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Changes in the expression of plasma proteins associated with thrombosis in BRCA1 mutation carriers.
- Published in:
- Journal of Cancer Research & Clinical Oncology, 2012, v. 138, n. 5, p. 867, doi. 10.1007/s00432-012-1161-y
- By:
- Publication type:
- Article
Sex Ratios in Families With BRCA Mutations—Reply.
- Published in:
- 2003
- By:
- Publication type:
- Letter
Association Between BRCA1 Mutations and Ratio of Female to Male Births in Offspring of Families With Breast Cancer, Ovarian Cancer, or Both.
- Published in:
- JAMA: Journal of the American Medical Association, 2003, v. 290, n. 7, p. 929, doi. 10.1001/jama.290.7.929
- By:
- Publication type:
- Article
Study of KRAS new predictive marker in a clinical laboratory.
- Published in:
- Clinical & Translational Oncology, 2012, v. 14, n. 12, p. 937, doi. 10.1007/s12094-012-0886-z
- By:
- Publication type:
- Article
Topoisomerase 2 alpha: a real predictor of anthracycline efficacy?
- Published in:
- Clinical & Translational Oncology, 2012, v. 14, n. 3, p. 163, doi. 10.1007/s12094-012-0779-1
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- Publication type:
- Article
Risk-reduction surgery in BRCA mutation carriers in a Spanish population: adherence and results.
- Published in:
- Clinical & Translational Oncology, 2008, v. 10, n. 10, p. 660, doi. 10.1007/s12094-008-0267-9
- By:
- Publication type:
- Article
IGF-I and the IGF-I receptor in development of nonmammalian vertebrates.
- Published in:
- Molecular Reproduction & Development, 1993, v. 35, n. 4, p. 427, doi. 10.1002/mrd.1080350418
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- Publication type:
- Article
Reassessing the TARBP2 mutation rate in hereditary nonpolyposis colorectal cancer.
- Published in:
- 2010
- By:
- Publication type:
- Letter
Frequency and Variability of Genomic Rearrangements on <i>MSH2</i> in Spanish Lynch Syndrome Families.
- Published in:
- PLoS ONE, 2013, v. 8, n. 9, p. 1, doi. 10.1371/journal.pone.0072195
- By:
- Publication type:
- Article
Differential distribution and enrichment of non-coding RNAs in exosomes from normal and Cancer-associated fibroblasts in colorectal cancer.
- Published in:
- Molecular Cancer, 2018, v. 17, n. 1, p. N.PAG, doi. 10.1186/s12943-018-0863-4
- By:
- Publication type:
- Article
Low prevalence of SLX4 loss-of-function mutations in non-BRCA1/2 breast and/or ovarian cancer families.
- Published in:
- European Journal of Human Genetics, 2013, v. 21, n. 8, p. 883, doi. 10.1038/ejhg.2012.268
- By:
- Publication type:
- Article
Limited family structure and triple-negative breast cancer (TNBC) subtype as predictors of BRCA mutations in a genetic counseling cohort of early-onset sporadic breast cancers.
- Published in:
- Breast Cancer Research & Treatment, 2014, v. 148, n. 2, p. 415, doi. 10.1007/s10549-014-3167-4
- By:
- Publication type:
- Article
Characterization of four novel BRCA2 large genomic rearrangements in Spanish breast/ovarian cancer families: review of the literature, and reevaluation of the genetic mechanisms involved in their origin.
- Published in:
- Breast Cancer Research & Treatment, 2012, v. 133, n. 1, p. 273, doi. 10.1007/s10549-011-1909-0
- By:
- Publication type:
- Article
A HRM-based screening method detects RAD51C germ-line deleterious mutations in Spanish breast and ovarian cancer families.
- Published in:
- Breast Cancer Research & Treatment, 2011, v. 129, n. 3, p. 939, doi. 10.1007/s10549-011-1543-x
- By:
- Publication type:
- Article
Parity and the risk of breast and ovarian cancer in BRCA1 and BRCA2 mutation carriers.
- Published in:
- Breast Cancer Research & Treatment, 2010, v. 119, n. 1, p. 221, doi. 10.1007/s10549-009-0394-1
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- Publication type:
- Article
Analysis of FANCB and FANCN/PALB2 Fanconi Anemia genes in BRCA1/2-negative Spanish breast cancer families.
- Published in:
- Breast Cancer Research & Treatment, 2009, v. 113, n. 3, p. 545, doi. 10.1007/s10549-008-9945-0
- By:
- Publication type:
- Article
Screening for large rearrangements of the BRCA2 gene in Spanish families with breast/ovarian cancer.
- Published in:
- Breast Cancer Research & Treatment, 2007, v. 103, n. 1, p. 103, doi. 10.1007/s10549-006-9376-8
- By:
- Publication type:
- Article
Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing.
- Published in:
- Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46403-5
- By:
- Publication type:
- Article
Mutant BRCA1 alleles transmission: Different approaches and different biases.
- Published in:
- International Journal of Cancer, 2005, v. 113, n. 1, p. 166, doi. 10.1002/ijc.20541
- By:
- Publication type:
- Article
The breast cancer low-penetrance allele 1100delC in the CHEK2 gene is not present in Spanish familial breast cancer population.
- Published in:
- International Journal of Cancer, 2004, v. 108, n. 1, p. 54, doi. 10.1002/ijc.11414
- By:
- Publication type:
- Article
No mutations in the XRCC2 gene in BRCA1/2-negative high-risk breast cancer families.
- Published in:
- International Journal of Cancer, 2003, v. 103, n. 1, p. 136, doi. 10.1002/ijc.10766
- By:
- Publication type:
- Article
Clustering of cancer-related mutations in a subset of BRCA1 alleles: A study in the Spanish population.
- Published in:
- International Journal of Cancer, 2002, v. 100, n. 5, p. 618, doi. 10.1002/ijc.10527
- By:
- Publication type:
- Article
Loss of heterozygosity analysis at the BRCA loci in tumor samples from patients with familial breast cancer.
- Published in:
- International Journal of Cancer, 2002, v. 99, n. 2, p. 305, doi. 10.1002/ijc.10337
- By:
- Publication type:
- Article
Association between BRCA1 and BRCA2 mutations and cancer phenotype in Spanish breast/ovarian cancer families: Implications for genetic testing.
- Published in:
- International Journal of Cancer, 2002, v. 97, n. 4, p. 466, doi. 10.1002/ijc.1627
- By:
- Publication type:
- Article
Spanish family study on hereditary breast and/or ovarian cancer: Analysis of the BRCA1 gene.
- Published in:
- International Journal of Cancer, 2001, v. 91, n. 1, p. 137, doi. 10.1002/1097-0215(20010101)91:1<137::AID-IJC1020>3.0.CO;2-R
- By:
- Publication type:
- Article
Prognostic Value of BRAF, PI3K, PTEN, EGFR Copy Number, Amphiregulin and Epiregulin Status in Patients with KRAS Codon 12 Wild-Type Metastatic Colorectal Cancer Receiving First-Line Chemotherapy with Anti-EGFR Therapy.
- Published in:
- Molecular Diagnosis & Therapy, 2015, v. 19, n. 6, p. 397, doi. 10.1007/s40291-015-0165-0
- By:
- Publication type:
- Article
Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes.
- Published in:
- British Journal of Cancer, 2017, v. 117, n. 7, p. 1048, doi. 10.1038/bjc.2017.286
- By:
- Publication type:
- Article
Characterisation of the novel deleterious RAD51C p.Arg312Trp variant and prioritisation criteria for functional analysis of RAD51C missense changes.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Influence of KRAS p.G13D mutation in patients with metastatic colorectal cancer treated with cetuximab.
- Published in:
- 2012
- By:
- Publication type:
- journal article
SETD6 dominant negative mutation in familial colorectal cancer type X.
- Published in:
- Human Molecular Genetics, 2017, v. 26, n. 22, p. 4481, doi. 10.1093/hmg/ddx336
- By:
- Publication type:
- Article
Predominance of pathogenic missense variants in the RAD51C gene occurring in breast and ovarian cancer families.
- Published in:
- Human Molecular Genetics, 2012, v. 21, n. 13, p. 2889, doi. 10.1093/hmg/dds115
- By:
- Publication type:
- Article
Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer.
- Published in:
- International Journal of Cancer, 2020, v. 146, n. 6, p. 1568, doi. 10.1002/ijc.32683
- By:
- Publication type:
- Article
About 1% of the breast and ovarian Spanish families testing negative for BRCA1 and BRCA2 are carriers of RAD51D pathogenic variants.
- Published in:
- International Journal of Cancer, 2014, v. 134, n. 9, p. 2088, doi. 10.1002/ijc.28540
- By:
- Publication type:
- Article
A novel TP53 germline inframe deletion identified in a Spanish series of Li-fraumeni syndrome suspected families.
- Published in:
- Familial Cancer, 2017, v. 16, n. 4, p. 567, doi. 10.1007/s10689-017-9990-0
- By:
- Publication type:
- Article
Cancer risk and overall survival in mismatch repair proficient hereditary non-polyposis colorectal cancer, Lynch syndrome and sporadic colorectal cancer.
- Published in:
- Familial Cancer, 2014, v. 13, n. 1, p. 109, doi. 10.1007/s10689-013-9683-2
- By:
- Publication type:
- Article
Association of MUTYH and MSH6 germline mutations in colorectal cancer patients.
- Published in:
- Familial Cancer, 2009, v. 8, n. 4, p. 525, doi. 10.1007/s10689-009-9282-4
- By:
- Publication type:
- Article
Lack of Germ-line Mutations at the Specific BRCA1-IRIS Coding Sequence in 114 Spanish High-risk Breast/ovarian Families.
- Published in:
- Familial Cancer, 2005, v. 4, n. 4, p. 317, doi. 10.1007/s10689-005-1236-x
- By:
- Publication type:
- Article
The CHEK2 1100delC allele is not relevant for risk assessment in HNPCC and HBCC Spanish families.
- Published in:
- Familial Cancer, 2005, v. 4, n. 2, p. 183
- By:
- Publication type:
- Article
RECQL5: Another DNA helicase potentially involved in hereditary breast cancer susceptibility.
- Published in:
- Human Mutation, 2019, v. 40, n. 5, p. 566, doi. 10.1002/humu.23732
- By:
- Publication type:
- Article
Capillary Electrophoresis Analysis of Conventional Splicing Assays: IARC Analytical and Clinical Classification of 31 BRCA2 Genetic Variants.
- Published in:
- Human Mutation, 2014, v. 35, n. 1, p. 53, doi. 10.1002/humu.22456
- By:
- Publication type:
- Article
Evaluation of Rare Variants in the New Fanconi Anemia Gene ERCC4 ( FANCQ) as Familial Breast/Ovarian Cancer Susceptibility Alleles.
- Published in:
- Human Mutation, 2013, v. 34, n. 12, p. 1615, doi. 10.1002/humu.22438
- By:
- Publication type:
- Article
BRCA1 Alternative splicing landscape in breast tissue samples.
- Published in:
- BMC Cancer, 2015, v. 15, n. 1, p. 1, doi. 10.1186/s12885-015-1145-9
- By:
- Publication type:
- Article
BRCA1 Alternative splicing landscape in breast tissue samples.
- Published in:
- 2015
- By:
- Publication type:
- journal article
Eight novel germline MLH1 and MSH2 mutations in hereditary non-polyposis colorectal cancer families from Spain.
- Published in:
- Human Mutation, 2001, v. 18, n. 6, p. 549, doi. 10.1002/humu.1240
- By:
- Publication type:
- Article
Role of GALNT12 in the genetic predisposition to attenuated adenomatous polyposis syndrome.
- Published in:
- PLoS ONE, 2017, v. 12, n. 11, p. 1, doi. 10.1371/journal.pone.0187312
- By:
- Publication type:
- Article
New Mutation in the hMSH2 Gene in a Spanish Muir-Torre Syndrome.
- Published in:
- 2000
- By:
- Publication type:
- Letter