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Hoffmann, R. A wiki for the life sciences where authorship matters. Nature Genetics (2008)
 
MeSH Review

Reticulocytes

 
 
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Disease relevance of Reticulocytes

 

High impact information on Reticulocytes

  • Silenced LOX mRNA in rabbit reticulocytes specifically coimmunoprecipitated with hnRNP K [6].
  • We have purified two proteins from rabbit reticulocytes that specifically mediate LOX silencing and identified them as hnRNPs K and E1 [6].
  • In vitro experiments with a fusion construct using reticulocyte lysates demonstrate polyamine-dependent expression with a frameshift efficiency of 19% at the optimal concentration of spermidine [7].
  • There was a 28 percent increase in the number of reticulocytes containing fetal hemoglobin and a 48 percent increase in the percentage of fetal hemoglobin, as compared with the maximal values obtained with hydroxyurea alone [8].
  • Treatment with erythropoietin, either alone or in combination with hydroxyurea, had no significant effect on the percentage of hemoglobin F-containing reticulocytes (F reticulocytes) or red cells (F cells) [9].
 

Chemical compound and disease context of Reticulocytes

 

Biological context of Reticulocytes

 

Anatomical context of Reticulocytes

 

Associations of Reticulocytes with chemical compounds

 

Gene context of Reticulocytes

  • In the rad6 delta 1-9 mutant, beta-galactosidase proteins bearing destabilizing amino-terminal residues become long lived, and purified rad6 delta 1-9 protein is ineffective in ubiquitin-protein ligase (E3)-dependent protein degradation in the proteolytic system derived from rabbit reticulocytes [29].
  • Sequence analysis using PCR-amplified cDNA revealed that the 5'-end of the coding sequence of G6PD mRNA in reticulocytes is identical to those in other tissues [30].
  • In contrast, PMN and MNL IL-1 alpha and beta mRNAs were translated with equal efficiency in rabbit reticulocyte lysates, suggesting that synthesis of IL-1 in PMN is subject to some form of translational control [31].
  • Curcumin, a CSN kinase inhibitor, blocks E6-dependent p53 degradation in reticulocyte lysates [32].
  • Mutation of Thr155 to valine is sufficient to stabilize p53 against E6-dependent degradation in reticulocyte lysates and to reduce binding to Mdm2 [32].
 

Analytical, diagnostic and therapeutic context of Reticulocytes

References

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