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المؤلفون: Ignacio Blanco, Heli Nevanlinna, Norbert Arnold, Gad Rennert, Catherine Noguès, Javier Benitez, Etienne Rouleau, Embrace, Gemo, Irene Konstantopoulou, David J. Hughes, Flavio Lejbkowicz, kConFab, Rita K. Schmutzler, Mercedes Durán, Carole Brewer, Beatrix Versmold, Georgia Chenevix-Trench, Paolo Radice, Trevor Cole, Alfons Meindl, Ivan Bièche, Rosalind A. Eeles, Isabelle Coupier, Olga M. Sinilnikova, Hebon, A L Laborde, Florence Coulet, Kristiina Aittomäki, M. Cook, Ana Osorio, D. G. Evans, Dieter Schaefer, S. Giraud, Craig Luccarini, Jacques Simard, Hans J. J. P. Gille, Fiona Lalloo, Liliane Demange, Xiaoqing Chen, Florent Soubrier, Susan Peock, Amanda B. Spurdle, Rosemarie Davidson, Lesley McGuffog, T. A. M. van Os, Henry T. Lynch, Jacqueline Cook, Ursula G. Froster, Douglas F. Easton, Sara Dishon, Siranoush Manoukian, Christian Sutter, Gabriella Pichert, Frans B. L. Hogervorst, Mélanie Léoné, Jonathan Beesley, Katherine L. Nathanson, Rosette Lidereau, Sue Healey, Daniel Sinnett, Gc-Hboc, Christoph Engel, Joan Paterson, Chrystelle Colas, Mark H. Greene, U Hamann, Dominique Stoppa-Lyonnet, Ocgn, Irene L. Andrulis, Helmut Deissler, Jennifer T. Loud, A C Antoniou, Susan M. Domchek
المساهمون: Universitat de Barcelona, Human genetics, CCA - Oncogenesis
المصدر: Dipòsit Digital de la UB
Universidad de Barcelona
BRITISH JOURNAL OF CANCER
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
Recercat. Dipósit de la Recerca de Catalunya
British Journal of Cancer
Sinilnikova, O M, Antoniou, A C, Simard, J, Healey, S, Leone, M, Sinnett, D, Spurdle, A B, Beesley, J, Chen, X, Greene, M H, Loud, J T, Lejbkowicz, F, Rennert, G, Dishon, S, Andrulis, I L, Domchek, S M, Nathanson, K L, Manoukian, S, Radice, P, Konstantopoulou, I, Blanco, I, Laborde, A L, Duran, M, Osorio, A, Benitez, J, Hamann, U, Hogervorst, F B L, van Os, T A M, Gille, J J P, Peock, S, Cook, M, Luccarini, C, Evans, D G, Lalloo, F, Eeles, R, Pichert, G, Davidson, R, Cole, T, Cook, J, Paterson, J, Brewer, C, Hughes, D J, Coupier, I, Giraud, S, Coulet, F, Colas, C, Soubrier, F, Rouleau, E, Bieche, I, Lidereau, R, Demange, L, Nogues, C, Lynch, H T, Schmutzler, R K, Versmold, B, Engel, C, Meindl, A, Arnold, N, Sutter, C, Deissler, H, Schaefer, D, Froster, U G, Aittomaki, K, Nevanlinna, H, McGuffog, L, Easton, D F, Chenevix-Trench, G & Stoppa-Lyonnet, D 2009, ' The TP53 Arg72Pro and MDM2 309G > T polymorphisms are not associated with breast cancer risk in BRCA1 and BRCA2 mutation carriers ', British Journal of Cancer, vol. 101, no. 8, pp. 1456-1460 . https://doi.org/10.1038/sj.bjc.6605279Test
British Journal of Cancer, 101(8), 1456-1460. Nature Publishing Groupمصطلحات موضوعية: Oncology, Cancer Research, endocrine system diseases, Genes, BRCA2, Genes, BRCA1, polymorphism, 0302 clinical medicine, Breast cancer, Risk Factors, Genotype, TP53, skin and connective tissue diseases, risk, 0303 health sciences, Nucleotides, Hazard ratio, Proto-Oncogene Proteins c-mdm2, 3. Good health, 030220 oncology & carcinogenesis, Female, Breast disease, medicine.medical_specialty, Heterozygote, Single-nucleotide polymorphism, Breast Neoplasms, Biology, Polymorphism, Single Nucleotide, Càncer de mama, 03 medical and health sciences, breast cancer, MDM2, BRCA1/2, Internal medicine, medicine, Genetics, SNP, Humans, Genetic Predisposition to Disease, neoplasms, 030304 developmental biology, Proportional hazards model, Mutació (Biologia), Cancer, Genetics and Genomics, Mutation (Biology), medicine.disease, Genes, p53, Nucleòtids, Mutation, Cancer research, Genètica
وصف الملف: application/pdf
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dc2176476f08ccdf42bfc7391bc1cac4Test
https://doi.org/10.1038/sj.bjc.6605279Test -
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المؤلفون: W. Hofmann, Gemma Llort, Jan Lubinski, Marina Pollán, Dieter Niederacher, Orland Diez, Heli Nevanlinna, Sabine Preisler-Adams, Norbert Arnold, Paolo Radice, Cezary Cybulski, P L Mai, Christoph Engel, Anna Jakubowska, Alfons Meindl, Drakoulis Yannoukakos, Bernard Peissel, Paolo Peterlongo, Javier Benítez, Dorothea Gadzicki, Lesley McGuffog, Tuomas Heikkinen, Ute Hamann, Rita K. Schmutzler, J T Loud, Tadeusz Dębniak, Aleksandra Tołoczko-Grabarek, Ana Osorio, G Pita, Antonis C. Antoniou, Beatrix Versmold
المصدر: British Journal of Cancer
مصطلحات موضوعية: Adult, p53, Heterozygote, Cancer Research, Genotype, endocrine system diseases, Breast Neoplasms, Biology, breast cancer, BRCA2 Mutation, Breast cancer, Risk Factors, Polymorphism (computer science), medicine, Humans, Genetic Predisposition to Disease, skin and connective tissue diseases, Gene, Germ-Line Mutation, BRCA2 Protein, Ovarian Neoplasms, Genetics, Polymorphism, Genetic, BRCA1 Protein, Haplotype, Genetics and Genomics, Heterozygote advantage, BRCA1, medicine.disease, BRCA2, Haplotypes, Oncology, Mutation (genetic algorithm), Cancer research, Female, Tumor Suppressor Protein p53
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b296aa65b6036a9c2c043d2276bf454aTest
https://doi.org/10.1038/sj.bjc.6604624Test -
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المؤلفون: Paolo Radice, Daniele Calistri, M. A. Pierotti, Laura Cortesi, Dino Amadori, Valeria Pensotti, Silvia Casadei
المصدر: British Journal of Cancer
مصطلحات موضوعية: mutational analysis, Cancer Research, CFLP, DNA Mutational Analysis, Breast Neoplasms, Biology, Polymerase Chain Reaction, Sensitivity and Specificity, DNA sequencing, law.invention, chemistry.chemical_compound, law, Coding region, Humans, Genetic Predisposition to Disease, Gene, Polymerase chain reaction, Germ-Line Mutation, DNA Primers, Fluorescent Dyes, Ovarian Neoplasms, Polymorphism, Genetic, BRCA1 Protein, Reproducibility of Results, Regular Article, hereditary breast cancer, DNA, Neoplasm, Exons, Amplicon, BRCA1, Molecular biology, Oncology, chemistry, Nucleic Acid Conformation, Female, Restriction fragment length polymorphism, DNA
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ae1381d51eb49763fb94905e4fe373Test
http://europepmc.org/articles/PMC2375072Test -
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المؤلفون: M. Giarola, J. D. A. Delhanty, Lucio Bertario, Paola Sala, Paolo Radice, P. Mondini, M. A. Pierotti, Alberto Azzarelli, D. Wells, S. Pilotti
المصدر: British Journal of Cancer
Scopus-Elsevierمصطلحات موضوعية: Adult, Male, Cancer Research, Pathology, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Genes, APC, Adolescent, Adenomatous polyposis coli, Population, Fibromatosis, Abdominal, Familial adenomatous polyposis, Exon, Germline mutation, Neoplastic Syndromes, Hereditary, medicine, Humans, Allele, education, Gene, Polymorphism, Single-Stranded Conformational, Aged, education.field_of_study, biology, Single-strand conformation polymorphism, Middle Aged, medicine.disease, body regions, Fibromatosis, Aggressive, Oncology, Adenomatous Polyposis Coli, Mutation, biology.protein, Female, Research Article
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0ecf6e6fdaf531ed85ef75cf1c766b3eTest
https://pubmed.ncbi.nlm.nih.gov/9744495Test