A comparison of genomic profiles of complex diseases under different models

por Potenciano, Víctor, Abad-Grau, María Mar, Alcina, Antonio, Matesanz, Fuencisla
Publicado 2016

High ACSL5 Transcript Levels Associate with Systemic Lupus Erythematosus and Apoptosis in Jurkat T Lymphocytes and Peripheral Blood Cells

por Catalá-Rabasa, Antonio, Ndagire, Dorothy, Sabio, Jose Mario, Fedetz, Maria, Matesanz, Fuencisla, Alcina, Antonio
Publicado 2011

Sample Reproducibility of Genetic Association Using Different Multimarker TDTs in Genome-Wide Association Studies: Characterization and a New Approach

por Abad-Grau, Mara M., Medina-Medina, Nuria, Montes-Soldado, Rosana, Matesanz, Fuencisla, Bafna, Vineet
Publicado 2012

Genome-wide association filtering using a highly locus-specific transmission/disequilibrium test

por Abad-Grau, María M., Medina-Medina, Nuria, Montes-Soldado, Rosana, Moreno-Ortega, José, Matesanz, Fuencisla
Publicado 2010

Splice-site variant in ACSL5: a marker promoting opposing effect on cell viability and protein expression

por Pérez-Núñez, Iván, Karaky, Mohamad, Fedetz, María, Barrionuevo, Cristina, Izquierdo, Guillermo, Matesanz, Fuencisla, Alcina, Antonio
Publicado 2019

Interaction of PLP with GFP-MAL2 in the Human Oligodendroglial Cell Line HOG

por Bello-Morales, Raquel, Pérez-Hernández, Marta, Rejas, María Teresa, Matesanz, Fuencisla, Alcina, Antonio, López-Guerrero, José Antonio
Publicado 2011

Polymorphisms in ARNTL/BMAL1 and CLOCK Are Not Associated with Multiple Sclerosis in Spanish Population

por de Rojas, Isabel, Martin-Montero, César, Fedetz, Maria, González-Jiménez, Adela, Matesanz, Fuencisla, Urcelay, Elena, Espino-Paisán, Laura
Publicado 2022

A splice variant in the ACSL5 gene relates migraine with fatty acid activation in mitochondria

por Matesanz, Fuencisla, Fedetz, María, Barrionuevo, Cristina, Karaky, Mohamad, Catalá-Rabasa, Antonio, Potenciano, Victor, Bello-Morales, Raquel, López-Guerrero, Jose-Antonio, Alcina, Antonio
Publicado 2016

Multifaceted Analysis of Cerebrospinal Fluid and Serum from Progressive Multiple Sclerosis Patients: Potential Role of Vitamin C and Metal Ion Imbalance in the Divergence of Primar...

por Pomary, Precious Kwadzo, Eichau, Sara, Amigó, Núria, Barrios, Laura, Matesanz, Fuencisla, García-Valdecasas, Marta, Hrom, Ioana, García Sánchez, María Isabel, Garcia-Martin, Maria Luisa
Publicado 2023

Impact of Multiple Sclerosis Risk Polymorphism rs7665090 on MANBA Activity, Lysosomal Endocytosis, and Lymphocyte Activation

por González-Jiménez, Adela, López-Cotarelo, Pilar, Agudo-Jiménez, Teresa, Casanova, Ignacio, de Silanes, Carlos López, Martín-Requero, Ángeles, Matesanz, Fuencisla, Urcelay, Elena, Espino-Paisán, Laura
Publicado 2022

IL2RA/CD25 Gene Polymorphisms: Uneven Association with Multiple Sclerosis (MS) and Type 1 Diabetes (T1D)

por Alcina, Antonio, Fedetz, María, Ndagire, Dorothy, Fernández, Oscar, Leyva, Laura, Guerrero, Miguel, Abad-Grau, María M., Arnal, Carmen, Delgado, Concepción, Lucas, Miguel, Izquierdo, Guillermo, Matesanz, Fuencisla
Publicado 2009

Multiple Sclerosis Risk Variant HLA-DRB1*1501 Associates with High Expression of DRB1 Gene in Different Human Populations

por Alcina, Antonio, Abad-Grau, María del Mar, Fedetz, María, Izquierdo, Guillermo, Lucas, Miguel, Fernández, Óscar, Ndagire, Dorothy, Catalá-Rabasa, Antonio, Ruiz, Agustín, Gayán, Javier, Delgado, Concepción, Arnal, Carmen, Matesanz, Fuencisla
Publicado 2012

Human Endogenous Retrovirus HERV-Fc1 Association with Multiple Sclerosis Susceptibility: A Meta-Analysis

por de la Hera, Belén, Varadé, Jezabel, García-Montojo, Marta, Alcina, Antonio, Fedetz, María, Alloza, Iraide, Astobiza, Ianire, Leyva, Laura, Fernández, Oscar, Izquierdo, Guillermo, Antigüedad, Alfredo, Arroyo, Rafael, Álvarez-Lafuente, Roberto, Vandenbroeck, Koen, Matesanz, Fuencisla, Urcelay, Elena
Publicado 2014

HERV-W polymorphism in chromosome X is associated with multiple sclerosis risk and with differential expression of MSRV

por García-Montojo, Marta, de la Hera, Belén, Varadé, Jezabel, de la Encarnación, Ana, Camacho, Iris, Domínguez-Mozo, María, Arias-Leal, Ana, García-Martínez, Ángel, Casanova, Ignacio, Izquierdo, Guillermo, Lucas, Miguel, Fedetz, Maria, Alcina, Antonio, Arroyo, Rafael, Matesanz, Fuencisla, Urcelay, Elena, Alvarez-Lafuente, Roberto
Publicado 2014

Influence of the LILRA3 Deletion on Multiple Sclerosis Risk: Original Data and Meta-Analysis

por Ortiz, Miguel A., Núñez, Concepción, Ordóñez, David, Alvarez-Cermeño, José C., Martínez-Rodriguez, José E., Sánchez, Antonio J., Arroyo, Rafael, Izquierdo, Guillermo, Malhotra, Sunny, Montalban, Xavier, García-Merino, Antonio, Munteis, Elvira, Alcina, Antonio, Comabella, Manuel, Matesanz, Fuencisla, Villar, Luisa M., Urcelay, Elena
Publicado 2015

Identification of the genetic mechanism that associates L3MBTL3 to multiple sclerosis

por Alcina, Antonio, Fedetz, Maria, Vidal-Cobo, Isabel, Andrés-León, Eduardo, García-Sánchez, Maria-Isabel, Barroso-del-Jesus, Alicia, Eichau, Sara, Gil-Varea, Elia, Luisa-Maria Villar, Saiz, Albert, Leyva, Laura, Vandenbroeck, Koen, Otaegui, David, Izquierdo, Guillermo, Comabella, Manuel, Urcelay, Elena, Matesanz, Fuencisla
Publicado 2022

CD40: Novel Association with Crohn's Disease and Replication in Multiple Sclerosis Susceptibility

por Blanco-Kelly, Fiona, Matesanz, Fuencisla, Alcina, Antonio, Teruel, María, Díaz-Gallo, Lina M., Gómez-García, María, López-Nevot, Miguel A., Rodrigo, Luis, Nieto, Antonio, Cardeña, Carlos, Alcain, Guillermo, Díaz-Rubio, Manuel, de la Concha, Emilio G., Fernandez, Oscar, Arroyo, Rafael, Martín, Javier, Urcelay, Elena
Publicado 2010

Correction: CD40: Novel Association with Crohn's Disease and Replication in Multiple Sclerosis Susceptibility

por Blanco-Kelly, Fiona, Matesanz, Fuencisla, Alcina, Antonio, Teruel, María, Díaz-Gallo, Lina M., Gómez-García, María, López-Nevot, Miguel A., Rodrigo, Luis, Nieto, Antonio, Cardeña, Carlos, Alcain, Guillermo, Díaz-Rubio, Manuel, de la Concha, Emilio G., Fernandez, Oscar, Arroyo, Rafael, Martín, Javier, Urcelay, Elena
Publicado 2010

Fine Mapping and Functional Analysis of the Multiple Sclerosis Risk Gene CD6

por Swaminathan, Bhairavi, Cuapio, Angélica, Alloza, Iraide, Matesanz, Fuencisla, Alcina, Antonio, García-Barcina, Maria, Fedetz, Maria, Fernández, Óscar, Lucas, Miguel, Órpez, Teresa, Pinto-Medel, Mª Jesus, Otaegui, David, Olascoaga, Javier, Urcelay, Elena, Ortiz, Miguel A., Arroyo, Rafael, Oksenberg, Jorge R., Antigüedad, Alfredo, Tolosa, Eva, Vandenbroeck, Koen
Publicado 2013

A New Risk Variant for Multiple Sclerosis at 11q23.3 Locus Is Associated with Expansion of CXCR5+ Circulating Regulatory T Cells

por Gil-Varea, Elia, Fedetz, Maria, Eixarch, Herena, Spataro, Nino, Villar, Luisa María, Urcelay, Elena, Saiz, Albert, Fernández, Óscar, Leyva, Laura, Ramió-Torrentà, Lluís, Vandenbroeck, Koen, Otaegui, David, Castillo-Triviño, Tamara, Izquierdo, Guillermo, Malhotra, Sunny, Bosch, Elena, Navarro, Arcadi, Alcina, Antonio, Montalban, Xavier, Matesanz, Fuencisla, Comabella, Manuel
Publicado 2020