Biochemical mechanisms of aggregation in TGFBI-linked corneal dystrophies

Author:

Nielsen Nadia Sukusu,Poulsen Ebbe ToftgaardORCID,Lukassen Marie V.,Chao Shern ConnieORCID,Mogensen Emilie Hage,Weberskov Christian E.,DeDionisio LarryORCID,Schauser LeifORCID,Moore Tara C.B.,Otzen Daniel E.ORCID,Hjortdal Jesper,Enghild Jan J.ORCID

Funder

VELUX Foundation

LEO Foundation

Danish Council for Independent Research

Publisher

Elsevier BV

Subject

Sensory Systems,Ophthalmology

Reference231 articles.

1. Survey of patients with granular, lattice, avellino, and Reis-Bucklers corneal dystrophies for mutations in the BIGH3 and gelsolin genes;Afshari;Arch. Ophthalmol.,2001

2. Atypical asymmetric lattice corneal dystrophy associated with a novel homozygous mutation (Val624Met) in the TGFBI gene;Afshari;Mol. Vis.,2008

3. Initial suppression of transforming growth factor-beta signaling and loss of TGFBI causes early alveolar structural defects resulting in bronchopulmonary dysplasia;Ahlfeld;Am. J. Pathol.,2016

4. Unilateral lattice corneal dystrophy associated with the novel His572del mutation in the TGFBI gene;Aldave;Mol. Vis.,2006

5. A clinical and histopathologic examination of accelerated TGFBIp deposition after LASIK in combined granular-lattice corneal dystrophy;Aldave;Am. J. Ophthalmol.,2007

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