Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Clara Ruiz-Ponte"'
Autor:
Clara Esteban-Jurado, Sebastià Franch-Expósito, Clara Ruiz-Ponte, Sergi Castellví-Bel, Maria Marti-Solano, Sabela Carballal, Joaquín Cubiella, David Giménez-Zaragoza, Teresa Ocaña, Gemma Llort, Jenifer Muñoz, Rosa Aligué, María López-Cerón, Francesc Balaguer, Tom van Wezel, Luis Bujanda, Miriam Cuatrecasas, Judith Balmaña, Victoria Gonzalo, Antoni Castells, Miriam Alvarez-Barona, Marcos Díaz-Gay
Publikováno v:
Oncotarget, 8(16), 26732-26743
Oncotarget
Oncotarget
// Clara Esteban-Jurado 1 , David Gimenez-Zaragoza 2 , Jenifer Munoz 1 , Sebastia Franch-Exposito 1 , Miriam Alvarez-Barona 3 , Teresa Ocana 1 , Miriam Cuatrecasas 4 , Sabela Carballal 1 , Maria Lopez-Ceron 1 , Maria Marti-Solano 5 , Marcos Diaz-Gay
Autor:
Pedro Pérez-Segura, David Marrupe, Carmen Poves, Vanesa García-Barberán, Patricia Llovet, Víctor Lorca, Miguel de la Hoya, Daniel Rueda, Beatriz García-Paredes, María Jesús Fernández-Aceñero, Pilar Garre, Clara Ruiz-Ponte, Eduardo Díaz-Rubio, Trinidad Caldés, Lorena Martín-Morales
Publikováno v:
PLoS ONE
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS ONE, Vol 12, Iss 11, p e0187312 (2017)
Repositorio Institucional de la Consejería de Sanidad de la Comunidad de Madrid
Consejería de Sanidad de la Comunidad de Madrid
PLoS ONE, Vol 12, Iss 11, p e0187312 (2017)
The involvement of GALNT12 in colorectal carcinogenesis has been demonstrated but it is not clear to what extent it is implicated in familial CRC susceptibility. Partially inactivating variant, NM_024642.4:c.907G>A, p.(D303N), has been previously det
Autor:
Roland P. Kuiper, Kevin Sweet, Robbert D.A. Weren, Robert Hüneburg, Alois Lang, Jan Lubinski, Hildegunn Høberg-Vetti, Janet R. Vos, Erik A. M. Jansen, Marija Staninova, Barbara Rivera, Stefan Aretz, M. Elisa Vink-Börger, Claire Palles, Noel F C C de Miranda, Daniel D. Buchanan, Wenche Sjursen, William D. Foulkes, Kornelia Neveling, Clara Ruiz-Ponte, Ad Geurts van Kessel, Sue Kenwrick, Renske A. Kuiper, Laura Valle, Aleksandar Dimovski, Judith E. Grolleman, Paul A. James, Isabel Spier, David Cockburn, Maartje Nielsen, Hans Morreau, Hans K. Schackert, Nicoline Hoogerbrugge, Tom van Wezel, Helen Lindsay, Ian G. Campbell, Isabell Popp, Dagmara Dymerska, Na Li, Rolf H. Sijmons, Frederik J. Hes, Marjolijn J. L. Ligtenberg, Marjolijn C.J. Jongmans, Detlev Schindler, Ian Tomlinson, Eveline J. Kamping, Mark Clendenning, Olivera Spasic-Boskovic, Richarda M. de Voer, Sanne W. ten Broeke, Julian Adlard, Gabriel Capellá, Fadwa A. Elsayed
Publikováno v:
Cancer Cell, 35, 256
Cancer Cell, 35, 2, pp. 256
Cancer Cell, 35(2), 256-+. CELL PRESS
Cancer cell, 35(2), 256-266.e5. CELL PRESS
Cancer Cell, 35(2), 256. Cell Press
Cancer Cell, 35, 2, pp. 256
Cancer Cell, 35(2), 256-+. CELL PRESS
Cancer cell, 35(2), 256-266.e5. CELL PRESS
Cancer Cell, 35(2), 256. Cell Press
Biallelic germline mutations affecting NTHL1 predispose carriers to adenomatous polyposis and colorectal cancer, but the complete phenotype is unknown. We describe 29 individuals carrying biallelic germline NTHL1 mutations from 17 families, of which
Autor:
Elena Gallardo, Luis Bujanda, Rosa M. Xicola, Antoni Castells, María I. García, Lucía Cortejoso, Montserrat Andreu, Laia Paré, Josep-Maria Reñé, Victor Moreno, Elisabeth Guino, Ceres Fernandez-Rozadilla, David Páez, Victoria Gonzalo, Clara Ruiz-Ponte, Montserrat Baiget, Jean-Baptiste Cazier, Alejandro Brea-Fernández, Xavier Bessa, Luis A. López-Fernández, María Jesús Lamas, Xavier Llor, Dolors Gonzalez, Claire Palles, Sonia Candamio, R. Jover, Sergi Castellví-Bel, Luis Rodrigo, Goretti Duran, Marta Crous-Bou, Rafael López, Ian Tomlinson, Angel Carracedo
Publikováno v:
PHARMACOGENOMICS JOURNAL
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
The development of genotyping technologies has allowed for wider screening for inherited causes of variable outcomes following drug administration. We have performed a genome-wide association study (GWAS) on 221 colorectal cancer (CRC) patients that
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dfee7bb772359573fde439ee1248eb3e
https://ora.ox.ac.uk/objects/uuid:33723795-f3a8-4604-84a3-ecfe2d1726be
https://ora.ox.ac.uk/objects/uuid:33723795-f3a8-4604-84a3-ecfe2d1726be
Autor:
Manuela Pinheiro, Manuel R. Teixeira, Helga Westers, Tom van Wezel, D. Timothy Bishop, Kari Hemminki, Emma Northwood, Daniel Chubb, Ben Kinnersley, Richard S. Houlston, Robert M.W. Hofstra, Clemens Schafmayer, Claire Palles, Jochen Hampe, Susan M. Farrington, Malcolm G. Dunlop, Matthew Frampton, Clara Ruiz-Ponte, Maria Timofeeva, Asta Försti, Sara E. Dobbins, Ian Tomlinson, Stephan Buch, Sergi Castellví-Bel
Publikováno v:
Nature Communications
Nature Communications, Vol 7, Iss 1, Pp 1-3 (2016)
Nature Communications, 7:10611. Nature Publishing Group
Nature Communications, 7
Nature Communications, Vol 7, Iss 1, Pp 1-3 (2016)
Nature Communications, 7:10611. Nature Publishing Group
Nature Communications, 7
Sill and co-workers1 report that germline variation in semaphorin 4A (SEMA4A) influences colorectal cancer (CRC) risk. This stems from identifying the SEMA4A p.Val78Met variant in one kindred with familial colorectal cancer type X (FCCTX) and subsequ
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:
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:
Sari Tuupanen, Melissa C. Southey, Ian Chandler, Enric Domingo, Paul D.P. Pharoah, Luis G. Carvajal-Carmona, D. Gareth Evans, Malcolm G. Dunlop, Trinidad Caldés, Graham G. Giles, Zoe Kemp, Harry Campbell, David J. Kerr, Alan M. Pittman, Eamonn R. Maher, D. Timothy Bishop, Jayaram Vijayakrishnan, Hans Morreau, Albert Tenesa, Asta Försti, Jean-Baptiste Cazier, Kimberley Howarth, Ella Barclay, Rebecca A. Barnetson, Tom van Wezel, Juul T. Wijnen, James G. D. Prendergast, Maggie Gorman, Julian Peto, Anneke Lucassen, Antoni Castells, Jochen Hampe, José A. G. Agúndez, Susan M. Farrington, Kate Sullivan, Henry Völzke, Richard Gray, Ulrich John, King Yip Cheng, Pavel Vodicka, Emma Jaeger, Peter Broderick, Judy W. C. Ho, Mobshra Qureshi, Lauri A. Aaltonen, Stephan Buch, Sarah Fielding, Sarah L. Spain, Lynn Martin, Andrew Rowan, Wendy Wood, Emily L. Webb, John M. Luk, Angel Carracedo, Clara Ruiz-Ponte, Alessio Naccarati, Steven J. Lubbe, Ian Tomlinson, Lara Lipton, John L. Hopper, Iina Niittymäki, Axel Walther, José M. Ladero, Pak C. Sham, Stefan Schreiber, Sergi Castellví-Bel, Miguel de la Hoya, Clemens Schafmayer, Gianluca Severi, Auli Karhu, Steven Penegar, Thibaud Koessler, Kari Hemminki, Richard S. Houlston, Huw Thomas
Publikováno v:
Nature Genetics. 40:623-630
To identify colorectal cancer (CRC) susceptibility alleles, we conducted a genome-wide association study. In phase 1, we genotyped 550,163 tagSNPs in 940 familial colorectal tumor cases (627 CRC, 313 high-risk adenoma) and 965 controls. In phase 2, w