Onderzoeker
Sarah Delbaere
- Trefwoorden:biotechnologie, biomedische, proefdieren, genetica, zebravis, biochemie
- Disciplines:Genetica, Cellulaire interacties en extracellulaire matrix, Ontwikkelingsbiologie, Klinische genetica en moleculaire diagnostiek, Biologie van gewervelden, Dierlijke ontwikkelings- en reproductieve biologie, Dierlijke genetica, Ontwikkelingsgenetica
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf1 okt 2018 → 20 sep 2020 - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 sep 2015 → 30 sep 2018
Publicaties
1 - 10 van 12
- Alterations in glycosaminoglycan biosynthesis associated with the Ehlers-Danlos syndromes(2022)
Auteurs: Sarah Delbaere, Catherine Bui, Göran Larson, Shuji Mizumoto, Tomoki Kosho, Sylvie Fournel-Gigleux, Fransiska Malfait
Pagina's: C1843 - C1859 - Hypomorphic zebrafish models mimic the musculoskeletal phenotype of β4GalT7-deficient Ehlers-Danlos syndrome(2020)
Auteurs: Sarah Delbaere, Tim Van Damme, Delfien Syx, Sofie Symoens, Paul Coucke, Andy Willaert, Fransiska Malfait
Pagina's: 59 - 75 - 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(2020)
Auteurs: Sarah Delbaere, Tibbe Dhooge, Florence Petit, Nathalie Goemans, Anne Destrée, Olivier Vanakker, Fransiska Malfait
Pagina's: 112 - 123 - b3galt6 Knock-out zebrafish recapitulate β3GalT6-deficiency disorders in human and reveal a trisaccharide proteoglycan linkage region(2020)
Auteurs: Sarah Delbaere, Adelbert De Clercq, Shuji Mizumoto, Fredrik Noborn, Jan Willem Bek, Charlotte Gistelinck, Delfien Syx, Phil L. Salmon, Paul Coucke, Göran Larson, et al.
- Fishing for pathogenic mechanisms underlying rare Ehlers-Danlos syndrome subtypes(2020)
Auteurs: Sarah Delbaere
- Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type(2018)
Auteurs: Sarah Delbaere, Phil L Salmon, Fransiska Malfait
Aantal pagina's: 1 - Zebrafish modeling for spondylodysplastic Ehlers-Danlos syndrome, the B4GALT7 type : mimicking the human hypomorphic phenotype in a validated knock-down model(2018)
Auteurs: Sarah Delbaere, Tim Van Damme, Fransiska Malfait
Aantal pagina's: 1 - Knockdown and knockout zebrafish models for the β4GalT7-deficient type of Ehlers-Danlos syndrome reveal distinctive and overlapping phenotypic features(2018)
Auteurs: Sarah Delbaere, Tim Van Damme, Delfien Syx, Sofie Symoens, Andy Willaert, Fransiska Malfait
Aantal pagina's: 1 - Loss of galactosyltransferase II, encoded by B3GALT6, causes skeletal abnormalities in a zebrafish model for spondylodysplastic Ehlers-Danlos syndrome, the B3GALT6 type(2018)
Auteurs: Sarah Delbaere, Phil L Salmon, Fransiska Malfait
Aantal pagina's: 1 - Myopathic Ehlers-Danlos syndrome : expanding the clinical and mutational spectrum with five new families(2018)
Auteurs: Tibbe Dhooge, Sarah Delbaere, Fransiska Malfait
Aantal pagina's: 1