Discover Community Create You

Loading publication...

Noodle always counts identifier-free feature events for service operation. With your permission, Google Analytics can also estimate audience and engagement. Search text, publication identifiers, cookies, IP addresses and browser fingerprints are never included in Noodle's first-party event counters.

Privacy details

Article

Engineered mutations in fibrillin-1 leading to Marfan syndrome act at the protein, cellular and organismal levels

5 May 2015

Abstract excerpt

No abstract is available from the source.

Read the complete abstract on PubMed

Topics

Share this publication in a Topic to start or enrich a Post.

Share to Connective tissue disorders research
Share to Peptidase Inhibition and Analysis
Share to Protease and Inhibitor Mechanisms

Source

Methodology Data sources Editorial policy Privacy Delete account & data About Contact Helena Bioinformatics

Identifiers

PMID: 26281765
DOI: 10.1016/j.mrrev.2015.04.002

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 24 Oct 2026.

Related research

Semantic proximity does not establish scientific evidence. Graph snapshot: 2026-09-29.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Engineered mutations in fibrillin-1 leading to Marfan syndrome act at the protein, cellular and organismal levelsPMID 26281765Read ↗

Marfan syndrome: new clues to genotype-phenotype correlations.Semantic proximity Read ↗

The Multiple Functions of Fibrillin-1 Microfibrils in Organismal Physiology.Semantic proximity Read ↗

FBN1: The disease-causing gene for Marfan syndrome and other genetic disorders.Semantic proximity Read ↗

Marfan syndrome in the third Millennium.Semantic proximity Read ↗

Marfan syndrome. Part 1: pathophysiology and diagnosis.Semantic proximity Read ↗

The molecular genetics of Marfan syndrome and related microfibrillopathies.Semantic proximity Read ↗

The fibrillin-Marfan syndrome connection.Semantic proximity Read ↗

Fibrillin microfibril structure identifies long-range effects of inherited pathogenic mutations affecting a key regulatory TGFβ-binding siteSemantic proximity Read ↗

[Molecular biological aspects of Marfan syndromes].Semantic proximity Read ↗

Marfan syndrome: from gene to therapy.Semantic proximity Read ↗

Mutations in the human gene for fibrillin-1 (FBN1) in the Marfan syndrome and related disorders.Semantic proximity Read ↗

Genetic models of fibrillinopathies.Semantic proximity Read ↗

⌁Select a neighboring publication to make it the new centre.