(Q24294570)

25 June 2017

title

Stac3 is a component of the excitation-contraction coupling machinery and mutated in Native American myopathy (English)

1 reference

SH3 and cysteine rich domain 3

25 June 2017

main subject

1 reference

neuromuscular synaptic transmission

1 reference

Calcium channel, voltage-dependent, L type, alpha 1S subunit, b

1 reference

SH3 and cysteine rich domain 3

1 reference

Native American myopathy

1 reference

5

0 references

Eric J. Horstick

1

0 references

Allison Ashley-Koch

6

0 references

Clara Franzini-Armstrong

15

object named as

Clara Franzini-Armstrong

1 reference

25 June 2017

Hiromi Hirata

16

1 reference

ORCID Public Data File 2021

author name string

Jeremy W Linsley

2

1 reference

25 June 2017

James J Dowling

3

1 reference

25 June 2017

Michael A Hauser

4

1 reference

25 June 2017

Louis Saint-Amant

7

1 reference

25 June 2017

Akhila Satish

8

1 reference

25 June 2017

Wilson W Cui

9

1 reference

25 June 2017

Weibin Zhou

10

1 reference

25 June 2017

Shawn M Sprague

11

1 reference

25 June 2017

Demetra S Stamm

12

1 reference

25 June 2017

Cynthia M Powell

13

1 reference

25 June 2017

Marcy C Speer

14

1 reference

25 June 2017

John Y Kuwada

17

1 reference

25 June 2017

language of work or name

English

0 references

publication date

1 January 2013

1 reference

25 June 2017

published in

Nature Communications

1 reference

25 June 2017

volume

4

1 reference

25 June 2017

page(s)

1952

1 reference

describes a project that uses

25 June 2017

ImageJ

1 reference

11 June 2022

https://www.ebi.ac.uk/europepmc/webservices/rest/PMC4056023/fullTextXML

inferred from PubMed Central ID database lookup

cites work

Regulation of voltage-gated calcium channel activity by the Rem and Rad GTPases

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

Stac, a novel neuron-specific protein with cysteine-rich and SH3 domains

19 March 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

FK506 binding protein associated with the calcium release channel (ryanodine receptor)

19 March 2017

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Loss of myotubularin function results in T-tubule disorganization in zebrafish and human myotubular myopathy

19 March 2017

1 reference

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Selenoprotein N is required for ryanodine receptor calcium release channel activity in human and zebrafish muscle

19 March 2017

1 reference

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Ablation of triadin causes loss of cardiac Ca2+ release units, impaired excitation-contraction coupling, and cardiac arrhythmias

19 March 2017

1 reference

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A statistical model for identifying proteins by tandem mass spectrometry

19 March 2017

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19 March 2017

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Primary structure of the receptor for calcium channel blockers from skeletal muscle

19 March 2017

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Casq2 deletion causes sarcoplasmic reticulum volume increase, premature Ca2+ release, and catecholaminergic polymorphic ventricular tachycardia

19 March 2017

1 reference

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Imaging neural activity in worms, flies and mice with improved GCaMP calcium indicators

19 March 2017

1 reference

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Stac3 is required for myotube formation and myogenic differentiation in vertebrate skeletal muscle.

7 April 2017

1 reference

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Ryanodine receptors: structure, expression, molecular details, and function in calcium release.

27 September 2017

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Rem, a member of the RGK GTPases, inhibits recombinant CaV1.2 channels using multiple mechanisms that require distinct conformations of the GTPase

27 September 2017

1 reference

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Non-Ca2+-conducting Ca2+ channels in fish skeletal muscle excitation-contraction coupling

27 September 2017

1 reference

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Characterization of domain-peptide interaction interface: a generic structure-based model to decipher the binding specificity of SH3 domains

27 September 2017

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Characterization of housekeeping genes in zebrafish: male-female differences and effects of tissue type, developmental stage and chemical treatment

27 September 2017

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Rem inhibits skeletal muscle EC coupling by reducing the number of functional L-type Ca2+ channels

27 September 2017

1 reference

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Bridging the myoplasmic gap: recent developments in skeletal muscle excitation-contraction coupling

27 September 2017

1 reference

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The beta 1a subunit is essential for the assembly of dihydropyridine-receptor arrays in skeletal muscle

27 September 2017

1 reference

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Zebrafish bandoneon mutants display behavioral defects due to a mutation in the glycine receptor beta-subunit

27 September 2017

1 reference

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Evidence for conformational coupling between two calcium channels

27 September 2017

1 reference

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Calsequestrin and the calcium release channel of skeletal and cardiac muscle

27 September 2017

1 reference

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Beta subunits of voltage-gated calcium channels

27 September 2017

1 reference

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Mutations in SEPN1 cause congenital muscular dystrophy with spinal rigidity and restrictive respiratory syndrome.

27 September 2017

1 reference

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27 September 2017

1 reference

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Structural evidence for direct interaction between the molecular components of the transverse tubule/sarcoplasmic reticulum junction in skeletal muscle

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

Primary structure and expression from complementary DNA of skeletal muscle ryanodine receptor.

27 September 2017

1 reference

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Intramembrane charge movement restored in dysgenic skeletal muscle by injection of dihydropyridine receptor cDNAs

27 September 2017

1 reference

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Stabilization of calcium release channel (ryanodine receptor) function by FK506-binding protein

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

Novel congenital myopathy locus identified in Native American Indians at 12q13.13-14.1.

27 September 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

The identification of genes with unique and essential functions in the development of the zebrafish, Danio rerio.

30 May 2018

1 reference

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Enhanced dihydropyridine receptor channel activity in the presence of ryanodine receptor.

30 May 2018

1 reference

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accordion, a zebrafish behavioral mutant, has a muscle relaxation defect due to a mutation in the ATPase Ca2+ pump SERCA1.

30 May 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

The zebrafish shocked gene encodes a glycine transporter and is essential for the function of early neural circuits in the CNS.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

Non-sense mutations in the dihydropyridine receptor beta1 gene, CACNB1, paralyze zebrafish relaxed mutants

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

Zebrafish relatively relaxed mutants have a ryanodine receptor defect, show slow swimming and provide a model of multi-minicore disease.

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

Developmental transition of touch response from slow muscle-mediated coilings to fast muscle-mediated burst swimming in zebrafish

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

De novo occurrence of novel SPG3A/atlastin mutation presenting as cerebral palsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

Physiological properties of zebrafish embryonic red and white muscle fibers during early development

21 January 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

Time course of the development of motor behaviors in the zebrafish embryo

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

A genetic screen for mutations affecting embryogenesis in zebrafish.

29 November 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4056023

Involvement of dihydropyridine receptors in excitation–contraction coupling in skeletal muscle

29 November 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

Slow inward calcium currents have no obvious role in muscle excitation–contraction coupling

21 January 2018

1 reference

https://api.crossref.org/works/10.1038%2FNCOMMS2952

Regulation of voltage-gated Ca2+ channels by calmodulin

21 January 2018

1 reference

12 December 2020

Native American myopathy: congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia

1 reference

12 December 2020

Congenital myopathies

1 reference

12 December 2020

The Cavβ subunit prevents RFP2-mediated ubiquitination and proteasomal degradation of L-type channels

1 reference

12 December 2020

Identifiers

DOI

10.1038/NCOMMS2952

1 reference

Dimensions Publication ID

25 June 2017

0 references

1018214413

0 references

OpenCitations bibliographic resource ID

1603631

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1 reference

Consolidated OpenCitations Corpus – April 2017

OpenCitations bibliographic resource ID

1603631

1 reference