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Eye (London, England)|February 15, 2019
Evaluation of TGFBI corneal dystrophy and molecular diagnostic testingConnie Chao-Shern, Lawrence A DeDionisio, Jun-Heok Jang, et al.
The Journal of Clinical Endocrinology and Metabolism|January 10, 2003
Genetic mapping studies of familial juvenile hyperuricemic nephropathy on chromosome 16p11-p13Joanna M Stacey, Jeremy J O Turner, Brian Harding, et al.
Scientific Reports|November 25, 2017
Towards personalised allele-specific CRISPR gene editing to treat autosomal dominant disordersKathleen A Christie, David G Courtney, Larry A DeDionisio, et al.
Disease Models & Mechanisms|March 23, 2017
A mouse model for inherited renal fibrosis associated with endoplasmic reticulum stressSian E Piret, Eric Olinger, Anita A C Reed, et al.
Proteomics. Clinical Applications|June 20, 2020
Protein Analysis of the TGFBI<sup>R124H</sup> Mouse Model Gives Insight into Phenotype Development of Granular Corneal DystrophyMarie V Lukassen, Ebbe T Poulsen, Jack Donaghy, et al.
Investigative Ophthalmology & Visual Science|July 25, 2015
Protein Composition of TGFBI-R124C- and TGFBI-R555W-Associated Aggregates Suggests Multiple Mechanisms Leading to Lattice and Granular Corneal DystrophyDavid G Courtney, Ebbe Toftgaard Poulsen, Susan Kennedy, et al.
Journal of Controlled Release : Official Journal of the Controlled Release Society|July 13, 2020
Topical siRNA delivery to the cornea and anterior eye by hybrid silicon-lipid nanoparticlesPaulina Baran-Rachwalska, Nissim Torabi-Pour, Flavia Maria Sutera, et al.
Microvascular Research|January 23, 2023
Assessment of hemodynamic indices of conjunctival microvascular function in patients with coronary microvascular dysfunctionJonathan A Mailey, Julie S Moore, Paul F Brennan, et al.
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