Zobrazeno 1 - 9 of 9 pro vyhledávání: '"Ana, Aguinaga"'
1
Akademický článek
The Spanish Fabry women study: a retrospective observational study describing the phenotype of females with GLA variants
Autor: Rosario Sánchez, Tomás Ripoll-Vera, Manuel López-Mendoza, Joaquín de Juan-Ribera, Juan Ramón Gimeno, Álvaro Hermida, María Aurora Ruz-Zafra, José Vicente Torregrosa, Antonia Mora, José Manuel García-Pinilla, Elena Fortuny, Ana Aguinaga-Barrilero, Roser Torra
Publikováno v: Orphanet Journal of Rare Diseases, Vol 18, Iss 1, Pp 1-10 (2023)
Abstract Background Fabry disease (FD) is an X-linked condition caused by variants in the GLA gene. Since females have two X chromosomes, they were historically thought to be carriers. Although increased knowledge has shown that females often develop
Externí odkaz: https://doaj.org/article/97d9b7378eee421696d9ada54b59aa94
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2
Akademický článek
Defects at the Posttranscriptional Level Account for the Low TCRζ Chain Expression Detected in Gastric Cancer Independently of Caspase-3 Activity
Autor: Ana Aguinaga-Barrilero, Patricia Castro-Sánchez, Ignacio Juárez, Alberto Gutiérrez-Calvo, Noelia Rodríguez-Pérez, Adela Lopez, Remedios Gómez, José M. Martin-Villa
Publikováno v: Journal of Immunology Research, Vol 2020 (2020)
Background. Reduced TCRζ chain surface has been reported in T cells from patients with different inflammatory conditions and cancer. However, the causes of this diminished expression in cancer remain elusive. Methods. T cell-enriched populations of
Externí odkaz: https://doaj.org/article/07fb59270df346d0ba693f5068494631
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3
Defects at the Posttranscriptional Level Account for the Low TCRζ Chain Expression Detected in Gastric Cancer Independently of Caspase-3 Activity
Autor: Remedios Gómez, Ana Aguinaga-Barrilero, José Manuel Martín-Villa, Ignacio Juarez, Patricia Castro-Sánchez, Alberto Gutierrez-Calvo, Adela López, Noelia Rodríguez-Pérez
Publikováno v: Journal of Immunology Research
Journal of Immunology Research, Vol 2020 (2020)
Background. Reduced TCRζ chain surface has been reported in T cells from patients with different inflammatory conditions and cancer. However, the causes of this diminished expression in cancer remain elusive. Methods. T cell-enriched populations of
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::36a4620236d14eccb2a9462f8f4d7350
https://doi.org/10.1155/2020/1039458
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4
Higher prevalence of LAP+ (Latency TGFβ-Associated Peptide) T cells at the tissue level in patients with early gastric cancer
Autor: Ana, Aguinaga-Barrilero, Ignacio, Juarez, Christian, Vaquero-Yuste, Marta, Molina-Alejandre, Alberto, Gutiérrez-Calvo, Inmaculada, Lasa, Adela, López, Remedios, Gómez, Elisa M, Molanes-López, José M, Martin-Villa
Publikováno v: E-Prints Complutense. Archivo Institucional de la UCM
instname
The presence of cells with regulatory functions in patients with cancer is one of the mechanisms whereby the immune system cannot confront tumor growth. We sought to determine the prevalence of immunoregulatory Tcell subpopulations, expressing the la
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cfcbbb7e761c556243439d831380c5aa
https://doi.org/10.1016/j.cellimm.2022.104635
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5
The cellular resistance against oxidative stress (H2O2) is independent of neutral trehalase (Ntc1p) activity inCandida albicans
Autor: Yolanda, Pendreño, Y, Pedreño, Pilar, González-Párraga, P, González-Párraga, Sergio, Conesa, S, Conesa, María, Martínez-Esparza, M, Martínez-Esparza, Ana, Aguinaga, A, Aguinaga, José A, Hernández, J A, Hernández, Juan Carlos, Argüelles
Publikováno v: FEMS Yeast Research. 6:57-62
The protective role of trehalose against oxidative stress caused by hydrogen peroxide in Candida albicans has been investigated in the homozygous mutant ntc1Delta/ntc1Delta, disrupted in the NTC1 gene, which encodes the neutral (cytosolic) trehalase
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::220853d3a0acf25472a631b342adfe96
https://doi.org/10.1111/j.1567-1364.2005.00025.x
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6
Blau Syndrome-Related CARD15/NOD2 Mutations Are Not Linked to Idiopathic Uveitis in Spanish Patients
Autor: Noelia Rodríguez-Pérez, Ana Aguinaga-Barrilero, Marina B. Gorroño-Echebarría, Mercedes Pérez-Blas, José M. Martín-Villa
Publikováno v: Disease Markers, Vol 27, Iss 1, Pp 1-5 (2009)
Disease markers
Uveitis is a clinical feature of the Blau syndrome, a disease linked to CARD15 (also referred to as NOD2) mutations. Three main mutations in this gene (R334W, R334Q and L469F) have been reported as Blau syndrome risk factors, a disease that manifests
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d3f02e3c12c297c765bb4d0fd8480992
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7
Analysis of Crohn's disease-related CARD15 polymorphisms in Spanish patients with idiopathic uveitis
Autor: José Manuel Martín-Villa, Noelia Rodríguez-Pérez, Ana Aguinaga-Barrilero, Mercedes Pérez-Blas, Marina Begoña Gorroño-Echebarría
Publikováno v: Disease markers
Scopus-Elsevier
Disease Markers, Vol 24, Iss 2, Pp 111-117 (2008)
We wished to analyse the frequency of Crohn’s disease-linked CARD15 polymorphisms (P268S, R702W, G908R and 1007fs) in a group of Spanish patients with idiopathic uveitis. To this aim, DNA samples were obtained from 111 unrelated patients. P268S, R7
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0433e73028edc08126e7d24876bcbb43
https://pubmed.ncbi.nlm.nih.gov/18219096
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