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Journal Article
Scientific Reports, ISSN 2045-2322, 12/2018, Volume 8, Issue 1, pp. 10821 - 12
Celiac disease (CD) is an autoimmune disease characterized by inflammation of the intestinal mucosa due to an immune response to wheat gliadins. Some gliadin... 
ALPHA | MULTIDISCIPLINARY SCIENCES | Celiac disease | α-Interferon | TLR7 protein | Immune response | Intestine | Mucosa | Gliadin | Toll-like receptors | Inflammation | Autoimmune diseases | Small intestine | Viral infections
Journal Article
Journal Article
Journal of Immunology, ISSN 0022-1767, 03/2017, Volume 198, Issue 5, pp. 1838 - 1845
Journal Article
Amino Acids, ISSN 0939-4451, 3/2017, Volume 49, Issue 3, pp. 541 - 550
Journal Article
PLoS ONE, ISSN 1932-6203, 07/2011, Volume 6, Issue 7, p. e21281
Journal Article
PLoS ONE, ISSN 1932-6203, 09/2012, Volume 7, Issue 9, p. e45209
Background: Celiac disease (CD) is an intestinal inflammatory condition that develops in genetically susceptible individuals after exposure to dietary wheat... 
INTESTINAL INFLAMMATION | OXIDATIVE STRESS | INFLAMMATORY-BOWEL-DISEASE | PROTEIN | EPITHELIAL-CELLS | MULTIDISCIPLINARY SCIENCES | CROSS-LINKING | FACTOR-KAPPA-B | ENDOPLASMIC-RETICULUM | HUNTINGTONS-DISEASE | CELIAC-DISEASE | Calcium - metabolism | GTP-Binding Proteins - agonists | Humans | Endoplasmic Reticulum - metabolism | Molecular Sequence Data | Transglutaminases - genetics | Peptide Fragments - pharmacology | GTP-Binding Proteins - genetics | Gliadin - chemistry | Heat-Shock Proteins - genetics | Endoplasmic Reticulum - drug effects | Biotin - metabolism | CCAAT-Enhancer-Binding Proteins - genetics | Single-Cell Analysis | Real-Time Polymerase Chain Reaction | CCAAT-Enhancer-Binding Proteins - metabolism | Caco-2 Cells | Amino Acid Sequence | Endoplasmic Reticulum Stress - drug effects | Heat-Shock Proteins - metabolism | Mitochondria - metabolism | Mitochondria - drug effects | Enzyme Activation - drug effects | Blotting, Western | Gene Expression Regulation - drug effects | Peptide Fragments - chemical synthesis | Signal Transduction - drug effects | Transglutaminases - metabolism | Gliadin - pharmacology | Biotin - analogs & derivatives | GTP-Binding Proteins - metabolism | Regulators | Peptides | Laboratories | Pathogenesis | Homeostasis | Homology | Biology | CCAAT/enhancer-binding protein | Kinases | Small intestine | Proteins | Mitochondria | Intestine | Rodents | Gastroenterology | Gliadin | Post-translation | Calcium homeostasis | Food | Stresses | Enzymes | Calcium mobilization | Calcium (intracellular) | Crosslinking | Biotin | Inflammation | Gene expression | Transglutaminase 2 | Stress | Inflammatory bowel disease | Polymerase chain reaction | Celiac disease | Enterocytes | Immunogenicity | Diet | Antigen-presenting cells | In vivo methods and tests | Intracellular | Autoimmune diseases | Endoplasmic reticulum | Wheat | Calcium (reticular) | Cancer | Apoptosis | Biochemical markers
Journal Article
PLoS ONE, ISSN 1932-6203, 2011, Volume 6, Issue 2, p. e17039
Background and Objectives: Damage to intestinal mucosa in celiac disease (CD) is mediated both by inflammation due to adaptive and innate immune responses,... 
JUXTACRINE | RESPONSES | INTERLEUKIN-15 | MULTIDISCIPLINARY SCIENCES | IL-15 | RECEPTOR | CYTOKINE | SECRETION | EXPRESSION | INTRAEPITHELIAL LYMPHOCYTES | CELL-DEATH | Interleukin-15 - physiology | Intestinal Mucosa - metabolism | Enterocytes - metabolism | Humans | Protein Transport - drug effects | Receptor, Epidermal Growth Factor - metabolism | Celiac Disease - immunology | Intestinal Mucosa - immunology | Enterocytes - pathology | Transport Vesicles - drug effects | Receptor, Epidermal Growth Factor - physiology | Caco-2 Cells | Immunity, Innate - drug effects | Cells, Cultured | Celiac Disease - physiopathology | Transport Vesicles - immunology | Enterocytes - immunology | Gene Expression Regulation - drug effects | Celiac Disease - pathology | Interleukin-15 - genetics | Biopsy | Transport Vesicles - metabolism | Interleukin-15 - metabolism | Cell Proliferation - drug effects | Gliadin - pharmacology | Celiac Disease - metabolism | Intestinal Mucosa - pathology | Celiac disease | Epidermal growth factor | RNA | Analysis | Protein biosynthesis | Inflammation | Protein binding | Cell proliferation | Flow cytometry | Pediatrics | Peptides | Disease | Laboratories | Mucosa | Trafficking | Hyperplasia | Bromodeoxyuridine | mRNA | Activation | Kinases | Cell surface | Small intestine | Cell activation | Cell growth | Intestine | Compartments | Rodents | Gliadin | Interleukin 1 | Protein transport | Active control | Enzyme-linked immunosorbent assay | Food | Immune system | Immunoglobulins | Immune response | Cytokines | Epidermal growth factor receptors | Immunoregulation | Interleukin 15 | Enterocytes | Protein synthesis | Crypts | Cell lines | Interleukin 5 receptors | Autoimmune diseases | Interleukin 15 receptors | Apoptosis
Journal Article
Methods in Molecular Biology, ISSN 1064-3745, 2018, Volume 1723, pp. 139 - 154
Journal Article
PLoS ONE, ISSN 1932-6203, 11/2013, Volume 8, Issue 11, p. e79763
Journal Article
PLoS ONE, ISSN 1932-6203, 2010, Volume 5, Issue 8, p. e12246
Journal Article