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

Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiency

14 Apr 2010

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 Bone and Dental Protein Studies
Share to Connective tissue disorders research
Share to Protease and Inhibitor Mechanisms

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 20389311
DOI: 10.1038/ejhg.2010.45

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 8 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Altered TGFβ signaling and cardiovascular manifestations in patients with autosomal recessive cutis laxa type I caused by fibulin-4 deficiencyPMID 20389311Read ↗

Decoding clinical diversity in monogenic TGFBR1 and TGFBR2 mutations: insights into the interplay of molecular mechanisms and hypomorphicitySemantic proximity Read ↗

Identification of a novel TGFBR1 mutation in a Loeys-Dietz syndrome type II patient with vascular Ehlers-Danlos syndrome phenotype.Semantic proximity Read ↗

Extracellular Interactions between Fibulins and Transforming Growth Factor (TGF)-β in Physiological and Pathological ConditionsSemantic proximity Read ↗

LTBP4 in Health and Disease.Semantic proximity Read ↗

Cardiovascular manifestations in Marfan syndrome and related diseases; multiple genes causing similar phenotypesSemantic proximity Read ↗

Loeys-Dietz Syndrome.Semantic proximity Read ↗

TGFβ Signaling and Cardiovascular DiseasesSemantic proximity Read ↗

Loeys-Dietz syndrome.Semantic proximity Read ↗

Connective tissue disorders and cardiovascular complications: the indomitable role of transforming growth factor-beta signaling.Semantic proximity Read ↗

Bi-allelic premature truncating variants in LTBP1 cause cutis laxa syndrome.Semantic proximity Read ↗

Cutis laxa: A comprehensive overview of clinical characteristics and pathophysiology.Semantic proximity Read ↗

Role of transforming growth factor-beta superfamily signaling pathways in human disease.Semantic proximity Read ↗

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