Researcher
Sanne D'hondt
- Disciplines:Cellular interactions and extracellular matrix, Clinical genetics and molecular diagnostics, Dermatology, Genetics, Animal cell and molecular biology, Vascular diseases
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 15 Oct 2018 - Department of Pediatrics and medical genetics (Department)
Member
From17 Oct 2011 → 30 Sep 2018
Publications
1 - 7 of 7
- Aberrant binding of mutant HSP47 affects posttranslational modification of type I collagen and leads to osteogenesis imperfecta(2021)
Authors: Delfien Syx, Yoshihiro Ishikawa, Jan Gebauer, Sergei P. Boudko, Brecht Guillemyn, Tim Van Damme, Sanne D'hondt, Sofie Symoens, Sheela Nampoothiri, Douglas B. Gould, et al.
- Vascular phenotypes in nonvascular subtypes of the Ehlers-Danlos syndrome : a systematic review(2018)
Authors: Sanne D'hondt, Tim Van Damme, Fransiska Malfait
Pages: 562 - 573 - Type III collagen affects dermal and vascular collagen fibrillogenesis and tissue integrity in a mutant Col3a1 transgenic mouse model(2018)
Authors: Sanne D'hondt, Brecht Guillemyn, Leen Vanhoutte, Wendy Toussaint, Douglas R Keene, Yoshihiro Ishikawa, Hans Peter Bächinger, Mathieu Bertrand, Fransiska Malfait
Pages: 72 - 83 - Type III collagen : a major fibrillar collagen with major issues(2017)
Authors: Sanne D'hondt
- Genetic defects in TAPT1 disrupt ciliogenesis and cause a complex lethal osteochondrodysplasia(2015)
Authors: Aileen M Barnes, Charlotte Gistelinck, Fransiska Malfait, Brecht Guillemyn, Wouter Steyaert, Sanne D'hondt, Martine Biervliet, Paul Witten, Sergey Leikin, Elena Makareeva, et al.
Pages: 521 - 534 - Type III collagen is important for collagen fibrillogenesis and for dermal and cardiovascular development(2015)Volume: 23
Authors: Sanne D'hondt, Brecht Guillemyn, Sofie Symoens, Wendy Toussaint, Leen Vanhoutte, Riet De Rycke, Paul Coucke, Bart Lambrecht, Patrick Segers, Anne De Paepe, et al.
Pages: 110 - 110 - Deficiency for the ER-stress transducer OASIS causes severe recessive osteogenesis imperfecta in humans(2013)
Authors: Fransiska Malfait, Sanne D'hondt, Bert Callewaert, Annelies Dheedene, Wouter Steyaert, Hans Peter Bächinger, Hulya Kayserili