المؤلفون: Stephanie L Greville-Haygate, Emma R. Woodward, D. Gareth Evans, Andrew J Wallace, Helen Byers, Jamie M Ellingford, Fiona Lalloo, Anthony Howell, George J Burghel, Sasha J Howell, Miriam J. Smith, Elaine F. Harkness, William G. Newman, Naomi L. Bowers, Elke M van Veen, Diana Eccles, Sarah J Evans, Marta Pereira

المصدر: Journal of Medical Genetics

مصطلحات موضوعية: 0301 basic medicine, Oncology, Adult, medicine.medical_specialty, endocrine system diseases, PALB2, Genes, BRCA2, Genes, BRCA1, human genetics, Breast Neoplasms, Disease, genetic testing, 03 medical and health sciences, 0302 clinical medicine, Breast cancer, Internal medicine, Cancer Genetics, Medicine, Humans, genetics, Age of Onset, Prospective cohort study, skin and connective tissue diseases, CHEK2, Genetics (clinical), Genetic testing, medicine.diagnostic_test, business.industry, DNA, Neoplasm, Sequence Analysis, DNA, Ductal carcinoma, medicine.disease, Genes, p53, Checkpoint Kinase 2, 030104 developmental biology, 030220 oncology & carcinogenesis, Cohort, Mutation, Female, business

وصف الملف: text

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74b616e4efac02fce2b44a6198f63f53Test
http://europepmc.org/articles/PMC8788257Test

المؤلفون: Southey, MC, Goldgar, DE, Winqvist, R, Pylkäs, K, Couch, F, Tischkowitz, M, Foulkes, WD, Dennis, J, Michailidou, K, van Rensburg, EJ, Heikkinen, T, Nevanlinna, H, Hopper, JL, Dörk, T, Claes, KB, Reis-Filho, J, Teo, ZL, Radice, P, Catucci, I, Peterlongo, P, Tsimiklis, H, Odefrey, FA, Dowty, JG, Schmidt, MK, Broeks, A, Hogervorst, FB, Verhoef, S, Carpenter, J, Clarke, C, Scott, RJ, Fasching, PA, Haeberle, L, Ekici, AB, Beckmann, MW, Peto, J, Dos-Santos-Silva, I, Fletcher, O, Johnson, N, Bolla, MK, Sawyer, EJ, Tomlinson, I, Kerin, MJ, Miller, N, Marme, F, Burwinkel, B, Yang, R, Guénel, P, Truong, T, Menegaux, F, Sanchez, M, Bojesen, S, Nielsen, SF, Flyger, H, Benitez, J, Zamora, MP, Perez, JIA, Menéndez, P, Anton-Culver, H, Neuhausen, S, Ziogas, A, Clarke, CA, Brenner, H, Arndt, V, Stegmaier, C, Brauch, H, Brüning, T, Ko, Y-D, Muranen, TA, Aittomäki, K, Blomqvist, C, Bogdanova, NV, Antonenkova, NN, Lindblom, A, Margolin, S, Mannermaa, A, Kataja, V, Kosma, V-M, Hartikainen, JM, Spurdle, AB, Investigators, K, Australian Ovarian Cancer Study Group, Wauters, E, Smeets, D, Beuselinck, B, Floris, G, Chang-Claude, J, Rudolph, A, Seibold, P, Flesch-Janys, D, Olson, JE, Vachon, C, Pankratz, VS, McLean, C, Haiman, CA, Henderson, BE, Schumacher, F, Le Marchand, L, Kristensen, V, Alnæs, GG, Zheng, W, Hunter, DJ, Lindstrom, S, Hankinson, SE, Kraft, P, Andrulis, I, Knight, JA, Glendon, G, Mulligan, AM, Jukkola-Vuorinen, A, Grip, M, Kauppila, S, Devilee, P, Tollenaar, RAEM, Seynaeve, C, Hollestelle, A, Garcia-Closas, M, Figueroa, J, Chanock, SJ, Lissowska, J, Czene, K, Darabi, H, Eriksson, M, Eccles, DM, Rafiq, S, Tapper, WJ, Gerty, SM, Hooning, MJ, Martens, JWM, Collée, JM, Tilanus-Linthorst, M, Hall, P, Li, J, Brand, JS, Humphreys, K, Cox, A, Reed, MWR, Luccarini, C, Baynes, C, Dunning, AM, Hamann, U, Torres, D, Ulmer, HU, Rüdiger, T, Jakubowska, A, Lubinski, J, Jaworska, K, Durda, K, Slager, S, Toland, AE, Ambrosone, CB, Yannoukakos, D, Swerdlow, A, Ashworth, A, Orr, N, Jones, M, González-Neira, A, Pita, G, Alonso, MR, Álvarez, N, Herrero, D, Tessier, DC, Vincent, D, Bacot, F, Simard, J, Dumont, M, Soucy, P, Eeles, R, Muir, K, Wiklund, F, Gronberg, H, Schleutker, J, Nordestgaard, BG, Weischer, M, Travis, RC, Neal, D, Donovan, JL, Hamdy, FC, Khaw, K-T, Stanford, JL, Blot, WJ, Thibodeau, S, Schaid, DJ, Kelley, JL, Maier, C, Kibel, AS, Cybulski, C, Cannon-Albright, L, Butterbach, K, Park, J, Kaneva, R, Batra, J, Teixeira, MR, Kote-Jarai, Z, Olama, AAA, Benlloch, S, Renner, SP, Hartmann, A, Hein, A, Ruebner, M, Lambrechts, D, Van Nieuwenhuysen, E, Vergote, I, Lambretchs, S, Doherty, JA, Rossing, MA, Nickels, S, Eilber, U, Wang-Gohrke, S, Odunsi, K, Sucheston-Campbell, LE, Friel, G, Lurie, G, Killeen, JL, Wilkens, LR, Goodman, MT, Runnebaum, I, Hillemanns, PA, Pelttari, LM, Butzow, R, Modugno, F, Edwards, RP, Ness, RB, Moysich, KB, du Bois, A, Heitz, F, Harter, P, Kommoss, S, Karlan, BY, Walsh, C, Lester, J, Jensen, A, Kjaer, SK, Høgdall, E, Peissel, B, Bonanni, B, Bernard, L, Goode, EL, Fridley, BL, Vierkant, RA, Cunningham, JM, Larson, MC, Fogarty, ZC, Kalli, KR, Liang, D, Lu, KH, Hildebrandt, MAT, Wu, X, Levine, DA, Dao, F, Bisogna, M, Berchuck, A, Iversen, ES, Marks, JR, Akushevich, L, Cramer, DW, Schildkraut, J, Terry, KL, Poole, EM, Stampfer, M, Tworoger, SS, Bandera, EV, Orlow, I, Olson, SH, Bjorge, L, Salvesen, HB, van Altena, AM, Aben, KKH, Kiemeney, LA, Massuger, LFAG, Pejovic, T, Bean, Y, Brooks-Wilson, A, Kelemen, LE, Cook, LS, Le, ND, Górski, B, Gronwald, J, Menkiszak, J, Høgdall, CK, Lundvall, L, Nedergaard, L, Engelholm, SA, Dicks, E, Tyrer, J, Campbell, I, McNeish, I, Paul, J, Siddiqui, N, Glasspool, R, Whittemore, AS, Rothstein, JH, McGuire, V, Sieh, W, Cai, H, Shu, X-O, Teten, RT, Sutphen, R, McLaughlin, JR, Narod, SA, Phelan, CM, Monteiro, AN, Fenstermacher, D, Lin, H-Y, Permuth, JB, Sellers, TA, Chen, YA, Tsai, Y-Y, Chen, Z, Gentry-Maharaj, A, Gayther, SA, Ramus, SJ, Menon, U, Wu, AH, Pearce, CL, Van Den Berg, D, Pike, MC, Dansonka-Mieszkowska, A, Plisiecka-Halasa, J, Moes-Sosnowska, J, Kupryjanczyk, J, Pharoah, PD, Song, H, Winship, I, Chenevix-Trench, G, Giles, GG, Tavtigian, SV, Easton, DF, Milne, RL

المساهمون: Fletcher, Olivia, Johnson, Nichola, Garcia-Closas, Montserrat, Swerdlow, Anthony, Jones, Michael, Eeles, Rosalind, Kote-Jarai, Zsofia

مصطلحات موضوعية: Australian Ovarian Cancer Study Group, Humans, Breast Neoplasms, Ovarian Neoplasms, Prostatic Neoplasms, Genetic Predisposition to Disease, Tumor Suppressor Proteins, Nuclear Proteins, Risk, Case-Control Studies, Mutation, Female, Male, Genetic Association Studies, Ataxia Telangiectasia Mutated Proteins, Checkpoint Kinase 2, Fanconi Anemia Complementation Group N Protein

وصف الملف: Print-Electronic; 811; application/octet-stream

العلاقة: Journal of medical genetics, 2016, 53 (12), pp. 800 - 811; https://repository.icr.ac.uk/handle/internal/112Test

الإتاحة: https://doi.org/10.1136/jmedgenet-2016-103839Test
https://repository.icr.ac.uk/handle/internal/112Test

المؤلفون: Decker, Brennan, Allen, Jamie, Luccarini, Craig, Pooley, Karen A, Shah, Mitul, Bolla, Manjeet K, Wang, Qin, Ahmed, Shahana, Baynes, Caroline, Conroy, Don M, Brown, Judith, Luben, Robert, Ostrander, Elaine A, Pharoah, Paul DP, Dunning, Alison M, Easton, Douglas F

المصدر: Journal of Medical Genetics

مصطلحات موضوعية: Cancer: breast, Genetic Variation, Breast Neoplasms, Ataxia Telangiectasia Mutated Proteins, DNA-Binding Proteins, Checkpoint Kinase 2, Evidence Based Practice, Sequence Analysis, Protein, Genetic Epidemiology, Cancer Genetics, Humans, Female, Genetic Predisposition to Disease, Fanconi Anemia Complementation Group N Protein, Geneticscreening/counselling

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=pmid________::f66a7d8767bcda142e70616465225747Test
http://europepmc.org/articles/PMC5740532Test

المؤلفون: G. H. de Bock, Peter Devilee, J.G.M. Klijn, C. J. Cornelisse, Mieke Schutte, R.A.E.M. Tollenaar, Hanne Meijers-Heijboer, Caroline Seynaeve, J. Blom, C.T.M. Brekelmans, E M M Krol-Warmerdam, C. J. van Asperen

المساهمون: Human Genetics, Damage and Repair in Cancer Development and Cancer Treatment (DARE), Life Course Epidemiology (LCE), Medical Oncology, Clinical Genetics

المصدر: Journal of medical genetics, 41(10), 731-735. BMJ Publishing Group
JOURNAL OF MEDICAL GENETICS, 41(10), 731-735. BMJ PUBLISHING GROUP
Journal of Medical Genetics, 41, 731-735. BMJ Publishing Group

مصطلحات موضوعية: Oncology, Male, HEREDITARY BREAST, endocrine system diseases, SUSCEPTIBILITY, FAMILIES, Cohort Studies, Prospective cohort study, skin and connective tissue diseases, Genetics (clinical), POPULATION, Second-degree relative, Aged, 80 and over, RISK, education.field_of_study, Middle Aged, Prognosis, CARRIERS, CARCINOMAS, SURVIVAL, Original Article, Female, Adult, medicine.medical_specialty, Heterozygote, GENES, Population, Breast Neoplasms, Protein Serine-Threonine Kinases, Breast cancer, SDG 3 - Good Health and Well-being, Median follow-up, Internal medicine, Genetics, medicine, Humans, BRCA2 MUTATIONS, education, CHEK2, Survival analysis, Germ-Line Mutation, Aged, Neoplasm Staging, business.industry, Genetic Variation, medicine.disease, Survival Analysis, Checkpoint Kinase 2, Immunology, Ovarian cancer, business

الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::776418543274609fa6901369f0d24ac6Test
https://pure.eur.nl/en/publications/ba1a800b-9a66-4fc7-aa0c-fcd0bd975859Test

المؤلفون: Bougeard, Gaëlle, Limacher, J, Martin, C., Charbonnier, F., Killian, A., Delattre, O., Longy, M, Jonveaux, P., Fricker, J, Stoppa-Lyonnet, D., Flaman, J, Frébourg, T

المساهمون: Caractérisation structurale et fonctionnelle des mutations et des polymorphismes en cancérologie et neuro-psychiatrie, Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM), Institut Fédératif de Recherches Multidisciplinaires sur les Peptides (IFRMP 23), CHU Rouen, Normandie Université (NU)-Normandie Université (NU)-Université Le Havre Normandie (ULH), Normandie Université (NU)-Université de Rouen Normandie (UNIROUEN), Normandie Université (NU)-Institut National de la Santé et de la Recherche Médicale (INSERM)-Centre de Lutte Contre le Cancer Henri Becquerel Normandie Rouen (CLCC Henri Becquerel)-Centre National de la Recherche Scientifique (CNRS), Les Hôpitaux Universitaires de Strasbourg (HUS), Institut Curie Paris, Institut Bergonié Bordeaux, UNICANCER, Nutrition-Génétique et Exposition aux Risques Environnementaux (NGERE), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université de Lorraine (UL), Service de Génétique CHRU Nancy, Centre Hospitalier Régional Universitaire de Nancy (CHRU Nancy), Centre Paul Strauss (CRLCC Paul Strauss)

المصدر: ISSN: 0022-2593.

مصطلحات موضوعية: MESH: Checkpoint Kinase 2, MESH: DNA Mutational Analysis, MESH: Transcription Factors, MESH: Tumor Suppressor Protein p53, MESH: DNA-Binding Proteins, MESH: Tumor Suppressor Proteins, MESH: Family Health, MESH: Female, MESH: France, MESH: Genes, Tumor Suppressor, MESH: Germ-Line Mutation, MESH: Humans, MESH: Male, MESH: Li-Fraumeni Syndrome, MESH: Membrane Proteins, MESH: Mutation, MESH: Pedigree, MESH: Phosphoproteins, MESH: Protein Kinases, MESH: Protein-Serine-Threonine Kinases, MESH: Trans-Activators, [SDV.GEN.GH]Life Sciences [q-bio]/Genetics/Human genetics

العلاقة: info:eu-repo/semantics/altIdentifier/pmid/11370630; hal-03106956; https://hal.science/hal-03106956Test; PUBMED: 11370630; PUBMEDCENTRAL: PMC1734839

الإتاحة: https://doi.org/10.1136/jmg.38.4.253Test
https://hal.science/hal-03106956Test