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Pathology, Research and Practice|November 23, 2023
Circulating tumor cells as a predictor and prognostic tool for metastatic clear cell renal carcinoma: An immunocytochemistry and genomic analysisMilena Shizue Tariki, Caroline Correia Ghensev Barberan, Jacqueline Aparecida Torres, et al.
Plos One|June 18, 2014
Repair of oxidative DNA damage, cell-cycle regulation and neuronal death may influence the clinical manifestation of Alzheimer's diseaseAderbal R T Silva, Ana Cecília Feio Santos, Jose M Farfel, et al.
Nature Communications|June 10, 2014
Recurrent somatic mutation in DROSHA induces microRNA profile changes in Wilms tumourGiovana T Torrezan, Elisa N Ferreira, Adriana M Nakahata, et al.
Molecular Plant-Microbe Interactions : MPMI|June 7, 2008
Differential gene expression between the biotrophic-like and saprotrophic mycelia of the witches' broom pathogen Moniliophthora perniciosaJohana Rincones, Leandra M Scarpari, Marcelo F Carazzolle, et al.
Immunology|January 26, 2023
Systemic immune mediators reflect tumour-infiltrating lymphocyte intensity and predict therapeutic response in triple-negative breast cancerAnanda D Lopes, Nayane A L Galdino, Amanda B Figueiredo, et al.
NPJ Breast Cancer|January 18, 2022
Value of the loss of heterozygosity to BRCA1 variant classificationElizabeth Santana Dos Santos, Amanda B Spurdle, Dirce M Carraro, et al.
Oncogene|March 26, 2014
Intratumoral heterogeneity of ADAM23 promotes tumor growth and metastasis through LGI4 and nitric oxide signalsE T Costa, G F Barnabé, M Li, et al.
Brazilian Journal of Medical and Biological Research = Revista Brasileira De Pesquisas Medicas E Biologicas|August 15, 2006
Gene expression profiling of clinical stages II and III breast cancerM A A K Folgueira, H Brentani, M L H Katayama, et al.
Frontiers in Genetics|June 6, 2018
Complex Landscape of Germline Variants in Brazilian Patients With Hereditary and Early Onset Breast CancerGiovana T Torrezan, Fernanda G Dos Santos R de Almeida, Márcia C P Figueiredo, et al.
Human Mutation|December 16, 2020
Whole-exome sequencing of non-BRCA1/BRCA2 mutation carrier cases at high-risk for hereditary breast/ovarian cancerPaula S Felicio, Rebeca S Grasel, Natalia Campacci, et al.
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