Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Clara Esteban-Jurado"'
Autor:
Marc Vila Cuenca, Giacomo Marchi, Anna Barqué, Clara Esteban-Jurado, Alessandro Marchetto, Alejandro Giorgetti, Viorica Chelban, Henry Houlden, Nicholas W Wood, Chiara Piubelli, Marina Dorigatti Borges, Dulcinéia Martins de Albuquerque, Kleber Yotsumoto Fertrin, Ester Jové-Buxeda, Jordi Sanchez-Delgado, Neus Baena-Díez, Birute Burnyte, Algirdas Utkus, Fabiana Busti, Gintaras Kaubrys, Eda Suku, Kamil Kowalczyk, Bartosz Karaszewski, John B. Porter, Sally Pollard, Perla Eleftheriou, Patricia Bignell, Domenico Girelli, Mayka Sanchez
Publikováno v:
International Journal of Molecular Sciences, Vol 21, Iss 7, p 2374 (2020)
Aceruloplasminemia is a rare autosomal recessive genetic disease characterized by mild microcytic anemia, diabetes, retinopathy, liver disease, and progressive neurological symptoms due to iron accumulation in pancreas, retina, liver, and brain. The
Externí odkaz:
https://doaj.org/article/ff943e44ac60433cb447289feaaa3cff
Autor:
Marcos Díaz-Gay, Sebastià Franch-Expósito, Coral Arnau-Collell, Solip Park, Fran Supek, Jenifer Muñoz, Laia Bonjoch, Anna Gratacós-Mulleras, Paula A. Sánchez-Rojas, Clara Esteban-Jurado, Teresa Ocaña, Miriam Cuatrecasas, Maria Vila-Casadesús, Juan José Lozano, Genis Parra, Steve Laurie, Sergi Beltran, EPICOLON Consortium, Antoni Castells, Luis Bujanda, Joaquín Cubiella, Francesc Balaguer, Sergi Castellví-Bel
Publikováno v:
Cancers, Vol 11, Iss 3, p 362 (2019)
Colorectal cancer (CRC) shows aggregation in some families but no alterations in the known hereditary CRC genes. We aimed to identify new candidate genes which are potentially involved in germline predisposition to familial CRC. An integrated analysi
Externí odkaz:
https://doaj.org/article/e27f98e3059b46b4ab6ab503fc321b7a
Autor:
Anna Abulí, Antoni Castells, Luis Bujanda, Juan José Lozano, Xavier Bessa, Cristina Hernández, Cristina Álvarez-Urturi, Maria Pellisé, Clara Esteban-Jurado, Elizabeth Hijona, Andrea Burón, Francesc Macià, Jaume Grau, Rafael Guayta, Sergi Castellví-Bel, Montserrat Andreu, PROCOLON research group
Publikováno v:
PLoS ONE, Vol 11, Iss 4, p e0153084 (2016)
BACKGROUND:Common low-penetrance genetic variants have been consistently associated with colorectal cancer risk. AIM:To determine if these genetic variants are associated also with adenoma susceptibility and may improve selection of patients with inc
Externí odkaz:
https://doaj.org/article/31f74295138046c88a01528f00aae889
Autor:
Anna Abulí, Luis Bujanda, Jenifer Muñoz, Stephan Buch, Clemens Schafmayer, Maria Valeria Maiorana, Silvia Veneroni, Tom van Wezel, Tao Liu, Helga Westers, Clara Esteban-Jurado, Teresa Ocaña, Josep M Piqué, Montserrat Andreu, Rodrigo Jover, Angel Carracedo, Rosa M Xicola, Xavier Llor, Antoni Castells, EPICOLON Consortium, Malcolm Dunlop, Robert Hofstra, Annika Lindblom, Juul Wijnen, Paolo Peterlongo, Jochen Hampe, Clara Ruiz-Ponte, Sergi Castellví-Bel
Publikováno v:
PLoS ONE, Vol 9, Iss 4, p e95022 (2014)
Colorectal cancer is one of the most frequent neoplasms and an important cause of mortality in the developed world. Mendelian syndromes account for about 5% of the total burden of CRC, being Lynch syndrome and familial adenomatous polyposis the most
Externí odkaz:
https://doaj.org/article/346b83e22aca4a92b69ec2e743525b29
Autor:
Trinidad Caldés, Sergi Castellví-Bel, Miguel de la Hoya, Clara Esteban-Jurado, María Luisa González-Morales, Vanesa García-Barberan, Inmaculada Bando, Patricia Llovet, Marta Cazorla, Víctor Lorca, Pilar Garre, Lorena Martín-Morales
Supplementary data include a table with the primer sequences and three figures showing the validation and segregation study of the families carrying the BRIP1 variants.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8c5c9c218591706a6daab9206f48b5db
https://doi.org/10.1158/1940-6207.22533688
https://doi.org/10.1158/1940-6207.22533688
Autor:
Patricia Llovet, Vanesa García-Barberán, Víctor Lorca, Maria Luisa Gonzalez-Morales, Marta Cazorla, Lorena Martín-Morales, Clara Esteban-Jurado, Pilar Garre, Inmaculada Bando, Trinidad Caldés, Sergi Castellví-Bel, Miguel de la Hoya
Publikováno v:
Cancer Prevention Research. 14:185-194
Familial colorectal cancer Type X (FCCTX) comprises a heterogeneous group of families with an increased risk of developing colorectal cancer and other related tumors, but with mismatch repair–proficient, microsatellite-stable (MSS) tumors. Unfortun
Autor:
Anna Gratacós-Mulleras, Cristina Herrera-Pariente, Gabriel Capellá, Miriam Cuatrecasas, Jenifer Muñoz, Giulia Raimondi, Trinidad Caldés, Sebastià Franch-Expósito, Clara Esteban-Jurado, Sami Belhadj, Laia Bonjoch, Sergi Castellví-Bel, Francesc Balaguer, Marcos Díaz-Gay, Yasmin Soares de Lima, Laura Valle, Cristina Fillat, Pilar Garre, Antoni Castells, Teresa Ocaña, Coral Arnau-Collell
Publikováno v:
Gastroenterology
Dipòsit Digital de la UB
Universidad de Barcelona
Dipòsit Digital de la UB
Universidad de Barcelona
Background & Aims A significant proportion of colorectal cancer (CRC) cases have familial aggregation but little is known about the genetic factors that contribute to these cases. We performed an exhaustive functional characterization of genetic vari
Autor:
Algirdas Utkus, Domenico Girelli, Sally Pollard, Henry Houlden, Jordi Sánchez-Delgado, John B. Porter, Nicholas W. Wood, Dulcineia M. Albuquerque, Kamil Kowalczyk, Marc Vila Cuenca, Alessandro Marchetto, Birute Burnyte, Perla Eleftheriou, Alejandro Giorgetti, Bartosz Karaszewski, Eda Suku, Fabiana Busti, Giacomo Marchi, Neus Baena-Díez, Kleber Yotsumoto Fertrin, Clara Esteban-Jurado, Ester Jové-Buxeda, Chiara Piubelli, P Bignell, Mayka Sanchez, Viorica Chelban, Marina Dorigatti Borges, Anna Barqué, Gintaras Kaubrys
Publikováno v:
International Journal of Molecular Sciences
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
International Journal of Molecular Sciences, Vol 21, Iss 2374, p 2374 (2020)
Volume 21
Issue 7
International journal of molecular sciences, Basel : MDPI, 2020, vol. 21, no. 7, art. no. 2374, p. [1-14]
r-IGTP. Repositorio Institucional de Producción Científica del Instituto de Investigación Germans Trias i Pujol
instname
International Journal of Molecular Sciences, Vol 21, Iss 2374, p 2374 (2020)
Volume 21
Issue 7
International journal of molecular sciences, Basel : MDPI, 2020, vol. 21, no. 7, art. no. 2374, p. [1-14]
Aceruloplasminemia is a rare autosomal recessive genetic disease characterized by mild microcytic anemia, diabetes, retinopathy, liver disease, and progressive neurological symptoms due to iron accumulation in pancreas, retina, liver, and brain. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::816b90b81ea56ae7ab3b099bc22b677e
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=5283
https://fundanet.igtp.cat/Publicaciones/ProdCientif/PublicacionFrw.aspx?id=5283
Autor:
Steven Laurie, Maria Vila-Casadesús, Antoni Castells, Teresa Ocaña, Joaquín Cubiella, Clara Esteban-Jurado, Jordi Camps, Saray Duran-Sanchon, Jenifer Muñoz, Trinidad Caldés, Juan José Lozano, Sergi Beltran, Laia Bonjoch, Sergi Castellví-Bel, Pilar Garre, Isabel Quintanilla, Sophia Derdak, Francesc Balaguer, Marcos Díaz-Gay, María López-Cerón, Esther Samper, Luis Bujanda, Miriam Cuatrecasas, Sebastià Franch-Expósito, Sabela Carballal, Meritxell Gironella, Jaime J. Carvajal, Clara Ruiz-Ponte
Publikováno v:
Digital.CSIC. Repositorio Institucional del CSIC
instname
instname
EPICOLON consortium: et al.
Colorectal cancer (CRC) is one of the most common neoplasms and an important cause of mortality worldwide (http://globocan.iarc.fr/). Approximately 35% of the variation in CRC susceptibility is likely due to heritable
Colorectal cancer (CRC) is one of the most common neoplasms and an important cause of mortality worldwide (http://globocan.iarc.fr/). Approximately 35% of the variation in CRC susceptibility is likely due to heritable
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