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Human Mutation|January 12, 2017
Transdifferentiation of Human Dermal Fibroblasts to Smooth Muscle-Like Cells to Study the Effect of MYH11 and ACTA2 Mutations in Aortic AneurysmsKak K Yeung, Natalija Bogunovic, Niels Keekstra, et al.Journal of Medical Genetics|July 4, 2018
Novel pathogenic SMAD2 variants in five families with arterial aneurysm and dissection: further delineation of the phenotypeElyssa Cannaerts, Marlies Kempers, Alessandra Maugeri, et al.Scientific Reports|August 29, 2022
Osteogenic transdifferentiation of primary human fibroblasts to osteoblast-like cells with human platelet lysateFerdy K Cayami, Lauria Claeys, Ruben de Ruiter, et al.Proceedings of the National Academy of Sciences of the United States of America|March 7, 2024
Elucidating the role of water in collagen self-assembly by isotopically modulating collagen hydrationGiulia Giubertoni, Liru Feng, Kevin Klein, et al.Biomolecules|October 26, 2024
[18F]NaF PET/CT as a Marker for Fibrodysplasia Ossificans Progressiva: From Molecular Mechanisms to Clinical Applications in Bone DisordersJolien Zwama, Neeltje M Rosenberg, Vincent A Verheij, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|October 6, 2025
New Lens On Congenital Mild Bone Fragility: a Novel Col1a1 Knockout Mouse Model for Osteogenesis Imperfecta Type 1Lidiia Zhytnik, Laura Ventura, Anastasia Sclocco, et al.Scientific Reports|May 27, 2018
An in vitro method to keep human aortic tissue sections functionally and structurally intactJorn P Meekel, Menno E Groeneveld, Natalija Bogunovic, et al.Circulation. Cardiovascular Genetics|January 24, 2015
Beneficial Outcome of Losartan Therapy Depends on Type of FBN1 Mutation in Marfan SyndromeRomy Franken, Alexander W den Hartog, Teodora Radonic, et al.Bone|March 13, 2019
Evolution of heterotopic bone in fibrodysplasia ossificans progressiva: An [18F]NaF PET/CT studyEsmée Botman, Pieter G H M Raijmakers, Maqsood Yaqub, et al.American Journal of Human Genetics|December 25, 2012
Splice-site mutations in the axonemal outer dynein arm docking complex gene CCDC114 cause primary ciliary dyskinesiaAlexandros Onoufriadis, Tamara Paff, Dinu Antony, et al.Pageof 9