Onderzoeker
Lore Pottie
- Disciplines:Klinische genetica en moleculaire diagnostiek, Metabole ziekten, Dermatologie, Vasculaire ziekten, Dermatologie niet elders geclassificeerd
Affiliaties
- Vakgroep Biomoleculaire Geneeskunde (Departement)
Lid
Vanaf1 okt 2018 → 26 sep 2021 - Vakgroep Pediatrie en genetica (Departement)
Lid
Vanaf1 mrt 2017 → 30 sep 2018
Publicaties
1 - 10 van 19
- The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Auteurs: Michiel Vanhooydonck, Maxim Verlee, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Lisa Caboor, Matthias Van Impe, Delfien Syx, et al.
Aantal pagina's: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Auteurs: Michiel Vanhooydonck, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Matthias Van Impe, Delfien Syx, Andy Willaert, Lisa Caboor, et al.
Aantal pagina's: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Auteurs: Michiel Vanhooydonck, Maxim Verlee, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Lisa Caboor, Matthias Van Impe, Delfien Syx, et al.
Aantal pagina's: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2022)
Auteurs: Michiel Vanhooydonck, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Adelbert De Clercq, Lisa Caboor, Matthias Van Impe, Andy Willaert, Patrick Sips, et al.
Pagina's: 14 - 14 - EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis(2022)
Auteurs: Christin S. Adamo, Aude Beyens, Alvise Schiavinato, Douglas R. Keene, Sara F. Tufa, Matthias Morgelin, Jurgen Brinckmann, Takako Sasaki, Anja Niehoff, Maren Dreiner, et al.
Pagina's: 2230 - 2252 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2022)
Auteurs: Michiel Vanhooydonck, Lore Pottie, Annekatrien Boel, Piyanoot Tapaneeyaphan, Marta Guerreiro Santana Ramos Da Silva, Lisa Caboor, Adelbert De Clercq, Matthias Van Impe, Andy Willaert, Patrick Sips, et al.
Aantal pagina's: 1 - Loss-of-function variants in EFEMP1 cause a recognizable connective tissue disorder characterized by cutis laxa and multiple herniations(2021)
Auteurs: Maxim Verlee, Aude Beyens, Alper Gezdirici, Elif Gulec, Lore Pottie, Silke De Feyter, Michiel Vanhooydonck, Piyanoot Tapaneeyaphan, Bert Callewaert
- Exploring cutis laxa syndromes in vitro and in vivo through zebrafish modeling : lessons learnt from recently and newly discovered disease-causing genes(2021)
Auteurs: Lore Pottie
- Clinical and molecular delineation of cutis laxa syndromes : paradigms for elastic fiber homeostasis(2021)Edition: 2Series: Advances in Experimental Medicine and Biology (AEMB)
Auteurs: Aude Beyens, Lore Pottie, Patrick Sips, Bert Callewaert, Jaroslava Halper
Pagina's: 273 - 309 - Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome(2021)
Auteurs: Lore Pottie, Christin S. Adamo, Aude Beyens, Steffen Lütke, Piyanoot Tapaneeyaphan, Phil L. Salmon, Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, Jill E. Urquhart, et al.
Pagina's: 1095 - 1114