Associated Papers
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Elife, 2024
Association of genetic variation in COL11A1 with adolescent idiopathic scoliosis.
Yu H et al.
Biorxiv : the Preprint Server for Biology, 2023
Hepatitis B Virus Infection Among Leprosy Patients: A Case for Polymorphisms Compromising Activation of the Lectin Pathway and Complement Receptors.
Boldt ABW et al.
Frontiers in Immunology, 2020
Analysis of 75 Candidate SNPs Associated With Acute Rejection in Kidney Transplant Recipients: Validation of rs2910164 in MicroRNA MIR146A.
Oetting WS et al.
Transplantation, 2019
Host genetic variants in sepsis risk: a field synopsis and meta-analysis.
Lu H et al.
Critical Care (london, England), 2019
A Rare Genetic Defect of MBL2 Increased the Risk for Progression of IgA Nephropathy.
Ouyang Y et al.
Frontiers in Immunology, 2019
Actionable perturbations of damage responses by TCL1/ATM and epigenetic lesions form the basis of T-PLL.
Schrader A et al.
Nature Communications, 2018
Ficolin-2 Gene rs7851696 Polymorphism is Associated with Delayed Graft Function and Acute Rejection in Kidney Allograft Recipients.
Dabrowska-Zamojcin E et al.
Archivum Immunologiae Et Therapiae Experimentalis, 2018
The prevalence of the variants of the L-ficolin gene (FCN2) in the arctic populations of East Siberia.
Smolnikova MV et al.
Immunogenetics, 2017
Mannose-binding lectin and l-ficolin polymorphisms in patients with community-acquired pneumonia caused by intracellular pathogens.
van Kempen G et al.
Immunology, 2017
A journey through the lectin pathway of complement-MBL and beyond.
Garred P et al.
Immunological Reviews, 2016
FCN2 c.772G>T polymorphism is associated with chronic adenoiditis and/or tonsillitis, but not -4 A>G and -602 G>A.
Erkan AN et al.
International Journal of Pediatric Otorhinolaryngology, 2016
Low ficolin-2 levels in common variable immunodeficiency patients with bronchiectasis.
Metzger ML et al.
Clinical and Experimental Immunology, 2015
Multiple Infectious Complications in a Severely Injured Patient with Single Nucleotide Polymorphisms in Important Innate Immune Response Genes.
Bronkhorst MW et al.
The Open Orthopaedics Journal, 2015
Association of the FCN2 Gene Single Nucleotide Polymorphisms with Susceptibility to Pulmonary Tuberculosis.
Xu DD et al.
Plos One, 2015
Mannose-binding lectin-2 and ficolin-2 gene polymorphisms and clinical risk factors for acute rejection in kidney transplantation.
Wu X et al.
Transplant Immunology, 2014
Risk of infection and sepsis in severely injured patients related to single nucleotide polymorphisms in the lectin pathway.
Bronkhorst MW et al.
The British Journal of Surgery, 2013
Mannose-binding lectin 2 and ficolin-2 gene polymorphisms influence the susceptibility to bloodstream infections in kidney transplant recipients.
Wan QQ et al.
Transplantation Proceedings, 2013
Genetic variants of complement genes ficolin-2, mannose-binding lectin and complement factor H are associated with leprosy in Han Chinese from Southwest China.
Zhang DF et al.
Human Genetics, 2013
Cost-effective procedures for genotyping of human FCN2 gene single nucleotide polymorphisms.
Szala A et al.
Immunogenetics, 2013
Association of L-ficolin levels and FCN2 genotypes with chronic Chagas disease.
Luz PR et al.
Plos One, 2013
The functional polymorphism Ala258Ser in the innate receptor gene ficolin-2 in the donor predicts improved renal transplant outcome.
Eikmans M et al.
Transplantation, 2012
Ficolin-2 levels and FCN2 genetic polymorphisms as a susceptibility factor in schistosomiasis.
Ouf EA et al.
The Journal of Infectious Diseases, 2012
Reliable and rapid characterization of functional FCN2 gene variants reveals diverse geographical patterns.
Ojurongbe O et al.
Bmc Medical Genetics, 2012
Ficolin-2 levels and genetic polymorphisms of FCN2 in malaria.
Faik I et al.
Human Immunology, 2011
Ficolin-2 levels and FCN2 haplotypes influence hepatitis B infection outcome in Vietnamese patients.
Hoang TV et al.
Plos One, 2011
Leprosy and the human genome.
Misch EA et al.
Microbiology and Molecular Biology Reviews : Mmbr, 2010
MBL2, FCN1, FCN2 and FCN3-The genes behind the initiation of the lectin pathway of complement.
Garred P et al.
Molecular Immunology, 2009
Exploring the role of polymorphisms in ficolin genes in respiratory tract infections in children.
Ruskamp JM et al.
Clinical and Experimental Immunology, 2009
Host genetic susceptibility to pneumococcal and meningococcal disease: a systematic review and meta-analysis.
Brouwer MC et al.
The Lancet. Infectious Diseases, 2009
Functional SNPs in the human ficolin (FCN) genes reveal distinct geographical patterns.
Hummelshøj T et al.
Molecular Immunology, 2008
Extremes of L-ficolin concentration in children with recurrent infections are associated with single nucleotide polymorphisms in the FCN2 gene.
Cedzynski M et al.
Clinical and Experimental Immunology, 2007
Functional polymorphisms in the FCN2 gene are not associated with invasive pneumococcal disease.
Chapman SJ et al.
Molecular Immunology, 2007
Coding and non-coding polymorphisms in the lectin pathway activator L-ficolin gene in 188 Dutch blood bank donors.
Herpers BL et al.
Molecular Immunology, 2006
Polymorphisms in the FCN2 gene determine serum variation and function of Ficolin-2.
Hummelshoj T et al.
Human Molecular Genetics, 2005