Piyanoot Tapaneeyaphan
Overview
Explore the profile of Piyanoot Tapaneeyaphan including associated specialties, affiliations and a list of published articles.
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Articles
5
Citations
25
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0
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Recent Articles
1.
Syntaxin 18 Defects in Human and Zebrafish Unravel Key Roles in Early Cartilage and Bone Development
Guillemyn B, De Saffel H, Bek J, Tapaneeyaphan P, De Clercq A, Jarayseh T, et al.
J Bone Miner Res
. 2023 Sep;
38(11):1718-1730.
PMID: 37718532
SNARE proteins comprise a conserved protein family responsible for catalyzing membrane fusion during vesicle traffic. Syntaxin18 (STX18) is a poorly characterized endoplasmic reticulum (ER)-resident t-SNARE. Recently, together with TANGO1 and...
2.
Pottie L, Adamo C, Beyens A, Lutke S, Tapaneeyaphan P, De Clercq A, et al.
Am J Hum Genet
. 2021 Dec;
108(12):2386-2388.
PMID: 34861177
No abstract available.
3.
Pottie L, Adamo C, Beyens A, Lutke S, Tapaneeyaphan P, De Clercq A, et al.
Am J Hum Genet
. 2021 May;
108(6):1095-1114.
PMID: 33991472
Latent transforming growth factor β (TGFβ)-binding proteins (LTBPs) are microfibril-associated proteins essential for anchoring TGFβ in the extracellular matrix (ECM) as well as for correct assembly of ECM components. Variants...
4.
Verlee M, Beyens A, Gezdirici A, Gulec E, Pottie L, De Feyter S, et al.
Genes (Basel)
. 2021 Apr;
12(4).
PMID: 33807164
Hereditary disorders of connective tissue (HDCT) compromise a heterogeneous group of diseases caused by pathogenic variants in genes encoding different components of the extracellular matrix and characterized by pleiotropic manifestations,...
5.
Essawi O, Tapaneeyaphan P, Symoens S, Gistelinck C C, Malfait F, Eyre D, et al.
Eur J Med Genet
. 2020 Jun;
63(9):103980.
PMID: 32531462
To date 45 autosomal recessive disease-causing variants are reported in the FKBP10 gene. Those variant were found to be associated with Osteogenesis Imperfecta (OI) for which the hallmark phenotype is...