Researcher
Piyanoot Tapaneeyaphan
- Disciplines:Palliative care and end-of-life care, Laboratory medicine, Other translational sciences, Regenerative medicine, Nursing, Other clinical sciences, Other basic sciences, Other paramedical sciences, Other health sciences, Other medical and health sciences
Affiliations
- Department of Biomolecular Medicine (Department)
Member
From1 Oct 2018 → 31 May 2023 - Department of Pediatrics and medical genetics (Department)
Member
From15 Jan 2010 → 30 Sep 2018 - Department of Physiology (Department)
Member
From1 Mar 2009 → 31 Dec 2009
Publications
1 - 10 of 10
- 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 - 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
- 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 - New insights on the clinical variability of FKBP10 mutations(2020)
Authors: Osama Essawi, Piyanoot Tapaneeyaphan, Charlotte Gistelinck, Fransiska Malfait, David Eyre, Tamer Essawi, Bert Callewaert
- Bi-allelic loss-of-function variants in LTBP1cause autosomal recessive cutis laxa syndromeVolume: 30
Authors: Lore Pottie, Christin S. Adamo, Aude Beyens, Steffen Luetke, Piyanoot Tapaneeyaphan, Phil Salmon, Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, Jill E. Urquhart, et al.
Pages: 40 - 41 - Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome (vol 108, pg 1095, 2021)
Authors: Lore Pottie, Christin S. Adamo, Aude Beyens, Steffen Lutke, Piyanoot Tapaneeyaphan, Adelbert De Clercq, Phil L. Salmon, Alper Gezdirici, Elif Yilmaz Gulec, Naz Khan, et al.
Pages: 2386 - 2388