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1دورية أكاديمية
المؤلفون: Mette Nyegaard, Nanna D Rendtorff, Morten S Nielsen, Thomas J Corydon, Ditte Demontis, Anna Starnawska, Anne Hedemand, Annalisa Buniello, Francesco Niola, Michael T Overgaard, Suzanne M Leal, Wasim Ahmad, Friedrik P Wikman, Kirsten B Petersen, Dorthe G Crüger, Jaap Oostrik, Hannie Kremer, Niels Tommerup, Morten Frödin, Karen P Steel, Lisbeth Tranebjærg, Anders D Børglum
المصدر: PLoS Genetics, Vol 11, Iss 7, p e1005386 (2015)
وصف الملف: electronic resource
العلاقة: http://europepmc.org/articles/PMC4510537?pdf=renderTest; https://doaj.org/toc/1553-7390Test; https://doaj.org/toc/1553-7404Test
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المؤلفون: Dorthe G. Crüger, Anders Jakobsen, Jan Lindebjerg, Kathleen D. Danenberg, Hidekazu Kuramochi, Lene Byriel, Lars Henrik Jensen, Peter V. Danenberg, Anders Aamann Rasmussen
المصدر: Jensen, L H, Rasmussen, A A, Byriel, L, Kuramochi, H, Crüger, D G, Lindebjerg, J, Danenberg, P V, Jakobsen, A & Danenberg, K 2013, ' Regulation of MLH1 mRNA and protein expression by promoter methylation in primary colorectal cancer : a descriptive and prognostic cancer marker study ', Cellular Oncology, vol. 36, no. 5, pp. 411-419 . https://doi.org/10.1007/s13402-013-0148-2Test
مصطلحات موضوعية: Male, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Colorectal cancer, Biology, MLH1, Mismatch repair, Gene expression, medicine, Humans, RNA, Messenger, Promoter Regions, Genetic, neoplasms, Adaptor Proteins, Signal Transducing, Aged, Methylation specificMLPA, Nuclear Proteins, nutritional and metabolic diseases, Microsatellite instability, Promoter, General Medicine, DNA Methylation, Middle Aged, medicine.disease, digestive system diseases, Lynch syndrome, QPCR, Promoter hypermethylation, Oncology, DNA methylation, Cancer research, Molecular Medicine, Female, DNA mismatch repair, Colorectal Neoplasms, MutL Protein Homolog 1
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9351236416431d9a9c7905f2a5c6b659Test
https://doi.org/10.1007/s13402-013-0148-2Test -
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المؤلفون: A. Abele, Rosalind A. Eeles, Soo Hwang Teo, Marc Tischkowitz, Audrey Ardern-Jones, Ignacio Blanco, Elizabeth Bancroft, Gad Rennert, Nicola Nicolai, Graeme Suthers, R. Doherty, Huw Dorkins, Annelie Liljegren, Cezary Cybulski, S. Townshend, Yolanda Barbachano, L. Maehle, Dorthe G. Crüger, B. Newcombe, Peter R. Wilson, Alan Donaldson, David P. Dearnaley, Virginia E. Clowes, Irene Jobson, C. J. van Asperen, Vincent Khoo, Hans Lilja, Charles Jameson, Zsofia Kote-Jarai, Henrik Grönberg, A. Male, Carole Brewer, Wendy S. Rubinstein, Elizabeth Page, B. Bulman, Clare Moynihan, D G R Evans, T. Ramón y Cajal, Allan D. Spigelman, Jan Lubinski, Louise Izatt, Jorunn E. Eyfjord, Palle Jørn Sloth Osther, Y. J. Bignon, Eitan Friedman, Alan M. F. Stapleton, Fritz H. Schröder, Sara S. Strom, Geoffrey J. Lindeman, Alison Falconer, J Melia, Mónica Salinas, Christopher S. Foster, Colin Mercer, Katherine L. Tucker, Karol Axcrona, Freddie C. Hamdy, Lisa Walker, Judy Kirk, Saundra S. Buys, Susan M. Domchek, Mohnish Suri, Kyriacos Kyriacou, Susan Peock, D. Ilencikova, Chris H. Bangma, Neil K. Aaronson, A. Mitra, Paul Sibley, Fiona Douglas, Douglas F. Easton, Oskar T. Johannsson, Lambertus A. Kiemeney, Diana Eccles, Shirley Hodgson, Gillian Mitchell
المصدر: BJU International. 107:28-39
مصطلحات موضوعية: Oncology, Gynecology, medicine.medical_specialty, Prostate biopsy, medicine.diagnostic_test, business.industry, Urology, BRCA mutation, Cancer, medicine.disease, Prostate cancer, Prostate-specific antigen, Prostate cancer screening, medicine.anatomical_structure, Prostate, Internal medicine, medicine, Genetic predisposition, skin and connective tissue diseases, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::8e11f554b0b9c8a6d5f97f95c1786a42Test
https://doi.org/10.1111/j.1464-410x.2010.09648.xTest -
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المؤلفون: Maria J. Soares, Mauricio Magalhaes Costa, Ingrid Petroni Ewald, Rachel Kyle, Nelly Sabbaghian, Torben A Kruse, Leonor Gusmão, Mads Thomassen, Silvia Casadei, Annemarie H. van der Hout, Marc Tischkowitz, Patrícia Rocha, Ana Vega, Miguel de la Hoya, Patricia Ashton-Prolla, Lone Sunde, Sara Gutiérrez-Enríquez, Dirce Maria Carraro, Conxi Lázaro, Philippe Maillet, Maroulio Pertesi, Cindy Benson, Pedro Pinto, Alberto Gulino, Nancy Uhrhammer, Drakoulis Yannoukakos, William D. Foulkes, Lucie Cornil, Etienne Rouleau, Ana Peixoto, Ignacio Blanco, Gaelle Benais-Pont, Robert Royer, Mary Claire King, Montserrat Baiget, Thangarajan Rajkumar, María Dolores Miramar, Ana Rodriguez Valle, Maria Teresa Calvo, Judith Balmaña, Anne-Marie Gerdes, Rosette Lidereau, Giuseppe Giannini, Catarina Santos, Eladio Velasco, Maria Isabel Achatz, Dorthe G. Crüger, Luisa Mota-Vieira, Carmen Alonso, Orland Diez, Eitan Friedman, Manuela Pinheiro, Brigitte Bressac-de Paillerets, Yael Laitman, Steven A. Narod, Teresa Ramón y Cajal, Begoña Graña, António Amorim, Trinidad Caldés, Lídia Feliubadaló, Mercedes Durán, Bruno Pardo, Erik Teugels, Audrey Remenieras, Manuel R. Teixeira, Yves-Jean Bignon, Ana Blanco
المصدر: Digital.CSIC. Repositorio Institucional del CSIC
instname
Peixoto, A, Santos, C, Pinheiro, M, Pinto, P, Soares, M J, Rocha, P, Gusmão, L, Amorim, A, van der Hout, A, Gerdes, A-M, Thomassen, M, Kruse, T A, Cruger, D, Sunde, L E M, Bignon, Y-J, Uhrhammer, N, Cornil, L, Rouleau, E, Lidereau, R, Yannoukakos, D, Pertesi, M, Narod, S, Royer, R, Costa, M M, Lazaro, C, Feliubadaló, L, Graña, B, Blanco, I, de la Hoya, M, Caldés, T, Maillet, P, Benais-Pont, G, Pardo, B, Laitman, Y, Friedman, E, Velasco, E A, Durán, M, Miramar, M-D, Valle, A R, Calvo, M-T, Vega, A, Blanco, A, Diez, O, Gutiérrez-Enríquez, S, Balmaña, J, Ramon Y Cajal, T, Alonso, C, Baiget, M, Foulkes, W, Tischkowitz, M, Kyle, R, Sabbaghian, N, Ashton-Prolla, P, Ewald, I P, Rajkumar, T, Mota-Vieira, L, Giannini, G, Gulino, A, Achatz, M I, Carraro, D M, de Paillerets, B B, Remenieras, A, Benson, C, Casadei, S, King, M-C, Teugels, E & Teixeira, M R 2011, ' International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation ', Breast Cancer Research and Treatment, vol. 127, no. 3, pp. 671-9 . https://doi.org/10.1007/s10549-010-1036-3Test
Peixoto, A, Santos, C, Pinheiro, M, Pinto, P, Soares, M J, Rocha, P, Gusmão, L, Amorim, A, van der Hout, A, Gerdes, A-M, Thomassen, M, Kruse, T A, Cruger, D, Sunde, L, Bignon, Y-J, Uhrhammer, N, Cornil, L, Rouleau, E, Lidereau, R, Yannoukakos, D, Pertesi, M, Narod, S, Royer, R, Costa, M M, Lazaro, C, Feliubadaló, L, Graña, B, Blanco, I, de la Hoya, M, Caldés, T, Maillet, P, Benais-Pont, G, Pardo, B, Laitman, Y, Friedman, E, Velasco, E A, Durán, M, Miramar, M-D, Valle, A R, Calvo, M-T, Vega, A, Blanco, A, Diez, O, Gutiérrez-Enríquez, S, Balmaña, J, Ramon Y Cajal, T, Alonso, C, Baiget, M, Foulkes, W, Tischkowitz, M, Kyle, R, Sabbaghian, N, Ashton-Prolla, P, Ewald, I P, Rajkumar, T, Mota-Vieira, L, Giannini, G, Gulino, A, Achatz, M I, Carraro, D M, de Paillerets, B B, Remenieras, A, Benson, C, Casadei, S, King, M-C, Teugels, E & Teixeira, M R 2011, ' International distribution and age estimation of the Portuguese BRCA2 c.156_157insAlu founder mutation ', Breast Cancer Research and Treatment, vol. 127, no. 3, pp. 671-9 . https://doi.org/10.1007/s10549-010-1036-3Test
Breast Cancer Research and Treatment, 127(3), 671-679. SPRINGER
BREAST CANCER RESEARCH AND TREATMENT
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pauمصطلحات موضوعية: Proband, Reading Frames, Cancer Research, Genes, BRCA2, Polymerase Chain Reaction, DISEASE, 0302 clinical medicine, BREAST/OVARIAN CANCER FAMILIES, skin and connective tissue diseases, Predictive testing, Sequence Deletion, founder mutation, c.156_157insalu brca2 mutation, hereditary breast/ovarian cancer, age estimation, c.156-157insalu brca2 mutation, Ovarian Neoplasms, Genetics, 0303 health sciences, education.field_of_study, medicine.diagnostic_test, REARRANGEMENT, Founder Effect, 3. Good health, Oncology, 030220 oncology & carcinogenesis, Mutation (genetic algorithm), GENETIC-HETEROGENEITY, Female, Population, Breast Neoplasms, Polymorphism, Single Nucleotide, 03 medical and health sciences, Breast cancer, medicine, Humans, Genetic Predisposition to Disease, Amino Acid Sequence, Genetic Testing, RNA, Messenger, Founder mutation, education, 030304 developmental biology, Genetic testing, Portugal, business.industry, Haplotype, medicine.disease, Genetics, Population, Mutation, Age estimation, c.156_157insAlu BRCA2 mutation, business, Hereditary breast/ovarian cancer, Microsatellite Repeats, Founder effect
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f02e96ceaf1775d47c62e59d3f95ac1dTest
https://doi.org/10.1007/s10549-010-1036-3Test -
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المؤلفون: Anne-Marie Gerdes, Dorthe G. Crüger, Klaus Brusgaard, Maiken Thyregod Joergensen, Ove B. Schaffalitzky de Muckadell
المصدر: Jørgensen, M T, Brusgaard, K, Crüger, D G, Gerdes, A-M & Schaffalitzky de Muckadell, O B 2010, ' Incidence, Prevalence, Etiology, and Prognosis of First-Time Chronic Pancreatitis in Young Patients: A Nationwide Cohort Study ', Digestive Diseases and Sciences, vol. 55, no. 10, pp. 2988-2998 . https://doi.org/10.1007/s10620-009-1118-4Test
مصطلحات موضوعية: Adult, Male, medicine.medical_specialty, Pancreatic disease, Adolescent, Pancreatitis, Alcoholic, Physiology, Denmark, Genetic counseling, Comorbidity, Kaplan-Meier Estimate, Gastroenterology, Cohort Studies, Young Adult, Age Distribution, Cause of Death, Pancreatitis, Chronic, Internal medicine, Prevalence, Humans, Medicine, Registries, Sex Distribution, Hereditary pancreatitis, business.industry, Incidence, Incidence (epidemiology), Odds ratio, Prognosis, medicine.disease, Hospitalization, Endocrinology, Acute Disease, Chronic Disease, Cohort, Etiology, Pancreatitis, Exocrine Pancreatic Insufficiency, Female, business
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5b38b704c05124839b31e41508745a7dTest
https://doi.org/10.1007/s10620-009-1118-4Test -
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المؤلفون: Emma R. Woodward, Dorthe G. Crüger, Eamonn R. Maher, Anne-Bine Skytte
المصدر: Woodward, E R, Skytte, A-B, Cruger, D G & Maher, E R 2010, ' Population-based survey of cancer risks in chromosome 3 translocation carriers ', Genes, Chromosomes & Cancer, vol. 49, no. 1, pp. 52-8 . https://doi.org/10.1002/gcc.20718Test
مصطلحات موضوعية: Adult, Male, Risk, Oncology, Cancer Research, medicine.medical_specialty, Tumor suppressor gene, Denmark, Population, Chromosomal translocation, Biology, Translocation, Genetic, Germline mutation, Internal medicine, Genetics, medicine, Humans, Genetic Predisposition to Disease, Family history, education, Carcinoma, Renal Cell, Aged, Retrospective Studies, Aged, 80 and over, Family Health, education.field_of_study, Genetic heterogeneity, Cancer, Middle Aged, medicine.disease, Chromosome 3, Female, Chromosomes, Human, Pair 3
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2fe6f8ab352ca57fbe521ef44540415eTest
https://doi.org/10.1002/gcc.20718Test -
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المؤلفون: Emma R. Woodward, A M Considine, Dorthe G. Crüger, S Williamson, J M McHugo, H V Sleightholme
المصدر: Woodward, E R, Sleightholme, H V, Considine, A M, Williamson, S, McHugo, J M & Crüger, D G 2007, ' Annual surveillance by CA125 and transvaginal ultrasound for ovarian cancer in both high-risk and population risk women is ineffective ', British Journal of Obstetrics and Gynecology, vol. 114, no. 12, pp. 1500-1509 . https://doi.org/10.1111/j.1471-0528.2007.01499.xTest
مصطلحات موضوعية: Adult, medicine.medical_specialty, endocrine system diseases, Genes, BRCA2, Genes, BRCA1, DNA Mismatch Repair, Sensitivity and Specificity, Age Distribution, Risk Factors, medicine, Humans, Risk factor, Aged, Retrospective Studies, Ovarian Neoplasms, Gynecology, Incidental Findings, business.industry, Obstetrics, Endometrial cancer, Obstetrics and Gynecology, Cancer, Retrospective cohort study, Middle Aged, medicine.disease, female genital diseases and pregnancy complications, Endometrial Neoplasms, Pedigree, Early Diagnosis, CA-125 Antigen, Mutation, Cohort, Population study, Female, business, Ovarian cancer, Exploratory surgery
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::93dcfd28f4b9bde6f122c6d81d1eefb6Test
https://doi.org/10.1111/j.1471-0528.2007.01499.xTest -
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المصدر: Cancer Genetics and Cytogenetics. 168:168-171
مصطلحات موضوعية: Male, Cancer Research, endocrine system diseases, Sequence analysis, Denmark, Genes, BRCA2, Nonsense mutation, Genes, BRCA1, Breast Neoplasms, Biology, Genome, Germline mutation, Genetics, medicine, Humans, Multiplex ligation-dependent probe amplification, skin and connective tissue diseases, Molecular Biology, Gene, Sequence Deletion, Ovarian Neoplasms, Genome, Human, Exons, Sequence Analysis, DNA, medicine.disease, Molecular biology, Introns, Human genetics, Mutation, Female, Ovarian cancer
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::530fd89d2fb2ab4185ad413a6cbac59aTest
https://doi.org/10.1016/j.cancergencyto.2005.12.016Test -
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المؤلفون: Torben A Kruse, Dorthe G. Crüger, Anne-Marie Gerdes, Mads Thomassen
المصدر: Clinical Genetics. 69:171-178
مصطلحات موضوعية: Genetics, Myriad Model, business.industry, medicine.disease, BRCA2 Protein, language.human_language, Danish, Breast cancer, Mutation (genetic algorithm), Cohort, medicine, language, Family history, business, Genetics (clinical), Cohort study
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::e42e71d9930f4e43115077a370c55e5bTest
https://doi.org/10.1111/j.1399-0004.2006.00568.xTest -
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المؤلفون: Dorthe G. Crüger, Anne-Marie Gerdes, Torben A Kruse
المصدر: Clinical Genetics. 68:228-233
مصطلحات موضوعية: Genetics, Oncology, medicine.medical_specialty, medicine.diagnostic_test, Genetic counseling, Biology, medicine.disease, Prophylactic Surgery, Breast cancer, Internal medicine, Mutation (genetic algorithm), medicine, Family history, Predictive testing, Ovarian cancer, Genetics (clinical), Genetic testing
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::44a36d0fa3f35abc548032ab8667e096Test
https://doi.org/10.1111/j.1399-0004.2005.00484.xTest