A549 Cells [MESH]
  • |Animals [MESH]
  • |Base Sequence [MESH]
  • |Cell Line [MESH]
  • |Cells, Cultured [MESH]
  • |Exosomes/*genetics/metabolism [MESH]
  • |Female [MESH]
  • |Flow Cytometry [MESH]
  • |Gene Expression Profiling/methods [MESH]
  • |Guanine/*analysis [MESH]
  • |HCT116 Cells [MESH]
  • |Humans [MESH]
  • |K562 Cells [MESH]
  • |Macrophages/cytology/*metabolism [MESH]
  • |Membrane Proteins/metabolism [MESH]
  • |Mice, Inbred BALB C [MESH]
  • |MicroRNAs/*genetics [MESH]
  • |Neoplasms/genetics/metabolism/pathology [MESH]
  • |Oligonucleotide Array Sequence Analysis/methods [MESH]
  • |Reverse Transcriptase Polymerase Chain Reaction [MESH]


  • DeepDyve
  • Pubget Overpricing
  • suck abstract from ncbi

    Linkout box