Materials Map

Discover the materials research landscape. Find experts, partners, networks.

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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 (2/2 displayed)

  • 2011The distribution of exon 3-deleted/full-length growth hormone receptor polymorphism in the Turkish population.7citations
  • 2011Comparison of lipid profiles with APOA1 MspI polymorphism in obese children with hyperlipidemia.citations

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Chart of shared publication
Timirci, Ö.
1 / 1 shared
Keleşoğlu, F.
1 / 1 shared
Bozkurt, N.
1 / 1 shared
Kabataş Eryılmaz, S.
1 / 1 shared
Baş, F.
1 / 1 shared
Bundak, R.
1 / 1 shared
Küçükemre Aydın, B.
1 / 1 shared
Isbir, T.
2 / 4 shared
Keleşoglu, F.
1 / 1 shared
Gürkan, H.
1 / 1 shared
Bas, F.
1 / 1 shared
Toptas, B.
1 / 1 shared
Ergen, A.
1 / 2 shared
Görmüş, Uzay
1 / 1 shared
Izbirak, G.
1 / 1 shared
Ab, Dalan
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2011

Co-Authors (by relevance)

  • Timirci, Ö.
  • Keleşoğlu, F.
  • Bozkurt, N.
  • Kabataş Eryılmaz, S.
  • Baş, F.
  • Bundak, R.
  • Küçükemre Aydın, B.
  • Isbir, T.
  • Keleşoglu, F.
  • Gürkan, H.
  • Bas, F.
  • Toptas, B.
  • Ergen, A.
  • Görmüş, Uzay
  • Izbirak, G.
  • Ab, Dalan
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article

Comparison of lipid profiles with APOA1 MspI polymorphism in obese children with hyperlipidemia.

  • Keleşoglu, F.
  • Gürkan, H.
  • Bas, F.
  • Toptas, B.
  • Ergen, A.
  • Görmüş, Uzay
  • Izbirak, G.
  • Ab, Dalan
  • Darendeliler, F.
  • Isbir, T.
Abstract

<h4>Background</h4>Obesity is a multifactorial, chronic disorder leading to adverse metabolic effects on plasma lipid levels. Apolipoprotein AI (Apo AI) is the major structural component of high-density lipoprotein (HDL) and is involved in the esterification of cholesterol as a cofactor of lecithin-cholesterol acyltransferase (LCAT) and thus plays a major role in cholesterol efflux from peripheral cells. The APOA1 gene is associated with changes in lipid metabolism. A common gene polymorphism described in the APOA1 promoter region consists of the exchange of guanine (G) for adenine (A) at a position -75 bp upstream of the transcription origin. The relationship between lipid levels in obese children and the APOA1 MspI polymorphisms, was examined.<h4>Materials and methods</h4>Three separate groups were included, the patient group of obese children with hyperlipidemia; the obese control group (control group I) consisted of obese children without hyperlipidemia; and the healthy control group (control group II) contained healthy children with neither hyperlipidemia nor obesity. The related gene segments were amplified by polymerase chain reaction and determined different patterns were determined using denaturating gradient gel electrophoresis and positive results were confirmed automatic sequence analysis. All the results were analyzed by Proseq and BioEdit computer programmes.<h4>Results</h4>The A allele was found to be more frequent in control group I compared to the patient group (p=0.035). Very low-density lipoprotein (VLDL), LDL and triglyceride (TG), levels were statistically higher in the patients carrying the GA genotype than in control group I, and body mass index (BMI), VLDL and TG levels were statistically higher than in control group II (p<0.05). There was no relationship between -75(G/A) polymorphism and serum lipid HDL-cholesterol levels when patient values were compared to those of the controls (p>0.05). Additionally, according to the -75 GA genotypes, those in control group I with the GA genotype had elevated total cholesterol levels compared to those with the GG genotype (p<0.010). In conclusion, carrying the A allele could confer a higher risk of hyperlipidemia in obese children.

Topics
  • density
  • impedance spectroscopy
  • thermogravimetry