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

Human Calmodulin Mutations

13 Nov 2018

Abstract excerpt

Fluxes of Ca2+ across cell membranes enable fast cellular responses. Calmodulin (CaM) senses local changes in Ca2+ concentration and relays the information to numerous interaction partners. The critical role of accurate Ca2+ signaling on cellular function is underscored by the fact that there are three independent CaM genes (CALM1-3) in the human genome. All three genes are functional and encode the exact same...

Read the complete abstract on PubMed

Topics

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

Share to Cardiac electrophysiology and arrhythmias
Share to Genetics and Neurodevelopmental Disorders
Share to Signaling Pathways in Disease

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

Source

Identifiers

PMID: 30483049
DOI: 10.3389/fnmol.2018.00396

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 23 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

Human Calmodulin MutationsPMID 30483049Read ↗

Calmodulin Mutations in Human Disease.Semantic proximity Read ↗

Calmodulin Mutations Associated with Heart Arrhythmia: A Status ReportSemantic proximity Read ↗

Role of Calmodulin in Cardiac Disease: Insights on Genotype and Phenotype.Semantic proximity Read ↗

Spectrum and Prevalence of <i>CALM1</i> -, <i>CALM2</i> -, and <i>CALM3</i> -Encoded Calmodulin Variants in Long QT Syndrome and Functional Characterization of a Novel Long QT Syndrome–Associated Calmodulin Missense Variant, E141GSemantic proximity Read ↗

Calmodulinopathy: Functional Effects of CALM Mutations and Their Relationship With Clinical PhenotypesSemantic proximity Read ↗

The Crossroad of Ion Channels and Calmodulin in DiseaseSemantic proximity Read ↗

Brain voltage-gated Ca2+ channels and calmodulin: Teaming up in calmodulinopathies?Semantic proximity Read ↗

Novel CALM3 Variant Causing Calmodulinopathy With Variable Expressivity in a 4-Generation Family.Semantic proximity Read ↗

Divergent Regulation of Ryanodine Receptor 2 Calcium Release Channels by Arrhythmogenic Human Calmodulin Missense MutantsSemantic proximity Read ↗

Novel calmodulin mutations associated with congenital long QT syndrome affect calcium current in human cardiomyocytes.Semantic proximity Read ↗

Calmodulinopathy: A Novel, Life-Threatening Clinical Entity Affecting the YoungSemantic proximity Read ↗

Clinical presentation of calmodulin mutations: the International Calmodulinopathy Registry.Semantic proximity Read ↗

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