The Diversity of Fibrillin Functions: Lessons from the Periodontal Ligament
Marfan syndrome is caused by a mutation in the <i>FBN1</i> gene encoding fibrillin-1. This extracellular matrix glycoprotein, which assembles into microfibrils, is best known for its scaffolding role in the production of elastic fibers responsible for connective tissue elasticity and ten...
Saved in:
| Main Authors: | Elisabeth Genot, Tala Al Tabosh, Sylvain Catros, Florian Alonso, Damien Le Nihouannen |
|---|---|
| Format: | Article |
| Language: | English |
| Published: |
MDPI AG
2025-05-01
|
| Series: | Cells |
| Subjects: | |
| Online Access: | https://www.mdpi.com/2073-4409/14/11/764 |
| Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
The Biomechanics of Fibrillin Microfibrils: Lessons from the Ciliary Zonule
by: Pooja Rathaur, et al.
Published: (2024-12-01) -
DNA DIAGNOSTICS AND MUTATION SPECTRUM OF THE GENE FBN1 IN MARFAN’S SYNDROME
by: Yu. A. Rogozhina, et al.
Published: (2015-10-01) -
Case Report: A FBN1 frameshift-and-nonsense mutation and aortic dissection in Marfan syndrome
by: Chao Su, et al.
Published: (2025-04-01) -
Exploring thoracic aorta ECM alterations in Marfan syndrome: insights into aorta wall structure
by: Rodrigo Barbosa de Souza, et al.
Published: (2025-07-01) -
Corneal characteristics in children with Marfan syndrome with or without ectopia lentis
by: Marisa O'Brien, et al.
Published: (2025-06-01)