Riet De Rycke
Show
Sort by
-
- Journal Article
- A1
- open access
Cellular requirements for PIN polar cargo clustering in Arabidopsis thaliana
-
Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome
-
- Journal Article
- A1
- open access
Enhanced siRNA delivery and selective apoptosis induction in H1299 cancer cells by layer-by-layer-assembled Se nanocomplexes : toward more efficient cancer therapy
-
- Journal Article
- A1
- open access
Layer by layer assembled chitosan-coated gold nanoparticles for enhanced siRNA delivery and silencing
-
Nanoparticle-sensitized photoporation enables inflammasome activation studies in targeted single cells dagger
-
- Journal Article
- A1
- open access
Involvement of the choroid plexus in the pathogenesis of Niemann-Pick disease type C
-
- Journal Article
- A1
- open access
Importance of extracellular vesicle secretion at the blood-cerebrospinal fluid interface in the pathogenesis of Alzheimer’s disease
-
Mutations in LTBP1 cause autosomal recessive cutis laxa syndrome
-
Mutations in ATP6V1E1 or ATP6V1A cause autosomal-recessive cutis laxa (vol 100, pg 216, 2017)
-
Effect of sample preparation techniques upon single cell chemical imaging : a practical comparison between Synchrotron Radiation based X-ray Fluorescence (SR-XRF) and Nanoscopic Secondary Ion Mass Spectrometry (nano-SIMS)
-
- Journal Article
- A1
- open access
Zinc inhibits lethal inflammatory shock by preventing microbe-induced interferon signature in intestinal epithelium
-
- Journal Article
- A1
- open access
Comparison between Apicystis cryptica sp. n. and Apicystis bombi (Arthrogregarida, Apicomplexa): Gregarine parasites that cause fat body hypertrophism in bees
-
- Journal Article
- A1
- open access
A study of carry-over and histopathological effects after chronic dietary intake of citrinin in pigs, broiler chickens and laying hens
-
- Journal Article
- A1
- open access
Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy
-
Novel defects in collagen XII and VI expand the mixed myopathy/Ehlers-Danlos syndrome spectrum and lead to variant-specific alterations in the extracellular matrix