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)

  • 2021Lower androgen levels promote abnormal cartilage development in female patients with adolescent idiopathic scoliosis.1citations

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Yx, Wang
1 / 2 shared
Deng, A.
1 / 1 shared
Yj, Wang
1 / 1 shared
Yt, Wu
1 / 1 shared
Mx, Tang
1 / 1 shared
Li, J.
1 / 70 shared
Hq, Zhang
1 / 1 shared
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2021

Co-Authors (by relevance)

  • Yx, Wang
  • Deng, A.
  • Yj, Wang
  • Yt, Wu
  • Mx, Tang
  • Li, J.
  • Hq, Zhang
OrganizationsLocationPeople

article

Lower androgen levels promote abnormal cartilage development in female patients with adolescent idiopathic scoliosis.

  • Yx, Wang
  • Deng, A.
  • Yj, Wang
  • Yt, Wu
  • Mx, Tang
  • Li, J.
  • Cf, Guo
  • Hq, Zhang
Abstract

<h4>Background</h4>Adolescent idiopathic scoliosis (AIS) is a disease characterized by changes in the three-dimensional structure of the spine. Studies have shown that the development of AIS might be associated with genetic, biomechanics, endocrine factors and abnormal bone or cartilage development.<h4>Methods</h4>Blood samples collected from 301 female patients (161 females with AIS and 140 females without AIS) were used for genotyping. Forty-eight serum samples from 161 females with AIS and 40 serum samples from 140 females without AIS were subjected to enzyme-linked immunosorbent assays (ELISAs). We also evaluated 32 facet joints (18 females with AIS and 14 females without AIS from the 301 female patients) using immunohistochemistry, Western blotting, and isolation of human primary chondrocytes, among other methods. We treated the AIS primary chondrocytes with dihydrotestosterone (DHT) to verify the relationship among androgen, the androgen receptor (AR), and its downstream pathway proteins.<h4>Results</h4>The serum androgen level in the AIS group was significantly decreased (1.94±0.09 <i>vs.</i> 2.284±0.103) compared with that in the non-AIS (control) group. The single nucleotide polymorphism genotyping results showed that the mutation rates of rs6259 between the AIS and control groups were significantly different (G/G genotype: 48.4% <i>vs.</i> 42.1%, G/A genotype: 40.4% <i>vs.</i> 35.7%, P<0.05). The levels of interleukin (IL)-6 and metalloproteinase (MMP)-13 were increased in the cartilage of AIS patients, and these patients also exhibited decreased AR levels. The cell experiment results showed that androgen reduced the degree of abnormal cartilage development in female AIS patients through the AR/IL-6/signal transducer and activator of transcription 3 (STAT3) signaling pathway.<h4>Conclusions</h4>Our study provides a new perspective on the pathogenesis of AIS and indicates that decreased androgen levels in female AIS patients play a potential role in the development of AIS via the AR/IL-6/STAT3 signaling pathway.

Topics
  • impedance spectroscopy
  • experiment