about
Cooperation of the Cockayne syndrome group B protein and poly(ADP-ribose) polymerase 1 in the response to oxidative stress.Differential requirement for the ATPase domain of the Cockayne syndrome group B gene in the processing of UV-induced DNA damage and 8-oxoguanine lesions in human cells.Cell-free DNA in pregnancy with choriocarcinoma and coexistent live fetus: A case report.Functional IRF3 deficiency in a patient with herpes simplex encephalitis.XIAP deficiency and MEFV variants resulting in an autoinflammatory lymphoproliferative syndrome.Mutations in the TLR3 signaling pathway and beyond in adult patients with herpes simplex encephalitis.Ectodermal dysplasia with immunodeficiency caused by a branch-point mutation in IKBKG/NEMO.CBFA1 and topoisomerase I mRNA levels decline during cellular aging of human trabecular osteoblasts.A STAT1-gain-of-function mutation causing Th17 deficiency with chronic mucocutaneous candidiasis, psoriasiform hyperkeratosis and dermatophytosis.Report of the first nationally implemented clinical routine screening for fetal RHD in D- pregnant women to ascertain the requirement for antenatal RhD prophylaxis.Routine noninvasive prenatal screening for fetal RHD in plasma of RhD-negative pregnant women-2 years of screening experience from Denmark.Frequently used bioinformatics tools overestimate the damaging effect of allelic variants.The influence of HLA-types on disease progression among HIV-2 infected patients in Guinea-Bissau.Protein a Immunoadsorption May Hamper the Decision to Transplant Due to Interference With CDC Crossmatch Results.Vox Sanguinis International Forum on application of fetal blood grouping: summary.Vox Sanguinis International Forum on application of fetal blood grouping.Discovery of a novel HLA-B*15 allele, HLA-B*15:379, in a patient from Guinea-Bissau.Defective RNA sensing by RIG-I in severe influenza virus infection.Assessing a single targeted next generation sequencing for human leukocyte antigen typing protocol for interoperability, as performed by users with variable experience.RHD positive among C/E+ and D- blood donors in Denmark.The Cockayne syndrome group B protein is a functional dimer.Phylogeny of human T-lymphotropic virus-1 subtypes in Guinea-Bissau.The challenge of discriminating between HIV-1, HIV-2 and HIV-1/2 dual infections.Mutations in RNA Polymerase III genes and defective DNA sensing in adults with varicella-zoster virus CNS infection.The genetic component of preeclampsia: A whole-exome sequencing study.Whole Exome Sequencing of HIV-1 long-term non-progressors identifies rare variants in genes encoding innate immune sensors and signaling moleculesVaricella-zoster virus CNS vasculitis and RNA polymerase III gene mutation in identical twinsGene-specific DNA repair of pyrimidine dimers does not decline during cellular aging in vitroNeonatal-onset T(-)B(-)NK(+) severe combined immunodeficiency and neutropenia caused by mutated phosphoglucomutase 3Identification of Novel Genetic Variants in CVID Patients With Autoimmunity, Autoinflammation, or MalignancyHLA-DQB1*06:276, a novel HLA allele fund in a patient from Guinea-BissauTwo novel HLA-B alleles, HLA-B*53:01:17 and -B*58:83, found in patients from Guinea-BissauHTLV infected individuals have increased B-cell activation and proinflammatory regulatory T-cellsImpaired immune responses to herpesviruses and microbial ligands in patients with MonoMACAutoinflammatory disease with corneal and mucosal dyskeratosis caused by a novel NLRP1 variantHost Genetics, Innate Immune Responses, and Cellular Death Pathways in Poliomyelitis PatientsPattern Recognition Molecules of the Lectin Pathway-Screening of Patients with Suspected ImmunodeficiencyDiscriminatory rapid tests cause HIV-type misclassification-evaluation of three rapid tests using clinical samples from Guinea-BissauDefective interferon priming and impaired antiviral responses in a patient with an IRF7 variant and severe influenzaAutosomal Dominant Hyper-IgE Syndrome Without Significantly Elevated IgE
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description
researcher ORCID ID = 0000-0001-5158-3670
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wetenschapper
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name
Mette Christiansen
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Mette Christiansen
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Mette Christiansen
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Mette Christiansen
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type
label
Mette Christiansen
@ast
Mette Christiansen
@en
Mette Christiansen
@es
Mette Christiansen
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prefLabel
Mette Christiansen
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Mette Christiansen
@en
Mette Christiansen
@es
Mette Christiansen
@nl
P31
P496
0000-0001-5158-3670