David R. Eyre

2 ta ish

University of Washington

1. Mutations in FKBP10, which result in Bruck syndrome and recessive forms of osteogenesis imperfecta, inhibit the hydroxylation of telopeptide lysines in bone collagen

   U. Schwarze, Tim Cundy, Shawna M. Pyott +35

   MaqolaOAOchiq kirish20122 iqtibos

   ABIABI:AkademIndex/2026.other.036794

2. Loss of Type I Collagen Telopeptide Lysyl Hydroxylation Causes Musculoskeletal Abnormalities in a Zebrafish Model of Bruck Syndrome

   Charlotte Gistelinck, P. Eckhard Witten, Ann Huysseune +12

   MaqolaOAOchiq kirishConnective tissue disorders researchJournal of Bone and Mineral Research20160 iqtibos

   ABIABI:AkademIndex/2016.article.000011