Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Marta Alarcón-Riquelme"'
Autor:
Iris K. Madera‐Salcedo, Ada L. Ramírez‐Sánchez, Noé Rodríguez‐Rodríguez, Roberto García‐Quintero, Rosa M. Rubio, Gabriela Morales‐Montes de Oca, Emmanuel Dávalos, Rogelio Cuervo, Janette Furuzawa‐Carballeda, Jorge Alcocer‐Varela, Diana Gómez‐Martín, Marysol González‐Yáñez, Abigail de la Cruz, Adrián Albarrán‐Godínez, Gerardo Suárez‐Rojas, Juanita Romero‐Díaz, Norma O. Uribe‐Uribe, Marta Alarcón‐Riquelme, Mayra Furlan‐Magaril, Juan Manuel Mejía‐Vilet, José C. Crispín, Florencia Rosetti
Publikováno v:
Arthritis & Rheumatology.
Variants in STAT4 are associated with systemic lupus erythematosus (SLE) and other autoimmune diseases. How disease-associated variants affect STAT4 expression, in particular in CD4 T cells where STAT4 plays an essential role, is unknown.We compared
Autor:
Marisa Flook, Alba Escalera-Balsera, Paulina Rybakowska, Lidia Frejo, Angel Batuecas-Caletrio, Juan Carlos Amor-Dorado, Andres Soto-Varela, Marta Alarcón-Riquelme, Jose Antonio Lopez-Escamez
Background Meniere Disease (MD) is an inner ear syndrome, characterized by sensorineural hearing loss associated with episodes of vertigo, tinnitus, and aural fullness. The pathological mechanism leading to sporadic MD is still poorly understood, how
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9bbb04d1802cdda3ef55fbde10b92358
https://doi.org/10.21203/rs.3.rs-2210600/v1
https://doi.org/10.21203/rs.3.rs-2210600/v1
Autor:
Marisa Flook, Alba Escalera-Balsera, Paulina Rybakowska, Lidia Frejo, Angel Batuecas-Caletrio, Juan C. Amor-Dorado, Andres Soto-Varela, Marta Alarcón-Riquelme, Jose A. Lopez-Escamez
Publikováno v:
Clinical Immunology. 252:109632
This work was supported by B-CTS-68-UGR20 Grant by FEDER Funds, PI17/1644 and PI20-1126 grants from ISCIII by FEDER Funds from the EU, CLINMON-2 from the Meniere's Society UK, and Impact Data Science (IMP0001) . MF is funded by F18/00228 grant from I
Autor:
Lucas Le Lann, Pierre-Emmanuel Jouve, Marta Alarcón-Riquelme, Christophe Jamin, Jacques-Olivier Pers, Blanco Alonso, Ricardo, González-Gay Mantecón, Miguel Ángel
Publikováno v:
Scientific Reports 10, 11567 (2020).
UCrea Repositorio Abierto de la Universidad de Cantabria
instname
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
UCrea Repositorio Abierto de la Universidad de Cantabria
instname
Scientific Reports, Vol 10, Iss 1, Pp 1-8 (2020)
One of the most challenging objective for clinical cytometry in prospective multicenter immunomonitoring trials is to compare frequencies, absolute numbers of leukocyte populations and further the mean fluorescence intensities of cell markers, especi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=dedup_wf_001::6fe3f43a216c3734e7a3e0e294e194d3
https://www.nature.com/articles/s41598-020-68468-3.pdf
https://www.nature.com/articles/s41598-020-68468-3.pdf
Autor:
Rohan, Sharma, Valerie M, Harris, Joshua, Cavett, Biji T, Kurien, Ke, Liu, Kristi A, Koelsch, Anum, Fayaaz, Kaustubh S, Chaudhari, Lida, Radfar, David, Lewis, Donald U, Stone, C Erick, Kaufman, Shibo, Li, Barbara, Segal, Daniel J, Wallace, Michael H, Weisman, Swamy, Venuturupalli, Jennifer A, Kelly, Bernardo, Pons-Estel, Roland, Jonsson, Xianglan, Lu, Jacques-Eric, Gottenberg, Juan-Manuel, Anaya, Deborah S, Cunninghame-Graham, Andrew J W, Huang, Michael T, Brennan, Pamela, Hughes, Ilias, Alevizos, Corinne, Miceli-Richard, Edward C, Keystone, Vivian P, Bykerk, Gideon, Hirschfield, Gunnel, Nordmark, Sara Magnusson, Bucher, Per, Eriksson, Roald, Omdal, Nelson L, Rhodus, Maureen, Rischmueller, Michael, Rohrer, Marie, Wahren-Herlenius, Torsten, Witte, Marta, Alarcón-Riquelme, Xavier, Mariette, Christopher J, Lessard, John B, Harley, Wan-Fai, Ng, Astrid, Rasmussen, Kathy L, Sivils, R Hal, Scofield
Publikováno v:
Arthritis Rheumatol
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Repositorio EdocUR-U. Rosario
Universidad del Rosario
instacron:Universidad del Rosario
Objective: Sjögren's syndrome (SS) and systemic lupus erythematosus (SLE) are related by clinical and serologic manifestations as well as genetic risks. Both diseases are more commonly found in women than in men, at a ratio of ~10 to 1. Common X chr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid_dedup__::08e215409e94379e8724aa01011e4474
https://europepmc.org/articles/PMC8262088/
https://europepmc.org/articles/PMC8262088/
Autor:
Maureen D. Mayes, Lara Bossini-Castillo, Olga Gorlova, José Ezequiel Martin, Xiaodong Zhou, Wei V. Chen, Shervin Assassi, Jun Ying, Filemon K. Tan, Frank C. Arnett, John D. Reveille, Sandra Guerra, María Teruel, Francisco David Carmona, Peter K. Gregersen, Annette T. Lee, Elena López-Isac, Eguzkine Ochoa, Patricia Carreira, Carmen Pilar Simeón, Iván Castellví, Miguel Ángel González-Gay, Alexandra Zhernakova, Leonid Padyukov, Marta Alarcón-Riquelme, Cisca Wijmenga, Matthew Brown, Lorenzo Beretta, Gabriela Riemekasten, Torsten Witte, Nicolas Hunzelmann, Alexander Kreuter, Jörg H.W. Distler, Alexandre E. Voskuyl, Annemie J. Schuerwegh, Roger Hesselstrand, Annika Nordin, Paolo Airó, Claudio Lunardi, Paul Shiels, Jacob M. van Laar, Ariane Herrick, Jane Worthington, Christopher Denton, Fredrick M. Wigley, Laura K. Hummers, John Varga, Monique E. Hinchcliff, Murray Baron, Marie Hudson, Janet E. Pope, Daniel E. Furst, Dinesh Khanna, Kristin Phillips, Elena Schiopu, Barbara M. Segal, Jerry A. Molitor, Richard M. Silver, Virginia D. Steen, Robert W. Simms, Robert A. Lafyatis, Barri J. Fessler, Tracy M. Frech, Firas AlKassab, Peter Docherty, Elzbieta Kaminska, Nader Khalidi, Henry Niall Jones, Janet Markland, David Robinson, Jasper Broen, Timothy R.D.J. Radstake, Carmen Fonseca, Bobby P. Koeleman, Javier Martin, Norberto Ortego-Centeno, Raquel Ríos, José Luis Callejas, Nuria Navarrete, Rosa García Portales, María Teresa Camps, Antonio Fernández-Nebro, María F. González-Escribano, Julio Sánchez-Román, Francisco José García-Hernández, María Jesús Castillo, María Ángeles Aguirre, Inmaculada Gómez-Gracia, Benjamín Fernández-Gutiérrez, Luis Rodríguez-Rodríguez, Esther Vicente, José Luis Andreu, Mónica Fernández de Castro, Paloma García de la Peña, Francisco Javier López-Longo, Lina Martínez, Vicente Fonollosa, Gerard Espinosa, Carlos Tolosa, Anna Pros, Mónica Rodríguez Carballeira, Francisco Javier Narváez, Manel Rubio Rivas, Vera Ortiz Santamaría, Bernardino Díaz, Luis Trapiella, María del Carmen Freire, Adrián Sousa, María Victoria Egurbide, Patricia Fanlo Mateo, Luis Sáez-Comet, Federico Díaz, Vanesa Hernández, Emma Beltrán, José Andrés Román-Ivorra, Elena Grau, Juan José Alegre Sancho, Francisco J. Blanco García, Natividad Oreiro, Luis Fernández Sueiro
Publikováno v:
Mayes, M D, Bossini-Castillo, L, Gorlova, O, Martin, J E, Zhou, X D, Chen, W V, Assassi, S, Ying, J, Tan, F K, Arnett, F C, Reveille, J D, Guerra, S, Terue, M, Carmona, F D, Gregersen, P K, Lee, A T, Lopez-Isac, E, Ochoa, E, Carreira, P, Simeon, C P, Castellvi, I, Gonzalez-Gay, M A, Zhernakova, A, Padyukov, L, arcon-Riquelme, M, Wijmenga, C, Brown, M, Beretta, L, Riemekasten, G, Witte, T, Hunzelmann, N, Kreuter, A, Distler, J H W, Voskuyl, A E, Schuerwegh, A J, Hesselstrand, R, Nordin, A, Airo, P, Lunardi, C, Shiels, P, van Laar, J M, Herrick, A, Worthington, J, Denton, C, Wigley, F M, Hummers, L K, Varga, J, Hinchcliff, M E, Baron, M, Hudson, M, Pope, J E, Furst, DE, Khanna, D, Phillips, K, Schiopu, E, Segal, B M, Molitor, J A, Silver, R M, Steen, V D, Simms, R W, Lafyatis, R A, Fessler, B I J, Frech, T M, AlKassab, F, Docherty, P, Kaminska, E, Khalidi, N, Jones, H N, Markland, J, Robinson, D, Broen, J, Radstake, T R D J, Fonseca, C, Koeleman, BP & Martin, J 2014, ' Immunochip Analysis Identifies Multiple Susceptibility Loci for Systemic Sclerosis ', American journal of human genetics, vol. 94, no. 1, pp. 47-61 . https://doi.org/10.1016/j.ajhg.2013.12.002
American journal of human genetics, 94(1), 47-61. Cell Press
AMERICAN JOURNAL OF HUMAN GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
American Journal of Human Genetics, 94(1), 47-61. CELL PRESS
American Journal of Human Genetics, 94(1), 47-61
American journal of human genetics, 94(1), 47-61. Cell Press
AMERICAN JOURNAL OF HUMAN GENETICS
r-IIB SANT PAU. Repositorio Institucional de Producción Científica del Instituto de Investigación Biomédica Sant Pau
instname
American Journal of Human Genetics, 94(1), 47-61. CELL PRESS
American Journal of Human Genetics, 94(1), 47-61
In this study, 1,833 systemic sclerosis (SSc) cases and 3,466 controls were genotyped with the Immunochip array. Classical alleles, amino acid residues, and SNPs across the human leukocyte antigen (HLA) region were imputed and tested. These analyses
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6939d4b4c770d281595dee1bc71cee
https://research.vumc.nl/en/publications/81e9c026-1180-45c0-9c4c-8e4e9a9b7152
https://research.vumc.nl/en/publications/81e9c026-1180-45c0-9c4c-8e4e9a9b7152
Autor:
Pratyaksha, Wirapati, Karl, Forner, Angelica, Delgado-Vega, Marta, Alarcón-Riquelme, Mauro, Delorenzi, Jérôme, Wojcik
Publikováno v:
Annals of human genetics. 75(1)
Well-established examples of genetic epistasis between a pair of loci typically show characteristic patterns of phenotypic distributions in joint genotype tables. However, inferring epistasis given such data is difficult due to the lack of power in c
Autor:
Simanta Pathak, Yuyuan Guo, Huihua Ding, Yong Du, Soyoun Min, Kamala Vanarsa, Quanzhen Li, Sergey Kozyrev, Marta Alarcón-Riquelme, Chandra Mohan
Publikováno v:
The Journal of Immunology. 194:46.2-46.2
BANK1 is a B-cell adaptor protein that has been implicated in SLE and systemic sclerosis. Previous studies have interpreted that the overexpression of the full length BANK1 isoform plays a pathogenic and the truncated (∆BANK1) version plays a prote
Autor:
Eric Kai-Pang, Kong, Ludmila, Prokunina-Olsson, Wilfred Hing-Sang, Wong, Chak-Sing, Lau, Tak-Mao, Chan, Marta, Alarcón-Riquelme, Yu-Lung, Lau
Publikováno v:
Arthritis and rheumatism. 52(4)
The programmed death 1 (PD-1) molecule is a negative regulator of T cells, and a genetic association between PD-1 and systemic lupus erythematosus and rheumatoid arthritis (RA) in Caucasians has been reported. The aim of this study was to investigate
Autor:
Ludmila, Prokunina, Leonid, Padyukov, Anna, Bennet, Ulf, de Faire, Björn, Wiman, Jonathan, Prince, Lars, Alfredsson, Lars, Klareskog, Marta, Alarcón-Riquelme
Publikováno v:
Arthritis and rheumatism. 50(6)
To study the frequency of allele A of polymorphism PD-1.3 of the PDCD1 gene in patients with rheumatoid arthritis (RA) and its subsets, based on the presence of rheumatoid factor (RF) and the shared epitope (SE) alleles.A total of 1,175 patients with