Browsing by Author Estivill, Xavier, 1955-
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| Issue Date | Title | Author(s) |
|---|---|---|
| 2013 | A highly expressed miR-101 isomiR is a functional silencing small RNA | Llorens Torres, Franc; Bañez-Coronel, Mónica; Pantano, Lorena; Río Fernández, José Antonio del; Ferrer, Isidro (Ferrer Abizanda); Estivill, Xavier, 1955-; Martí Puig, Eulàlia |
| 23-Feb-2012 | A pathogenic mechanism in Huntington"s disease involves small CAG-repeated RNAs with neurotoxic activity | Bañez-Coronel, Mónica; Porta, Sílvia; Kagerbauer, Birgit; Mateu Huertas, Elisabet; Pantano, Lorena; Ferrer, Isidro (Ferrer Abizanda); Guzmán, Manuel; Estivill, Xavier, 1955-; Martí Puig, Eulàlia |
| 25-May-1990 | A polymorphic DNA probe from chromosome 7 (7q22) | Casals, T.; Nunes Martínez, Virginia; Estivill, Xavier, 1955- |
| 24-Oct-2018 | Allele balance bias identifies systematic genotyping errors and false disease associations | Muyas, Francesc; Bosio, Mattia; Puig, Anna; Susak, Hana; Domènech, Laura; Escaramís Babiano, Geòrgia; Zapata, Luis; Demidov, German; Estivill, Xavier, 1955-; Rabionet Janssen, Raquel; Ossowski, Stephan |
| 24-Nov-2004 | Anàlisi transcripcional de 15q24-q26: caracterització d'un nou gen expressat al sistema límbic, LRRN6A/LERN1 | Carim Todd, Laura |
| 3-Dec-2012 | Análisis de la herencia epigenética en trastornos neurológicos | Iraola Guzmán, Susana |
| 27-Feb-2003 | Contribució a l'estudi genètic de les malalties complexes: Asma i psoriasi a la població espanyola | Cid Ibeas, Rafael de |
| 2000 | Errors congènits del metabolisme (ECM). | Pàmpols i Ros, Teresa; Arranz, J. A.; Artuch Iriberri, Rafael; Baiget Bastús, Montserrat; Borja, F.; Briones, P.; Casals, T.; Chabás, A.; Coll, M. J.; Rio, E. del; Domínguez, C.; Estivill, Xavier, 1955-; Gallano, Pia; Giròs, Marisa; Martínez, M.; Maya, A.; Milà i Recasens, Montserrat; Margarit, E.; Nunes Martínez, Virginia; Oriola Ambrós, Josep |
| 25-Feb-2000 | Estudi clinicopatòlogic i genètic del melanoma maligne i de la síndrome del nevus displàstic. | Puig i Sardà, Susana |
| 11-Jan-2008 | Genetic and genomic analysis modeling of germline c-MYC overexpression and cancer susceptibility | Solé Acha, Xavier; Hernández, Pilar; López de Heredia, Miguel; Armengol, Lluís; Rodríguez Santiago, Benjamín; Gómez, Laia; Maxwell, Christopher A.; Aguiló Lúcia, Fernando; Condom i Mundó, Enric; Abril, Jesús; Pérez Jurado, Luis; Estivill, Xavier, 1955-; Nunes Martínez, Virginia; Capellá, G. (Gabriel); Gruber, Stephen B.; Moreno Aguado, Víctor; Pujana Genestar, M. Ángel |
| 23-Feb-2011 | Genetic variants of the FADS gene cluster and ELOVL gene family, colostrums LC-PUFA levels, breastfeeding, and child cognition | Morales, Eva; Bustamante Pineda, Mariona; González, Juan R.; Guxens, Mònica; Torrent, Maties; Méndez, Michelle; García-Esteban, Raquel; Julvez, Jordi; Forns, Joan; Vrijheid, Martine; Moltó-Puigmartí, Carolina; López Sabater, María del Carmen; Estivill, Xavier, 1955-; Sunyer Deu, Jordi |
| 12-Dec-2001 | Identificació de nous gens a la regió cromosòmica 21q22. Caracterització molecular de KCNE2 i KCNE3. | Domenech Gimeno, Anna |
| 16-Apr-2013 | Identification of genetic susceptibility factors for fibromyalgia | Docampo Martínez, Elisa |
| 19-Aug-2020 | In utero and childhood exposure to tobacco smoke and multi-layer molecular signatures in children | Vives, Marta; Hernández Ferrer, Carles; Maitre, Léa; Ruiz Arenas, Carlos; Andrusaityte, Sandra; Borràs, Eva; Carracedo Álvarez, Ángel; Casas, Maribel; Chatzi, Leda; Coen, Muireann; Estivill, Xavier, 1955-; González, Juan R.; Grazuleviciene, Regina; Gutzkow, Kristine B.; Keun, Hector C.; Lau, Chung-Ho E.; Cadiou, Solène; Lepeule, Johanna; Mason, Dan; Quintela, Inés; Robinson, Oliver; Sabidó Aguadé, Eduard; Santorelli, Gillian; Schwarze, Per E.; Siskos, Alexandros P.; Slama, Rémy; Vafeiadi, Marina; Martí Puig, Eulàlia; Vrijheid, Martine; Bustamante, Mariona |
| 11-Apr-1991 | Mspl restriction fragment length polymorphism near exon 10 of cystic fibrosis (CFTR) gene. | Bosch, A.; Kruyer, H.; Nunes Martínez, Virginia; Estivill, Xavier, 1955- |
| 5-Jul-1990 | Mutation analysis in cystic fibrosis | Gasparini, Paolo; Pignatti, P. F.; Novelli, Giuseppe; Dallapiccola, B.; Nunes Martínez, Virginia; Casals, T.; Estivill, Xavier, 1955-; Fernández Muñoz, Esteve; Balassopoulou, A.; Loukopoulos, D.; Lavinha, J.; Simova, L.; Komel, R. |
| 1-Jun-1995 | Mutations in the cystic fibrosis gene in patients with congenital absence of the vas deferens | Chillón, Miguel; Casals, T.; Mercier, Bernard; Bassas, Lluís; Lissens, Willy; Silber, Sherman; Romey, Marie Catherine; Ruiz Romero, Javier; Verlingue, Claudine; Claustres, Mireille; Nunes Martínez, Virginia; Férec, Claude; Estivill, Xavier, 1955- |
| 1996 | A nuclear defect in the 4p16 region predisposes to multiple mitochondrial DNA deletions in families with Wolfram syndrome. | Barrientos Rubio, Antoni; Volpini Bertrán, Víctor; Casademont i Pou, Jordi; Genís, David; Manzanares, Josep-Maria; Ferrer, Isidro (Ferrer Abizanda); Corral, Jordi; Cardellach, Francesc; Urbano Márquez, A. (Álvaro); Estivill, Xavier, 1955-; Nunes Martínez, Virginia |
| 27-Jan-2004 | Patologia molecular del gen CFTR: Fibrosi quística i fenotips relacionats | Casals Senent, Teresa |
| 25-Aug-1990 | PCR detection of the pKM.19/ScrfI RFLP (D7S23), a marker closely linked to the cystic fibrosis mutation | Nunes Martínez, Virginia; Chillón, Miguel; Lench, N.; Ramsay, M.; Estivill, Xavier, 1955- |