Bioquímica y Biología Molecular
Departamento
JOSE RAMON
BILBAO CATALA
PROFESORADO PLENO
Publicaciones en las que colabora con JOSE RAMON BILBAO CATALA (40)
2022
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Gluten-induced RNA methylation changes regulate intestinal inflammation via allele-specific XPO1 translation in epithelial cells
Gut, Vol. 71, Núm. 1, pp. 68-77
2021
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A Novel Noninvasive Method Based on Salivary Inflammatory Biomarkers for the Screening of Celiac Disease
Cellular and Molecular Gastroenterology and Hepatology
2019
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A novel RT-QPCR-based assay for the relative quantification of residue specific m6A RNA methylation
Scientific Reports, Vol. 9, Núm. 1
2018
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Celiac Diasease–associated lncRNA Named HCG14 Regulates NOD1 Expression in Intestinal Cells
Journal of Pediatric Gastroenterology and Nutrition, Vol. 67, Núm. 2, pp. 225-231
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Subcellular fractionation from fresh and frozen gastrointestinal specimens
Journal of Visualized Experiments, Vol. 2018, Núm. 137
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Transcription factor binding site enrichment analysis in co-expression modules in celiac disease
Genes, Vol. 9, Núm. 5
2011
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Upregulation of KIR3DL1 gene expression in intestinal mucosa in active celiac disease
Human Immunology, Vol. 72, Núm. 8, pp. 617-620
2010
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A regulatory single nucleotide polymorphism in the ubiquitin D gene associated with celiac disease
Human Immunology, Vol. 71, Núm. 1, pp. 96-99
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Long-term and acute effects of gliadin on small intestine of patients on potentially pathogenic networks in celiac disease
Autoimmunity, Vol. 43, Núm. 2, pp. 131-139
2009
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Exploring the diabetogenicity of the HLA-B18-DR3 CEH: Independent association with T1D genetic risk close to HLA-DOA
Genes and Immunity, Vol. 10, Núm. 6, pp. 596-600
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TH17 (and TH1) signatures of intestinal biopsies of CD patients in response to gliadin
Autoimmunity, Vol. 42, Núm. 1, pp. 69-73
2008
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Combined Functional and Positional Gene Information for the Identification of Susceptibility Variants in Celiac Disease
Gastroenterology, Vol. 134, Núm. 3, pp. 738-746
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Reply
Gastroenterology
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The functional R620W variant of the PTPN22 gene is associated with celiac disease
Tissue Antigens, Vol. 71, Núm. 3, pp. 247-249
2007
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Association of KIR2DL5B gene with celiac disease supports the susceptibility locus on 19q13.4
Genes and Immunity, Vol. 8, Núm. 2, pp. 171-176
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Epigenetic defects of GNAS in patients with pseudohypoparathyroidism and mild features of Albright's hereditary osteodystrophy
Journal of Clinical Endocrinology and Metabolism, Vol. 92, Núm. 6, pp. 2370-2373
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Mutations in GCK and HNF-1α explain the majority of cases with clinical diagnosis of MODY in Spain
Clinical Endocrinology, Vol. 67, Núm. 4, pp. 538-546
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The majority of cases of neonatal diabetes in Spain can be explained by known genetic abnormalities
Diabetic Medicine, Vol. 24, Núm. 7, pp. 707-713
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Toll-like receptor 4 (TLR4) gene polymorphisms in celiac disease
Tissue Antigens, Vol. 70, Núm. 6, pp. 495-498
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Two-year follow-up of anti-transglutaminase autoantibodies among celiac children on gluten-free diet: Comparison of IgG and IgA
Autoimmunity, Vol. 40, Núm. 2, pp. 117-121