Tamara Jarayseh
Overview
Explore the profile of Tamara Jarayseh including associated specialties, affiliations and a list of published articles.
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Articles
3
Citations
3
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Recent Articles
1.
Debaenst S, Jarayseh T, De Saffel H, Bek J, Boone M, Josipovic I, et al.
Elife
. 2025 Jan;
13.
PMID: 39817421
Heritable fragile bone disorders (FBDs), ranging from multifactorial to rare monogenic conditions, are characterized by an elevated fracture risk. Validating causative genes and understanding their mechanisms remain challenging. We assessed...
2.
Jarayseh T, Debaenst S, De Saffel H, Rosseel T, Milazzo M, Bek J, et al.
J Bone Miner Res
. 2024 Nov;
40(1):154-166.
PMID: 39566080
Rare monogenic disorders often exhibit significant phenotypic variability among individuals sharing identical genetic mutations. Bruck syndrome (BS), a prime example, is characterized by bone fragility and congenital contractures, although with...
3.
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...
4.
Jarayseh T, Guillemyn B, De Saffel H, Bek J, Syx D, Symoens S, et al.
Hum Genet
. 2023 Jan;
142(3):457-476.
PMID: 36697720
Bi-allelic mutations in the gene coding for human trans-membrane anterior-posterior transformation protein 1 (TAPT1) result in a broad phenotypic spectrum, ranging from syndromic disease with severe skeletal and congenital abnormalities...