Canlyniadau Chwilio - José Ramón Bilbao
- Dangos 1 - 14 canlyniadau o 14
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1
A novel RT-QPCR-based assay for the relative quantification of residue specific m6A RNA methylation gan Ainara Castellanos‐Rubio, Izortze Santín, Ane Olazagoitia‐Garmendia, Irati Romero‐Garmendia, Amaia Jauregi‐Miguel, María Legarda, José Ramón Bilbao
Cyhoeddwyd 2019Artigo -
2
A long noncoding RNA associated with susceptibility to celiac disease gan Ainara Castellanos‐Rubio, Nora Fernández‐Jiménez, Radomir Kratchmarov, Xiaobing Luo, Govind Bhagat, Peter H.R. Green, Robert J. Schneider, Megerditch Kiledjian, José Ramón Bilbao, Sankar Ghosh
Cyhoeddwyd 2016Artigo -
3
Functional Study of a Novel Single Deletion in the<i>TITF1/NKX2.1</i>Homeobox Gene That Produces Congenital Hypothyroidism and Benign Chorea But Not Pulmonary Distress gan Christian M. Moya, Guiomar Pérez de Nanclares, Luís Castaño, Neus Potau, José Ramón Bilbao, Antonio Carrascosa, María Bargadá, R. Coya, P. Martul, E Vicens-Calvet, Pilar Santisteban
Cyhoeddwyd 2006Artigo -
4
Human mitochondrial DNA is extensively methylated in a non-CpG context gan Vibha Patil, Cyrille Cuenin, Felicia Fei‐Lei Chung, Jesús Rafael Rodríguez‐Aguilera, Nora Fernández‐Jiménez, Irati Romero‐Garmendia, José Ramón Bilbao, Vincent Cahais, Joseph A. Rothwell, Zdenko Herceg
Cyhoeddwyd 2019Artigo -
5
Coregulation and modulation of NF B-related genes in celiac disease: uncovered aspects of gut mucosal inflammation gan Nora Fernández‐Jiménez, Ainara Castellanos‐Rubio, Leticia Plaza‐Izurieta, Iñaki Irastorza, Xabier Elcoroaristizabal, Amaia Jauregi‐Miguel, Tamara López-Euba, Carlos Tutau, Marian M. de Pancorbo, Juan Carlos Vitoria, José Ramón Bilbao
Cyhoeddwyd 2013Artigo -
6
Epigenetic Defects of<i>GNAS</i>in Patients with Pseudohypoparathyroidism and Mild Features of Albright’s Hereditary Osteodystrophy gan Guiomar Pérez de Nanclares, Eduardo Fernández‐Rebollo, Izortze Santín, Beatriz García‐Cuartero, Sonia Gaztambide, Edelmiro Menéndez Torre, María José Morales, Manuel Pombo, José Ramón Bilbao, Francisco Barros, Nuria Zazo, Wiebke Ahrens, Harald Jüppner, Olaf Hiort, Luís Castaño, Murat Bastepe
Cyhoeddwyd 2007Artigo -
7
Gluten-induced RNA methylation changes regulate intestinal inflammation via allele-specific <i>XPO1</i> translation in epithelial cells gan Ane Olazagoitia‐Garmendia, Linda Zhang, Paula Mera, J Godbout, Maialen Sebastian‐delaCruz, Iraia García‐Santisteban, Luis Manuel Mendoza, Alaín Huerta, Iñaki Irastorza, Govind Bhagat, Peter H. Green, Laura Herrero, Dolors Serra, José Antonio Rodríguez, Elena F. Verdú, Chuan He, José Ramón Bilbao, Ainara Castellanos‐Rubio
Cyhoeddwyd 2021Artigo -
8
Fine mapping of the celiac disease-associated LPP locus reveals a potential functional variant gan Rodrigo Coutinho de Almeida, Isis Ricaño-Ponce, Vinod Kumar, Patrick Deelen, Agata Szperl, Gosia Trynka, Javier Gutierrez‐Achury, Alexandros Kanterakis, Harm-Jan Westra, Lude Franke, Morris A. Swertz, Mathieu Platteel, José Ramón Bilbao, Donatella Barisani, Luigi Greco, Luisa Mearin, Victorien M. Wolters, Chris J. Mulder, Maria Cristina Mazzilli, Ajit Sood, Božena Cukrowská, Concepción Núñez, Riccardo Pratesi, Sebo Withoff, Cisca Wijmenga
Cyhoeddwyd 2013Revisão -
9
Improving coeliac disease risk prediction by testing non-HLA variants additional to HLA variants gan Jihane Romanos, Anna Rosén, Vinod Kumar, Gosia Trynka, Lude Franke, Agata Szperl, Javier Gutierrez‐Achury, Cleo C. van Diemen, Roan Kanninga, Soesma A. Jankipersadsing, Andrea K. Steck, Georges Eisenbarth, David A. van Heel, Božena Cukrowská, Valentina Bruno, Maria Cristina Mazzilli, Concepción Núñez, José Ramón Bilbao, M. L. Mearin, Donatella Barisani, Marian Rewers, Jill M. Norris, Anneli Ivarsson, H. Marieke Boezen, Edwin Liu, Cisca Wijmenga
Cyhoeddwyd 2013Artigo -
10
Potentially causal associations between placental DNA methylation and schizophrenia and other neuropsychiatric disorders gan Ariadna Cilleros‐Portet, Corina Lesseur, Sergi Marí, Marta Cosín‐Tomás, Manuel Lozano, Amaia Irizar, Amber Burt, Iraia García‐Santisteban, Diego Garrido-Martín, Geòrgia Escaramís, Alba Hernangomez‐Laderas, Raquel Soler-Blasco, Charles E. Breeze, Bárbara P. González‐García, Loreto Santa‐Marina, Jia Chen, Sabrina Llop, Mariana F. Fernández, Martine Vrijheid, Jesús Ibarluzea, Mónica Guxens, Carmen J. Marsit, Mariona Bustamante, José Ramón Bilbao, Nora Fernández‐Jiménez
Cyhoeddwyd 2025Artigo -
11
Dense genotyping identifies and localizes multiple common and rare variant association signals in celiac disease gan Gosia Trynka, Karen A. Hunt, Nicholas Bockett, Jihane Romanos, Vanisha Mistry, Agata Szperl, Sjoerd F. Bakker, Maria Teresa Bardella, Leena Bhaw, Gemma Castillejo, Emilio G. de la Concha, Rodrigo Coutinho de Almeida, Kerith‐Rae Dias, Cleo C. van Diemen, P Dubois, Richard H. Duerr, Sarah Edkins, Lude Franke, Karin Fransén, Javier Cuesta, Graham Heap, Barbara Hrdličková, Sarah Hunt, Leticia Plaza Izurieta, Valentina Izzo, Leo A. B. Joosten, Cordelia Langford, Maria Cristina Mazzilli, Charles A. Mein, Vandana Midah, Mitja Mitrovič, Barbara Mora, Marinita Morelli, Sarah Nutland, Concepción Núñez, Suna Önengüt-Gümüşcü, Kerra Pearce, Mathieu Platteel, Isabel Polanco, Simon Potter, Carmen Ribes‐Koninckx, Isis Ricaño-Ponce, Stephen S. Rich, Anna Rybak, José Luis Santiago, Sabyasachi Senapati, Ajit Sood, Hania Szajewska, Riccardo Troncone, Jezabel Varadé, Chris Wallace, Victorien M. Wolters, Alexandra Zhernakova, B.K. Thelma, Božena Cukrowská, Elena Urcelay, José Ramón Bilbao, M. L. Mearin, Donatella Barisani, Jeffrey C. Barrett, Vincent Plagnol, Panos Deloukas, Cisca Wijmenga, David A. van Heel
Cyhoeddwyd 2011Artigo -
12
DNA methylation in childhood asthma: an epigenome-wide meta-analysis gan Cheng‐Jian Xu, Cilla Söderhäll, Mariona Bustamante, Nour Baïz, Olena Gruzieva, Ulrike Gehring, Dan Mason, Leda Chatzi, Mikel Basterrechea, Sabrina Llop, Maties Torrent, Francesco Forastiere, Maria Pia Fantini, Karin C. Lødrup Carlsen, Tari Haahtela, Andréanne Morin, Marjan Kerkhof, Simon Kebede Merid, Bianca van Rijkom, Soesma A. Jankipersadsing, Marc Jan Bonder, Stéphane Ballereau, Cornelis J. Vermeulen, Raúl Aguirre‐Gamboa, Johan C. de Jongste, Henriëtte A. Smit, Ashish Kumar, Göran Pershagen, Stefano Guerra, Judith García‐Aymerich, Dario Greco, Lovisa E. Reinius, Rosemary McEachan, Raf Azad, Vegard Hovland, Petter Mowinckel, Harri Alenius, Nanna Fyhrquist, Nathanaël Lemonnier, Johann Pellet, Charles Auffray, Pieter van der Vlies, Cleo C. van Diemen, Yang Li, Cisca Wijmenga, Mihai G. Netea, Miriam F. Moffatt, William Cookson, Josep M. Antó, Jean Bousquet, Tiina Laatikainen, Catherine Laprise, Kai-Häkon Carlsen, Davide Gori, Daniela Porta, Carmen Íñiguez, José Ramón Bilbao, Yang Li, John Wright, Bert Brunekreef, Juha Kere, Martijn C. Nawijn, Isabella Annesi‐Maesano, Jordi Sunyer, Erik Melén, Gerard H. Koppelman
Cyhoeddwyd 2018Revisão -
13
Genome-wide association study of placental weight identifies distinct and shared genetic influences between placental and fetal growth gan Robin N. Beaumont, Christopher Flatley, Marc Vaudel, Xiaoping Wu, Jing Chen, Gunn-Helen Moen, Line Skotte, Øyvind Helgeland, Pol Solé-Navais, Karina Banasik, Clara Albiñana, Justiina Ronkainen, João Fadista, Sara Stinson, Katerina Trajanoska, Carol A. Wang, David Westergaard, Sundararajan Srinivasan, Carlos Sánchez-Soriano, José Ramón Bilbao, Catherine Allard, Marika Groleau, Teemu Kuulasmaa, Daniel J. Leirer, Frédérique White, Pierre‐Étienne Jacques, Haoxiang Cheng, Ke Hao, Ole A. Andreassen, Bjørn Olav Åsvold, Mustafa Atalay, Laxmi Bhatta, Luigi Bouchard, Ben Brumpton, Søren Brunak, Jonas Bybjerg‐Grauholm, Cathrine Ebbing, Paul Elliott, Line Engelbrechtsen, Christian Erikstrup, Marisa Estarlich, Paul W. Franks, Romy Gaillard, Frank Geller, Jakob Grove, David M. Hougaard, Eero Kajantie, Camilla S. Morgen, Ellen A. Nøhr, Mette Nyegaard, Colin N. A. Palmer, Ole Birger Pedersen, Fernando Rivadeneira, Sylvain Sebért, Beverley M. Shields, Camilla Stoltenberg, Ida Surakka, Lise Wegner Thørner, Henrik Ullum, Marja Vääräsmäki, Bjarni J. Vilhjálmsson, Cristen J. Willer, Timo A. Lakka, Dorte Jensen Gybel-Brask, Mariona Bustamante, Torben Hansen, Ewan R. Pearson, Rebecca M. Reynolds, Sisse Rye Ostrowski, Craig E. Pennell, Vincent W. V. Jaddoe, Janine F. Felix, Andrew T. Hattersley, Mads Melbye, Debbie A. Lawlor, Kristian Hveem, Thomas Werge, Henriette Svarre Nielsen, Per Magnus, David M. Evans, Bo Jacobsson, Marjo‐Riitta Järvelin, Ge Zhang, Marie‐France Hivert, Stefan Johansson, Rachel M. Freathy, Bjarke Feenstra, Pål R. Njølstad
Cyhoeddwyd 2023Artigo -
14
Novel loci for childhood body mass index and shared heritability with adult cardiometabolic traits gan Suzanne Vogelezang, Jonathan P. Bradfield, Tarunveer S. Ahluwalia, John A. Curtin, Timo A. Lakka, Niels Grarup, Markus Scholz, Peter J. van der Most, Claire Monnereau, Evie Stergiakouli, Anni Heiskala, Momoko Horikoshi, Iryna O. Fedko, Natàlia Vilor‐Tejedor, Diana L. Cousminer, Marie Standl, Carol A. Wang, Jorma Viikari, Frank Geller, Carmen Íñiguez, Niina Pitkänen, Alessandra Chesi, Jonas Bacelis, Loïc Yengo, Maties Torrent, Ιωάννα Ντάλλα, Øyvind Helgeland, Saskia Selzam, Judith M. Vonk, Mohammed H. Zafarmand, Barbara Heude, I. Sadaf Farooqi, Akram Alyass, Robin N. Beaumont, Henri Theil, Peter Rzehak, José Ramón Bilbao, Theresia M. Schnurr, Inês Barroso, Klaus Bønnelykke, Lawrence J. Beilin, Lisbeth Carstensen, Marie‐Aline Charles, Bo Chawes, Karine Clément, Ricardo Closa‐Monasterolo, Adnan Čustović, Johan G. Eriksson, Joaquín Escribano, Maria M. Groen‐Blokhuis, Veit Grote, Dariusz Gruszfeld, Hákon Hákonarson, Torben Hansen, Andrew T. Hattersley, Mette Hollensted, Jouke‐Jan Hottenga, Elina Hyppönen, Stefan Johansson, Raimo Joro, Mika Kähönen, Ville Karhunen, Wieland Kieß, Bridget Knight, Berthold Koletzko, Andreas Kühnapfel, Kathrin Landgraf, Jean‐Paul Langhendries, Terho Lehtimäki, Jaakko T. Leinonen, Aihuali Li, Virpi Lindi, Estelle Lowry, Mariona Bustamante, Carolina Medina‐Gómez, Mads Melbye, Kim F. Michaelsen, Camilla S. Morgen, Trevor A. Mori, Tenna Ruest Haarmark Nielsen, Harri Niinikoski, Albertine J. Oldehinkel, Katja Pahkala, Kalliope Panoutsopoulou, Oluf Pedersen, Craig E. Pennell, Christopher Power, Sijmen A. Reijneveld, Fernando Rivadeneira, Angela Simpson, Peter D. Sly, Jakob Stokholm, Koon Teo, Elisabeth Thiering, Nicholas J. Timpson, André G. Uitterlinden, C.E.M. van Beijsterveldt, Barbera D. C. van Schaik, Marc Vaudel, Elvira Verduci
Cyhoeddwyd 2020Revisão
Offerynnau Chwilio:
Pynciau Perthynol
Biology
Gene
Genetics
Medicine
Genotype
Single-nucleotide polymorphism
Gene expression
Internal medicine
Methylation
Disease
Antigen
DNA methylation
Genome-wide association study
Haplotype
Human leukocyte antigen
Immunology
Allele
Bioinformatics
Endocrinology
Genetic association
SNP
Coeliac disease
Computational biology
Context (archaeology)
CpG site
Demography
Genotyping
Gluten
Inflammation
Locus (genetics)