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1. Full Text Differential distribution and enrichment of non-coding RNAs in exosomes from normal and Cancer-associated fibroblasts in colorectal cancer
by Herrera, Mercedes and Llorens, Carlos and Rodríguez, Marta and Herrera, Alberto and Ramos, Ricardo and Gil, Beatriz and Candia, Antonio and Larriba, María Jesús and Garre, Pilar and Earl, Julie and Rodríguez-Garrote, Mercedes and Caldés, Trinidad and Bonilla, Félix and Carrato, Alfredo and García-Barberán, Vanesa and Peña, Cristina
Molecular cancer, ISSN 1476-4598, 08/2018, Volume 17, Issue 1, pp. 114 - 114
Non-coding RNAs | Liquid biopsy | Tumor microenvironment | Exosomes | Next generation sequencing | Colon Cancer | Biochemistry & Molecular Biology | Oncology | Life Sciences & Biomedicine | Science & Technology | Cell Proliferation | Prognosis | Colorectal Neoplasms - genetics | Humans | Cells, Cultured | Gene Expression Regulation, Neoplastic | Tumor Microenvironment | Exosomes - genetics | RNA, Untranslated - genetics | Sequence Analysis, RNA | Cancer-Associated Fibroblasts - chemistry | Biomarkers, Tumor - genetics | Fibroblasts - cytology | High-Throughput Nucleotide Sequencing - methods | Cancer-Associated Fibroblasts - cytology | Cell Movement | Fibroblasts - chemistry | Development and progression | MicroRNA | Research | Risk factors | Colorectal cancer | Cancer cells | Index Medicus | Medicin och hälsovetenskap
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2. Full Text Whole-exome sequencing identifies rare pathogenic variants in new predisposition genes for familial colorectal cancer
by Esteban-Jurado, Clara and Vila-Casadesus, Maria and Garre, Pilar and Lozano, Juan Jose and Pristoupilova, Anna and Beltran, Sergi and Munoz, Jenifer and Ocana, Teresa and Balaguer, Francesc and Lopez-Ceron, Maria and Cuatrecasas, Miriam and Franch-Exposito, Sebastia and Pique, Josep M and Castells, Antoni and Carracedo, Angel and Ruiz-Ponte, Clara and Abuli, Anna and Bessa, Xavier and Andreu, Montserrat and Bujanda, Luis and Caldes, Trinidad and Castellvi-Bel, Sergi and EPICOLON Consortium
Genetics in medicine, ISSN 1098-3600, 02/2015, Volume 17, Issue 2, pp. 131 - 142
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Genetic Predisposition to Disease | Reproducibility of Results | Colorectal Neoplasms - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Humans | Male | Loss of Heterozygosity | Genetic Counseling | Exome | Genetic Variation | Pedigree | Germ-Line Mutation | High-Throughput Nucleotide Sequencing | Index Medicus
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3. Full Text Using linkage studies combined with whole‐exome sequencing to identify novel candidate genes for familial colorectal cancer
by Toma, Claudio and Díaz‐Gay, Marcos and Franch‐Expósito, Sebastià and Arnau‐Collell, Coral and Overs, Bronwyn and Muñoz, Jenifer and Bonjoch, Laia and Soares de Lima, Yasmin and Ocaña, Teresa and Cuatrecasas, Miriam and Castells, Antoni and Bujanda, Luis and Balaguer, Francesc and Cubiella, Joaquín and Caldés, Trinidad and Fullerton, Janice M and Castellví‐Bel, Sergi
International journal of cancer, ISSN 0020-7136, 03/2020, Volume 146, Issue 6, pp. 1568 - 1577
colorectal cancer | genetic predisposition to disease | linkage analysis | whole‐exome sequencing | Life Sciences & Biomedicine | Oncology | Science & Technology | Genome-Wide Association Study | Colorectal Neoplasms - genetics | Humans | Middle Aged | Male | Penetrance | Whole Exome Sequencing - methods | Exome | Pedigree | Female | Chromosomes, Human | Polymorphism, Single Nucleotide | Genetic Linkage | Etiology | Genes | Colorectal carcinoma | Network analysis | Colorectal cancer | Genomes | Chromosomes | Gene sequencing | Cancer | Linkage analysis | Index Medicus | Cancer Genetics and Epigenetics
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4. Full Text Alternative splicing and ACMG-AMP-2015-based classification of PALB2 genetic variants: an ENIGMA report
by Lopez-Perolio, Irene and Leman, Raphaël and Behar, Raquel and Lattimore, Vanessa and Pearson, John F and Castéra, Laurent and Martins, Alexandra and Vaur, Dominique and Goardon, Nicolas and Davy, Grégoire and Garre, Pilar and García-Barberán, Vanesa and Llovet, Patricia and Pérez-Segura, Pedro and Díaz-Rubio, Eduardo and Caldés, Trinidad and Hruska, Kathleen S and Hsuan, Vickie and Wu, Sitao and Pesaran, Tina and Karam, Rachid and Vallon-Christersson, Johan and Borg, Ake and Investigators, kConFab and Valenzuela-Palomo, Alberto and Velasco, Eladio A and Southey, Melissa and Vreeswijk, Maaike P G and Devilee, Peter and Kvist, Anders and Spurdle, Amanda B and Walker, Logan C and Krieger, Sophie and de la Hoya, Miguel and kConFab Investigators
Journal of medical genetics, ISSN 0022-2593, 07/2019, Volume 56, Issue 7, pp. 453 - 460
pvs1 | variant classification | palb2 | acmg-amp guidelines | splicing | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | BRCA2 protein | Alternative splicing | AMP | Laboratories | Exons | Genomics | Genes | Breast cancer | Consortia | Polymerase chain reaction | Genetic variance | Pili | Classification | Trends | Index Medicus | Life Sciences | Human health and pathology | Cancer Genetics | 1506 | Clinical Medicine | Medical and Health Sciences | Medicin och hälsovetenskap | Klinisk medicin | Cancer and Oncology | Cancer och onkologi
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5. Full Text Germline Mutations in FAN1 Cause Hereditary Colorectal Cancer by Impairing DNA Repair
by Seguí, Nuria and Mina, Leonardo B and Lázaro, Conxi and Sanz-Pamplona, Rebeca and Pons, Tirso and Navarro, Matilde and Bellido, Fernando and López-Doriga, Adriana and Valdés-Mas, Rafael and Pineda, Marta and Guinó, Elisabet and Vidal, August and Soto, José Luís and Caldés, Trinidad and Durán, Mercedes and Urioste, Miguel and Rueda, Daniel and Brunet, Joan and Balbín, Milagros and Blay, Pilar and Iglesias, Silvia and Garré, Pilar and Lastra, Enrique and Sánchez-Heras, Ana Beatriz and Valencia, Alfonso and Moreno, Victor and Pujana, Miguel Ángel and Villanueva, Alberto and Blanco, Ignacio and Capellá, Gabriel and Surrallés, Jordi and Puente, Xose S and Valle, Laura
Gastroenterology (New York, N.Y. 1943), ISSN 0016-5085, 2015, Volume 149, Issue 3, pp. 563 - 566
Gastroenterology and Hepatology | Genetic Risk Factor | Lynch Syndrome | Susceptibility | DNA Mismatch Repair | Gastroenterology & Hepatology | Life Sciences & Biomedicine | Science & Technology | Genetic Predisposition to Disease | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Colorectal Neoplasms, Hereditary Nonpolyposis - pathology | Humans | Middle Aged | Child, Preschool | Male | Heredity | DNA Repair - genetics | Young Adult | Phenotype | Pedigree | Exodeoxyribonucleases - metabolism | HEK293 Cells | Aged, 80 and over | Cell Line, Tumor | Germ-Line Mutation | Adult | Colorectal Neoplasms, Hereditary Nonpolyposis - enzymology | Female | Aged | Exodeoxyribonucleases - genetics | Crosslinked polymers | Gene mutations | Analysis | Genomics | DNA | Colorectal cancer | Genetic aspects | Health aspects | DNA repair | Fanconi's anemia | Cancer | Index Medicus | Abridged Index Medicus
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6. Full Text SETD6 dominant negative mutation in familial colorectal cancer type X
by Martín-Morales, Lorena and Feldman, Michal and Vershinin, Zlata and Garre, Pilar and Caldés, Trinidad and Levy, Dan
Human molecular genetics, ISSN 0964-6906, 2017, Volume 26, Issue 22, pp. 4481 - 4493
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Frameshift Mutation | Colorectal Neoplasms, Hereditary Nonpolyposis - genetics | Humans | Middle Aged | Protein Methyltransferases - genetics | Male | NF-kappa B - metabolism | Protein Methyltransferases - metabolism | Whole Exome Sequencing | Colorectal Neoplasms, Hereditary Nonpolyposis - metabolism | NF-kappa B - genetics | Pedigree | Base Sequence | Adult | Colorectal Neoplasms, Hereditary Nonpolyposis - enzymology | Female | Aged | Mutation | Index Medicus
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7. Full Text The Fanconi anemia DNA damage repair pathway in the spotlight for germline predisposition to colorectal cancer
by Esteban-Jurado, Clara and Franch-Expósito, Sebastià and Muñoz, Jenifer and Ocaña, Teresa and Carballal, Sabela and López-Cerón, Maria and Cuatrecasas, Miriam and Vila-Casadesús, Maria and Lozano, Juan José and Serra, Enric and Beltran, Sergi and Brea-Fernández, Alejandro and Ruiz-Ponte, Clara and Castells, Antoni and Bujanda, Luis and Garre, Pilar and Caldés, Trinidad and Cubiella, Joaquín and Balaguer, Francesc and Castellví-Bel, Sergi and EPICOLON Consortium and The EPICOLON Consortium
European journal of human genetics : EJHG, ISSN 1018-4813, 10/2016, Volume 24, Issue 10, pp. 1501 - 1505
Biochemistry & Molecular Biology | Genetics & Heredity | Life Sciences & Biomedicine | Science & Technology | Colorectal Neoplasms - epidemiology | Genetic Predisposition to Disease | Colorectal Neoplasms - genetics | Humans | Fanconi Anemia Complementation Group E Protein - genetics | Male | Fanconi Anemia - epidemiology | DNA Repair - genetics | DNA-Binding Proteins - genetics | Fanconi Anemia Complementation Group C Protein - genetics | DNA-Directed DNA Polymerase - genetics | Spain | Exome | BRCA1 Protein - genetics | Genes, Dominant | Pedigree | Germ-Line Mutation | Fanconi Anemia - pathology | Female | Fanconi Anemia - genetics | Colorectal Neoplasms - pathology | Index Medicus | Short Report
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8. Full Text Assessment of Topoisomerase II α Status in Breast Cancer by Quantitative PCR, Gene Expression Microarrays, Immunohistochemistry, and Fluorescence in Situ Hybridization
by Romero, Atocha and Martín, Miguel and Cheang, Maggie C.U and López García-Asenjo, José Antonio and Oliva, Belén and He, Xiaping and de la Hoya, Miguel and García Sáenz, Jose Ángel and Arroyo Fernández, Manuel and Díaz Rubio, Eduardo and Perou, Charles M and Llopis, Trinidad Caldés
The American journal of pathology, ISSN 0002-9440, 2011, Volume 178, Issue 4, pp. 1453 - 1460
Pathology | Life Sciences & Biomedicine | Science & Technology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Investigative techniques, diagnostic techniques (general aspects) | Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques | Biological and medical sciences | Medical sciences | Tumors | Antigens, Neoplasm - genetics | Cell Proliferation | Oligonucleotide Array Sequence Analysis | Humans | Middle Aged | Antigens, Neoplasm - biosynthesis | Gene Expression Regulation, Neoplastic | Receptor, ErbB-2 - metabolism | DNA-Binding Proteins - genetics | Reverse Transcriptase Polymerase Chain Reaction | Polymerase Chain Reaction - methods | Gene Expression Regulation, Enzymologic | Immunohistochemistry - methods | Poly-ADP-Ribose Binding Proteins | Breast Neoplasms - enzymology | Biopsy | Adolescent | Adult | DNA Topoisomerases, Type II - genetics | Female | Aged | DNA Topoisomerases, Type II - biosynthesis | DNA-Binding Proteins - biosynthesis | In Situ Hybridization, Fluorescence - methods | Index Medicus | Abridged Index Medicus | Regular
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9. Full Text Contribution of New Adenomatous Polyposis Predisposition Genes in an Unexplained Attenuated Spanish Cohort by Multigene Panel Testing
by Lorca, Victor and Rueda, Daniel and Martin-Morales, Lorena and Jesus Fernandez-Acenero, Maria and Grolleman, J.E and Poves, Carmen and Voer, R.M. de and Caldes, Trinidad and Garre, Pilar
Scientific reports, ISSN 2045-2322, 2019, Volume 9, Issue 1, pp. 9814 - 10
Science & Technology - Other Topics | Multidisciplinary Sciences | Science & Technology | Genetic variance | Next-generation sequencing | Splicing | Etiology | Heritability | Adenoma | Ribonucleic acid--RNA | Patients | Genetic screening | Index Medicus
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10. Full Text Breast-Cancer Stromal Cells with TP53 Mutations and Nodal Metastases
by Patocs, Attila and Zhang, Li and Xu, Yaomin and Weber, Frank and Caldes, Trinidad and Mutter, George L and Platzer, Petra and Eng, Charis
The New England journal of medicine, ISSN 0028-4793, 12/2007, Volume 357, Issue 25, pp. 2543 - 2551
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Gynecology. Andrology. Obstetrics | Mammary gland diseases | Biological and medical sciences | General aspects | Medical sciences | Tumors | Receptor Cross-Talk | Breast - cytology | Neoplasm Invasiveness | Humans | Middle Aged | Genetic Diseases, Inborn - genetics | Genotype | Genetic Diseases, Inborn - pathology | Mutation, Missense | Loss of Heterozygosity | Allelic Imbalance | Stromal Cells | Genes, p53 | Breast Neoplasms - genetics | Breast Neoplasms - pathology | DNA Mutational Analysis | Lymphatic Metastasis - genetics | Polymerase Chain Reaction | Aged, 80 and over | Adult | Female | Aged | DNA, Neoplasm - analysis | Microsatellite Repeats | Tumor suppressor genes | Breast cancer | Genetic aspects | Research | Mutation (Biology) | Lasers | Cell cycle | Mutation | DNA repair | Apoptosis | Index Medicus | Abridged Index Medicus
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