Riet De Rycke
- Work address
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Proeftuinstraat 86, N1
9000 Gent - Riet.DeRycke@UGent.be
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Functional characterization of the first missense variant in CEP78 , a founder allele associated with cone‐rod dystrophy, hearing loss and reduced male fertility
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- Journal Article
- A1
- open access
Functional characterization of novel MFSD8 pathogenic variants anticipates neurological involvement in juvenile isolated maculopathy
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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
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Improved label-free identification of individual exosome-like vesicles with Au@Ag nanoparticles as SERS substrate
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Myhre syndrome : a first familial recurrence and broadening of the phenotypic spectrum
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- Journal Article
- A1
- open access
Defining the clinical, molecular and ultrastructural characteristics in occipital horn syndrome : two new cases and review of the literature
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Leveraging the low-dispersion COBALT/ARIS ablation system for multi-megapixel 3D images of single cells
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Striking effect of polymer end-group on C60 nanoparticle formation by high shear vibrational milling with alkyne-functionalized poly(2-oxazoline)s
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Bi-allelic AEBP1 mutations in two patients with Ehlers-Danlos syndrome
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Disruption of endocytosis through chemical inhibition of clathrin heavy chain function