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

Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation.

Circulation research - 23 Jul 2021

Yin Liheng, Zahradnikova Alexandra, Rizzetto Riccardo, Boncompagni Simona, Rabesahala de Meritens Camille, Zhang Yadan, Joanne Pierre, Marqués-Sulé Elena, Aguilar-Sánchez Yuriana, Fernández-Tenorio Miguel, Villejoubert Olivier, Li Linwei, Wang Yue Yi, Mateo Philippe, Nicolas Valérie, Gerbaud Pascale, Lai F Anthony, Perrier Romain, Álvarez Julio L, Niggli Ernst, Valdivia Héctor H, Valdivia Carmen R, Ramos-Franco Josefina, Zorio Esther, Zissimopoulos Spyros, Protasi Feliciano, Benitah Jean-Pierre, Gómez Ana M

Abstract excerpt

[Figure: see text].

Read the complete abstract on PubMed

Topics

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

Share to Action Potentials
Share to Binding Sites

Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

Share to Calcium Signaling

Share to HEK293 Cells

Share to Myocytes, Cardiac

Share to Polymorphic Catecholaminergic Ventricular Tachycardia

Share to Ryanodine Receptor Calcium Release Channel

Share to Tachycardia, Ventricular

Source

Open in PubMed Open full text

Identifiers

PMID: 34111951
DOI: 10.1161/CIRCRESAHA.121.319094
PMCID: PMC8320243

Provenance

PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026. Manifest publication-graph-cohort-2026-09-07.1.

Source receipt: pubmed, retrieved 7 Sept 2026.

Related research

Semantic proximity does not establish scientific evidence.

Research trail→

Click a neighbor to travelStep 1 · 12 closest

Impaired Binding to Junctophilin-2 and Nanostructural Alteration in CPVT Mutation.PMID 34111951Read ↗

TTC14 dysfunction contributing to microcephaly and lissencephaly spectrum features through protein mislocalization and impaired RNA processingSemantic proximity Read ↗

Insights into VPS13 properties and function reveal a new mechanism of eukaryotic lipid transport.Semantic proximity Read ↗

Pathologies at the gateway: exploring the link between nucleoporins and inherited diseases.Semantic proximity Read ↗

Cargos and genes: insights into vesicular transport from inherited human disease.Semantic proximity Read ↗

The role of junctophilin proteins in cellular functionSemantic proximity Read ↗

VPS13A and VPS13C influence lipid droplet abundanceSemantic proximity Read ↗

From the sideline: Tissue-specific nucleoporin function in health and disease, an update.Semantic proximity Read ↗

Valosin containing protein (VCP): initiator, modifier, and potential drug target for neurodegenerative diseases.Semantic proximity Read ↗

The junctophilin family of proteins: from bench to bedside.Semantic proximity Read ↗

Mutations in nucleoporins and their roles in human diseases: Integrating evidence on specific NUP functions.Semantic proximity Read ↗

A perspective from transport protein particle: vesicle tether and human diseases.Semantic proximity Read ↗

Characterization of Human Junctophilin Subtype GenesSemantic proximity Read ↗

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