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RNA assay identifies a previous misclassification of BARD1 c.1977A>G variant.
- Published in:
- Scientific Reports, 2021, v. 11, n. 1, p. 1, doi. 10.1038/s41598-021-02465-y
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- Publication type:
- Article
Clinical Management of COVID-19 in Cancer Patients with the STAT3 Inhibitor Silibinin.
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- Pharmaceuticals (14248247), 2022, v. 15, n. 1, p. 19, doi. 10.3390/ph15010019
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- Publication type:
- Article
Tumors defective in homologous recombination rely on oxidative metabolism: relevance to treatments with PARP inhibitors.
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- EMBO Molecular Medicine, 2020, v. 12, n. 6, p. 1, doi. 10.15252/emmm.201911217
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- Publication type:
- Article
Role of psychological background in cancer susceptibility genetic testing distress: It is not only about a positive result.
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- Journal of Genetic Counseling, 2023, v. 32, n. 4, p. 778, doi. 10.1002/jgc4.1687
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- Publication type:
- Article
Risk of endometrial cancer after RRSO in BRCA 1/2 carriers: a multicentre cohort study.
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- Clinical & Translational Oncology, 2024, v. 26, n. 4, p. 1033, doi. 10.1007/s12094-023-03312-4
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- Publication type:
- Article
SEOM clinical guideline on heritable TP53-related cancer syndrome (2022).
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- Clinical & Translational Oncology, 2023, v. 25, n. 9, p. 2627, doi. 10.1007/s12094-023-03202-9
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- Publication type:
- Article
SEOM clinical guidelines for hereditary cancer.
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- Clinical & Translational Oncology, 2011, v. 13, n. 8, p. 580, doi. 10.1007/s12094-011-0701-2
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- Publication type:
- Article
Giacomo Castelvetro’s salads. Anti-HER2 oncogene nutraceuticals since the 17th century?
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- Clinical & Translational Oncology, 2008, v. 10, n. 1, p. 30, doi. 10.1007/s12094-008-0151-7
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- Publication type:
- Article
Cancer screening and genetic counseling.
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- Clinical & Translational Oncology, 2004, v. 6, n. 3, p. 176, doi. 10.1007/BF02710121
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- Publication type:
- Article
What is the hereditary non-polyposis colorectal cancer syndrome?
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- Clinical & Translational Oncology, 2000, v. 2, n. 4, p. 191, doi. 10.1007/BF02979554
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- Publication type:
- Article
Characteristics of Adrenocortical Carcinoma Associated With Lynch Syndrome.
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- Journal of Clinical Endocrinology & Metabolism, 2021, v. 106, n. 2, p. 318, doi. 10.1210/clinem/dgaa833
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- Publication type:
- Article
Occupational exposure to pesticides and endometrial cancer in the Screenwide case-control study.
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- Environmental Health: A Global Access Science Source, 2023, v. 22, n. 1, p. 1, doi. 10.1186/s12940-023-01028-0
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- Publication type:
- Article
Silibinin and SARS-CoV-2: Dual Targeting of Host Cytokine Storm and Virus Replication Machinery for Clinical Management of COVID-19 Patients.
- Published in:
- Journal of Clinical Medicine, 2020, v. 9, n. 6, p. 1770, doi. 10.3390/jcm9061770
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- Publication type:
- Article
Modification of BRCA1-associated breast cancer risk by HMMR overexpression.
- Published in:
- Nature Communications, 2022, v. 13, n. 1, p. 1, doi. 10.1038/s41467-022-29335-z
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- Publication type:
- Article
Chemotherapy And Radiotherapy In Locally Advanced Cervical Cancer.
- Published in:
- Acta Oncologica, 1995, v. 34, n. 7, p. 941, doi. 10.3109/02841869509127209
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- Publication type:
- Article
Chop Chemotherapy of Intermediate and High-Grade Non-Hodgkin's Lymphoma.
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- Acta Oncologica, 1994, v. 33, n. 8, p. 935, doi. 10.3109/02841869409098460
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- Publication type:
- Article
Impact of SARS-CoV-2 vaccines and recent chemotherapy on COVID-19 morbidity and mortality in patients with soft tissue sarcoma: an analysis from the OnCovid registry.
- Published in:
- Therapeutic Advances in Medical Oncology, 2024, v. 16, p. 1, doi. 10.1177/17588359231225028
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- Publication type:
- Article
ZDHHC15 as a candidate gene for autism spectrum disorder.
- Published in:
- American Journal of Medical Genetics. Part A, 2023, v. 191, n. 4, p. 941, doi. 10.1002/ajmg.a.63099
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- Publication type:
- Article
A comprehensive custom panel design for routine hereditary cancer testing: preserving control, improving diagnostics and revealing a complex variation landscape.
- Published in:
- Scientific Reports, 2017, p. 39348, doi. 10.1038/srep39348
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- Publication type:
- Article
Erratum: Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
- Published in:
- Scientific Reports, 2016, p. 23880, doi. 10.1038/srep23880
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- Publication type:
- Article
Scarce evidence of the causal role of germline mutations in UNC5C in hereditary colorectal cancer and polyposis.
- Published in:
- Scientific Reports, 2016, p. 20697, doi. 10.1038/srep20697
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- Publication type:
- Article
Biological basis of extensive pleiotropy between blood traits and cancer risk.
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- Genome Medicine, 2024, v. 16, n. 1, p. 1, doi. 10.1186/s13073-024-01294-8
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- Publication type:
- Article
Specialist palliative and end-of-life care for patients with cancer and SARS-CoV-2 infection: a European perspective.
- Published in:
- Therapeutic Advances in Medical Oncology, 2021, p. 1, doi. 10.1177/17588359211042224
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- Publication type:
- Article
Specialist palliative and end-of-life care for patients with cancer and SARS-CoV-2 infection: a European perspective.
- Published in:
- Therapeutic Advances in Medical Oncology, 2021, p. 1, doi. 10.1177/17588359211042224
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- Publication type:
- Article
Assessing Associations between the AURKA-HMMR-TPX2-TUBG1 Functional Module and Breast Cancer Risk in BRCA1/2 Mutation Carriers.
- Published in:
- PLoS ONE, 2015, v. 10, n. 4, p. 1, doi. 10.1371/journal.pone.0120020
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- Publication type:
- Article
Analysis of <i>PALB2</i> Gene in <i>BRCA1</i>/<i>BRCA2</i> Negative Spanish Hereditary Breast/Ovarian Cancer Families with Pancreatic Cancer Cases.
- Published in:
- PLoS ONE, 2013, v. 8, n. 7, p. 1, doi. 10.1371/journal.pone.0067538
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- Publication type:
- Article
Functional and Structural Analysis of C-Terminal BRCA1 Missense Variants.
- Published in:
- PLoS ONE, 2013, v. 8, n. 4, p. 1, doi. 10.1371/journal.pone.0061302
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- Publication type:
- Article
Exploring the Link between Germline and Somatic Genetic Alterations in Breast Carcinogenesis.
- Published in:
- PLoS ONE, 2010, v. 5, n. 11, p. 1, doi. 10.1371/journal.pone.0014078
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- Publication type:
- Article
Clinically relevant combined effect of polygenic background, rare pathogenic germline variants, and family history on colorectal cancer incidence.
- Published in:
- BMC Medical Genomics, 2023, v. 16, n. 1, p. 1, doi. 10.1186/s12920-023-01469-z
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- Publication type:
- Article
Predicting Ovarian-Cancer Burden in Catalonia by 2030: An Age–Period–Cohort Modelling.
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- International Journal of Environmental Research & Public Health, 2022, v. 19, n. 3, p. 1404, doi. 10.3390/ijerph19031404
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- Article
Germline mutations in the spindle assembly checkpoint genes BUB1 and BUB3 are infrequent in familial colorectal cancer and polyposis.
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- 2018
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- Publication type:
- Letter to the Editor
Clinical and Sociodemographic Determinants of Adherence to World Cancer Research Fund/American Institute for Cancer Research (WCRF/AICR) Recommendations in Breast Cancer Survivors—Health-EpiGEICAM Study.
- Published in:
- Cancers, 2022, v. 14, n. 19, p. 4705, doi. 10.3390/cancers14194705
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- Publication type:
- Article
Non-Lynch Familial and Early-Onset Colorectal Cancer Explained by Accumulation of Low-Risk Genetic Variants.
- Published in:
- Cancers, 2021, v. 13, n. 15, p. 3857, doi. 10.3390/cancers13153857
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- Publication type:
- Article
Correction: Dueñas et al. Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals. Cancers 2020, 12 , 3419.
- Published in:
- 2021
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- Publication type:
- Correction Notice
Assessing Effectiveness of Colonic and Gynecological Risk Reducing Surgery in Lynch Syndrome Individuals.
- Published in:
- Cancers, 2020, v. 12, n. 11, p. 3419, doi. 10.3390/cancers12113419
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- Publication type:
- Article
Complete Loss of EPCAM Immunoexpression Identifies EPCAM Deletion Carriers in MSH2-Negative Colorectal Neoplasia.
- Published in:
- Cancers, 2020, v. 12, n. 10, p. 2803, doi. 10.3390/cancers12102803
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- Publication type:
- Article
Exploring the Role of Mutations in Fanconi Anemia Genes in Hereditary Cancer Patients.
- Published in:
- Cancers, 2020, v. 12, n. 4, p. 829, doi. 10.3390/cancers12040829
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- Publication type:
- Article
The Spectrum of FANCM Protein Truncating Variants in European Breast Cancer Cases.
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- Cancers, 2020, v. 12, n. 2, p. 292, doi. 10.3390/cancers12020292
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- Publication type:
- Article
Next-generation sequencing meets genetic diagnostics: development of a comprehensive workflow for the analysis of BRCA1 and BRCA2 genes.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 8, p. 864, doi. 10.1038/ejhg.2012.270
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- Publication type:
- Article
MLH1 methylation screening is effective in identifying epimutation carriers.
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- European Journal of Human Genetics, 2012, v. 20, n. 12, p. 1256, doi. 10.1038/ejhg.2012.136
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- Publication type:
- Article
MLH1 promoter hypermethylation in the analytical algorithm of Lynch syndrome: a cost-effectiveness study.
- Published in:
- European Journal of Human Genetics, 2012, v. 20, n. 7, p. 762, doi. 10.1038/ejhg.2011.277
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- Publication type:
- Article
Evolution of the predictive markers amphiregulin and epiregulin mRNAs during long-term cetuximab treatment of KRAS wild-type tumor cells.
- Published in:
- Investigational New Drugs, 2012, v. 30, n. 2, p. 846, doi. 10.1007/s10637-010-9612-2
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- Publication type:
- Article
An international survey of surveillance schemes for unaffected BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2016, v. 157, n. 2, p. 319, doi. 10.1007/s10549-016-3805-0
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- Publication type:
- Article
Investigating the effect of 28 BRCA1 and BRCA2 mutations on their related transcribed mRNA.
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- Breast Cancer Research & Treatment, 2016, v. 155, n. 2, p. 253, doi. 10.1007/s10549-015-3676-9
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- Publication type:
- Article
Assessing the RNA effect of 26 DNA variants in the BRCA1 and BRCA2 genes.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 132, n. 3, p. 979, doi. 10.1007/s10549-011-1661-5
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- Publication type:
- Article
Detection of a large rearrangement in PALB2 in Spanish breast cancer families with male breast cancer.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 132, n. 1, p. 307, doi. 10.1007/s10549-011-1842-2
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- Publication type:
- Article
Identification of a new complex rearrangement affecting exon 20 of BRCA1.
- Published in:
- 2011
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- Publication type:
- Report
Hereditary breast cancer and genetic counseling in young women.
- Published in:
- 2010
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- Publication type:
- Report
Identification and comprehensive characterization of large genomic rearrangements in the BRCA1 and BRCA2 genes.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 122, n. 3, p. 733, doi. 10.1007/s10549-009-0613-9
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- Publication type:
- Article
Fatty acid metabolism in breast cancer cells: differential inhibitory effects of epigallocatechin gallate (EGCG) and C75.
- Published in:
- Breast Cancer Research & Treatment, 2008, v. 109, n. 3, p. 471
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- Publication type:
- Article