Materials Map

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The Materials Map is an open tool for improving networking and interdisciplinary exchange within materials research. It enables cross-database search for cooperation and network partners and discovering of the research landscape.

The dashboard provides detailed information about the selected scientist, e.g. publications. The dashboard can be filtered and shows the relationship to co-authors in different diagrams. In addition, a link is provided to find contact information.

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The Materials Map is still under development. In its current state, it is only based on one single data source and, thus, incomplete and contains duplicates. We are working on incorporating new open data sources like ORCID to improve the quality and the timeliness of our data. We will update Materials Map as soon as possible and kindly ask for your patience.

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in Cooperation with on an Cooperation-Score of 37%

Topics

Publications (1/1 displayed)

  • 2022A functional microRNA binding site variant in IL-23R gene in systemic lupus erythematosus and rheumatoid arthritis: is there any correlation?3citations

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Ghorashi, Tahereh
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Soosanabadi, Mohsen
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Dizghandi, Saeed Esmaeili
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2022

Co-Authors (by relevance)

  • Ghorashi, Tahereh
  • Soosanabadi, Mohsen
  • Siri, Goli
  • Alesaeidi, Samira
  • Dizghandi, Saeed Esmaeili
  • Kenarangi, Taiebe
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article

A functional microRNA binding site variant in IL-23R gene in systemic lupus erythematosus and rheumatoid arthritis: is there any correlation?

  • Ghorashi, Tahereh
  • Soosanabadi, Mohsen
  • Siri, Goli
  • Alesaeidi, Samira
  • Mosallaei, Meysam
  • Dizghandi, Saeed Esmaeili
  • Kenarangi, Taiebe
Abstract

<AbstractText Label="BACKGROUND" NlmCategory="BACKGROUND">IL-23 receptor (IL-23R) dysregulation has been shown to have critical roles in pathogenesis of different autoimmune diseases including systemic lupus erythematosus (SLE) and rheumatoid arthritis (RA) via suppression of regulatory T cells (Tregs) as well as differentiation, expansion, and survival of T helper 17 (Th17) cells, followed by upregulation of interleukin 17 (IL-17). Here, we assessed the association of a functional microRNAs (miRNAs)-related single nucleotide polymorphism (miR-SNPs: rs10889677) in IL-23R, which was correlated with its overexpression and increased risk for SLE and RA in the Iranian population.</AbstractText><AbstractText Label="METHODS" NlmCategory="METHODS">Genotype and allele distribution of rs10889677 variant were investigated in 105 RA patients, 100 SLE cases and 105 healthy controls via polymerase chain reaction- restriction fragment length polymorphism (PCR-RFLP) method.</AbstractText><AbstractText Label="RESULTS" NlmCategory="RESULTS">Our findings suggested that AA genotype, but not AC genotype, was associated with increased risk of RA (AA vs. CC; OR: 3.27; 95%CI [1.467-7.551]). The allele A was more frequent in RA group compared to controls (A allele vs. C allele; OR: 1.92; 95%CI [1.282-2.894]). This common variant was not significantly correlated with SLE risk in our population (P &gt; 0.05). However, stratification analysis indicated that RA patients with AA genotype show higher serum concentration levels of C-reactive protein (CRP) (P: 0.008). No obvious correlation was noticed between different genotypes in SLE cases, except for a slight difference in terms of oral ulcer manifestation incidence (P: 0.038).</AbstractText><AbstractText Label="CONCLUSION" NlmCategory="CONCLUSIONS">This study suggests a significant relationship between rs10889677 variant in IL-23R with increased risk of RA and some clinical features in RA and SLE patients.</AbstractText><CopyrightInformation>© 2022. The Author(s), under exclusive licence to Springer Nature B.V.</CopyrightInformation>

Topics
  • impedance spectroscopy
  • reactive
  • chemical ionisation