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Selective Replacement of Cholesterol with Cationic Amphiphilic Drugs Enables the Design of Lipid Nanoparticles with Improved RNA Delivery
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Small heat shock proteins operate as molecular chaperones in the mitochondrial intermembrane space
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HSPB8 frameshift mutant aggregates weaken chaperone-assisted selective autophagy in neuromyopathies
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Endosperm cell death promoted by NAC transcription factors facilitates embryo invasion in Arabidopsis
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Syntaxin 18 defects in human and zebrafish unravel key roles in early cartilage and bone development
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Photothermal nanofibers enable macromolecule delivery in unstimulated human T cells
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GPIbα shedding in platelets is controlled by strict intracellular containment of both enzyme and substrate
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Autophagy promotes programmed cell death and corpse clearance in specific cell types of the Arabidopsis root cap
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Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndrome
(2022) EUROPEAN JOURNAL OF HUMAN GENETICS. In European Journal of Human Genetics 30(supplement 1). p.40-41 -
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EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis