Associated Papers
Role of Common Fractalkine Receptor Variants with Chronic Hepatitis B Patients in Tunisia.
Ben Dhifallah I et al.
Viruses, 2025
Human induced pluripotent stem cell-derived microglia with a CX3CR1-V249I genetic variant exhibit dysfunctional phenotypes and modulate neuronal growth and function.
Tutrow KD et al.
Biorxiv : the Preprint Server for Biology, 2025
Genetic factors associated with age-related macular degeneration modulating plasma inflammatory biomarker levels in patients with AIDS.
Sezgin E et al.
Ophthalmic Genetics, 2024
Integrating Common Risk Factors with Polygenic Scores Improves the Prediction of Type 2 Diabetes.
Timasheva Y et al.
International Journal of Molecular Sciences, 2023
Decoding the genetic relationship between Alzheimer's disease and type 2 diabetes: potential risk variants and future direction for North Africa.
Boukhalfa W et al.
Frontiers in Aging Neuroscience, 2023
Association between CX3CR1 rs3732378 polymorphism and neovascular age-related macular degeneration in a sample of Algerian population.
Messal A et al.
Molecular Biology Research Communications, 2023
Multi-omics analysis identifies osteosarcoma subtypes with distinct prognosis indicating stratified treatment.
Jiang Y et al.
Nature Communications, 2022
Genetic factors for survival in amyotrophic lateral sclerosis: an integrated approach combining a systematic review, pairwise and network meta-analysis.
Su WM et al.
Bmc Medicine, 2022
Effect of CX3CL1/CX3CR1 gene polymorphisms on the clinical efficacy of carboplatin therapy in Han patients with ovarian cancer.
Wang XC et al.
Frontiers in Genetics, 2022
An integrated multi-omic analysis of iPSC-derived motor neurons from C9ORF72 ALS patients.
Li J et al.
Iscience, 2021
The role of mycobiota-genotype association in inflammatory bowel diseases: a narrative review.
Mahmoudi E et al.
Gut Pathogens, 2021
Association of CX3CR1 Gene Polymorphisms with Fractalkine, Fractalkine Receptor, and C-Reactive Protein Levels in Patients with Kidney Failure.
Woźny Ł et al.
International Journal of Environmental Research and Public Health, 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
CX3CR1 at V249M and T280M Gene Polymorphism and Its Potential Risk for End-Stage Renal Diseases in Egyptian Patients.
Ibrahim AF et al.
International Journal of Nephrology, 2021
Systematic meta-analyses, field synopsis and global assessment of the evidence of genetic association studies in colorectal cancer.
Montazeri Z et al.
Gut, 2020
Functional fine-mapping of noncoding risk variants in amyotrophic lateral sclerosis utilizing convolutional neural network.
Yousefian-Jazi A et al.
Scientific Reports, 2020
Investigation of new candidate genes in retinoblastoma using the TruSight One "clinical exome" gene panel.
Akdeniz D et al.
Molecular Genetics & Genomic Medicine, 2019
CX3CR1-deficient microglia shows impaired signalling of the transcription factor NRF2: Implications in tauopathies.
Castro-Sánchez S et al.
Redox Biology, 2019
Cx3cr1-deficiency exacerbates alpha-synuclein-A53T induced neuroinflammation and neurodegeneration in a mouse model of Parkinson's disease.
Castro-Sánchez S et al.
Glia, 2018
Polymorphisms in the microglial marker molecule CX3CR1 affect the blood volume of the human brain.
Sakai M et al.
Psychiatry and Clinical Neurosciences, 2018
The Role of the Microglial Cx3cr1 Pathway in the Postnatal Maturation of Retinal Photoreceptors.
Jobling AI et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience, 2018
Polymorphisms in Selected Genes and Their Association with Age-Related Macular Degeneration in a Chinese Population.
Huang Q et al.
Medical Science Monitor : International Medical Journal of Experimental and Clinical Research, 2018
Association of the CX3CR1-V249I Variant with Neurofibrillary Pathology Progression in Late-Onset Alzheimer's Disease.
López-López A et al.
Molecular Neurobiology, 2018
Common polymorphisms of chemokine (C-X3-C motif) receptor 1 gene modify amyotrophic lateral sclerosis outcome: A population-based study.
Calvo A et al.
Muscle & Nerve, 2018
The Association of Fractalkine Receptor (T280M) Polymorphism in the Pathogenesis of Acute Coronary Syndrome in the Egyptian Population.
Hassan DS et al.
Current Pharmaceutical Biotechnology, 2018
Role of the Fractalkine Receptor in CNS Autoimmune Inflammation: New Approach Utilizing a Mouse Model Expressing the Human CX3CR1I249/M280 Variant.
Cardona SM et al.
Frontiers in Cellular Neuroscience, 2018
ENPP1 121Q functional variant enhances susceptibility to coronary artery disease in South Indian patients with type 2 diabetes mellitus.
Sumi S et al.
Molecular and Cellular Biochemistry, 2017
Rare genetic variants in CX3CR1 and their contribution to the increased risk of schizophrenia and autism spectrum disorders.
Ishizuka K et al.
Translational Psychiatry, 2017
Investigation of DNA repair-related SNPs underlying susceptibility to papillary thyroid carcinoma reveals MGMT as a novel candidate gene in Belarusian children exposed to radiation.
Lonjou C et al.
Bmc Cancer, 2017
CX3CR1 polymorphisms associated with an increased risk of developmental dysplasia of the hip in human.
Li L et al.
Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society, 2017
Genome-Wide Association Study of Polymorphisms Predisposing to Bronchiolitis.
Pasanen A et al.
Scientific Reports, 2017
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
Associations of fractalkine receptor (CX3CR1) and CCR5 gene variants with hypertension, diabetes and atherosclerosis in chronic renal failure patients undergoing hemodialysis.
Bagci B et al.
International Urology and Nephrology, 2016
Common and Rare Genetic Variation in CCR2, CCR5, or CX3CR1 and Risk of Atherosclerotic Coronary Heart Disease and Glucometabolic Traits.
Golbus JR et al.
Circulation. Cardiovascular Genetics, 2016
Association of CX3CR1 (V249I and T280M) polymorphisms with age-related macular degeneration: a meta-analysis.
Li D et al.
Canadian Journal of Ophthalmology. Journal Canadien D'ophtalmologie, 2015
Associations Between the T280M and V249I SNPs in CX3CR1 and the Risk of Age-Related Macular Degeneration.
Zhang R et al.
Investigative Ophthalmology & Visual Science, 2015
Association between the CX3CR1 gene V249I polymorphism and delayed kidney allograft function.
Dabrowska-Zamojcin E et al.
Transplant Immunology, 2015
Fractalkine receptor polymorphism may not be associated with the development and clinical course of ulcerative colitis.
Gokcan H et al.
Bosnian Journal of Basic Medical Sciences, 2015
CX3CR1 polymorphisms and the risk of age-related macular degeneration.
Ma B et al.
International Journal of Clinical and Experimental Pathology, 2015
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
Immunity genes and susceptibility to otitis media: a comprehensive review.
Mittal R et al.
Journal of Genetics and Genomics = Yi Chuan Xue Bao, 2014
CCR2, CX3CR1, RANTES and SDF1 genetic polymorphisms influence HIV infection in a Zimbabwean pediatric population.
Mhandire K et al.
Journal of Infection in Developing Countries, 2014
Maternal genotype and severe preeclampsia: a HuGE review.
Fong FM et al.
American Journal of Epidemiology, 2014
Study of Polymorphisms in CX3CR1, PLEKHA1 and VEGF genes as risk factors for age-related macular degeneration in Indian patients.
Gupta D et al.
Archives of Medical Research, 2014
Fractalkine receptor polymorphism and chronic tonsillitis.
Babakurban ST et al.
European Archives of Oto-rhino-laryngology : Official Journal of the European Federation of Oto-rhino-laryngological Societies (eufos) : Affiliated With the German Society for Oto-rhino-laryngology - Head and Neck Surgery, 2014