Associated Papers
RNA-sequencing based gene variants observed in patients with hyperlipidemia and premature coronary heart disease: A preliminary study.
Dechkhajorn W et al.
Biochemistry and Biophysics Reports, 2026
IFNAR2 p.F8S Variant Associates with Severe COVID-19 and Adaptive Immune Cell Activation Modulation.
Malvestiti F et al.
International Journal of Molecular Sciences, 2026
The Role of TLR2/TLR4 Receptors in Host Genetic Susceptibility to Recurrent Vulvovaginitis.
Routsias J et al.
Journal of Fungi (basel, Switzerland), 2025
Truncated variant rs373056577 confers increased risk of type 2 diabetes and missense variant rs121912717 is associated with hypertriglyceridemia in Bangladeshi population.
Sayed S et al.
Metabolism Open, 2025
Polymorphic pseudogenes in the human genome - a comprehensive assessment.
Lopes-Marques M et al.
Human Genetics, 2024
Phenotype wide association study links bronchopulmonary dysplasia with eosinophilia in children.
Kelchtermans J et al.
Scientific Reports, 2024
Lack of Association of TLR1 and TLR5 Coding Variants with Mortality in a Large Multicenter Cohort of Melioidosis Patients.
Yimthin T et al.
The American Journal of Tropical Medicine and Hygiene, 2024
ACE Phenotyping in Human Blood and Tissues: Revelation of ACE Outliers and Sex Differences in ACE Sialylation.
Enyedi EE et al.
Biomedicines, 2024
Impact of Gene Modifiers on Cystic Fibrosis Phenotypic Profiles: A Systematic Review.
Ward A et al.
Human Mutation, 2024
Lung Inflammatory Genes in Cystic Fibrosis and Their Relevance to Cystic Fibrosis Transmembrane Conductance Regulator Modulator Therapies.
Carbone A et al.
Genes, 2023
Global analysis of suppressor mutations that rescue human genetic defects.
Ünlü B et al.
Genome Medicine, 2023
rs67047829 genotypes of ERV3-1/ZNF117 are associated with lower body mass index in the Polish population.
Clark JSC et al.
Scientific Reports, 2023
Genetic Susceptibility to Fungal Infections.
Yazdi M et al.
Advanced Biomedical Research, 2023
Sensitization of Patient-Derived Colorectal Cancer Organoids to Photon and Proton Radiation by Targeting DNA Damage Response Mechanisms.
Pape K et al.
Cancers, 2022
Flagellin From Pseudomonas aeruginosa Modulates SARS-CoV-2 Infectivity in Cystic Fibrosis Airway Epithelial Cells by Increasing TMPRSS2 Expression.
Ruffin M et al.
Frontiers in Immunology, 2021
Genetic Variants Assessing Crohn's Disease Pattern in Pediatric Inflammatory Bowel Disease Patients by a Clinical Exome Survey.
Noel DD et al.
Bioinformatics and Biology Insights, 2021
Clustering of known low and moderate risk alleles rather than a novel recessive high-risk gene in non-BRCA1/2 sib trios affected with breast cancer.
Hilbers FS et al.
International Journal of Cancer, 2020
Whole‑exome sequencing identifies a novel mutation of SLC20A2 (c.C1849T) as a possible cause of hereditary multiple exostoses in a Chinese family.
Li Y et al.
Molecular Medicine Reports, 2020
The GenomeAsia 100K Project enables genetic discoveries across Asia.
Unknown Author
Nature, 2019
Pattern recognition receptor polymorphisms in early periodontitis.
Leite FRM et al.
Journal of Periodontology, 2019
Flagellin-independent effects of a Toll-like receptor 5 polymorphism in the inflammatory response to Burkholderia pseudomallei.
Dickey AK et al.
Plos Neglected Tropical Diseases, 2019
Genetic defects in fungal recognition and susceptibility to invasive pulmonary aspergillosis.
Cunha C et al.
Medical Mycology, 2019
Host genetic variants in sepsis risk: a field synopsis and meta-analysis.
Lu H et al.
Critical Care (london, England), 2019
In Silico Analysis of nsSNPs of Carp TLR22 Gene Affecting its Binding Ability with Poly I:C.
Chakrapani V et al.
Interdisciplinary Sciences, Computational Life Sciences, 2018
Toll-like receptor 2, 4 and 9 polymorphisms and their association with ICU-acquired infections in Central Greece.
Chatzi M et al.
Journal of Critical Care, 2018
TLR5 decoy receptor as a novel anti-amyloid therapeutic for Alzheimer's disease.
Chakrabarty P et al.
The Journal of Experimental Medicine, 2018
Genetically defined variants of toll-like receptors 3, 7 and 9 as phenotype and risk modifier factors for psoriasis.
Julià M et al.
Journal of Dermatological Science, 2018
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
Allele-specific expression reveals interactions between genetic variation and environment.
Knowles DA et al.
Nature Methods, 2017
A nonsense mutation in TLR5 is associated with survival and reduced IL-10 and TNF-α levels in human melioidosis.
Chaichana P et al.
Plos Neglected Tropical Diseases, 2017
Genetic variation of the Toll-like receptors in a Swedish allergic rhinitis case population.
Henmyr V et al.
Bmc Medical Genetics, 2017
Genetic alterations in necrotizing enterocolitis.
Cuna A et al.
Seminars in Perinatology, 2017
Association of TLR polymorphisms with bronchopulmonary dysplasia.
Malash AH et al.
Gene, 2016
Rapidity of fibrosis progression in liver transplant recipients with recurrent hepatitis C is influenced by toll-like receptor 3 polymorphism.
Citores MJ et al.
Clinical Transplantation, 2016
Deep resequencing of 131 Crohn's disease associated genes in pooled DNA confirmed three reported variants and identified eight novel variants.
Hong SN et al.
Gut, 2016
Premature termination codons in modern human genomes.
Fujikura K
Scientific Reports, 2016
Association of Single Nucleotide Polymorphisms in Toll-like Receptors with Acinetobacter baumanii Infectionin a Chinese Population.
He L et al.
Iranian Journal of Public Health, 2016
A toll-like receptor 9 (rs352140) variant is associated with placental inflammation in newborn infants.
Karody V et al.
The Journal of Maternal-fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians, 2016
Toll-like receptor cascade and gene polymorphism in host-pathogen interaction in Lyme disease.
Rahman S et al.
Journal of Inflammation Research, 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