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BMJ Open|December 1, 2022
SARS-CoV-2 antibody responses post-vaccination in UK healthcare workers with pre-existing medical conditions: a cohort studyVictoria Ward, Jia Wei, William Gordon, et al.The Journal of Biological Chemistry|May 17, 2015
Lysyl Oxidase Activity Is Required for Ordered Collagen Fibrillogenesis by Tendon CellsAndreas Herchenhan, Franziska Uhlenbrock, Pernilla Eliasson, et al.Plos One|September 1, 2017
Asporin-deficient mice have tougher skin and altered skin glycosaminoglycan content and structureMarco Maccarana, René B Svensson, Anki Knutsson, et al.The Journal of Biological Chemistry|May 26, 2015
Molecular Consequences of the SERPINH1/HSP47 Mutation in the Dachshund Natural Model of Osteogenesis ImperfectaUschi Lindert, Mary Ann Weis, Jyoti Rai, et al.Human Molecular Genetics|December 17, 2014
HSP47 and FKBP65 cooperate in the synthesis of type I procollagenIvan Duran, Lisette Nevarez, Anna Sarukhanov, et al.Journal of Anatomy|February 28, 2014
3-D ultrastructure and collagen composition of healthy and overloaded human tendon: evidence of tenocyte and matrix bucklingJessica Pingel, Yinhui Lu, Tobias Starborg, et al.Human Mutation|June 22, 2012
Absence of FKBP10 in recessive type XI osteogenesis imperfecta leads to diminished collagen cross-linking and reduced collagen deposition in extracellular matrixAileen M Barnes, Wayne A Cabral, MaryAnn Weis, et al.Human Mutation|August 8, 2019
Dominant-negative SOX9 mutations in campomelic dysplasiaFabiana Csukasi, Ivan Duran, Wenjuan Zhang, et al.Euro Surveillance : Bulletin Europeen Sur Les Maladies Transmissibles = European Communicable Disease Bulletin|February 28, 2019
Genetic relatedness of ceftriaxone-resistant and high-level azithromycin resistant Neisseria gonorrhoeae cases, United Kingdom and Australia, February to April 2018Amy V Jennison, David Whiley, Monica M Lahra, et al.Journal of Bone and Mineral Research : the Official Journal of the American Society for Bone and Mineral Research|September 25, 2014
A transgenic mouse model of OI type V supports a neomorphic mechanism of the IFITM5 mutationCaressa D Lietman, Ronit Marom, Elda Munivez, et al.Pageof 5