Structured Summary
Abstract
A fibrillin (FBN1) that functions as a structural support protein for MICROFIBRILS. It also regulates the maturation of OSTEOBLASTS by controlling the availability and concentration of TGF-BETA and BONE MORPHOGENETIC PROTEINS. Mutations in the FBN1 gene are associated with MARFAN SYNDROME.
MeSH Record
Classification
Broader headings
Related Concepts
Knowledge Graph
Drag nodes to rearrange; hover to trace links; click a node to open its page.
MeSH Record
Synonyms
4 entry terms
- Fibrillin 1
- Asprosin
- Profibrillin 1
- Profibrillin-1
MeSH Record
Aspects Covered
30 allowable subheadings
Indexed with the subheadings administration & dosage, adverse effects, agonists, analysis, antagonists & inhibitors, biosynthesis, blood, cerebrospinal fluid, chemical synthesis, chemistry, classification, deficiency, drug effects, economics, genetics, history, immunology, isolation & purification, metabolism, pharmacokinetics, pharmacology, physiology, poisoning, radiation effects, standards, supply & distribution, therapeutic use, toxicity, ultrastructure, urine.
MeSH Record
History Note
2017; use FIBRILLIN 1985-2016
MeSH Hierarchy
Tree Numbers
AMA Style
References
- National Library of Medicine. Fibrillin-1. Medical Subject Headings (MeSH). 2026. Unique ID D000071838. http://id.nlm.nih.gov/mesh/2026/D000071838
- Fibrillin-1. In: Wikidata. https://www.wikidata.org/wiki/Q21118138