Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Clara Ruiz-Ponte"'
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:
Sneha Bontu, Esther Lee, Francesc Balaguer, Pilar Garre, Brian J. Doyle, John A. Baron, Xavier Bessa, Nathan A. Ellis, Luis Bujanda, Jamie Rawson, Sergi Castellví-Bel, Miguel de la Hoya, Trinidad Caldés, Montserrat Andreu, Polly A. Newcomb, Joan Clofent, Xavier Llor, John D. Potter, Sapna Syngal, Clara Ruiz-Ponte, Antoni Castells, Rosa M. Xicola, Angel Carracedo, Cristina Alenda, Noralane M. Lindor, Rodrigo Jover
Publikováno v:
CARCINOGENESIS
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
r-FISABIO. Repositorio Institucional de Producción Científica
instname
r-ISABIAL. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica y Sanitaria de Alicante
r-FISABIO: Repositorio Institucional de Producción Científica
Fundación para el Fomento de la Investigación Sanitaria y Biomédica de la Comunitat Valenciana (FISABIO)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
We describe an association between TGFBR1 polymorphism rs868 and mismatch repair proficient hereditary colorectal cancers. This polymorphism results in more binding of TGFBR1 to let-7b-5p miRNA, which would result in lower expression of TGFBR1 and th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f04b7e9a9dbc950abb2743608552d6b
https://fundanet.fisabio.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2338
https://fundanet.fisabio.san.gva.es/publicaciones/ProdCientif/PublicacionFrw.aspx?id=2338
Autor:
Graham Casey, Henry Völzke, Hermann Brenner, Thomas J. Hudson, Albert Tenesa, David J. Kerr, Clara Ruiz-Ponte, Stephane Ballereau, Luis G. Carvajal-Carmona, Anna Abulí, Jenny Chang-Claude, Lynn Martin, Maggie Gorman, Clemens Schafmayer, Steven Gallinger, John L. Hopper, Ian Tomlinson, Iina Niittymäki, Richard S. Houlston, Simone Picelli, Ella Barclay, Jochen Hampe, Xavier Bessa, Alan M. Pittman, Lauri A. Aaltonen, Susanna von Holst, Auli Karhu, Brent W. Zanke, Malcolm G. Dunlop, Michael Hoffmeister, Polly A. Newcomb, Harry Campbell, Steven Penegar, Sari Tuupanen, Steven J. Lubbe, Annika Lindblom, Axel Walther, Ian Chandler, David Duggan, Paul D.P. Pharoah, Peter Broderick, Mark A. Jenkins, Sergi Castellví-Bel, Susan M. Farrington, David H. Brewster, Thibaud Koessler
Publikováno v:
Gut. 62:871-881
OBJECTIVE: Colorectal cancer (CRC) has a substantial heritable component. Common genetic variation has been shown to contribute to CRC risk. A study was conducted in a large multi-population study to assess the feasibility of CRC risk prediction usin
Autor:
Stefan Schreiber, Markus M. Lerch, Malcolm G. Dunlop, T. van Wezel, Albert Tenesa, Paul D.P. Pharoah, S. Tuupanenx, Clemens Schafmayer, Jwc Ho, Pavel Vodicka, Rodney J. Scott, Koichi Matsuda, Brent W. Zanke, Jochen Hampe, Stephan Buch, Luis G. Carvajal-Carmona, Paolo Radice, Steven Penegar, Lara Lipton, Asta Försti, Magdalena Echeverry, Henry Völzke, Ian Tomlinson, Juul T. Wijnen, Pak C. Sham, Harry Campbell, C. A. Schmidt, Antoni Castells, Robert M.W. Hofstra, Thibaud Koessler, Yusuke Nakamura, Hans Morreau, Hermann Brenner, Annika Lindblom, I. Niittymäkix, Steve Gallinger, Oliver M. Sieber, Victor Moreno, Peter Devilee, Cristina M. Villanueva, Lauri A. Aaltonen, Angel Carracedo, Peter Broderick, Sergi Castellví-Bel, Jürgen Tepel, Paolo Peterlongo, Kari Hemminki, Richard S. Houlston, Alejandro Vélez, Thomas J. Hudson, Clara Ruiz-Ponte
Publikováno v:
Tomlinson, I P M, Dunlop, M, Campbell, H, Zanke, B, Gallinger, S, Hudson, T, Koessler, T, Pharoah, P D, Niittymaki, I, Tuupanen, S, Aaltonen, L A, Hemminki, K, Lindblom, A, Forsti, A, Sieber, O, Lipton, L, van Wezel, T, Morreau, H, Wijnen, J T, Devilee, P, Matsuda, K, Nakamura, Y, Castellvi-Bel, S, Ruiz-Ponte, C, Castells, A, Carracedo, A, Ho, J W C, Sham, P, Hofstra, R M W, Vodicka, P, Brenner, H, Hampe, J, Schafmayer, C, Tepel, J, Schreiber, S, Volzke, H, Lerch, M M, Schmidt, C A, Buch, S, Moreno, V, Villanueva, C M, Peterlongo, P, Radice, P, Echeverry, M M, Velez, A, Carvajal-Carmona, L, Scott, R, Penegar, S, Broderick, P, Tenesa, A & Houlston, R S 2010, ' COGENT (COlorectal cancer GENeTics): an international consortium to study the role of polymorphic variation on the risk of colorectal cancer ', British Journal of Cancer, vol. 102, no. 2, pp. 447-454 . https://doi.org/10.1038/sj.bjc.6605338
Europe PubMed Central
British journal of cancer, vol 102, iss 2
British Journal of Cancer
British Journal of Cancer, 102(2), 447-454
Recercat. Dipósit de la Recerca de Catalunya
instname
British Journal of Cancer; Vol 102
British Jounal of Cancer, 102(2), 447-454. Nature Publishing Group
Dipòsit Digital de la UB
Universidad de Barcelona
Europe PubMed Central
British journal of cancer, vol 102, iss 2
British Journal of Cancer
British Journal of Cancer, 102(2), 447-454
Recercat. Dipósit de la Recerca de Catalunya
instname
British Journal of Cancer; Vol 102
British Jounal of Cancer, 102(2), 447-454. Nature Publishing Group
Dipòsit Digital de la UB
Universidad de Barcelona
It is now recognised that a part of the inherited risk of colorectal cancer (CRC) can be explained by the co-inheritance of low-penetrance genetic variants. The accumulated experience to date in identifying these variants has served to highlight diff
Autor:
Lara Lipton, Amy Price, Enric Domingo, Trinidad Caldés, Gianluca Severi, Emma Jaeger, Sarah Fielding, Auli Karhu, José M. Ladero, Alan M. Pittman, David J. Kerr, Axel Walther, Mobshra Qureshi, Ian Tomlinson, Sergi Castellví-Bel, King Yip Cheng, Miguel de la Hoya, Wendy Wood, Emily L. Webb, John M. Luk, G Evans, Philip Twiss, Timothy Bishop, Hans Morreau, Steven Penegar, Pak C. Sham, Angel Carracedo, Melissa C. Southey, Eamonn R. Maher, Maria Chiara Di Bernardo, Sarah L. Spain, Julian Peto, Anneke Lucassen, Kari Hemminki, Lynn Martin, Richard Gray, Ian Chandler, Luis G. Carvajal-Carmona, Jean-Baptiste Cazier, Steven J. Lubbe, Kimberley Howarth, Richard S. Houlston, Graham G. Giles, Maggie Gorman, Kate Sullivan, Zoe Kemp, Pavel Vodicka, Judy W. C. Ho, Lauri A. Aaltonen, Clara Ruiz-Ponte, Jayaram Vijayakrishnan, Asta Försti, Huw Thomas, Alessio Naccarati, Peter Broderick, Juul T. Wijnen, Antoni Castells, Tom van Wezel, John L. Hopper, Iina Niittymäki, José A. G. Agúndez, Sari Tuupanen, Andrew Rowan, Ella Barclay
Publikováno v:
Human Molecular Genetics. 17:3720-3727
The common single-nucleotide polymorphism (SNP) rs3802842 at 11q23.1 has recently been reported to be associated with risk of colorectal cancer (CRC). To examine this association in detail we genotyped rs3802842 in eight independent case-control seri
Autor:
Rosa M. Xicola, Xavier Bessa, Xavier Llor, Juan Clofent, Luis G. Carvajal-Carmona, Angel Carracedo, Claire Palles, Rodrigo Jover, Montserrat Andreu, Ceres Fernandez-Rozadilla, Ian Tomlinson, Montserrat Baiget, Antoni Castells, Sergi Castellví-Bel, Jean-Baptiste Cazier, María Jesús Lamas, Dolors Gonzalez, Luis A. López-Fernández, Victor Moreno, Alejandro Brea-Fernández, Luis Bujanda, Clara Ruiz-Ponte, Anna Abulí
Publikováno v:
BMC genomics, vol 14, iss 1
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
Addi. Archivo Digital para la Docencia y la Investigación
instname
Recercat. Dipósit de la Recerca de Catalunya
BMC Genomics
BMC GENOMICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Dipòsit Digital de la UB
Universidad de Barcelona
RUNA. Repositorio da Consellería de Sanidade e Sergas
Servizo Galego de Saúde (SERGAS)
Addi. Archivo Digital para la Docencia y la Investigación
instname
Recercat. Dipósit de la Recerca de Catalunya
BMC Genomics
BMC GENOMICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
Dipòsit Digital de la UB
Universidad de Barcelona
Background: Colorectal cancer (CRC) is a disease of complex aetiology, with much of the expected inherited risk being due to several common low risk variants. Genome-Wide Association Studies (GWAS) have identified 20 CRC risk variants. Nevertheless,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0bf4bc4b6080228a9f39d00c529bc1b5
https://escholarship.org/uc/item/9z6163kh
https://escholarship.org/uc/item/9z6163kh
Autor:
Jean G. Ford, Tom D. Brutsaert, Enrique Vargas, Jose R. Rodriguez-Santana, Lorna G. Moore, F.L. Moreno, Y. Ruiz, Clara Ruiz–Ponte, Celeste Eng, A. Ibarra, Guillermo Barreto, Fabiola León-Velarde, Carlos Bustamante, Lisbeth Borjas, Laura Uribe Figueroa, Irma Silva Zolezzi, Esteban J. Parra, María Dolores Torres, Abigail W. Bigham, Gerardo Gutiérrez, Angel Carracedo, Jill S. Barnholtz-Sloan, Daniela Seminara, Elizabeth A. Nguyen, Mark D. Shriver, Paola Raska, William Rodriguez-Cintron, Elad Ziv, Fernando Rondóo González, Alejandra V. Contreras, William Zabala, Robert W. Haile, Christopher R. Gignoux, Antonio Salas, Esteban G. Burchard, Marc Via, Juan Carlos Fernández-López, Ceres Fernandez-Rozadilla, Miguel Cruz, Jorge Escobedo, Alfredo Hidalgo-Miranda, Gerardo Jimenez-Sanchez, Rocio Chapela, Patricia Taboada, Joshua Galanter, L. Porras
Publikováno v:
PLOS GENETICS
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
PLoS Genetics
PLoS Genetics; Vol 8
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
PLoS genetics, vol 8, iss 3
PLoS Genetics, Vol 8, Iss 3, p e1002554 (2012)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
r-FSJD. Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
instname
PLoS Genetics
PLoS Genetics; Vol 8
Repositorio UdeA
Universidad de Antioquia
instacron:Universidad de Antioquia
PLoS genetics, vol 8, iss 3
PLoS Genetics, Vol 8, Iss 3, p e1002554 (2012)
Dipòsit Digital de la UB
Universidad de Barcelona
Recercat. Dipósit de la Recerca de Catalunya
r-FSJD: Repositorio Institucional de Producción Científica de la Fundació Sant Joan de Déu
Fundació Sant Joan de Déu
Most individuals throughout the Americas are admixed descendants of Native American, European, and African ancestors. Complex historical factors have resulted in varying proportions of ancestral contributions between individuals within and among ethn
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ee2f406b27451ad5824e9d13a06bb2
https://hdl.handle.net/20.500.12866/11058
https://hdl.handle.net/20.500.12866/11058