Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease

Title Publication Date Language Citations
Rhythm gene PER1 mediates ferroptosis and lipid metabolism through SREBF2/ALOX15 axis in polycystic ovary syndrome2024/04/01English
Pre-eclamptic foetal programming predisposes offspring to hepatic steatosis via DNA methylation2024/04/01English
Calcium signaling induces partial EMT and renal fibrosis in a Wnt4 knock-in mouse model2024/04/01English
Decorin suppresses stemness and migration potential of malignant peripheral nerve sheath tumor through inhibiting epidermal growth factor receptor signalingEnglish
The IRE1α-XBP1 arm of the unfolded protein response is a host factor activated in SARS-CoV-2 infectionEnglish
miR-519a-3p, found to regulate cellular prion protein during Alzheimer's disease pathogenesis, as a biomarker of asymptomatic stagesEnglish
Mechano-sensor Piezo1 inhibits glucagon production in pancreatic α-cellsEnglish
Hippo pathway activated by circulating reactive oxygen species mediates cardiac diastolic dysfunction after acute kidney injury2024/04/01English
Therapeutic benefits of central LH receptor agonism in the APP/PS1 AD model involve trophic and immune regulation and reproductive status dependent2024/04/01English
CPEB2 inhibits preeclampsia progression by regulating SSTR3 translation through polyadenylation2024/04/01English
Targeting JUNB to modulate M2 macrophage polarization in preeclampsia2024/04/01English
Pan-neuronal expression of human mutant SOD1 in Drosophila impairs survival and motor performance, induces early neuroinflammation and chromosome aberrationsEnglish
High phosphate and calcium induce osteoblastic phenotype switching and calcification of corneal epithelial cells in a Runx2-dependent and synergistic manner; a possible mechanism of chronic kidney disease-associated corneal calcificationEnglish
Caveolin-2 palmitoylation turnover facilitates insulin receptor substrate-1-directed lipid metabolism by insulin receptor tyrosine kinaseEnglish
Tcf4 dysfunction alters dorsal and ventral cortical neurogenesis in Pitt-Hopkins syndrome mouse model showing sexual dimorphismEnglish
Molecular and cellular consequences of mevalonate kinase deficiencyEnglish
Similar metabolic pathways are affected in both Congenital Myasthenic Syndrome-22 and Prader-Willi SyndromeEnglish
Caldesmon and heat shock protein 20 phosphorylation in nitroglycerin- and magnesium-induced relaxation of swine carotid artery2000/03/01English
Protective effects of 5,6,7,8-tetrahydroneopterin against X-ray radiation injury in mice1999/03/01English
Biochemical and molecular study of mentally retarded patient with partial deficiency of hypoxanthine-guanine phosphoribosyltransferase2002/05/01English
The mechanism of inhibition of β-oxidation by aspirin metabolites in skin fibroblasts from Reye’s syndrome patients and controls1999/05/01English
Lipopolysaccharide-induced increase in plasma nitrotyrosine concentrations in rats1997/11/01English
Quantitative analysis of mitochondrial DNA deletion in paraffin embedded muscle tissues from patients with KSS and CPEO1997/05/01English
Oleic and linoleic acids promote chondrocyte apoptosis by inhibiting autophagy via downregulation of SIRT1/FOXO1 signaling2024/04/01English
Accumulation of neutral lipids in dystrophic neurites surrounding amyloid plaques in Alzheimer's disease2024/04/01English
GDI2 deletion alleviates neurodegeneration and memory loss in the 5xFAD mice model of Alzheimer's disease2024/04/01English
Terminal glycosylation in cystic fibrosis1999/10/01English
Antimycin resistance and ubiquinol cytochrome c reductase instability associated with a human cytochrome b mutation1996/12/01English
Kelley-Seegmiller syndrome due to a unique variant of hypoxanthine-guanine phosphoribosyltransferase: reduced affinity for 5-phosphoribosyl-1-pyrophosphate manifested only at low, physiological substrate concentrations2000/02/01English
Expression and intracellular processing of chimeric and mutant CFTR molecules11This work is dedicated to the memory of the late pediatrician R. Van Geffel who pioneered the treatment of CF children in Belgium.2000/01/01English