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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Materials Map under construction

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 (6/6 displayed)

  • 2019Inhibitory effect of 5-aminoimidazole-4-carbohydrazonamides derivatives against Candida spp biofilm on nanohydroxyapatite substrate7citations
  • 2018Relationship between clinical toxicities and ERCC1 rs3212986 and XRCC3 rs861539 polymorphisms in cervical cancer patients9citations
  • 2018TP53 Arg72Pro polymorphism is associated with increased overall survival but not response to therapy in Portuguese/Caucasian patients with advanced cervical cancer9citations
  • 2014FASL polymorphism is associated with response to bacillus Calmette-Guerin immunotherapy in bladder cancer20citations
  • 2006Association of the A870G cyclin D1 gene polymorphism with genetic susceptibility to nasopharyngeal carcinoma29citations
  • 2003Association between CYP2E1 polymorphisms and susceptibility to prostate cancercitations

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Chart of shared publication
Ribeiro, Ana I.
1 / 1 shared
Cerqueira, Fátima
1 / 3 shared
Sousa, João C.
1 / 1 shared
Proença, M. Fernanda R. P.
1 / 6 shared
Fernandes, M. H.
1 / 1 shared
Dias, Alice
1 / 3 shared
Grenho, L.
1 / 1 shared
Monteiro, F. J.
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Gabriel, Carla
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Pereira, D.
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Coelho, A.
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Assis, J.
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Bravo, I.
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Nogueira, A.
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Soares, S.
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Catarino, R.
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Ferreira, Ja
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Santos, L.
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Oliveira, D.
1 / 5 shared
Tavares, A.
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Videira, Pa
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Morais, A.
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Lima, L.
1 / 2 shared
Coelho, V.
1 / 1 shared
Catarino, Rj
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Lopes, C.
2 / 27 shared
Pinto, D.
2 / 9 shared
Breda, E.
1 / 1 shared
Sousa, H.
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Oliveira, J.
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Ferreira, Pm
1 / 1 shared
Vasconcelos, A.
1 / 1 shared
Costa, S.
1 / 18 shared
Chart of publication period
2019
2018
2014
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Co-Authors (by relevance)

  • Ribeiro, Ana I.
  • Cerqueira, Fátima
  • Sousa, João C.
  • Proença, M. Fernanda R. P.
  • Fernandes, M. H.
  • Dias, Alice
  • Grenho, L.
  • Monteiro, F. J.
  • Gabriel, Carla
  • Pereira, D.
  • Coelho, A.
  • Assis, J.
  • Bravo, I.
  • Nogueira, A.
  • Soares, S.
  • Catarino, R.
  • Ferreira, Ja
  • Santos, L.
  • Oliveira, D.
  • Tavares, A.
  • Videira, Pa
  • Morais, A.
  • Lima, L.
  • Coelho, V.
  • Catarino, Rj
  • Lopes, C.
  • Pinto, D.
  • Breda, E.
  • Sousa, H.
  • Oliveira, J.
  • Ferreira, Pm
  • Vasconcelos, A.
  • Costa, S.
OrganizationsLocationPeople

article

TP53 Arg72Pro polymorphism is associated with increased overall survival but not response to therapy in Portuguese/Caucasian patients with advanced cervical cancer

  • Medeiros, Rui
  • Pereira, D.
  • Coelho, A.
  • Assis, J.
  • Bravo, I.
  • Catarino, R.
  • Nogueira, A.
  • Soares, S.
Abstract

Identification of mechanisms that influence the therapeutic response and survival in patients with cancer is important. It is known that the genetic variability of the host, including presence of genetic polymorphisms in genes involved in DNA damage response, serves a crucial role in the prognosis of these patients. The present hospital-based retrospective cohort study aimed to evaluate the influence of TP53 Arg72Pro (rs1042522) polymorphism in the clinical outcome of 260 Caucasian patients diagnosed with cervical cancer and treated with concomitant radiotherapy and chemotherapy. The polymorphism genotyping was assessed using allelic discrimination by quantiative polymerase chain reaction. The results indicate that the TP53 Arg72Pro polymorphism did not significantly impact the response to therapy (P= 0.571) nor disease-free survival (P= 0.081). However, the polymorphism did influence overall survival, as increased median survival time was observed for patients carrying Arg/Pro genotype when compared with patients with Arg/Arg and Pro/Pro genotypes (126 months vs. 111 months, respectively; P= 0.047). To conclude, the present findings suggest that a pharmacogenomic profile based on the genetic background of patients, including the analysis of the TP53 genotypes, may individualize treatment nad assist in the selection of therapies that may improve clinical outcome and lower toxicity for the patients.

Topics
  • impedance spectroscopy
  • toxicity