Associated Papers
Somatic mutations reveal hyperactive Notch signaling and racial disparities in prurigo nodularis.
Rajeh A et al.
Medrxiv : the Preprint Server for Health Sciences, 2023
Understanding the genetic basis of immune responses to fungal infection.
Gonçalves SM et al.
Expert Review of Anti-infective Therapy, 2022
Association of single nucleotide polymorphisms in CXCR1, CXCR2 and CXCL5 with Behçet disease: a study in the Denizli province of Turkey.
Arıkan S et al.
Clinical and Experimental Dermatology, 2021
Prioritization of candidate genes for a South African family with Parkinson's disease using in-silico tools.
Sebate B et al.
Plos One, 2021
Long-Range Coupled Motions Underlie Ligand Recognition by a Chemokine Receptor.
Sepuru KM et al.
Iscience, 2020
Pharmacogenomics, biomarker network, and allele frequencies in colorectal cancer.
López-Cortés A et al.
The Pharmacogenomics Journal, 2020
Uniparental disomy causes deficiencies of vitamin K-dependent proteins.
Dasi MA et al.
Journal of Thrombosis and Haemostasis : Jth, 2016
Impact of genetic variations in C-C chemokine receptors and ligands on infectious diseases.
Qidwai T et al.
Human Immunology, 2016
Polymorphisms in Host Immunity-Modulating Genes and Risk of Invasive Aspergillosis: Results from the AspBIOmics Consortium.
Lupiañez CB et al.
Infection and Immunity, 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
Symptom clusters of pain, depressed mood, and fatigue in lung cancer: assessing the role of cytokine genes.
Reyes-Gibby CC et al.
Supportive Care in Cancer : Official Journal of the Multinational Association of Supportive Care in Cancer, 2013
Next generation exome sequencing of paediatric inflammatory bowel disease patients identifies rare and novel variants in candidate genes.
Christodoulou K et al.
Gut, 2013
Genetic variations of interleukin-8, CXCR1 and CXCR2 genes and risk of acute pyelonephritis in children.
Javor J et al.
International Journal of Immunogenetics, 2012
Genetic and functional evaluation of the role of CXCR1 and CXCR2 in susceptibility to visceral leishmaniasis in north-east India.
Mehrotra S et al.
Bmc Medical Genetics, 2011
Variation in the CXCR1 gene (IL8RA) is not associated with susceptibility to chronic periodontitis.
Scarel-Caminaga RM et al.
Journal of Negative Results in Biomedicine, 2011
Genetic variants in inflammation-related genes are associated with radiation-induced toxicity following treatment for non-small cell lung cancer.
Hildebrandt MA et al.
Plos One, 2010
CXCR1 and SLC11A1 polymorphisms affect susceptibility to cutaneous leishmaniasis in Brazil: a case-control and family-based study.
Castellucci L et al.
Bmc Medical Genetics, 2010
Genetic risk for recurrent urinary tract infections in humans: a systematic review.
Zaffanello M et al.
Journal of Biomedicine & Biotechnology, 2010
Genetic variation of the human urinary tract innate immune response and asymptomatic bacteriuria in women.
Hawn TR et al.
Plos One, 2009
Role of inflammation gene polymorphisms on pain severity in lung cancer patients.
Reyes-Gibby CC et al.
Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association for Cancer Research, Cosponsored by the American Society of Preventive Oncology, 2009
Common variants in immune and DNA repair genes and risk for human papillomavirus persistence and progression to cervical cancer.
Wang SS et al.
The Journal of Infectious Diseases, 2009
Variants in inflammation genes and the risk of biliary tract cancers and stones: a population-based study in China.
Hsing AW et al.
Cancer Research, 2008
A report of cytokine polymorphisms and COPD risk in Xuan Wei, China.
Shen M et al.
International Journal of Hygiene and Environmental Health, 2008
Genotype frequency and F ST analysis of polymorphisms in immunoregulatory genes in Chinese and Caucasian populations.
Lan Q et al.
Immunogenetics, 2007
Polymorphisms in chemokine receptor genes and susceptibility to Kawasaki disease.
Breunis WB et al.
Clinical and Experimental Immunology, 2007
Polymorphisms in immunoregulatory genes, smoky coal exposure and lung cancer risk in Xuan Wei, China.
Lee KM et al.
Carcinogenesis, 2007
Evidence of potential interaction of chemokine genes in susceptibility to systemic sclerosis.
Lee EB et al.
Arthritis and Rheumatism, 2007
Impact of IL8 and IL8-receptor alpha polymorphisms on the genetics of bronchial asthma and severe RSV infections.
Puthothu B et al.
Clinical and Molecular Allergy : Cma, 2006
Polymorphisms in interleukin 8 and its receptors (IL8, IL8RA and IL8RB) and association of common IL8 receptor variants with peripheral blood eosinophil counts.
Cheong HS et al.
Journal of Human Genetics, 2006
Association of interleukin-8 receptor alpha polymorphisms with chronic obstructive pulmonary disease and asthma.
Stemmler S et al.
Genes and Immunity, 2005
Single nucleotide polymorphisms in CXCR1 gene and its association with hepatitis B infected patients in Saudi Arabia.
Almajhdi FN et al.
Annals of Hepatology, 0