Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Ana T. Pinto"'
Autor:
Ana T Pinto, Marta L Pinto, Sérgia Velho, Marta T Pinto, Ana P Cardoso, Rita Figueira, Armanda Monteiro, Margarida Marques, Raquel Seruca, Mário A Barbosa, Marc Mareel, Maria J Oliveira, Sónia Rocha
Publikováno v:
PLoS ONE, Vol 11, Iss 8, p e0160891 (2016)
Both cancer and tumour-associated host cells are exposed to ionizing radiation when a tumour is subjected to radiotherapy. Macrophages frequently constitute the most abundant tumour-associated immune population, playing a role in tumour progression a
Externí odkaz:
https://doaj.org/article/84edee5aeb8c49a1a2a0419b348a0e0f
Autor:
Branca M. Cavaco, Lúcia Roque, Carmo Martins, Ana T. Pinto, José Cabeçadas, Valeriano Leite, Saudade André, Ana Saramago, Marta Pojo, Ruben Roque, Joana Simões-Pereira
Publikováno v:
Endocrine. 66:288-300
Anaplastic thyroid cancer (ATC) is among the most aggressive and unresectable tumors, presenting a bad prognosis. A better comprehension of the functional and molecular mechanisms behind the aggressiveness of this cancer, as well as new biomarkers fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::68c0895513da216922fbd79ab0a182ac
https://doi.org/10.1007/s12020-019-02009-5
https://doi.org/10.1007/s12020-019-02009-5
Publikováno v:
European Journal of Medical Genetics. 61:294-299
Germline mutations in the WT1 gene have been identified in some families with Wilms tumor. Recently, the CTR9 gene was found to be mutated in three families with Wilms tumor, thus representing a novel predisposition gene for this disease. We identifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::139aef85950a92aa6c013f821ab16520
https://doi.org/10.1016/j.ejmg.2017.12.010
https://doi.org/10.1016/j.ejmg.2017.12.010
Autor:
Branca M. Cavaco, Marta Pojo, Ana T. Pinto, Ana Teresa Serra, Valeriano Leite, Diana P. Sousa
Publikováno v:
Nutrition and cancer. 72(2)
Aim: Anaplastic thyroid cancer (ATC) is the most aggressive subtype of thyroid cancer, presenting high mortality. Currently, no curative treatments exist and new therapeutic strategies are required. Although nutraceuticals were reported to have antic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ba7cb2350db8cd511913544c22aac6f9
https://pubmed.ncbi.nlm.nih.gov/31287730
https://pubmed.ncbi.nlm.nih.gov/31287730
Publikováno v:
Endocrine. 65(2)
Germline mutations in the four genes that encode the succinate dehydrogenase complex (SDHx) are a risk factor for developing pheochromocytomas and/or paragangliomas. The precise genotype–phenotype correlations are still uncertain and the most commo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b4a1e719b71ad457ad234abc9daf92f2
https://pubmed.ncbi.nlm.nih.gov/31104306
https://pubmed.ncbi.nlm.nih.gov/31104306
Publikováno v:
Endocrine Abstracts.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d30b6fa186f850a83bf20539dc24f8e9
https://doi.org/10.1530/endoabs.49.gp23
https://doi.org/10.1530/endoabs.49.gp23