The mgΔlpn mouse model for Marfan syndrome recapitulates the ocular phenotypes of the disease-Reference-Cited by-同舟云学术

The mgΔlpn mouse model for Marfan syndrome recapitulates the ocular phenotypes of the disease

Published:2021-03 Issue: Volume:204 Page:108461
ISSN:0014-4835
Container-title:Experimental Eye Research
language:en
Short-container-title:Experimental Eye Research

Author:

Souza Rodrigo Barbosa de,Gyuricza Isabela Gerdes^ORCID,Cassiano Luara Lucena,Farinha-Arcieri Luis Ernesto,Alvim Liberatore Ana Maria,Schuindt do Carmo Sheila,Caldeira Waldir,Cruz Marcio V.,Ribeiro Alberto F.,Tedesco Roberto Carlos,Reinhardt Dieter P.,Smith Ricardo,Jun Koh Ivan Hong^ORCID,Pereira Lygia V.

Funder

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior

Publisher

Elsevier BV

Subject

Cellular and Molecular Neuroscience,Sensory Systems,Ophthalmology

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4. Marfan syndrome;Dietz,2017

5. Management strategies of ocular abnormalities in patients with marfan syndrome: current perspective;Esfandiari;J. Ophthalmic Vis. Res.,2019

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1. The Fbn1 gene variant governs passive ascending aortic mechanics in the mgΔlpn mouse model of Marfan syndrome when superimposed to perlecan haploinsufficiency;Frontiers in Cardiovascular Medicine;2024-03-13

2. Genetic mutation and aqueous humor metabolites alterations in a family with Marfan syndrome;Heliyon;2024-01

3. Genetic models of fibrillinopathies;GENETICS;2023-11-16

4. Extracellular matrix and vascular dynamics in the kidney of a murine model for Marfan syndrome;PLOS ONE;2023-05-09

5. Hyperkyphosis is not dependent on bone mass and quality in the mouse model of Marfan syndrome;Bone;2021-11