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Fuencisla Matesanz

Showing results (41-50 of 58) with videos related to

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Scientific Reports|August 30, 2020
Predictive factors and early biomarkers of response in multiple sclerosis patients treated with natalizumabMaria Inmaculada Dominguez-Mozo, Silvia Perez-Perez, Luisa María Villar, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 24, 2011
Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genesJezabel Varadé, Manuel Comabella, Miguel A Ortiz, et al.
Plos One|May 10, 2012
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1Fuencisla Matesanz, Antonio González-Pérez, Miguel Lucas, et al.
Frontiers in Immunology|February 25, 2025
CD38 deficiency leads to a defective short-lived transcriptomic response to chronic graft-versus-host disease induction, involving purinergic signaling-related genes and distinct transcriptomic signatures associated with lupusMercedes Zubiaur, Laura C Terrón-Camero, Fernando Gordillo-González, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 14, 2014
A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bandsMercedes Delgado-García, Fuencisla Matesanz, Antonio Alcina, et al.
Nature Structural & Molecular Biology|May 24, 2011
Genome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genesDavid Martin, Cristina Pantoja, Ana Fernández Miñán, et al.
Journal of Medical Genetics|November 20, 2012
Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosisAntonio Alcina, Maria Fedetz, Oscar Fernández, et al.
Journal of Neuroinflammation|September 16, 2018
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease courseElia Gil-Varea, Elena Urcelay, Carles Vilariño-Güell, et al.
Brain : a Journal of Neurology|November 30, 2022
Not all roads lead to the immune system: the genetic basis of multiple sclerosis severityVilija G Jokubaitis, Maria Pia Campagna, Omar Ibrahim, et al.
Cells|January 16, 2020
The Rare <i>IL22RA2</i> Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple SclerosisPaloma Gómez-Fernández, Aitzkoa Lopez de Lapuente Portilla, Ianire Astobiza, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
Scientific Reports|August 30, 2020
Predictive factors and early biomarkers of response in multiple sclerosis patients treated with natalizumabMaria Inmaculada Dominguez-Mozo, Silvia Perez-Perez, Luisa María Villar, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|December 24, 2011
Replication study of 10 genes showing evidence for association with multiple sclerosis: validation of TMEM39A, IL12B and CBLB [correction of CLBL] genesJezabel Varadé, Manuel Comabella, Miguel A Ortiz, et al.
Plos One|May 10, 2012
Genome-wide association study of multiple sclerosis confirms a novel locus at 5p13.1Fuencisla Matesanz, Antonio González-Pérez, Miguel Lucas, et al.
Frontiers in Immunology|February 25, 2025
CD38 deficiency leads to a defective short-lived transcriptomic response to chronic graft-versus-host disease induction, involving purinergic signaling-related genes and distinct transcriptomic signatures associated with lupusMercedes Zubiaur, Laura C Terrón-Camero, Fernando Gordillo-González, et al.
Multiple Sclerosis (Houndmills, Basingstoke, England)|November 14, 2014
A new risk variant for multiple sclerosis at the immunoglobulin heavy chain locus associates with intrathecal IgG, IgM index and oligoclonal bandsMercedes Delgado-García, Fuencisla Matesanz, Antonio Alcina, et al.
Nature Structural & Molecular Biology|May 24, 2011
Genome-wide CTCF distribution in vertebrates defines equivalent sites that aid the identification of disease-associated genesDavid Martin, Cristina Pantoja, Ana Fernández Miñán, et al.
Journal of Medical Genetics|November 20, 2012
Identification of a functional variant in the KIF5A-CYP27B1-METTL1-FAM119B locus associated with multiple sclerosisAntonio Alcina, Maria Fedetz, Oscar Fernández, et al.
Journal of Neuroinflammation|September 16, 2018
Exome sequencing study in patients with multiple sclerosis reveals variants associated with disease courseElia Gil-Varea, Elena Urcelay, Carles Vilariño-Güell, et al.
Brain : a Journal of Neurology|November 30, 2022
Not all roads lead to the immune system: the genetic basis of multiple sclerosis severityVilija G Jokubaitis, Maria Pia Campagna, Omar Ibrahim, et al.
Cells|January 16, 2020
The Rare <i>IL22RA2</i> Signal Peptide Coding Variant rs28385692 Decreases Secretion of IL-22BP Isoform-1, -2 and -3 and Is Associated with Risk for Multiple SclerosisPaloma Gómez-Fernández, Aitzkoa Lopez de Lapuente Portilla, Ianire Astobiza, et al.
Pageof 6