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المؤلفون: Seçil Aksoy, Michael O. Woods, Heinric Williams, Bruno Buecher, Finlay A. Macrae, Lotte N. Krogh, Jay Qiu, Wan K.W. Juhari, Jan T. Lowery, Anne-Marie Gerdes, Magnus von Knebel Doeberitz, Luigi Ricciardiello, Karsten Schulmann, Jose Luis Soto, Kristina Lagerstedt-Robinson, Kiwamu Akagi, Raj Ramesar, Uffe Birk Jensen, Angel Alonso, Robert Hüneburg, Olivier Caron, Michel Longy, Jan Lubinski, Kate Green, Annabel Goodwin, D. Gareth Evans, Julie Wods, Leigha Senter, Matthew F. Kalady, Mark Clendenning, Barbara A. Leggett, Ravindran Ankathil, Swati G. Patel, Julian Barwell, Katherine M. Tucker, Grant Lee, Pascaline Berthet, Dawn M. Nixon, Sonia S. Kupfer, Naohiro Tomita, Susan Parry, Trinidad Caldés, Robert W. Haile, Edenir Inêz Palmero, Karin Alvarez, Cassandra B. Nichols, Mark A. Jenkins, N. Jewel Samadder, Loic LeMarchand, John Burn, Francisco Lopez, Rodney J. Scott, Pierre Laurent-Puig, Julie Arnold, Christina Therkildsen, Hans K. Schackert, Pilar Garre, Reinhard Buettner, Adriana Della Valle, Patricia Esperon, Wolff Schmiegel, Karl Heinimann, Inge Bernstein, Matthias Kloor, Nicoline Hoogerbrugge, Rui Manuel Reis, Fränzel J.B. Van Duijnhoven, Christoph Engel, Mohd Nizam Zahary, Sylviane Olschwang, Sapna Syngal, Valérie Bonadona, Nicholas Pachter, Matilde Navarro, Albert de la Chapelle, Beate Betz, Jukka-Pekka Mecklin, Catherine Noguès, Elena M. Stoffel, Toni T. Seppälä, Chrystelle Colas, Anneke Lucassen, Allan D. Spigelman, Youenn Drouet, Elisa J. Cops, Uri Ladabaum, Steve Thibodeau, Jeffrey N. Weitzel, Fiona Lalloo, Patrick J. Morrison, Maurizio Genuardi, Kohji Tanakaya, Patrick M. Lynch, Frederik J. Hes, William D. Foulkes, Carmen Guillén-Ponce, Jenny von Salomé, Emilia Rogoża-Janiszewska, Andrew Latchford, John L. Hopper, Carrie Snyder, Verónica Barca-Tierno, Gabriela Möslein, Lauren M. Gima, Melissa C. Southey, Paul A. James, Marion Dhooge, Claudia Perne, Steven Gallinger, Heather Hampel, Amanda B. Spurdle, Ingrid Winship, Emmanuelle Fourme, Rish K. Pai, Daniela Turchetti, Marta Pineda, Jürgen Weitz, James Hill, Daniel D. Buchanan, Carlos A. Vaccaro, Noralane M. Lindor, Rachel Pearlman, Pål Møller, Christian P. Strassburg, Jane C. Figueiredo, Aída Falcón de Vargas, Silke Zachariae, Karolin Bucksch, Joanne Ngeow, Silke Redler, Henrik Okkels, Maija R.J. Kohonen-Corish, Hans F. A. Vasen, Verena Steinke-Lange, Roselyne Guimbaud, Deepak Vangala, Isabelle Coupier, Nils Rahner, Berrin Tunca, Sanne W. Bajwa-ten Broeke, Niels de Wind, Sophie Lejeune, José Gaston Guillem, Karin Wadt, Polly A. Newcomb, Elke Holinski-Feder, Florencia Neffa, Rodrigo Santa Cruz Guindalini, Paul E. Wise, Julian R. Sampson, Graham Casey, Lene Juel Rasmussen, Rolf H. Sijmons, Tadeusz Dębniak, Ann-Sofie Backman, Joji Utsunomiya, Melyssa Aronson, Aung Ko Win, Yves-Jean Bignon, Judy W. C. Ho, Robyn L. Ward, Mev Dominguez-Valentin, Karolina Malińska, Elizabeth E. Half, John-Paul Plazzer, Marjolijn J. L. Ligtenberg, Rachel Austin, Nicola K. Poplawski, Marcia Cruz-Correa, Nagahide Matsubara, Charlotte Kvist Lautrup, Thomas Hansen, Tatsuro Yamaguchi, Thomas John, David J. Amor, Ilana Solomon, Yun-Hee Choi, Meghan J. van Wanzeele, Rakefet Shtoyerman, Vanessa Huntley, Maartje Nielsen, Deborah Neklason, Kevin J. Monahan, Gülçin Tezcan, Stefan Aretz, Talya Boisjoli, Sophie Giraud, Thierry Frebourg, Christophe Rosty, Heike Görgens, Lone Sunde, Allyson Templeton, Jacob Nattermann, Mala Pande, Joan Brunet, Nancy Uhrhammer, James M. Church, Florencia Spirandelli, Laurent Briollais, James G. Dowty, Jeanette C. Reece, Rachel Susman, Fay Kastrinos, Kirsi Pylvänäinen, Gabriel Capellá, Helène Schuster, Min H. Chew, Markus Loeffler, Christine Lasset, Michael J. Hall, Capuccine Delnatte, Floor A. Duijkers
المساهمون: Imagerie Moléculaire et Stratégies Théranostiques (IMoST), Institut National de la Santé et de la Recherche Médicale (INSERM)-Université Clermont Auvergne (UCA), Centre Jean Perrin [Clermont-Ferrand] (UNICANCER/CJP), UNICANCER, Digital Precision Cancer Medicine (iCAN), ATG - Applied Tumor Genomics, HUS Abdominal Center, Clinical sciences, Medical Genetics, Win A.K., Dowty J.G., Reece J.C., Lee G., Templeton A.S., Plazzer J.-P., Buchanan D.D., Akagi K., Aksoy S., Alonso A., Alvarez K., Amor D.J., Ankathil R., Aretz S., Arnold J.L., Aronson M., Austin R., Backman A.-S., Bajwa-ten Broeke S.W., Barca-Tierno V., Barwell J., Bernstein I., Berthet P., Betz B., Bignon Y.-J., Boisjoli T., Bonadona V., Briollais L., Brunet J., Bucksch K., Buecher B., Buettner R., Burn J., Caldes T., Capella G., Caron O., Casey G., Chew M.H., Choi Y.-H., Church J., Clendenning M., Colas C., Cops E.J., Coupier I., Cruz-Correa M., de la Chapelle A., de Wind N., Debniak T., Della Valle A., Delnatte C., Dhooge M., Dominguez-Valentin M., Drouet Y., Duijkers F.A., Engel C., Esperon P., Evans D.G., Falcon de Vargas A., Figueiredo J.C., Foulkes W., Fourme E., Frebourg T., Gallinger S., Garre P., Genuardi M., Gerdes A.-M., Gima L.M., Giraud S., Goodwin A., Gorgens H., Green K., Guillem J., Guillen-Ponce C., Guimbaud R., Guindalini R.S.C., Half E.E., Hall M.J., Hampel H., Hansen T.V.O., Heinimann K., Hes F.J., Hill J., Ho J.W.C., Holinski-Feder E., Hoogerbrugge N., Huneburg R., Huntley V., James P.A., Jensen U.B., John T., Juhari W.K.W., Kalady M., Kastrinos F., Kloor M., Kohonen-Corish M.R., Krogh L.N., Kupfer S.S., Ladabaum U., Lagerstedt-Robinson K., Lalloo F., Lasset C., Latchford A., Laurent-Puig P., Lautrup C.K., Leggett B.A., Lejeune S., LeMarchand L., Ligtenberg M., Lindor N., Loeffler M., Longy M., Lopez F., Lowery J., Lubinski J., Lucassen A.M., Lynch P.M., Malinska K., Matsubara N., Mecklin J.-P., Moller P., Monahan K., Morrison P.J., Nattermann J., Navarro M., Neffa F., Neklason D., Newcomb P.A., Ngeow J., Nichols C., Nielsen M., Nixon D.M., Nogues C., Okkels H., Olschwang S., Pachter N., Pai R.K., Palmero E.I., Pande M., Parry S., Patel S.G., Pearlman R., Perne C., Pineda M., Poplawski N.K., Pylvanainen K., Qiu J., Rahner N., Ramesar R., Rasmussen L.J., Redler S., Reis R.M., Ricciardiello L., Rogoza-Janiszewska E., Rosty C., Samadder N.J., Sampson J.R., Schackert H.K., Schmiegel W., Schulmann K., Schuster H., Scott R., Senter L., Seppala T.T., Shtoyerman R., Sijmons R.H., Snyder C., Solomon I.B., Soto J.L., Southey M.C., Spigelman A., Spirandelli F., Spurdle A.B., Steinke-Lange V., Stoffel E.M., Strassburg C.P., Sunde L., Susman R., Syngal S., Tanakaya K., Tezcan G., Therkildsen C., Thibodeau S., Tomita N., Tucker K.M., Tunca B., Turchetti D., Uhrhammer N., Utsunomiya J., Vaccaro C., van Duijnhoven F.J.B., van Wanzeele M.J., Vangala D.B., Vasen H.F.A., von Knebel Doeberitz M., von Salome J., Wadt K.A.W., Ward R.L., Weitz J., Weitzel J.N., Williams H., Winship I., Wise P.E., Wods J., Woods M.O., Yamaguchi T., Zachariae S., Zahary M.N., Hopper J.L., Haile R.W., Macrae F.A., Moslein G., Jenkins M.A.
المصدر: The Lancet Oncology, 22(7), 1014-1022. ELSEVIER SCIENCE INC
International Mismatch Repair Consortium, Sunde, L E M, Lautrup, C K, Okkels, H & Bernstein, I 2021, ' Variation in the risk of colorectal cancer in families with Lynch syndrome : a retrospective cohort study ', The Lancet. Oncology, vol. 22, no. 7, pp. 1014-1022 . https://doi.org/10.1016/S1470-2045(21)00189-3
The International Mismatch Repair Consortium 2021, ' Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study ', The Lancet Oncology, vol. 22, no. 7, pp. 1014-1022 . https://doi.org/10.1016/S1470-2045(21)00189-3
Lancet Oncology
Lancet Oncology, Elsevier, 2021, 22 (7), pp.1014-1022. ⟨10.1016/S1470-2045(21)00189-3⟩
The International Mismatch Repair Consortium 2021, ' Variation in the risk of colorectal cancer in families with Lynch syndrome : a retrospective cohort study ', The Lancet Oncology, vol. 22, no. 7, pp. 1014-1022 . https://doi.org/10.1016/S1470-2045(21)00189-3
Lancet Oncology, 22, 7, pp. 1014-1022
Lancet Oncology, 22, 1014-1022مصطلحات موضوعية: 0301 basic medicine, Proband, Oncology, Male, Heredity, DNA mismatch repair, [SDV]Life Sciences [q-bio], SUSCEPTIBILITY, Settore MED/03 - GENETICA MEDICA, 0302 clinical medicine, Residence Characteristics, Risk Factors, Tumours of the digestive tract Radboud Institute for Molecular Life Sciences [Radboudumc 14], PMS2, ComputingMilieux_MISCELLANEOUS, MLH1, Age Factors, Middle Aged, Penetrance, Lynch syndrome, 3. Good health, Pedigree, Phenotype, 030220 oncology & carcinogenesis, Colorectal Neoplasms, Hereditary Nonpolyposis/diagnosis, Female, Adult, medicine.medical_specialty, PENETRANCE, congenital, hereditary, and neonatal diseases and abnormalities, GENES, 3122 Cancers, colorectal cancer, BREAST, Risk Assessment, 03 medical and health sciences, Sex Factors, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Retrospective Studies, business.industry, MUTATIONS, Cancer, medicine.disease, digestive system diseases, MSH2, MSH6, MODEL, INDIVIDUALS, 030104 developmental biology, Lynch Syndrome, Gene-Environment Interaction, business
وصف الملف: application/pdf; STAMPA
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المؤلفون: Einar Andreas Rødland, Joan B. Vida, Heike Görgens, Eivind Hovig, Kirsi Pylvänäinen, Monika Morak, Wouter H. de Vos tot Nederveen Cappel, Lone Sunde, Mark A. Jenkins, Lucio Bertario, Patricia Esperon, Reinhard Büttner, Finlay A. Macrae, Inge Bernstein, Marc S. Greenblatt, Wolff Schmiegel, Giulia Martina Cavestro, Maria Grazia Tibiletti, Silke Redler, Zohreh Ketabi, Karl Heinimann, Fiona Lalloo, Huw Thomas, Christina Therkildsen, Deepak Vangala, Magnus von Knebel Doeberitz, Matilde Navarro, Erik Rokkones, Douglas Tjandra, D. G. Evans, Marta Pineda, Marian J.E. Mourits, Lior H. Katz, Bernardo Bonanni, Pablo Kalfayan, Stephen N. Thibodeau, Loic Le Marchand, Revital Kariv, Maartje Nielsen, Emma J Crosbie, Oliver G. Denton, Stefanie Holzapfel, Guy Rosner, Mev Dominguez-Valentin, John Burn, Verena Steinke-Lange, Carlos A. Vaccaro, Gabriela Möslein, Elke Holinski-Feder, Gabriel Capellá, Johanna Tecklenburg, Karin Wadt, Kate Green, Christoph Engel, Miriam Mints, Anna Lepistö, Tamara Alejandra Piñero, Jukka-Pekka Mecklin, John L. Hopper, Robert Hüneburg, Markus Loeffler, Florencia Neffa, Toni T. Seppälä, Claudia Perne, Polly A. Newcomb, Karin Alvarez, Adriana Della Valle, Julian R. Sampson, Sanne W. ten Broeke, Francisco Lopez-Koestner, John-Paul Plazzer, James Hill, Hans Georg Strauß, Ingrid Winship, Nathan Gluck, Aung Ko Win, Jane C. Figueiredo, Jürgen Weitz, Hans F. A. Vasen, Rolf H. Sijmons, Walter Hernán Pavicic, Stefan Aretz, Steven Gallinger, Noralane M. Lindor, Pål Møller, Laura Renkonen-Sinisalo
المساهمون: Guided Treatment in Optimal Selected Cancer Patients (GUTS), Damage and Repair in Cancer Development and Cancer Treatment (DARE), Targeted Gynaecologic Oncology (TARGON), Seppala, T. T., Dominguez-Valentin, M., Crosbie, E. J., Engel, C., Aretz, S., Macrae, F., Winship, I., Capella, G., Thomas, H., Hovig, E., Nielsen, M., Sijmons, R. H., Bertario, L., Bonanni, B., Tibiletti, M. G., Cavestro, G. M., Mints, M., Gluck, N., Katz, L., Heinimann, K., Vaccaro, C. A., Green, K., Lalloo, F., Hill, J., Schmiegel, W., Vangala, D., Perne, C., Strauss, H. -G., Tecklenburg, J., Holinski-Feder, E., Steinke-Lange, V., Mecklin, J. -P., Plazzer, J. -P., Pineda, M., Navarro, M., Vida, J. B., Kariv, R., Rosner, G., Pinero, T. A., Pavicic, W., Kalfayan, P., ten Broeke, S. W., Jenkins, M. A., Sunde, L., Bernstein, I., Burn, J., Greenblatt, M., de Vos tot Nederveen Cappel, W. H., Della Valle, A., Lopez-Koestner, F., Alvarez, K., Buttner, R., Gorgens, H., Morak, M., Holzapfel, S., Huneburg, R., von Knebel Doeberitz, M., Loeffler, M., Redler, S., Weitz, J., Pylvanainen, K., Renkonen-Sinisalo, L., Lepisto, A., Hopper, J. L., Win, A. K., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Therkildsen, C., Wadt, K. A. W., Mourits, M. J. E., Ketabi, Z., Denton, O. G., Rodland, E. A., Vasen, H., Neffa, F., Esperon, P., Tjandra, D., Moslein, G., Rokkones, E., Sampson, J. R., Evans, D. G., Moller, P., Genome-Scale Biology (GSB) Research Program, HUS Abdominal Center, Clinicum, II kirurgian klinikka, Department of Surgery, Doctoral Programme in Clinical Research
المصدر: Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Thomas, H, Hovig, E, Nielsen, M, Sijmons, R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J P, Plazzer, J P, Pineda, M, Navarro, M, Vida, J B, Kariv, R, Rosner, G, Piñero, T A, Pavicic, W, Kalfayan, P, ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Redler, S, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Hopper, J L, Win, A K, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Therkildsen, C, Wadt, K A W, Mourits, M J E, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Rokkones, E, Sampson, J R, Evans, D G & Møller, P 2021, ' Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report ', European Journal of Cancer, vol. 148, pp. 124-133 . https://doi.org/10.1016/j.ejca.2021.02.022
European Journal of Cancer, 148, 124-133. ELSEVIER SCI LTD
Dipòsit Digital de la UB
Universidad de Barcelona
Seppälä, T T, Dominguez-Valentin, M, Crosbie, E J, Engel, C, Aretz, S, Macrae, F, Winship, I, Capella, G, Hovig, E, Nielsen, M, Sijmons, R H, Bertario, L, Bonanni, B, Tibiletti, M G, Cavestro, G M, Mints, M, Gluck, N, Katz, L, Heinimann, K, Vaccaro, C A, Green, K, Lalloo, F, Hill, J, Schmiegel, W, Vangala, D, Perne, C, Strauß, H-G, Tecklenburg, J, Holinski-Feder, E, Steinke-Lange, V, Mecklin, J-P, Plazzer, J-P, Pineda, M, Navarro, M, Vida, J B, Kariv, R, Rosner, G, Piñero, T A, Pavicic, W, Kalfayan, P, Ten Broeke, S W, Jenkins, M A, Sunde, L, Bernstein, I, Burn, J, Greenblatt, M, de Vos Tot Nederveen Cappel, W H, Della Valle, A, Lopez-Koestner, F, Alvarez, K, Büttner, R, Görgens, H, Morak, M, Holzapfel, S, Hüneburg, R, von Knebel Doeberitz, M, Loeffler, M, Redler, S, Weitz, J, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Hopper, J L, Win, A K, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Therkildsen, C, Wadt, K A W, Mourits, M J E, Ketabi, Z, Denton, O G, Rødland, E A, Vasen, H, Neffa, F, Esperon, P, Tjandra, D, Möslein, G, Rokkones, E, Sampson, J R, Evans, D G & Møller, P 2021, ' Uptake of hysterectomy and bilateral salpingo-oophorectomy in carriers of pathogenic mismatch repair variants : a Prospective Lynch Syndrome Database report ', European Journal of Cancer, vol. 148, pp. 124-133 . https://doi.org/10.1016/j.ejca.2021.02.022
European Journal of Cancerمصطلحات موضوعية: 0301 basic medicine, Cancer Research, Oophorectomy, Databases, Factual, Colorectal cancer, SURGERY, medicine.medical_treatment, Càncer d'ovari, computer.software_genre, DNA Mismatch Repair, 0302 clinical medicine, Endometrial cancer, munasarjasyöpä, Medicine, Prospective Studies, Colectomy, Salpingo-oophorectomy/methods, Database, Manchester Cancer Research Centre, COLON-CANCER, MLH1, WOMEN, Middle Aged, Prognosis, Lynch syndrome, 3. Good health, kohdunrungon syöpä, Oncology, COLECTOMY, 030220 oncology & carcinogenesis, Female, Biomarkers, Tumor/genetics, Adult, Heterozygote, Genital Neoplasms, Female, Salpingo-oophorectomy, Hysterectomy, 03 medical and health sciences, Genital Neoplasms, Female/prevention & control, Ovarian cancer, Colorectal Neoplasms, Hereditary Nonpolyposis/genetics, Biomarkers, Tumor, Mortalitat, Humans, Hysterectomy/methods, Mortality, Lynchin oireyhtymä, Risk-reducing surgery, Aged, business.industry, ResearchInstitutes_Networks_Beacons/mcrc, Cancer, MSH6, 3126 Surgery, anesthesiology, intensive care, radiology, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, MSH2, 030104 developmental biology, Cross-Sectional Studies, PMS2, Càncer d'endometri, Mutation, kohdunpoisto, business, computer, Follow-Up Studies
وصف الملف: application/pdf; fulltext
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المؤلفون: Gabriel Capellá, Patricia Esperon, Christoph Engel, Rolf H. Sijmons, María Laura Gonzalez, Matilde Navarro, Francisco López-Köstner, Julian R. Sampson, Miquel Serra-Burriel, Karin Alvarez, Ingrid Winship, Nathan Gluck, Lone Sunde, Reinhard Büttner, Giulia Martina Cavestro, Wouter H. de Vos tot Nederveen Cappel, Jukka-Pekka Mecklin, Marc S. Greenblatt, Kate Green, Robert Hüneburg, Markus Loeffler, Maria Grazia Tibiletti, Tamara Alejandra Piñero, Florencia Neffa, Lucio Bertario, Ariadna Sánchez, Verena Steinke-Lange, Christina Therkildsen, Jane C. Figueiredo, Douglas Tjandra, Magnus von Knebel Doeberitz, Lior H. Katz, Steven Gallinger, Noralane M. Lindor, Gabriela Möslein, Adriana Della Valle, John L. Hopper, Einar Andreas Rødland, Miriam Mints, Annika Lindblom, Ian M. Frayling, Polly A. Newcomb, Pål Møller, Sanne W. ten Broeke, Laura Renkonen-Sinisalo, Sigve Nakken, Stefanie Holzapfel, Finlay A. Macrae, Stefan Aretz, Nils Rahner, Karin Wadt, Robert W. Haile, Francesc Balaguer, Revital Kariv, Stephen N. Thibodeau, Huw D. Thomas, Emma J Crosbie, Deepak Vangala, Monika Morak, Ignacio Blanco, Hans K. Schackert, Henrik Okkels, Mev Dominguez-Valentin, Oliver G. Denton, John-Paul Plazzer, Zohreh Ketabi, James Hill, Loic Le Marchand, Mark A. Jenkins, Inge Bernstein, D. Gareth Evans, Heike Görgens, Marta Pineda, John Burn, Kirsi Pylvänäinen, Eivind Hovig, Hans F. A. Vasen, Pablo Kalfayan, Toni T. Seppälä, Aung Ko Win, Maartje Nielsen, Wolff Schmiegel, Guy Rosner, Karl Heinimann, Fiona Lalloo, Carlos A. Vaccaro, Elke Holinski-Feder, Leticia Moreira
المساهمون: HUS Abdominal Center, Clinicum, II kirurgian klinikka, University of Helsinki, Department of Surgery, ATG - Applied Tumor Genomics, Research Programs Unit, Dominguez-Valentin, M., Sampson, J. R., Seppala, T. T., ten Broeke, S. W., Plazzer, J. -P., Nakken, S., Engel, C., Aretz, S., Jenkins, M. A., Sunde, L., Bernstein, I., Capella, G., Balaguer, F., Thomas, H., Evans, D. G., Burn, J., Greenblatt, M., Hovig, E., de Vos tot Nederveen Cappel, W. H., Sijmons, R. H., Bertario, L., Tibiletti, M. G., Cavestro, G. M., Lindblom, A., Della Valle, A., Lopez-Kostner, F., Gluck, N., Katz, L. H., Heinimann, K., Vaccaro, C. A., Buttner, R., Gorgens, H., Holinski-Feder, E., Morak, M., Holzapfel, S., Huneburg, R., Knebel Doeberitz, M., Loeffler, M., Rahner, N., Schackert, H. K., Steinke-Lange, V., Schmiegel, W., Vangala, D., Pylvanainen, K., Renkonen-Sinisalo, L., Hopper, J. L., Win, A. K., Haile, R. W., Lindor, N. M., Gallinger, S., Le Marchand, L., Newcomb, P. A., Figueiredo, J. C., Thibodeau, S. N., Wadt, K., Therkildsen, C., Okkels, H., Ketabi, Z., Moreira, L., Sanchez, A., Serra-Burriel, M., Pineda, M., Navarro, M., Blanco, I., Green, K., Lalloo, F., Crosbie, E. J., Hill, J., Denton, O. G., Frayling, I. M., Rodland, E. A., Vasen, H., Mints, M., Neffa, F., Esperon, P., Alvarez, K., Kariv, R., Rosner, G., Pinero, T. A., Gonzalez, M. L., Kalfayan, P., Tjandra, D., Winship, I. M., Macrae, F., Moslein, G., Mecklin, J. -P., Nielsen, M., Moller, P., Guided Treatment in Optimal Selected Cancer Patients (GUTS)
المصدر: Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M & Okkels, H 2020, ' Correction : Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 9 . https://doi.org/10.1038/s41436-020-0892-4
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, Ten Broeke, S W, Plazzer, J-P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos Tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J-P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Dipòsit Digital de la UB
Universidad de Barcelona
Evans, D G, Crosbie, E, Hill, J & et al. 2019, ' Cancer risks by gene, age and gender in 6,350 carriers of pathogenic mismatch repair variants: findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine . https://doi.org/10.1038/s41436-019-0596-9
Genetics in Medicine, 22(1), 15-25. NATURE PUBLISHING GROUP
Genetics in Medicine
Dominguez-Valentin, M, Sampson, J R, Seppälä, T T, ten Broeke, S W, Plazzer, J P, Nakken, S, Engel, C, Aretz, S, Jenkins, M A, Sunde, L, Bernstein, I, Capella, G, Balaguer, F, Thomas, H, Evans, D G, Burn, J, Greenblatt, M, Hovig, E, de Vos tot Nederveen Cappel, W H, Sijmons, R H, Bertario, L, Tibiletti, M G, Cavestro, G M, Lindblom, A, Della Valle, A, Lopez-Köstner, F, Gluck, N, Katz, L H, Heinimann, K, Vaccaro, C A, Büttner, R, Görgens, H, Holinski-Feder, E, Morak, M, Holzapfel, S, Hüneburg, R, Knebel Doeberitz, M V, Loeffler, M, Rahner, N, Schackert, H K, Steinke-Lange, V, Schmiegel, W, Vangala, D, Pylvänäinen, K, Renkonen-Sinisalo, L, Hopper, J L, Win, A K, Haile, R W, Lindor, N M, Gallinger, S, Le Marchand, L, Newcomb, P A, Figueiredo, J C, Thibodeau, S N, Wadt, K, Therkildsen, C, Okkels, H, Ketabi, Z, Moreira, L, Sánchez, A, Serra-Burriel, M, Pineda, M, Navarro, M, Blanco, I, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Denton, O G, Frayling, I M, Rødland, E A, Vasen, H, Mints, M, Neffa, F, Esperon, P, Alvarez, K, Kariv, R, Rosner, G, Pinero, T A, Gonzalez, M L, Kalfayan, P, Tjandra, D, Winship, I M, Macrae, F, Möslein, G, Mecklin, J P, Nielsen, M & Møller, P 2020, ' Cancer risks by gene, age, and gender in 6350 carriers of pathogenic mismatch repair variants : findings from the Prospective Lynch Syndrome Database ', Genetics in Medicine, vol. 22, no. 1, pp. 15-25 . https://doi.org/10.1038/s41436-019-0596-9
Genetics in Medicine, 22(1), 15-25. Nature Publishing Groupمصطلحات موضوعية: Oncology, Male, Colorectal cancer, Lynch syndrome, Penetrance, DNA Mismatch Repair, 0302 clinical medicine, Databases, Genetic, Malalties hereditàries, Prospective Studies, Càncer, PMS2, Genetics (clinical), Mismatch Repair Endonuclease PMS2, Cancer, 0303 health sciences, Sex Characteristics, Factors de risc en les malalties, 1184 Genetics, developmental biology, physiology, MLH1, Middle Aged, 16. Peace & justice, 3. Good health, DNA-Binding Proteins, MutS Homolog 2 Protein, syöpägeenit, MSH2, 030220 oncology & carcinogenesis, MSH6, 030211 gastroenterology & hepatology, DNA mismatch repair, Female, geneettiset tekijät, MutL Protein Homolog 1, Genetic diseases, Adult, medicine.medical_specialty, congenital, hereditary, and neonatal diseases and abnormalities, Risk factors in diseases, suolistosyövät, MUTATION CARRIERS, Risk Assessment, Article, sukupuoli, Age and gender, 03 medical and health sciences, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Lynchin oireyhtymä, Gene, 030304 developmental biology, Aged, business.industry, Endometrial cancer, Correction, nutritional and metabolic diseases, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Survival Analysis, digestive system diseases, Mutation, 3111 Biomedicine, ikä, business, Ovarian cancer
وصف الملف: application/pdf; fulltext
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المؤلفون: Mev Dominguez-Valentin, Lone Sunde, John-Paul Plazzer, Nils Rahner, Deepak Vangala, Robert Hüneburg, Douglas Tjandra, Verena Steinke-Lange, Ignacio Blanco, Rodney J. Scott, Lior H. Katz, Christoph Engel, Inge Bernstein, Matthias Kloor, Maartje Nielsen, John Burn, Toni T. Seppälä, Wolff Schmiegel, Karl Heinimann, Eivind Hovig, Fiona Lalloo, Stefan Aretz, D. Gareth Evans, Emma J Crosbie, Elke Holinski-Feder, James Hill, Gabriela Möslein, Ken Ljungmann, Marta Pineda, Noralane M. Lindor, Huw Thomas, Aysel Ahadova, Florencia Neffa, Julian R. Sampson, Ian M. Frayling, Pål Møller, Laura Renkonen-Sinisalo, Anna Lepistö, Jukka-Pekka Mecklin, Kate Green, Finlay A. Macrae, Monika Morak, Ingrid Winship, Nathan Gluck, Adriana Della Valle, Hans F. A. Vasen, Annika Lindblom, Charlotte Kvist Lautrup, Sanne W. ten Broeke, Matilde Navarro, Christina Therkildsen, Mette Kalager, Sigve Nakken, Stefanie Holzapfel, Gabriel Capellá, Kirsi Pylvänäinen, Wouter H. de Vos tot Nederveen Cappel
المساهمون: Clinicum, University of Helsinki, Department of Surgery, II kirurgian klinikka, HUS Abdominal Center
المصدر: Seppala, T T, Ahadova, A, Dominguez-Valentin, M, Macrae, F, Evans, D G, Therkildsen, C, Sampson, J, Scott, R, Burn, J, Moeslein, G, Bernstein, I, Holinski-Feder, E, Pylvanainen, K, Renkonen-Sinisalo, L, Lepisto, A, Lautrup, C K, Lindblom, A, Plazzer, J-P, Winship, I, Tjandra, D, Katz, L H, Aretz, S, Hueneburg, R, Holzapfel, S, Heinimann, K, Della Valle, A, Neffa, F, Gluck, N, Cappel, W H D V T N, Vasen, H, Morak, M, Steinke-Lange, V, Engel, C, Rahner, N, Schmiegel, W, Vangala, D, Thomas, H, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Capella, G, Pineda, M, Navarro, M, Blanco, I, ten Broeke, S, Nielsen, M, Ljungmann, K, Nakken, S, Lindor, N, Frayling, I M, Hovig, E, Sunde, L, Kloor, M, Mecklin, J-P, Kalager, M & Møller, P 2019, ' Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; a prospective Lynch syndrome database report ', Hereditary Cancer in Clinical Practice, vol. 17, 8 . https://doi.org/10.1186/s13053-019-0106-8
Seppälä, T T, Ahadova, A, Dominguez-Valentin, M, Macrae, F, Evans, D G, Therkildsen, C, Sampson, J, Scott, R, Burn, J, Möslein, G, Bernstein, I, Holinski-Feder, E, Pylvänäinen, K, Renkonen-Sinisalo, L, Lepistö, A, Lautrup, C K, Lindblom, A, Plazzer, J P, Winship, I, Tjandra, D, Katz, L H, Aretz, S, Hüneburg, R, Holzapfel, S, Heinimann, K, Valle, A D, Neffa, F, Gluck, N, De Vos Tot Nederveen Cappel, W H, Vasen, H, Morak, M, Steinke-Lange, V, Engel, C, Rahner, N, Schmiegel, W, Vangala, D, Thomas, H, Green, K, Lalloo, F, Crosbie, E J, Hill, J, Capella, G, Pineda, M, Navarro, M, Blanco, I, Ten Broeke, S, Nielsen, M, Ljungmann, K, Nakken, S, Lindor, N, Frayling, I, Hovig, E, Sunde, L, Kloor, M, Mecklin, J P, Kalager, M & Møller, P 2019, ' Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis; A prospective Lynch syndrome database report ', Hereditary Cancer in Clinical Practice, vol. 17, no. 1, 8, pp. 1-8 . https://doi.org/10.1186/s13053-019-0106-8
Hereditary Cancer in Clinical Practice
Hereditary Cancer in Clinical Practice, Vol 17, Iss 1, Pp 1-8 (2019)
Hereditary cancer in clinical practice, 17:8. BioMed Central Ltd.
Hereditary Cancer in Clinical Practice, 17. BMC
Evans, D G, Crosbie, E, Hill, J & et al. 2019, ' Lack of association between screening interval and cancer stage in Lynch syndrome may be accounted for by over-diagnosis : a Prospective Lynch Syndrome Database report ', Hereditary cancer in clinical practice . https://doi.org/10.1186/s13053-019-0106-8
Dipòsit Digital de la UB
Universidad de Barcelonaمصطلحات موضوعية: 0301 basic medicine, COLONOSCOPIC SURVEILLANCE, Colorectal cancer, Colonoscopy, 030105 genetics & heredity, computer.software_genre, FAMILIES, COLORECTAL-CANCER, Breast cancer screening, 0302 clinical medicine, 610 Medical sciences Medicine, Epidemiology, tähystys, Stage (cooking), Hereditary nonpolyposis colorectal cancer, MUTATION, Genetics (clinical), RISK, Surveillance, Database, medicine.diagnostic_test, Incidence (epidemiology), lcsh:Neoplasms. Tumors. Oncology. Including cancer and carcinogens, Lynch syndrome, 3. Good health, Oncology, 030220 oncology & carcinogenesis, endoskopia, Screening, syöpätaudit, koloskopia, medicine.medical_specialty, lcsh:QH426-470, 3122 Cancers, suolistosyövät, mikrosatelliitit, lcsh:RC254-282, Mismatch repair, 03 medical and health sciences, Càncer colorectal, medicine, Endoscòpia, Lynchin oireyhtymä, perinnölliset taudit, seulontatutkimus, business.industry, Research, Colonoscòpia, Microsatellite instability, Endoscopy, DNA, diagnostiikka, medicine.disease, digestive system diseases, Hereditary cancer, ADENOMA, lcsh:Genetics, Over-diagnosis, tarkkailu, business, computer
وصف الملف: application/pdf; fulltext
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a87d576e3fb9e3dcbdd2dcab126ab6fe
https://pure.au.dk/portal/da/publications/lack-of-association-between-screening-interval-and-cancer-stage-in-lynch-syndrome-may-be-accounted-for-by-overdiagnosis-a-prospective-lynch-syndrome-database-report(5e685588-68dd-4773-aeff-5d891bcb370f).html -
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المؤلفون: Karl Heinimann, Ian Tomlinson, Rui Henrique, Helena Baldaia, Fátima Carneiro, Michal Kovac, Ana Peixoto, Manuela Pinheiro, Manuel R. Teixeira, Paula Lopes, Isabel Veiga, Raquel Seruca, Carla M. A. Pinto
المصدر: British Journal of Cancer
مصطلحات موضوعية: Adult, Male, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, Adolescent, Carcinogenesis, Activin Receptors, Type II, Protein Serine-Threonine Kinases, Biology, Bone Morphogenetic Protein Receptors, Type II, Genetics & Genomics, MLH1, Young Adult, Germline mutation, medicine, Humans, neoplasms, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Aged, Genetics, Receptor, Transforming Growth Factor-beta Type II, Nuclear Proteins, nutritional and metabolic diseases, Microsatellite instability, Middle Aged, 16. Peace & justice, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, target genes, digestive system diseases, Lynch syndrome, 3. Good health, DNA-Binding Proteins, MSH6, MutS Homolog 2 Protein, Oncology, MSH3, MSH2, MutS Homolog 3 Protein, Female, microsatellite instability, DNA mismatch repair, Colorectal Neoplasms, MutL Protein Homolog 1, Receptors, Transforming Growth Factor beta
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المؤلفون: Michal Kovac, Päivi Peltomäki, Giancarlo Marra, Friedel Wenzel, Luigi Terracciano, Annette Gylling, Salvatore Piscuoglio, Hans Joerg Altermatt, Mihaela Zavolan, Francesca Trapani, Karl Heinimann, Valentina Mele, Shivendra Kishore
المساهمون: University of Zurich, Zavolan, Mihaela
المصدر: Cancer Research
مصطلحات موضوعية: Untranslated region, congenital, hereditary, and neonatal diseases and abnormalities, Cancer Research, EWING SARCOMA BREAKPOINT REGION 1, Locus (genetics), Biology, Transfection, DNA Mismatch Repair, medicine, Humans, 1306 Cancer Research, RNA, Messenger, 3' Untranslated Regions, Gene, Genetics, Three prime untranslated region, 10061 Institute of Molecular Cancer Research, RNA-Binding Proteins, Microsatellite instability, HCT116 Cells, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, DNA Repair-Deficiency Disorders, Phenotype, digestive system diseases, 3. Good health, Oncology, 570 Life sciences, biology, 2730 Oncology, Calmodulin-Binding Proteins, Microsatellite Instability, DNA mismatch repair, RNA-Binding Protein EWS, biology.gene, Colorectal Neoplasms, HT29 Cells, HeLa Cells
وصف الملف: Cancer_Res-2014-Kishore-224-34.pdf - application/pdf; Cancer_Res-2013-Kishore-0008-5472.CAN-13-2100.pdf - application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc544989e815b10d4476ccecd8771a0a
https://doi.org/10.1158/0008-5472.can-13-2100 -
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المؤلفون: Sandro J. Stoeckli, Jeannette Greiner, Daniel S. Engeler, Michael Brändle, Christian Rothermundt, Silke Gillessen, Michael Christian Sulz, Karin van Leyen, Johannes Weber, Claudia Hader, Isabelle Binet, Thomas Hundsberger, Patrik Kloos, W. Krek, Ina Krull, Karl Heinimann, Sabine Schmid
المصدر: Schmid, S, Gillessen, S, Binet, I, Brändle, M, Engeler, D, Greiner, J, Hader, C, Heinimann, K, Kloos, P, Krek, W, Krull, I, Stoeckli, S J, Sulz, M C, van Leyen, K, Weber, J, Rothermundt, C & Hundsberger, T 2014, ' Management of von hippel-lindau disease : an interdisciplinary review ', Oncology Research and Treatment, vol. 37, no. 12, pp. 761-71 . https://doi.org/10.1159/000369362
Oncology research and treatmentمصطلحات موضوعية: Cancer Research, Pediatrics, medicine.medical_specialty, Pathology, von Hippel-Lindau Disease, Genetic counseling, MEDLINE, Disease, 03 medical and health sciences, 0302 clinical medicine, Germline mutation, medicine, Screening programs, Humans, Von Hippel–Lindau disease, 030304 developmental biology, Genetic testing, 0303 health sciences, medicine.diagnostic_test, Manchester Cancer Research Centre, business.industry, von Hippel-Lindau Disease/diagnosis, Incidence (epidemiology), ResearchInstitutes_Networks_Beacons/mcrc, Hematology, medicine.disease, 3. Good health, Oncology, 030220 oncology & carcinogenesis, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::69409d9f2206b07f562da7ddeb0c7d60
https://pubmed.ncbi.nlm.nih.gov/25765507 -
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المؤلفون: Stefanie Kalt, Mauro Delorenzi, Monika E. Hegi, Pierre Bady, Annie-Claire Diserens, Vincent Castella, Karl Heinimann, Marie-France Hamou
المصدر: Neuro-Oncology
Neuro-oncologyمصطلحات موضوعية: Cancer Research, Biology, medicine.disease_cause, Polymerase Chain Reaction, law.invention, Loss of heterozygosity, 03 medical and health sciences, chemistry.chemical_compound, 0302 clinical medicine, Similarity (network science), law, Glioma, medicine, Biomarkers, Tumor, Tumor Cells, Cultured, Humans, Polymerase chain reaction, 030304 developmental biology, Genetics, 0303 health sciences, Mutation, Brain Neoplasms, DNA, Neoplasm, medicine.disease, DNA Fingerprinting, 3. Good health, Editorial, Oncology, chemistry, DNA profiling, 030220 oncology & carcinogenesis, Microsatellite, Neurology (clinical), DNA, Microsatellite Repeats
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39a1d1bd66cfb6304c3e76814c1bef4c
https://pubmed.ncbi.nlm.nih.gov/22669103 -
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المؤلفون: Josef Jiricny, Karl Heinimann, Michal Kovac, Giancarlo Marra, Endre Laczko, Ritva Haider, Hansjakob Mueller
المساهمون: University of Zurich, Heinimann, K
المصدر: Familial Cancer
Familial cancer, 10 (3)
Europe PubMed Centralمصطلحات موضوعية: Male, Oncology, Proband, Cancer Research, Time Factors, Colorectal cancer, DNA Mismatch Repair, Polymerase Chain Reaction, 0302 clinical medicine, 1306 Cancer Research, Prospective Studies, Registries, Prospective cohort study, Genetics (clinical), Amsterdam Criteria II, Aged, 80 and over, Genetics, 0303 health sciences, medicine.diagnostic_test, 10061 Institute of Molecular Cancer Research, DNA, Neoplasm, Middle Aged, Lynch syndrome, Neoplasm Proteins, 3. Good health, Colorectum, Familial cancer, Mismatch repair, Switzerland, Phenotype, 030220 oncology & carcinogenesis, Female, 2730 Oncology, DNA mismatch repair, Adult, 2716 Genetics (clinical), medicine.medical_specialty, Young Adult, 03 medical and health sciences, 1311 Genetics, Internal medicine, medicine, Humans, Genetic Predisposition to Disease, Genetic Testing, Germ-Line Mutation, Aged, 030304 developmental biology, Genetic testing, business.industry, medicine.disease, Colorectal Neoplasms, Hereditary Nonpolyposis, Human genetics, digestive system diseases, 570 Life sciences, biology, business, Follow-Up Studies, Microsatellite Repeats
وصف الملف: application/application/pdf; ZORA_NL_48807.pdf - application/pdf
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0181f8b60f28cdb3c532712e8de6b9ee
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المؤلفون: Chang Won Hong, Wendy McKinnon, Marc S. Greenblatt, Duck Woo Kim, Marie Luise Bisgaard, Paul Rozen, Malcolm G. Dunlop, Gregor Brown, Fiona Douglas, Finlay A. Macrae, Melyssa Aronson, John Burn, Gabriela Moeslein, Sung Hye Hong, Juul T. Wijnen, Elizabeth Chow, Elly Lynch, Seok Byung Lim, Young Kyoung Shin, Hans F. A. Vasen, Alessandra Viel, Jae-Gahb Park, Peggy Conrad, Benedito Mauro Rossi, Mary E. Velthuizen, Jarvinen Heikki, Lyn Schofield, James M. Ford, Il-Jin Kim, Karl Heinimann, Byung-Ho Nam, Carlos A. Vaccaro
المصدر: Clinical cancer research : an official journal of the American Association for Cancer Research. 12(11 Pt 1)
مصطلحات موضوعية: Oncology, Male, Cancer Research, Gastroenterology, DNA Mismatch Repair, 0302 clinical medicine, Duodenal Neoplasms, Surveys and Questionnaires, PMS2, Child, Mismatch Repair Endonuclease PMS2, Adenosine Triphosphatases, Aged, 80 and over, Nuclear Proteins, Neoplasms, Second Primary, Middle Aged, 3. Good health, DNA-Binding Proteins, MutS Homolog 2 Protein, 030220 oncology & carcinogenesis, 030211 gastroenterology & hepatology, DNA mismatch repair, Female, MutL Protein Homolog 1, Adult, congenital, hereditary, and neonatal diseases and abnormalities, medicine.medical_specialty, Adolescent, Genotype, MLH1, 03 medical and health sciences, Germline mutation, Predictive Value of Tests, Internal medicine, medicine, Humans, neoplasms, Germ-Line Mutation, Adaptor Proteins, Signal Transducing, Aged, Jejunal Neoplasms, business.industry, nutritional and metabolic diseases, Colorectal Neoplasms, Hereditary Nonpolyposis, digestive system diseases, MSH6, Ileal Neoplasms, DNA Repair Enzymes, MSH2, business
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::56b243219336a1e3a3a53f622ce8053c
https://pubmed.ncbi.nlm.nih.gov/16740762