Cargando…

Triadin/Junctin Double Null Mouse Reveals a Differential Role for Triadin and Junctin in Anchoring CASQ to the jSR and Regulating Ca(2+) Homeostasis

Triadin (Tdn) and Junctin (Jct) are structurally related transmembrane proteins thought to be key mediators of structural and functional interactions between calsequestrin (CASQ) and ryanodine receptor (RyRs) at the junctional sarcoplasmic reticulum (jSR). However, the specific contribution of each...

Descripción completa

Detalles Bibliográficos
Autores principales:	Boncompagni, Simona, Thomas, Monique, Lopez, Jose R., Allen, Paul D., Yuan, Qunying, Kranias, Evangelia G., Franzini-Armstrong, Clara, Perez, Claudio F.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Public Library of Science 2012
Materias:	Research Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3388061/ https://www.ncbi.nlm.nih.gov/pubmed/22768324 http://dx.doi.org/10.1371/journal.pone.0039962

Ejemplares similares

A unique triadin exon deletion causing a null phenotype
por: O’Callaghan, Barry M., et al.
Publicado: (2018)

A new cytoplasmic interaction between junctin and ryanodine receptor Ca(2+) release channels
por: Li, Linwei, et al.
Publicado: (2015)

Quantification of the calcium signaling deficit in muscles devoid of triadin
por: Manno, Carlo, et al.
Publicado: (2022)

A Skeletal Muscle Ryanodine Receptor Interaction Domain in Triadin
por: Wium, Elize, et al.
Publicado: (2012)

Generation of a Triadin KnockOut Syndrome Zebrafish Model
por: Vecchi, Vanilla Martina, et al.
Publicado: (2021)

Caveolin 3 Is Associated with the Calcium Release Complex and Is Modified via in Vivo Triadin Modification†
por: Vassilopoulos, Stéphane, et al.
Publicado: (2010)

Dynamics of triadin, a muscle-specific triad protein, within sarcoplasmic reticulum subdomains
por: Sébastien, Muriel, et al.
Publicado: (2020)

Immunolocalization of sarcolemmal dihydropyridine receptor and sarcoplasmic reticular triadin and ryanodine receptor in rabbit ventricle and atrium
Publicado: (1995)

Association of decreased triadin expression level with apoptosis of dopaminergic cells in Parkinson’s disease mouse model
por: Seo, Min Hyung, et al.
Publicado: (2021)

Absence of triadin, a protein of the calcium release complex, is responsible for cardiac arrhythmia with sudden death in human
por: Roux-Buisson, Nathalie, et al.
Publicado: (2012)

Cellular and electrophysiological characterization of triadin knockout syndrome using induced pluripotent stem cell-derived cardiomyocytes
por: Clemens, Daniel J., et al.
Publicado: (2023)

Triad formation: organization and function of the sarcoplasmic reticulum calcium release channel and triadin in normal and dysgenic muscle in vitro
Publicado: (1993)

Triadin Binding to the C-Terminal Luminal Loop of the Ryanodine Receptor is Important for Skeletal Muscle Excitation–Contraction Coupling
por: Goonasekera, Sanjeewa A., et al.
Publicado: (2007)

Triadin Decrease Impairs the Expression of E-C Coupling Related Proteins in Muscles of MPTP-Induced Parkinson’s Disease Mice
por: Seo, Min Hyung, et al.
Publicado: (2021)

Status Of A Compact Electron Storage Ring Jsr
por: Harada, S, et al.
Publicado: (1990)

An Association Study of CASQ1 Gene Polymorphisms and Heat Stroke
por: Li, Ying, et al.
Publicado: (2014)

JsrNet: A Joint Sampling–Reconstruction Framework for Distributed Compressive Video Sensing
por: Chen, Can, et al.
Publicado: (2019)

CASQ2 variants in Chinese children with catecholaminergic polymorphic ventricular tachycardia
por: Li, Qirui, et al.
Publicado: (2019)

Noncatalytic Oxidative Coupling of Methane (OCM): Gas-Phase Reactions in a Jet Stirred Reactor (JSR)
por: Wang, Haoyi, et al.
Publicado: (2021)

CASQ1‐related myopathy: The first report from China and the literature review
por: Zhang, Kai‐Yue, et al.
Publicado: (2022)

The Evolution of the Mitochondria-to-Calcium Release Units Relationship in Vertebrate Skeletal Muscles
por: Franzini-Armstrong, Clara, et al.
Publicado: (2011)

Automated inference of Boolean models from molecular interaction maps using CaSQ
por: Aghamiri, Sara Sadat, et al.
Publicado: (2020)

Cancer Appetite and Symptom Questionnaire (CASQ) for Brazilian Patients: Cross-Cultural Adaptation and Validation Study
por: Spexoto, Maria Claudia Bernardes, et al.
Publicado: (2016)

Compound heterozygous CASQ2 mutations and long‐term course of catecholaminergic polymorphic ventricular tachycardia
por: Josephs, Katherine, et al.
Publicado: (2017)

A Homozygous CASQ2 Mutation in a Japanese Patient with Catecholaminergic Polymorphic Ventricular Tachycardia
por: Fujisawa, Taishi, et al.
Publicado: (2019)

Ca(2+) entry units in a superfast fish muscle
por: Kittelberger, J. Matthew, et al.
Publicado: (2022)

Joint system relaxometry (JSR) and Crámer‐Rao lower bound optimization of sequence parameters: A framework for enhanced precision of DESPOT T(1) and T(2) estimation
por: Teixeira, Rui Pedro A.G., et al.
Publicado: (2017)

Anchored phosphatases modulate glucose homeostasis
por: Hinke, Simon A, et al.
Publicado: (2012)

Adeno-associated virus-mediated CASQ2 delivery rescues phenotypic alterations in a patient-specific model of recessive catecholaminergic polymorphic ventricular tachycardia
por: Lodola, Francesco, et al.
Publicado: (2016)

Null Mutation in PGAP1 Impairing Gpi-Anchor Maturation in Patients with Intellectual Disability and Encephalopathy
por: Murakami, Yoshiko, et al.
Publicado: (2014)

The role of CaMKII regulation of phospholamban activity in heart disease
por: Mattiazzi, Alicia, et al.
Publicado: (2014)

Calcium-Mediated Oscillation in Membrane Potentials and Atrial-Triggered Activity in Atrial Cells of Casq2(R33Q/R33Q) Mutation Mice
por: Zhang, Jian-cheng, et al.
Publicado: (2018)

Lipid-anchored proteasomes control membrane protein homeostasis
por: Zhang, Ruizhu, et al.
Publicado: (2023)

Basonuclin-Null Mutation Impairs Homeostasis and Wound Repair in Mouse Corneal Epithelium
por: Zhang, Xiaohong, et al.
Publicado: (2007)

Persistence of improved glucose homeostasis in Gclm null mice with age and cadmium treatment
por: Schaupp, Christopher M., et al.
Publicado: (2021)

Pacing Dynamics Determines the Arrhythmogenic Mechanism of the CPVT2-Causing CASQ2(G112+5X) Mutation in a Guinea Pig Ventricular Myocyte Computational Model
por: Paudel, Roshan, et al.
Publicado: (2022)

Calcium Homeostasis and Muscle Energy Metabolism Are Modified in HspB1-Null Mice
por: Picard, Brigitte, et al.
Publicado: (2016)

Molecular adaptation to calsequestrin 2 (CASQ2) point mutations leading to catecholaminergic polymorphic ventricular tachycardia (CPVT): comparative analysis of R33Q and D307H mutants
por: Valle, Giorgia, et al.
Publicado: (2020)

Altered Spinal Homeostasis and Maladaptive Plasticity in GFAP Null Mice Following Peripheral Nerve Injury
por: De Luca, Ciro, et al.
Publicado: (2022)

Targeting an anchored phosphatase-deacetylase unit restores renal ciliary homeostasis
por: Gopalan, Janani, et al.
Publicado: (2021)

Cannot write session to /tmp/vufind_sessions/sess_j2a7kh1v67jp76ikbd9dqepfh7