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 (2/2 displayed)

  • 2009Paraoxonase 1 gene polymorphisms contribute to coronary artery disease risk among north Indians.citations
  • 2006Association of APOE (Hha1) and ACE (I/D) gene polymorphisms with type 2 diabetes mellitus in North West India.43citations

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Chart of shared publication
Prajnya, R.
1 / 1 shared
Sinha, N.
1 / 2 shared
Agrawal, S.
1 / 4 shared
Mastana, Sarabjit
2 / 2 shared
Bush, L.
1 / 1 shared
Singh, M.
1 / 14 shared
Pp, Singh
1 / 1 shared
Naz, I.
1 / 1 shared
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2009
2006

Co-Authors (by relevance)

  • Prajnya, R.
  • Sinha, N.
  • Agrawal, S.
  • Mastana, Sarabjit
  • Bush, L.
  • Singh, M.
  • Pp, Singh
  • Naz, I.
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article

Paraoxonase 1 gene polymorphisms contribute to coronary artery disease risk among north Indians.

  • Prajnya, R.
  • Sinha, N.
  • Agrawal, S.
  • Mastana, Sarabjit
  • Bush, L.
  • Gilmour, A.
Abstract

<h4>Background</h4>Polymorphisms in paraoxonase 1 (PON1) coding for PON1 enzyme have been studied as genetic markers of coronary artery disease (CAD). PON1 Q192R and PON1 L55M polymorphisms have been analyzed extensively, but data on association and role of these polymorphisms in the etiology of CAD are conflicting. In this study, we tested the genetic association between PON1 Q192R and PON1 L55M polymorphisms and CAD among north Indians.<h4>Materials and methods</h4>Two hundred eighty-five angiographically proven patients with coronary artery disease and 200 sex-matched and ethnically matched controls were genotyped for 2 PON1 polymorphisms by the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) technique. Genotype/ allele frequencies were compared in patients and controls using the chi-square test.<h4>Results</h4>At PON1-192 locus, there were significant differences between patients and controls (P< 0.05), leading to significant odds ratios for RR genotype (OR= 1.92, CI: 1.19-3.10) and *R allele (OR= 1.30, CI: 1.00-1.70). These odds ratios were higher in the sub-sample of smokers (2.84 and 1.45, respectively). Binary logistic regression analysis also confirmed that *R allele carriers (QR and RR) have a higher risk of CAD (OR= 3.54, CI: 1.67-5.53). PON1-55 locus did not show significant differences between patients and controls, but LL genotype and *L allele were significant risk factors in the nonsmoker group. RL haplotype was also significantly associated with CAD risk (OR= 1.44, CI: 1.08-1.93).<h4>Conclusions</h4>PON1-192R allele and RR genotype are significantly associated with CAD patients from the north Indian population (Uttar Pradesh). This association was stronger in smokers, supporting the conclusion that an interaction between PON1 activity and smoking augments CAD risk. Further studies with larger sample size are warranted to confirm these associations in different Indian populations.

Topics
  • chemical ionisation
  • collision-induced dissociation