Show
Sort by
-
- Journal Article
- A2
- open access
The landscape of drug resistance in Plasmodium falciparum malaria in the Democratic Republic of Congo : a mapping systematic review
-
Chapter 2 : host polymorphisms and COVID-19 infection
-
A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis
-
The effect of polymorphisms in FSHR gene on late follicular phase progesterone and estradiol serum levels in predicted normoresponders
-
Is monitoring of antiplatelet therapy by light transmission aggregometry dependent on instrument and reagent used?
-
The effect of polymorphisms in FSHR and FSHB genes on ovarian response : a prospective multicenter multinational study in Europe and Asia
-
Personalized proteome : comparing proteogenomics and open variant search approaches for single amino acid variant detection
-
Evaluation of the usefulness of intermittent preventive treatment of malaria in pregnancy with sulfadoxine-pyrimethamine in a context with increased resistance of Plasmodium falciparum in Kingasani Hospital, Kinshasa in the Democratic Republic of Congo
-
- Journal Article
- A1
- open access
A randomized phase II study comparing the efficacy and safety of the glyco-optimized anti-EGFR antibody tomuzotuximab against cetuximab in patients with recurrent and/or metastatic squamous cell cancer of the head and neck : the RESGEX study
-
ADRB2 haplotypes and asthma exacerbations in children and young adults : an individual participant data meta-analysis
-
Population pharmacokinetics and pharmacogenetics of ritonavir-boosted darunavir in the presence of raltegravir or tenofovir disoproxil fumarate/emtricitabine in HIV-infected adults and the relationship with virological response : a sub-study of the NEAT001/ANRS143 randomized trial
-
- Journal Article
- A1
- open access
Response to IL‐17A inhibitors secukinumab and ixekizumab cannot be explained by genetic variation in the protein‐coding and untranslated regions of the IL‐17A gene : results from a multicentre study of four European psoriasis cohorts
-
- Journal Article
- A1
- open access
Cost-effective and robust genotyping using double-mismatch allele-specific quantitative PCR
-
- Journal Article
- A2
- open access
Genetic biomarkers in the VEGF pathway predicting response to anti-VEGF therapy in age-related macular degeneration
-
A new approach for modeling patient overall radiosensitivity and predicting multiple toxicity endpoints for breast cancer patients
-
- Journal Article
- A1
- open access
Biallelic and monoallelic ESR2 variants associated with 46,XY disorders of sex development
-
A simple colorimetric assay for measuring fructosamine 3 kinase activity
-
Complete overview of protein-inactivating sequence variations in 36 sequenced mouse inbred strains
(2017) PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 114(34). p.9158-9163 -
Genome-wide association study on the FEV1/FVC ratio in never-smokers identifies HHIP and FAM13A
-
Genome-wide copy number variation scan identifies complement component C4 as novel susceptibility gene for Crohn's disease
-
- Journal Article
- A1
- open access
Chromosomal radiosensitivity of human immunodeficiency virus positive/negative cervical cancer patients in South Africa
-
No clinical utility of KRAS variant rs61764370 for ovarian or breast cancer
-
Androgen-sensitive hypertension associated with soluble guanylate cyclase-α₁ deficiency is mediated by 20-HETE
-
- Journal Article
- A1
- open access
GWAS analysis of handgrip and lower body strength in older adults in the CHARGE consortium
-
- Journal Article
- A1
- open access
Protocadherin-1 localization and cell-adhesion function in airway epithelial cells in asthma
-
Somatic cell count and milk neutrophil viability of dairy heifers with specific CXCR1 genotypes following experimental intramammary infection with Staphylococcus chromogenes originating from milk
-
- Journal Article
- A1
- open access
Differential expression of CXCR1 and commonly used reference genes in bovine milk somatic cells following experimental intramammary challenge
-
- Journal Article
- A1
- open access
Reactive oxygen species generation by bovine blood neutrophils with different CXCR1 (IL8RA) genotype following Interleukin-8 incubation
-
- Journal Article
- A1
- open access
Migration and interaction in a contact zone: mtDNA variation among Bantu-speakers in Southern Africa
-
- Journal Article
- A1
- open access
Factors modifying the risk for developing acute skin toxicity after whole-breast intensity modulated radiotherapy
-
- Journal Article
- A1
- open access
Kinetics of leptin binding to the Q223R leptin receptor
-
The effect of enterotoxigenic Escherichia coli F4ab,ac on early-weaned piglets: a gene expression study
-
High resolution melting analysis as a rapid and highly sensitive method for Cichorium plasmotype characterization
-
Acute radiation-induced nocturia in prostate cancer patients is associated with pretreatment symptoms, radical prostatectomy, and genetic markers in the TGFβ1 gene
-
A predictive model for dysphagia following IMRT for head and neck cancer: introduction of the EMLasso technique
-
Investigating the genetic association between ERAP1 and spondyloarthritis
-
Ribosomal protein SA and its pseudogenes in ruminants : an extremely conserved gene family
-
Polymorphisms in the lectin pathway genes as a possible cause of early chronic Pseudomonas aeruginosa colonization in cystic fibrosis patients
-
17q24.2 microdeletions: a new syndromal entity with intellectual disability, truncal obesity, mood swings and hallucinations
-
Combined FAM-labeled TaqMan probe detection and SYBR green I melting curve analysis in multiprobe qPCR genotyping assays
-
No association between TGF-β1 polymorphisms and radiation-induced lung toxicity in a European cohort of lung cancer patients
-
- Journal Article
- A1
- open access
Evidence for local dendritic cell activation in pulmonary sarcoidosis
-
Persistent glucose transporter expression on pancreatic beta cells from longstanding type 1 diabetic individuals
-
Genome-wide association and large-scale follow up identifies 16 new loci influencing lung function
-
Anti-NMDA-receptor encephalitis in a 3 year old patient with chromosome 6p21.32 microdeletion including the HLA cluster
-
Confirmation of association of the macrophage migration inhibitory factor gene with systemic sclerosis in a large European population
-
A multiplex microsatellite marker kit for diversity assessment of large cassava (Manihot esculenta Crantz) germplasm collections
-
Association analysis of PPARGC1A mutations with meat quality parameters in a commercial hybrid pig population
-
Parsing the effects of individual SNPs in candidate genes with family data
-
Association of TGFβ1 polymorphisms involved in radiation toxicity with TGFβ1 secretion in vitro
-
Analysis of the high affinity IgE receptor genes reveals epistatic effects of FCER1A variants on eczema risk
-
Prediction of late normal tissue complications in RT treated gynaecological cancer patients: potential of the γ-H2AX foci assay and association with chromosomal radiosensitivity
-
An illegitimate microRNA target site within the 3' UTR of MDM4 affects ovarian cancer progression and chemosensitivity
-
How neuroscience and behavioral genetics improve psychiatric assessment: report on a violent murder case
-
Evaluation of a candidate breast cancer associated SNP in ERCC4 as a risk modifier in BRCA1 and BRCA2 mutation carriers. Results from the Consortium of Investigators of Modifiers of BRCA1/BRCA2 (CIMBA)
-
Variations in HSP70 genes associated with noise-induced hearing loss in two independent populations
-
Acute normal tissue reactions in head-and-neck cancer patients treated with IMRT: influence of dose and association with genetic polymorphisms in DNA DSB repair genes
-
Complete genomic sequence of the goat prion protein gene (PRNP)
-
Matrix Metalloproteinase 12, Asthma, and COPD
-
Genotyping of Frequent BRCA1/2 SNPs with Unlabeled Probes A Supplement to HRMCA Mutation Scanning, Allowing the Strong Reduction of Sequencing Burden
-
Response to serotonin reuptake inhibitors in OCD is not influenced by common CYP2D6 polymorphisms
-
Inherited traits affecting platelet function
-
Acute kidney injury in the intensive care unit: it's the gene, stupid!
-
Polymorphisms in base-excision repair and nucleotide-excision repair genes in relation to lung cancer risk
-
Association between variations in CAT and noise-induced hearing loss in two independent noise-exposed populations
-
Glucocorticoid receptor gene-based SNP analysis in patients with recurrent major depression
-
Role of mannose-binding lectin (MBL2) genotyping in predicting the risk of recurrent otitis media (ROM)
-
Postglacial migration of Populus nigra L.: lessons learnt from chloroplast DNA
-
The influence of genetic variation in oxidative stress genes on human noise susceptibility
-
Ex-situ conservation of Black poplar in Europe : genetic diversity in nine gene bank collections and their value for nature development
-
Polymorphisms in the prion protein gene and in the doppel gene increase susceptibility for Creutzfeldt-Jakob disease
-
Introducing the multivariate dale model in population-based genetic association studies
-
Three unrelated individuals with perinatally lethal osteogenesis imperfecta resulting from identical glycine 502 serine substitutions in the α2 chain of type I collagen