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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
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A lipid nanoparticle platform for mRNA delivery through repurposing of cationic amphiphilic drugs
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KIL1 terminates fertility in maize by controlling silk senescence
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Knockout of RSN1, TVP18 or CSC1-2 causes perturbation of Golgi cisternae in Pichia pastoris
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Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome (vol 108, pg 1095, 2021)
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Macrophages are metabolically heterogeneous within the tumor microenvironment
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Cellular requirements for PIN polar cargo clustering in Arabidopsis thaliana
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Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome
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Enhanced siRNA delivery and selective apoptosis induction in H1299 cancer cells by layer-by-layer-assembled Se nanocomplexes : toward more efficient cancer therapy
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Layer by layer assembled chitosan-coated gold nanoparticles for enhanced siRNA delivery and silencing
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Nanoparticle-sensitized photoporation enables inflammasome activation studies in targeted single cells dagger
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Involvement of the choroid plexus in the pathogenesis of Niemann-Pick disease type C