2004
DOI: 10.1038/sj.gene.6364141
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Combined haplotype analysis of the interleukin-19 and -20 genes: relationship to plaque-type psoriasis

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Cited by 58 publications
(59 citation statements)
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References 28 publications
(28 reference statements)
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“…30 In the present study, we attempted to elucidate the role of the IL-24 gene in predicting risk for psoriasis and to describe the linkage disequilibrium (LD) pattern of the IL-19, IL-20 and IL-24 genes. The association and haplotype analyses of the IL-24 gene were carried out.…”
Section: Introductionmentioning
confidence: 99%
“…30 In the present study, we attempted to elucidate the role of the IL-24 gene in predicting risk for psoriasis and to describe the linkage disequilibrium (LD) pattern of the IL-19, IL-20 and IL-24 genes. The association and haplotype analyses of the IL-24 gene were carried out.…”
Section: Introductionmentioning
confidence: 99%
“…2,5,6 In monocytes IL-19 secretion in response to LPS and GM-CSF has been shown to induce monocyte production of proinflammatory cytokines. 7 IL-19 expression is also upregulated in psoriatic lesions, [8][9][10] in sera from asthmatic patients, and in the urine of uremic patients, although the source of IL-19 production has not yet been identified. 11,12 Very little is known about the roles and the cellular sources of IL-19 in the lung.…”
mentioning
confidence: 99%
“…7,8,10,16 Psoriatic lesions are characterized by increased expression of IL-19 and IL-20, which is normalized after treatment with cyclosporine or calcipotriol parallel to the clinical improvement of psoriatic lesions. 7,8 Although the data on the expression of IL-20R types I and II in psoriasis are somewhat controversial it seems possible that changes in the expression and/or function of IL-20-RI contribute to the changes of the IL-19 cytokine system that are part of psoriasis pathophysiology.…”
Section: Discussionmentioning
confidence: 99%
“…11,[15][16][17] For each SNP, a set of four primers was designed using the online program available at http: //cedar.genetics.soton.ac.uk/public_html/primer1.html. Each PCR reaction was carried out in a total volume of 10 ml, containing 100 ng of template DNA, 20 pmol of each inner primer, 2 pmol of each outer primer, 0.2 mM deoxyribonucleotide triphosphate, 1 Â reaction buffer (75 mM Tris-HCl, pH 8.8, 20 mM (NH 4 ) 2 SO 4 , 0.01% Tween 20, 0.1 mg ml À1 Tartrazine, 1% Sucrose (Naxo, Tartu, Estonia), 0.5 U Smart-Taq DNA polymerase (Naxo).…”
Section: Ethical Considerationsmentioning
confidence: 99%
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