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

Next-generation sequencing of prolidase gene identifies novel and common variants associated with low prolidase in coronary artery ectasia

3 Dec 2022

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 Kawasaki Disease and Coronary Complications
Share to Peptidase Inhibition and Analysis

Source

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Identifiers

PMID: 36462085
DOI: 10.1007/s11033-022-08142-1

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Next-generation sequencing of prolidase gene identifies novel and common variants associated with low prolidase in coronary artery ectasiaPMID 36462085Read ↗

Clinical Genetics of Prolidase Deficiency: An Updated ReviewSemantic proximity Read ↗

Molecular characterisation of six patients with prolidase deficiency: identification of the first small duplication in the prolidase gene and of a mutation generating symptomatic and asymptomatic outcomes within the same family.Semantic proximity Read ↗

Coding Variation in ANGPTL4, LPL, and SVEP1 and the Risk of Coronary Disease.Semantic proximity Read ↗

Exome Sequencing,<i>ANGPTL3</i>Mutations, and Familial Combined HypolipidemiaSemantic proximity Read ↗

The role of rs267606943 polymorphism in the prolidase gene and plasma prolidase in polycystic ovary syndrome.Semantic proximity Read ↗

Inframe insertion and splice site variants in MFGE8 associate with protection against coronary atherosclerosis.Semantic proximity Read ↗

Comprehensive in-silico prediction of damage associated SNPs in Human Prolidase gene.Semantic proximity Read ↗

Mammalian Glutamyl Aminopeptidase Genes (ENPEP) and Proteins: Comparative Studies of a Major Contributor to Arterial HypertensionSemantic proximity Read ↗

Harnessing natural diversity to identify key amino acid residues in prolidaseSemantic proximity Read ↗

PROLIDASE: A Review from Discovery to its Role in Health and DiseaseSemantic proximity Read ↗

Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activity.Semantic proximity Read ↗

Human prolidase and prolidase deficiency: an overview on the characterization of the enzyme involved in proline recycling and on the effects of its mutations.Semantic proximity Read ↗

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