Associated Papers
Next-Generation Sequencing Identifies Novel Germline Mutations in Patients with Budd-Chiari Syndrome-Associated Hepatocellular Carcinoma.
Kumar S et al.
Digestive Diseases and Sciences, 2025
TLR5 Variants Are Associated with the Risk for COPD and NSCLC Development, Better Overall Survival of the NSCLC Patients and Increased Chemosensitivity in the H1299 Cell Line.
Baranašić J et al.
Biomedicines, 2022
Case report: Two unique nonsense mutations in HTRA1-related cerebral small vessel disease in a Chinese population and literature review.
Chen W et al.
Frontiers in Neurology, 2022
Hereditary Haemorrhagic Telangiectasia (HHT) Marked by ACVRL1C1120T Variant Displays Hypopigmented Naevi and Frequent Bleeding Episodes if CYP2C9 Co-Mutated: Clinical Notes & Rationale of Patient Registry.
Minarik L et al.
Folia Biologica, 2020
Introducing the first whole genomes of nationals from the United Arab Emirates.
AlSafar HS et al.
Scientific Reports, 2019
Toll-like receptor polymorphism in host immune response to infectious diseases: A review.
Mukherjee S et al.
Scandinavian Journal of Immunology, 2019
Pattern recognition receptor polymorphisms in early periodontitis.
Leite FRM et al.
Journal of Periodontology, 2019
Toll-like receptor 5 gene polymorphism is associated with breast cancer susceptibility.
Shuang C et al.
Oncotarget, 2017
TLR5 Polymorphisms rs2072493, rs5744174, and rs5744168 Are Not Genetic Risk Factors for Chronic Helicobacter pylori Infection in Indian Tamils.
Goda V et al.
Immunological Investigations, 2017
Evaluation of Toll-like-receptor gene family variants as prognostic biomarkers in rheumatoid arthritis.
Torices S et al.
Immunology Letters, 2017
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.
Henmyr V et al.
Bmc Medical Genetics, 2017
Three-dimensional modelling identifies novel genetic dependencies associated with breast cancer progression in the isogenic MCF10 model.
Maguire SL et al.
The Journal of Pathology, 2016
Characterization of Disease-Associated Mutations in Human Transmembrane Proteins.
Molnár J et al.
Plos One, 2016
Pooled Resequencing of 122 Ulcerative Colitis Genes in a Large Dutch Cohort Suggests Population-Specific Associations of Rare Variants in MUC2.
Visschedijk MC et al.
Plos One, 2016
Gene/environment interactions in the pathogenesis of autoimmunity: new insights on the role of Toll-like receptors.
Gianchecchi E et al.
Autoimmunity Reviews, 2015
Polymorphisms in TLR9 but not in TLR5 increase the risk for duodenal ulcer and alter cytokine expression in the gastric mucosa.
Trejo-de la O A et al.
Innate Immunity, 2015
Personal exposure to PM2.5, genetic variants and DNA damage: a multi-center population-based study in Chinese.
Chu M et al.
Toxicology Letters, 2015
Pooled sequencing of 531 genes in inflammatory bowel disease identifies an associated rare variant in BTNL2 and implicates other immune related genes.
Prescott NJ et al.
Plos Genetics, 2015
Association of TLR5 gene polymorphisms in ulcerative colitis patients of north India and their role in cytokine homeostasis.
Meena NK et al.
Plos One, 2015
Linking genetic variation in human Toll-like receptor 5 genes to the gut microbiome's potential to cause inflammation.
Leifer CA et al.
Immunology Letters, 2014
Association of TLR4 and TLR5 gene polymorphisms with Graves' disease in Chinese Cantonese population.
Xiao W et al.
Human Immunology, 2014
Functional TLR5 genetic variants affect human colorectal cancer survival.
Klimosch SN et al.
Cancer Research, 2013
Genetic variations in toll-like receptor pathway and lung function decline in Cystic fibrosis patients.
Haerynck F et al.
Human Immunology, 2013
Integrating precision medicine in the study and clinical treatment of a severely mentally ill person.
O'Rawe JA et al.
Peerj, 2013
Rule-based models of the interplay between genetic and environmental factors in childhood allergy.
Bornelöv S et al.
Plos One, 2013
Association of toll-like receptor 5 gene polymorphism with susceptibility to ossification of the posterior longitudinal ligament of the spine in korean population.
Chung WS et al.
Journal of Korean Neurosurgical Society, 2011
Genetic variants in toll-like receptors are not associated with rheumatoid arthritis susceptibility or anti-tumour necrosis factor treatment outcome.
Coenen MJ et al.
Plos One, 2010
Can immunogenetics illuminate the diverse manifestations of respiratory infections?
Affandi JS et al.
Therapeutic Advances in Respiratory Disease, 2010
The heterogeneous allelic repertoire of human toll-like receptor (TLR) genes.
Georgel P et al.
Plos One, 2009
Multiple sclerosis and polymorphisms of innate pattern recognition receptors TLR1-10, NOD1-2, DDX58, and IFIH1.
Enevold C et al.
Journal of Neuroimmunology, 2009
Toll-like receptor polymorphisms and susceptibility to urinary tract infections in adult women.
Hawn TR et al.
Plos One, 2009
A history of recurrent positive selection at the toll-like receptor 5 in primates.
Wlasiuk G et al.
Molecular Biology and Evolution, 2009
Biased distribution of single nucleotide polymorphisms (SNPs) in porcine Toll-like receptor 1 (TLR1), TLR2, TLR4, TLR5, and TLR6 genes.
Shinkai H et al.
Immunogenetics, 2006
Characterization and functional investigation of single nucleotide polymorphisms (SNPs) in the human TLR5 gene.
Merx S et al.
Human Mutation, 2006
Polymorphism report: identification of two common single nucleotide polymorphisms in the human toll-like receptor 5 (TLR5) gene.
Kao YL et al.
Molecular and Cellular Probes, 2004
A common dominant TLR5 stop codon polymorphism abolishes flagellin signaling and is associated with susceptibility to legionnaires' disease.
Hawn TR et al.
The Journal of Experimental Medicine, 2003