Researcher
Lore Pottie
- Disciplines:Clinical genetics and molecular diagnostics, Metabolic diseases, Dermatology, Vascular diseases, Dermatology not elsewhere classified
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 26 Sep 2021 - Department of Pediatrics and medical genetics (Department)
Member
From1 Mar 2017 → 30 Sep 2018
Publications
1 - 10 of 19
- The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Authors: 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.
Number of pages: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Authors: 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.
Number of pages: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2023)
Authors: 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.
Number of pages: 1 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2022)
Authors: 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.
Pages: 14 - 14 - EMILIN1 deficiency causes arterial tortuosity with osteopenia and connects impaired elastogenesis with defective collagen fibrillogenesis(2022)
Authors: 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.
Pages: 2230 - 2252 - The establishment of the first reported zebrafish model for thoracic aortic dissection and rupture(2022)
Authors: 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.
Number of pages: 1 - Loss-of-function variants in EFEMP1 cause a recognizable connective tissue disorder characterized by cutis laxa and multiple herniations(2021)
Authors: 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)
Authors: 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)
Authors: Aude Beyens, Lore Pottie, Patrick Sips, Bert Callewaert, Jaroslava Halper
Pages: 273 - 309 - Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome(2021)
Authors: 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.
Pages: 1095 - 1114