Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Pavel Vodicka"'
Autor:
Alicja Wolk, Edward Giovannucci, Li Li, Polly A. Newcomb, Kenneth Offit, Clemens Schafmayer, Vicente Martín, Sergi Castellví-Bel, Daniel D. Buchanan, Mingyang Song, Qianchuan He, Martha L. Slattery, Volker Arndt, Anna H. Wu, Amit Joshi, David A. Drew, D. Timothy Bishop, Annika Lindblom, Temitope O. Keku, Jochen Hampe, Ozan Dikilitas, Douglas A. Corley, John B. Harley, Hakon Hakonarson, Steven Gallinger, Noralane M. Lindor, Ian B. Stanaway, Jeffrey K. Lee, Sonja I. Berndt, Veronika Vymetalkova, Syed H.E. Zaidi, Jessica Minnier, Daniel J. Schaid, Ludmila Vodickova, John D. Potter, Heather Hampel, Christopher I. Li, Frank D. Mentch, Wei-Qi Wei, Cornelia M. Ulrich, Marc J. Gunter, Robert E. Schoen, Catherine M. Tangen, Victor Moreno, Shuji Ogino, Tabitha A. Harrison, Albert de la Chapelle, Pavel Vodicka, Andrew T. Chan, Keith R. Curtis, Elisabeth A. Rosenthal, Jenny Chang-Claude, David C. Muller, Paul D.P. Pharoah, Roger L. Milne, David Duggan, Eric B. Larson, David R. Crosslin, Andrea Gsur, Stéphane Bézieau, Graham G. Giles, Robert J. MacInnis, Bahram Namjou, Christopher H. Dampier, Gail P. Jarvik, Andrea N. Burnett-Hartman, Richard B. Hayes, Fränzel J.B. Van Duijnhoven, Wendy K. Chung, Michael Hoffmeister, Mark A. Jenkins, Mathieu Lemire, Thomas J. Hudson, Elizabeth A. Platz, Neil Murphy, Graham Casey, Michael O. Woods, Aung Ko Win, Flora Qu, Li Hsu, Emily White, Peter T. Campbell, Lori C. Sakoda, Jane C. Figueiredo, Minta Thomas, Jeroen R. Huyghe, Bethany Van Guelpen, Kala Visvanathan, Loic Le Marchand, Corinne E. Joshu, Yu Ru Su, Ulrike Peters, Stephen B. Gruber, Demetrius Albanes, Stephen N. Thibodeau, Antoni Castells, Hermann Brenner
Publikováno v:
Am J Hum Genet
American Journal of Human Genetics, 107(3), 432-444
American Journal of Human Genetics 107 (2020) 3
American Journal of Human Genetics, 107(3), 432-444
American Journal of Human Genetics 107 (2020) 3
Accurate colorectal cancer (CRC) risk prediction models are critical for identifying individuals at low and high risk of developing CRC, as they can then be offered targeted screening and interventions to address their risks of developing disease (if
Autor:
Pavel Rossner, Roger W. L. Godschalk, Lada Živković, Gunnar Brunborg, Mahara Valverde, Juliana da Silva, Emilio Rojas, E. S. Kuznetsova, Serena Galati, Palma Lamonaca, Mirta Milić, Ekaterina I. Surikova, Helga Stopper, Bozena Novotna, Ninoslav Djelic, Sabine A. S. Langie, Katarina Volkovova, Pierre Lebailly, Delia Cavallo, Karl-Heinz Wagner, Stefano Bonassi, Monica Neri, Malgorzata Dobrzyńska, Hervé Perdry, Carina Ladeira, Alena Kažimı́rová, Rudolf Stetina, Mojgan Najafzadeh, Diana Anderson, Amaya Azqueta, Semra Sardas, Zdenka Durackova, Paula Rohr, Cristiana Pereira, Bozena Smolkova, Annamaria Buschini, Andrew Collins, Dwi Ramadhani, Anna Safar, Goran Gajski, N. P. Sirota, Idoia Ibero-Baraibar, Avdulla J. Alija, Kirsten B. Holven, Ezgi Eyluel Bangkoglu, Marcello Ceppi, Cristian Del Boˊ, Francesca Marcon, Stine Marie Ulven, Elisa Boutet-Robinet, Inger Ottestad, Biljana Spremo-Potparević, Fisnik Asllani, Annemarie Grindel, Irina A. Goroshinskaya, Maria Dusinska, Zsuzsanna Nemeth, Ricard Marcos, Tania Mandina Cardoso, Lisa Giovannelli, Vanessa Moraes de Andrade, Cinzia Lucia Ursini, Maria João Silva, Massimo Moretti, Magdalena Barancokova, Nurşen Başaran, Monika Dvořáková, Solange Costa, Vesna Dimitrijević Srećković, Susana Pastor, Omar García Lima, Marta Staruchova, Vanessa Valdiglesias, Patrizia Riso, Carlos Hernández, Cristina Andreoli, Blanca Laffon, Alba Hernández, Kristine B. Gutzkow, Carla Costa, Marco Bruzzone, Zuzana Paduchova, Peter Møller, Ela Kadioglu, João Paulo Teixeira, Gudrun Koppen, Pavel Vodicka, Henriqueta Louro, Irene Orlow, Silvia Moretti
Publikováno v:
Mutation Research-Reviews
Mutation Research-Reviews, Elsevier, 2021, 787, pp.108371. ⟨10.1016/j.mrrev.2021.108371⟩
Mutation research. Reviews in mutation research
Mili, M, Ceppi, M, Bruzzone, M, Azqueta, A, Brunborg, G, Godschalk, R, Koppen, G, Langie, S, Møller, P, Teixeira, J P, Alija, A, Anderson, D, Andrade, V, Andreoli, C, Asllani, F, Bangkoglu, E E, Barancokova, M, Basaran, N, Boutet-Robinet, E, Buschini, A, Cavallo, D, Pereira, C C, Costa, C, Costa, S, Silva, J D, Bo, C D, Sreckovic, V D, Djelic, N, Durackova, Z, Dvorakova, M, Gajski, G, Galati, S, Lima, O G, Giovannelli, L, Goroshinskaya, I A, Grindel, A, Gutzkow, K B, Hernandez, A, Hernandez, C, Holven, K B, Ibero-Baraibar, I, Ottestad, I, Kadioglu, E, Kazimirova, A, Kuznetsova, E, Ladeira, C, Laffon, B, Lamonaca, P, Lebailly, P, Louro, H, Cardoso, T M, Marcon, F, Marcos, R, Moretti, M, Moretti, S, Najafzadeh, M, Nemeth, Z, Neri, M, Novotna, B, Orlow, I, Paduchova, Z, Pastor, S, Perdry, H, Spremo-Potparevic, B, Ramadhani, D, Riso, P, Rohr, P, Rojas, E, Rossner, P, Safar, A, Sardas, S, Silva, M J, Sirota, N, Smolkova, B, Staruchova, M, Stetina, R, Stopper, H, Surikova, E I, Ulven, S M, Ursini, C L, Valdiglesias, V, Valverde, M, Vodicka, P, Volkovova, K, Wagner, K-H, Zivkovic, L, Dusinska, M, Collins, A R & Bonassi, S 2021, ' The hCOMET project : International database comparison of results with the comet assay in human biomonitoring. Baseline frequency of DNA damage and effect of main confounders ', Mutation Research-Reviews, vol. 787, 108371 . https://doi.org/10.1016/j.mrrev.2021.108371
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Mutation Research-Reviews in Mutation Research
RUC. Repositorio da Universidade da Coruña
instname
Mutation Research/Reviews in Mutation Research
Mutation Research-Reviews, Elsevier, 2021, 787, pp.108371. ⟨10.1016/j.mrrev.2021.108371⟩
Mutation research. Reviews in mutation research
Mili, M, Ceppi, M, Bruzzone, M, Azqueta, A, Brunborg, G, Godschalk, R, Koppen, G, Langie, S, Møller, P, Teixeira, J P, Alija, A, Anderson, D, Andrade, V, Andreoli, C, Asllani, F, Bangkoglu, E E, Barancokova, M, Basaran, N, Boutet-Robinet, E, Buschini, A, Cavallo, D, Pereira, C C, Costa, C, Costa, S, Silva, J D, Bo, C D, Sreckovic, V D, Djelic, N, Durackova, Z, Dvorakova, M, Gajski, G, Galati, S, Lima, O G, Giovannelli, L, Goroshinskaya, I A, Grindel, A, Gutzkow, K B, Hernandez, A, Hernandez, C, Holven, K B, Ibero-Baraibar, I, Ottestad, I, Kadioglu, E, Kazimirova, A, Kuznetsova, E, Ladeira, C, Laffon, B, Lamonaca, P, Lebailly, P, Louro, H, Cardoso, T M, Marcon, F, Marcos, R, Moretti, M, Moretti, S, Najafzadeh, M, Nemeth, Z, Neri, M, Novotna, B, Orlow, I, Paduchova, Z, Pastor, S, Perdry, H, Spremo-Potparevic, B, Ramadhani, D, Riso, P, Rohr, P, Rojas, E, Rossner, P, Safar, A, Sardas, S, Silva, M J, Sirota, N, Smolkova, B, Staruchova, M, Stetina, R, Stopper, H, Surikova, E I, Ulven, S M, Ursini, C L, Valdiglesias, V, Valverde, M, Vodicka, P, Volkovova, K, Wagner, K-H, Zivkovic, L, Dusinska, M, Collins, A R & Bonassi, S 2021, ' The hCOMET project : International database comparison of results with the comet assay in human biomonitoring. Baseline frequency of DNA damage and effect of main confounders ', Mutation Research-Reviews, vol. 787, 108371 . https://doi.org/10.1016/j.mrrev.2021.108371
Dipòsit Digital de Documents de la UAB
Universitat Autònoma de Barcelona
Repositório Científico de Acesso Aberto de Portugal
Repositório Científico de Acesso Aberto de Portugal (RCAAP)
instacron:RCAAP
Mutation Research-Reviews in Mutation Research
RUC. Repositorio da Universidade da Coruña
instname
Mutation Research/Reviews in Mutation Research
[Abstract] The alkaline comet assay, or single cell gel electrophoresis, is one of the most popular methods for assessing DNA damage in human population. One of the open issues concerning this assay is the identification of those factors that can exp
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1560aa5f9072ffa2ca3906292955490b
https://hal.inrae.fr/hal-03164976/file/nihms-1739355.pdf
https://hal.inrae.fr/hal-03164976/file/nihms-1739355.pdf
Autor:
Asta Försti, Alena Kazimirova, Yasmeen Niazi, Per Hoffmann, Hauke Thomsen, Katarina Volkovova, Magdalena Barancokova, Veronika Vymetalkova, Kari Hemminki, Maria Dusinska, Pavel Vodicka, Markus M. Nöthen, Marta Staruchova, Soňa Vodenkova, Ludmila Vodickova, Ludovit Musak, Michal Kroupa, Bozena Smolkova
Publikováno v:
DNA repair. 101
Nonspecific structural chromosomal aberrations (CAs) can be found at around 1% of circulating lymphocytes from healthy individuals but the frequency may be higher after exposure to carcinogenic chemicals or radiation. The frequency of CAs has been me
Autor:
John P. Neoptolemos, Markus W. Büchler, Jakob R. Izbicki, Ben Schöttker, Cosmeri Rizzato, Cornelia Schroeder, Salvatore Paiella, Hanneke W. M. van Laarhoven, William Greenhalf, Simona Bursi, Renata Talar-Wojnarowska, Christos Dervenis, Ludmila Vodickova, Francesca Tavano, Giulia Martina Cavestro, Thilo Hackert, Claudio Pasquali, Ewa Małecka-Panas, Gabriele Capurso, Andrea Mambrini, Daniele Campa, Andrea Padoan, Ioannis S. Papanikolaou, Raffaele Pezzilli, Péter Hegyi, Beatrice Mohelnikova-Duchonova, Federica Gemignani, Michael F. Nentwich, Pavel Vodicka, Stefano Landi, Richárd Szmola, Anna Caterina Milanetto, Eithne Costello, Rudolf Kaaks, Laura Ginocchi, Bernd Holleczek, Erika Darvasi, Verena Katzke, Evaristo Maiello, Manuel Gentiluomo, Ondrej Strouhal, Orazio Palmieri, Juozas Kupcinskas, Alice Alessandra Galeotti, Viktor Hlavac, George Theodoropoulos, Audrius Ivanauskas, Maria Gazouli, Ferenc Izbéki, Federico Canzian, Oliver Strobel, Ofure Obazee, Martin Lovecek, Timothy J. Key, Domenica Gioffreda, Pavel Soucek, Ugo Boggi, Krzysztof Jamroziak, Cosimo Sperti, Maarten F. Bijlsma, Yogesh K. Vashist, Andrea Szentesi, Hermann Brenner, Livia Archibugi, Giuseppe Vanella, Daniela Basso
Publikováno v:
Journal of medical genetics, 58(6), 369-377. BMJ Publishing Group
JOURNAL OF MEDICAL GENETICS
JOURNAL OF MEDICAL GENETICS
BackgroundMost cases of pancreatic ductal adenocarcinoma (PDAC) are asymptomatic in early stages, and the disease is typically diagnosed in advanced phases, resulting in very high mortality. Tools to identify individuals at high risk of developing PD
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a267bd63e2a9e7418632e88a73d56f47
https://hdl.handle.net/11568/1072532
https://hdl.handle.net/11568/1072532
Autor:
Pavel Vodicka, Ludmila Vodickova, Ludovit Musak, Veronika Vymetalkova, Alessio Naccarati, Giovanni Fiorito
Publikováno v:
Mutation Research/Reviews in Mutation Research. 770:26-34
The lymphocyte cytokinesis-block micronucleus (CBMN) assay has been applied in hundreds of in vivo biomonitoring studies of humans exposed either environmentally or occupationally to genotoxic chemicals. However, there is an emerging need to re-evalu
Autor:
Asta Försti, Ludmila Vodickova, Alena Kazimirova, Markus M. Nöthen, Marta Staruchova, Per Hoffmann, Yasmeen Niazi, Katarina Volkovova, Kari Hemminki, Maria Dusinska, Veronika Vymetalkova, Soňa Vodenkova, Ludovit Musak, Hauke Thomsen, Pavel Vodicka, Michal Kroupa, Bozena Smolkova, Magdalena Barancokova
Publikováno v:
Mutagenesis. 34(4)
Non-specific structural chromosomal aberrations (CAs) observed in peripheral blood lymphocytes of healthy individuals can be either chromosome-type aberrations (CSAs) or chromatid-type aberrations (CTAs) depending on the stage of cell division they a
Autor:
Arantza Farina Sarasqueta, Tom van Wezel, Clara Ruiz-Ponte, Stephanie A. Schubert, Juul T. Wijnen, Sergi Castellví-Bel, Rolf H. Sijmons, Hans Morreau, Bruce H. R. Wolffenbuttel, Stijn Crobach, Melanie M. van der Klauw, Arnoud Boot, Jan Oosting, Noel F C C de Miranda, Fadwa A. Elsayed, Frederik J. Hes, Hans F. A. Vasen, Maartje Nielsen, Pavel Vodicka, Rolf H. A. M. Vossen, Carli M. J. Tops, Ronald van Eijk, Malcolm G. Dunlop, Ian Tomlinson, Dina Ruano
Publikováno v:
British Journal of Cancer
Schubert, S A, Ruano, D, Elsayed, F A, Boot, A, Crobach, S, Sarasqueta, A F, Wolffenbuttel, B, van der Klauw, M M, Oosting, J, Tops, C M, van Eijk, R, Vasen, H F, Vossen, R H, Nielsen, M, Castellví-Bel, S, Ruiz-Ponte, C, Tomlinson, I, Dunlop, M G, Vodicka, P, Wijnen, J T, Hes, F J, Morreau, H, de Miranda, N F, Sijmons, R H & van Wezel, T 2017, ' Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia ', British Journal of Cancer . https://doi.org/10.1038/bjc.2017.240
British Jounal of Cancer, 117(8), 1215-1223. Nature Publishing Group
British Journal of Cancer, 117(8), 1215-1223
British journal of cancer, 117(6), 876-884. Nature Publishing Group
Schubert, S A, Ruano, D, Elsayed, F A, Boot, A, Crobach, S, Sarasqueta, A F, Wolffenbuttel, B, van der Klauw, M M, Oosting, J, Tops, C M, van Eijk, R, Vasen, H F, Vossen, R H, Nielsen, M, Castellví-Bel, S, Ruiz-Ponte, C, Tomlinson, I, Dunlop, M G, Vodicka, P, Wijnen, J T, Hes, F J, Morreau, H, de Miranda, N F, Sijmons, R H & van Wezel, T 2017, ' Evidence for genetic association between chromosome 1q loci and predisposition to colorectal neoplasia ', British Journal of Cancer . https://doi.org/10.1038/bjc.2017.240
British Jounal of Cancer, 117(8), 1215-1223. Nature Publishing Group
British Journal of Cancer, 117(8), 1215-1223
British journal of cancer, 117(6), 876-884. Nature Publishing Group
BACKGROUND: A substantial fraction of familial colorectal cancer (CRC) and polyposis heritability remains unexplained. This study aimed to identify predisposing loci in patients with these disorders.METHODS: Homozygosity mapping was performed using 2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c27b339caa03287c7a985f07c59a3502
https://hdl.handle.net/1887/115104
https://hdl.handle.net/1887/115104
Autor:
Alena Kazimirova, Veronika Vymetalkova, Alexandra Horska, Kari Hemminki, Pavel Vodicka, Pavel Soucek, Magdalena Barancokova, Christoph Frank, Ludmila Vodickova, Zdenek Smerhovsky, Ludovit Musak, Asta Försti, Alessio Naccarati, Bozena Smolkova, J. Buchancova, Maria Dusinska
Publikováno v:
Genes, Chromosomes and Cancer. 54:260-266
Nonspecific chromosomal aberrations (CAs) are found in about 1% of lymphocytes drawn from healthy individuals. They include chromosome-type aberrations (CSAs), which are increased in exposure to ionizing radiation, and chromatid-type aberrations (CTA
Autor:
Beatrice Mohelnikova-Duchonova, Simona Susova, Ludmila Vodickova, Jolanta Gromadzinska, Pavel Soucek, A Moraviec-Sztandera, Pavel Vodicka
Publikováno v:
Neoplasma. 57:415-421
The question of susceptibility to squamous cell carcinoma of head and neck (SCCHN) in the environmental context was addressed by analysis of functional polymorphisms in enzymes metabolizing smoke constituents and/or alcohol (CYP2A13, CYP1B1, EPHX1, N
Autor:
Kari Hemminki, Rajesh Kumar, Ludmila Vodickova, Rudolf Stetina, Vincent Haufroid, Maria Dusinska, Pavel Vodicka, Katerina Trtkova, Alessio Naccarati, Pavel Soucek
Publikováno v:
Mutation Research/Fundamental and Molecular Mechanisms of Mutagenesis. 593:22-31
We investigated in a central European population, the association between genetic polymorphisms in several genes coding for xenobiotic metabolizing enzymes (CYP1A1, CYP2E1, EPHX1, GSTP1, GSTM1 and GSTT1) and in DNA repair genes (XPD, XPG, XPC and XRC