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Management of type 2 diabetes mellitus in older adults : eight case studies with focus SGLT-2 inhibitors and metformin
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- Journal Article
- A1
- open access
Clinical implementation of RNA sequencing for Mendelian disease diagnostics
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- Journal Article
- A1
- open access
Clinical heterogeneity in MT-ATP6 pathogenic variants : same genotype—different onset
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Clinical and molecular features of 66 patients with musculocontractural Ehlers−Danlos syndrome caused by pathogenic variants in CHST14 (mcEDS-CHST14)
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- Journal Article
- A1
- open access
Persistent hypercobalaminemia three months after successful gradual attenuation of extrahepatic shunts in dogs: a prospective cohort study
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- Miscellaneous
- open access
Editorial : micronutrients : the borderline between their beneficial role and toxicity in plants
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- Journal Article
- A1
- open access
The role of albumin and the extracellular matrix on the pathophysiology of oedema formation in severe malnutrition
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- Journal Article
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- open access
Whole genome duplication of wild-type and CINNAMYL ALCOHOL DEHYDROGENASE1-downregulated hybrid poplar reduces biomass yield and causes a brittle apex phenotype in field-grown wild types
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Soybean response and profitability upon inoculation and nitrogen fertilisation in Belgium
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- Journal Article
- A1
- open access
Dietary resistant starch alleviates Escherichia coli-induced bone loss in meat ducks by promoting short-chain fatty acid production and inhibiting Malt1/NF-kappa B inflammasome activation
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- Journal Article
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- open access
ADAR1 prevents autoinflammation by suppressing spontaneous ZBP1 activation
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Timing of blood sampling for butyrylcholinesterase phenotyping in patients with prolonged neuromuscular block after mivacurium or suxamethonium
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- Journal Article
- A1
- open access
Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta
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- Journal Article
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- open access
Vitamin D and lung outcomes in elderly COVID-19 patients
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- Journal Article
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- open access
Approach to the virilizing girl at puberty
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- Journal Article
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- open access
The hepatocyte IKK:NF-kB axis promotes liver steatosis by stimulating de novo lipogenesis and cholesterol synthesis
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IGF1 haploinsufficiency in children with short stature : a case series
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- Journal Article
- A1
- open access
Metabolic engineering provides insight into the regulation of thiamin biosynthesis in plants
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Dissecting the facts about the impact of contaminant iron in human nutrition : a review
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- Journal Article
- A1
- open access
Long-term environmental hypoxia exposure and haematopoietic prolyl hydroxylase-1 deletion do not impact experimental Crohn's like ileitis
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The influence of the genetic background of the host on vitamin D deficiency in children with COVID-19
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A case of clubbed down syndrome in broilers
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- Journal Article
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- open access
Course and survival of COVID-19 patients with comorbidities in relation to the trace element status at hospital admission
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- Journal Article
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- open access
A novel non-coding variant in DCLRE1C results in deregulated splicing and induces SCID through the generation of a truncated ARTEMIS protein that fails to support V(D)J recombination and DNA damage repair
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- Journal Article
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- open access
ADAR1 interaction with Z-RNA promotes editing of endogenous double-stranded RNA and prevents MDA5-dependent immune activation
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- Journal Article
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- open access
A mutation in DNA polymerase α rescues WEE1KO sensitivity to HU
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- Journal Article
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- open access
Interplay between the EMT transcription factors ZEB1 and ZEB2 regulates hematopoietic stem and progenitor cell differentiation and hematopoietic lineage fidelity
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Diagnostic muscle biopsies in the era of genetics : the added value of myopathology in a selection of limb-girdle muscular dystrophy patients
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Association of unbalanced translocation der(1;7) with germline GATA2 mutations
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- Journal Article
- A1
- open access
Inborn errors of type I IFN immunity in patients with life-threatening COVID-19
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Contribution of rare and predicted pathogenic gene variants to childhood-onset lupus : a large, genetic panel analysis of British and French cohorts
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DNGR1-Cre-mediated deletion of Tnfaip3/A20 in conventional dendritic cells induces pulmonary hypertension in mice
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Biochemical thresholds for pathological presentation of ATP synthase deficiencies
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- Journal Article
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- open access
Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathy
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- Journal Article
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- open access
Three-dimensional correction of fibular hemimelia using a computer-assisted planning : technical report and literature review
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- Journal Article
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- open access
Respiratory Syncytial Virus infection promotes necroptosis and HMGB1 release by airway epithelial cells
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- Journal Article
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- open access
Long-term MALT1 inhibition in adult mice without severe systemic autoimmunity
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Estrogen receptor alpha signaling in extrahypothalamic neurons during late puberty decreases bone size and strength in female but not in male mice
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A century-old mystery unveiled : Sekizaisou is a natural lignin mutant
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- Journal Article
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- open access
Two distinct ubiquitin-binding motifs in A20 mediate its anti-inflammatory and cell-protective activities
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- Journal Article
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- open access
Selenium deficiency risk in central Kenya highlands : an assessment from the soil to the body
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- Journal Article
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- open access
Urinary amine and organic acid metabolites evaluated as markers for childhood aggression : the ACTION biomarker study
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Crtap and p3h1 knock out zebrafish support defective collagen chaperoning as the cause of their osteogenesis imperfecta phenotype
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- Journal Article
- A2
- open access
Exercise-induce hyperalgesia, complement system and elastase activation in myalgic encephalomyelitis/chronic fatigue syndrome : a secondary analysis of experimental comparative studies
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Enhancement of co-production of nutritional protein and carotenoids in Dunaliella salina using a two-phase cultivation assisted by nitrogen level and light intensity
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Single-cell RNA sequencing of the T helper cell response to house dust mites defines a distinct gene expression signature in airway Th2 cells
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Long-term results of the Delta Xtend reverse shoulder prosthesis
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- Journal Article
- A1
- open access
Hepatic symptoms and histology in 13 patients with a Zellweger spectrum disorder
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A20 prevents inflammasome-dependent arthritis by inhibiting macrophage necroptosis through its ZnF7 ubiquitin-binding domain
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Targeting filamin A reduces macrophage activity and atherosclerosis
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Low serum IgA and airway injury in World Trade Center-exposed firefighters : a 17-year longitudinal study
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- Journal Article
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- open access
Mepazine inhibits RANK-induced osteoclastogenesis independent of its MALT1 inhibitory function
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- Journal Article
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- open access
Nanoscopic X-ray fluorescence imaging and quantification of intracellular key-elements in cryofrozen Friedreich's ataxia fibroblasts
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- Journal Article
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Current understanding and future research priorities in malignancy associated with inborn errors of immunity and DNA repair disorders : the perspective of an interdisciplinary working group
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Pathogenic variants in the ABCC6 gene are associated with an increased risk for ischemic stroke
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Clinical and genetic predictors of atypical hemolytic uremic syndrome phenotype and outcome
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- Journal Article
- A1
- open access
LPCAT1 controls phosphate homeostasis in a zinc-dependent manner
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- Journal Article
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- open access
Ikaros family zinc finger 1 regulates dendritic cell development and function in humans
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Role of glutamine synthetase in angiogenesis beyond glutamine synthesis
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Bariatric surgery does not appear to affect women's breast-milk composition
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- Journal Article
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- open access
A CARD9 founder mutation disrupts NF-κB signaling by inhibiting BCL10 and MALT1 recruitment and signalosome formation
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A novel LPS-responsive beige-like anchor protein (LRBA) mutation presents with normal cytotoxic T lymphocyte-associated protein 4 (CTLA-4) and overactive TH17 immunity
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Germline gain-of-function myeloid differentiation primary response gene-88 (MYD88) mutation in a child with severe arthritis
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- Journal Article
- A1
- open access
Associations between insulin resistance and three B-vitamins in European adolescents : the HELENA study = Asociaciones entre la resistencia a la insulina y tres vitaminas del grupo B en adolescentes europeos : el estudio HELENA
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A20 deletion in T cells modulates acute graft-versus-host disease in mice
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Heme oxygenase activity and heme binding in a neonatal mouse model
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Cellular redox profiling using high-content microscopy
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- Journal Article
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- open access
Severe congenital microcephaly with AP4M1 mutation, a case report
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- Journal Article
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- open access
Dietary practices in propionic acidemia : a European survey
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- Journal Article
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- open access
Staple crops biofortified with increased vitamins and minerals : considerations for a public health strategy
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- Journal Article
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A critical assessment of the therapeutic potential of resveratrol supplements for treating mitochondrial disorders
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International forum : an investigation of iron status in blood donors
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Mutations in CDC45, encoding an essential component of the pre-initiation complex, cause Meier-Gorlin syndrome and craniosynostosis
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- Journal Article
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- open access
AURORA : bariatric surgery registration in women of reproductive age : a multicenter prospective cohort study
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The role of vitamin K in vascular calcification of patients with chronic kidney disease
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- Journal Article
- A1
- open access
Wars2 is a determinant of angiogenesis
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International forum regarding practices related to donor haemoglobin and iron
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Prevalence, clinical characteristics and prognosis of GATA2-related myelodysplastic syndromes (MDS) in children and adolescents
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Development and validation of a small single-domain antibody that effectively inhibits matrix metalloproteinase 8
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ALG1-CDG: clinical and molecular characterization of 39 unreported patients
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- Journal Article
- A1
- open access
Biomarkers of selenium status in dogs
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Colour vision in Stargardt disease
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- Journal Article
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- open access
Mutations in the mitochondrial cysteinyl-tRNA synthase gene, CARS2, lead to a severe epileptic encephalopathy and complex movement disorder
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The androgen receptor has no direct antiresorptive actions in mouse osteoclasts
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Impact of a trace element supplementation programme on health and performance of cross-breed (Bos indicus x Bos taurus) dairy cattle under tropical farming conditions: a double-blinded randomized field trial
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- Journal Article
- A1
- open access
Iodine status of young Burkinabe children receiving small-quantity lipid-based nutrient supplements and iodised salt : a cluster-randomised trial
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- Journal Article
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- open access
Leptin's metabolic and immune functions can be uncoupled at the ligand/receptor interaction level
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XEDAR activates the non-canonical NF-κB pathway
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- Journal Article
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- open access
Citrulline supplementation improves organ perfusion and arginine availability under conditions with enhanced arginase activity
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- Journal Article
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- open access
Botpathologie bij apen van de Nieuwe en Oude Wereld
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MAT2A Mutations predispose individuals to thoracic aortic aneurysms
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy
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Present and future of folate biofortification of crop plants
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- Journal Article
- A1
- open access
Gelokaliseerde steatitis als complicatie na dystokie bij een merrie
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A disparate trace element metabolism in zebu (Bos indicus) and crossbred (Bos indicus × Bos taurus) cattle in response to a copper-deficient diet
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The tumor necrosis factor alpha-induced protein 3 (TNFAIP3, A20) imposes a brake on antitumor activity of CD8 T cells
(2014) PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA. 111(30). p.11115-11120 -
Proton-pump inhibitors do not influence serum magnesium levels in renal transplant recipients
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes severe myopathy and encephalopathy
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Effects of trace element supplementation on apparent nutrient digestibility and utilisation in grass-fed zebu (Bos indicus) cattle
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Complement factor H functional assay may help to monitor atypical haemolytic uraemic syndrome : a pilot study