Page 36 - Read Online
P. 36

Page 228       Bergara-Muguruza et al. J Transl Genet Genom 2023;7:213-229  https://dx.doi.org/10.20517/jtgg.2023.14

                    associated with multiple sclerosis risk: mechanistic insights and potential clinical impact. ACS Chem Neurosci 2020;11:1651-60.
                    DOI  PubMed
               55.       Husby S, Koletzko S, Korponay-Szabó IR, et al. European society for pediatric gastroenterology, hepatology, and nutrition guidelines
                    for the diagnosis of coeliac disease. J Pediatr Gastroenterol Nutr 2012;54:136-60.  DOI
               56.       Gutierrez-Achury J, Zhernakova A, Pulit SL, et al. Fine mapping in the MHC region accounts for 18% additional genetic risk for
                    celiac disease. Nat Genet 2015;47:577-8.  DOI  PubMed  PMC
               57.       Dubois PCA, Trynka G, Franke L, et al. Multiple common variants for celiac disease influencing immune gene expression. Nat Genet
                    2010;42:295-302.  DOI
               58.       Plaza-Izurieta L, Fernandez-Jimenez N, Irastorza I, et al. Expression analysis in intestinal mucosa reveals complex relations among
                    genes under the association peaks in celiac disease. Eur J Hum Genet 2015;23:1100-5.  DOI  PubMed  PMC
               59.       Santin I, Jauregi-Miguel A, Velayos T, et al. Celiac diasease-associated lncRNA named HCG14 regulates NOD1 expression in
                    intestinal cells. J Pediatr Gastroenterol Nutr 2018;67:225-31.  DOI
               60.       Jauregi-Miguel A, Santin I, Garcia-Etxebarria K, et al. MAGI2 gene region and celiac disease. Front Nutr 2019;6:187.  DOI  PubMed
                    PMC
               61.       Castellanos-Rubio A, Fernandez-Jimenez N, Kratchmarov R, et al. A long noncoding RNA associated with susceptibility to celiac
                    disease. Science 2016;352:91-5.  DOI  PubMed  PMC
               62.       Zhernakova A, Festen EM, Franke L, et al. Genetic analysis of innate immunity in Crohn's disease and ulcerative colitis identifies two
                    susceptibility loci harboring CARD9 and IL18RAP. Am J Hum Genet 2008;82:1202-10.  DOI  PubMed  PMC
               63.       Coenen MJH, Trynka G, Heskamp S, et al. Common and different genetic background for rheumatoid arthritis and coeliac disease.
                    Hum Mol Genet 2009;18:4195-203.  DOI
               64.       Smyth DJ, Plagnol V, Walker NM, et al. Shared and distinct genetic variants in type 1 diabetes and celiac disease. N Engl J Med
                    2008;359:2767-77.  DOI  PubMed  PMC
               65.       Eizirik DL, Colli ML, Ortis F. The role of inflammation in insulitis and beta-cell loss in type 1 diabetes. Nat Rev Endocrinol
                    2009;5:219-26.  DOI
               66.       Santin I, Eizirik DL. Candidate genes for type 1 diabetes modulate pancreatic islet inflammation and β-cell apoptosis. Diabetes Obes
                    Metab 2013;15 Suppl 3:71-81.  DOI  PubMed
               67.       Carpenter S, Aiello D, Atianand MK, et al. A long noncoding RNA mediates both activation and repression of immune response
                    genes. Science 2013;341:789-92.  DOI  PubMed  PMC
               68.       Zhang Q, Chao TC, Patil VS, et al. The long noncoding RNA ROCKI regulates inflammatory gene expression. EMBO J
                    2019;38:e100041.  DOI  PubMed  PMC
               69.       Gonzalez-Moro I, Olazagoitia-Garmendia A, Colli ML, et al. The T1D-associated lncRNA Lnc13 modulates human pancreatic β cell
                    inflammation by allele-specific stabilization of STAT1 mRNA. Proc Natl Acad Sci USA 2020;117:9022-31.  DOI  PubMed  PMC
               70.       Krogvold L, Edwin B, Buanes T, et al. Detection of a low-grade enteroviral infection in the islets of langerhans of living patients
                    newly diagnosed with type 1 diabetes. Diabetes 2015;64:1682-7.  DOI
               71.       González-Moro I, Garcia-Etxebarria K, Mendoza LM, et al. LncRNA ARGI contributes to virus-induced pancreatic β cell
                    inflammation through transcriptional activation of IFN-stimulated genes. Adv Sci 2023;10:e2300063.  DOI  PubMed  PMC
               72.       Ayala-Fontánez N, Soler DC, McCormick TS. Current knowledge on psoriasis and autoimmune diseases. Psoriasis 2016;6:7-32.
                    DOI  PubMed  PMC
               73.       Barrea L, Nappi F, Di Somma C, et al. Environmental risk factors in psoriasis: the point of view of the nutritionist. Int J Environ Res
                    Public Health 2016;13:743.  DOI  PubMed  PMC
               74.       Gupta R, Ahn R, Lai K, et al. Landscape of long noncoding RNAs in psoriatic and healthy skin. J Invest Dermatol 2016;136:603-9.
                    DOI  PubMed  PMC
               75.       Rakhshan A, Zarrinpour N, Moradi A, et al. A single nucleotide polymorphism within HOX transcript antisense RNA (HOTAIR) is
                    associated with risk of psoriasis. Int J Immunogenet 2020;47:430-4.  DOI
               76.       Yao X, Hao S, Xue T, Zhou K, Zhang Y, Li H. Association of HOTAIR polymorphisms with susceptibility to psoriasis in a Chinese
                    Han population. Biomed Res Int 2021;2021:5522075.  DOI  PubMed  PMC
               77.       Obaid M, Udden SMN, Deb P, Shihabeddin N, Zaki MH, Mandal SS. LncRNA HOTAIR regulates lipopolysaccharide-induced
                    cytokine expression and inflammatory response in macrophages. Sci Rep 2018;8:15670.  DOI  PubMed  PMC
               78.       Lizzul PF, Aphale A, Malaviya R, et al. Differential expression of phosphorylated NF-kappaB/RelA in normal and psoriatic
                    epidermis and downregulation of NF-kappaB in response to treatment with etanercept. J Invest Dermatol 2005;124:1275-83.  DOI
               79.       Guo W, Dong Z, Bai Y, et al. Associations between polymorphisms of HOTAIR and risk of gastric cardia adenocarcinoma in a
                    population of north China. Tumour Biol 2015;36:2845-54.  DOI
               80.       Zhang DD, Wang WT, Xiong J, et al. Long noncoding RNA LINC00305 promotes inflammation by activating the AHRR-NF-κB
                    pathway in human monocytes. Sci Rep 2017;7:46204.  DOI  PubMed  PMC
               81.       Gao W, Zhu M, Wang H, et al. Association of polymorphisms in long non-coding RNA H19 with coronary artery disease risk in a
                    Chinese population. Mutat Res 2015;772:15-22.  DOI
               82.       Han DKM, Khaing ZZ, Pollock RA, Haudenschild CC, Liau G. H19, a marker of developmental transition, is reexpressed in human
                    atherosclerotic plaques and is regulated by the insulin family of growth factors in cultured rabbit smooth muscle cells. J Clin Invest
                    1996;97:1276-85.  DOI  PubMed  PMC
   31   32   33   34   35   36   37   38   39   40   41