Drupal-Biblio17<style face="normal" font="default" size="100%">A genetic variant of NLRP1 gene is associated with asbestos body burden in patients with malignant pleural mesothelioma.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HLA-G regulatory polymorphisms are associated with susceptibility to HCV infection.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">LTF and DEFB1 polymorphisms are associated with susceptibility toward chronic periodontitis development.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Polymorphisms in key bone modulator cytokines genes influence bisphosphonates therapy in postmenopausal women.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Association of the HLA-G 3'UTR polymorphisms with colorectal cancer in Italy: a first insight.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MBL2 Genetic Variants in HCV Infection Susceptibility, Spontaneous Viral Clearance and Pegylated Interferon Plus Ribavirin Treatment Response.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Role of inflammasome genetics in susceptibility to HPV infection and cervical cancer development.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Comprehensive analysis of polymorphisms in the HLA-G 5' upstream regulatory and 3' untranslated regions in Brazilian patients with systemic lupus erythematosus.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Distribution of forensic marker allelic frequencies in Pernambuco, Northestern Brazil.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Interleukin-18, interleukin-12B and interferon-γ gene polymorphisms in Brazilian patients with rheumatoid arthritis: a pilot study.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A rapid screening of ancestry for genetic association studies in an admixed population from Pernambuco, Brazil.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short Communication FYB polymorphisms in Brazilian patients with type I diabetes mellitus and autoimmune polyglandular syndrome type III.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Trace samples of human blood in mosquitoes as a forensic investigation tool.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Tumor necrosis factor-α and interleukin-6 gene polymorphism association with susceptibility to celiac disease in Italian patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Unusual onset of a case of chronic recurrent multifocal osteomyelitis.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HLA-B35, a common genetic trait, in a familial case of Henoch-Schoenlein purpura and Berger's disease.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HLA-G 14 bp deletion/insertion polymorphism and mother-to-child transmission of HIV.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HLA-G gene polymorphisms associated with susceptibility to rheumatoid arthritis disease and its severity in Brazilian patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Short communication: novel truncating mutations in the CFTR gene causing a severe form of cystic fibrosis in Italian patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">A comparative analysis of serologic parameters and oxidative stress in osteoarthritis and rheumatoid arthritis: reply to Mishra and colleagues.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Association of MBL2 gene exon 1 variants with autoimmune thyroid disease in Brazilian patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">CD14 polymorphisms correlate with an augmented risk for celiac disease in Italian patients.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Frequency of human papillomavirus types 16, 18, 31, and 33 and sites of cervical lesions in gynecological patients from Recife, Brazil.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Functional single-nucleotide polymorphisms in the DEFB1 gene are associated with systemic lupus erythematosus in Southern Brazilians.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">HLA-G 14bp del/ins genetic variation: association with susceptibility to human immunodeficiency virus-1 vertical transmission but not with human immunodeficiency virus-1 infection through horizontal transmission.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Letter: inflammatory bowel disease, complementary and alternative medicine, and genetics.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mannose-binding lectin and MBL-associated serine protease-2 gene polymorphisms in a Brazilian population from Rio de Janeiro.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Anti-α-enolase Antibodies in Serum from Pediatric Patients Affected by Inflammatory Diseases: Diagnostic and Pathogenetic Insights.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">MBL2 polymorphisms and the choice of controls for association studies: just another story?</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Analysis of DEFB1 regulatory SNPs in cystic fibrosis patients from North-Eastern Italy.</style>Drupal-Biblio17<style face="normal" font="default" size="100%">Mannose-binding lectin is produced by vaginal epithelial cells and its level in the vaginal fluid is influenced by progesterone.</style>