(Q40454423)

English

A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties.

scientific article published on 24 February 2005

A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

A human congenital myasthenia-causing mutation (epsilon L78P) of the muscle nicotinic acetylcholine receptor with unusual single channel properties. (English)

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

congenital disorder

0 references

David Colquhoun

2

object named as

David Colquhoun

0 references

author name string

Christopher Shelley

1

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

David Colquhoun

2

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

language of work or name

0 references

publication date

24 February 2005

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Journal of Physiology

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

564

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Pt 2

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

377-396

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

Contributions of the non-alpha subunit residues (loop D) to agonist binding and channel gating in the muscle nicotinic acetylcholine receptor

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Inorganic, monovalent cations compete with agonists for the transmitter binding site of nicotinic acetylcholine receptors

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

A mutational analysis of the acetylcholine receptor channel transmitter binding site

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

The activation mechanism of alpha1 homomeric glycine receptors

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Crystal structure of an ACh-binding protein reveals the ligand-binding domain of nicotinic receptors

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Single-channel behavior of heteromeric alpha1beta glycine receptors: an attempt to detect a conformational change before the channel opens

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Nicotine and carbamylcholine binding to nicotinic acetylcholine receptors as studied in AChBP crystal structures

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Gating dynamics of the acetylcholine receptor extracellular domain.

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Binding, gating, affinity and efficacy: the interpretation of structure-activity relationships for agonists and of the effects of mutating receptors

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

The quality of maximum likelihood estimates of ion channel rate constants

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

On the stochastic properties of bursts of single ion channel openings and of clusters of bursts

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Fast events in single-channel currents activated by acetylcholine and its analogues at the frog muscle end-plate

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Function and structure in glycine receptors and some of their relatives

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Improved technique for studying ion channels expressed in Xenopus oocytes, including fast superfusion.

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Recessive inheritance and variable penetrance of slow-channel congenital myasthenic syndromes

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Mutations in different functional domains of the human muscle acetylcholine receptor alpha subunit in patients with the slow-channel congenital myasthenic syndrome

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

End-plate currents and acetylcholine noise at normal and myasthenic human end-plates

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Desensitization of diliganded mouse muscle nicotinic acetylcholine receptor channels

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

End-plate acetylcholine receptor deficiency due to nonsense mutations in the epsilon subunit

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Congenital myasthenic syndromes: A diverse array of molecular targets.

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Sleuthing molecular targets for neurological diseases at the neuromuscular junction

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

The dissociation of acetylcholine from open nicotinic receptor channels

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Properties of the human muscle nicotinic receptor, and of the slow-channel myasthenic syndrome mutant epsilonL221F, inferred from maximum likelihood fits

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Dependence of acetylcholine receptor channel kinetics on agonist concentration in cultured mouse muscle fibres

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Diseases of the neuromuscular junction

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Structure and gating mechanism of the acetylcholine receptor pore

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Congenital myasthenic syndromes due to heteroallelic nonsense/missense mutations in the acetylcholine receptor epsilon subunit gene: identification and functional characterization of six new mutations

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

A re-examination of adult mouse nicotinic acetylcholine receptor channel activation kinetics

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Activation of Torpedo acetylcholine receptors expressed in mouse fibroblasts. Single channel current kinetics reveal distinct agonist binding affinities

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Mutation of the acetylcholine receptor alpha subunit causes a slow-channel myasthenic syndrome by enhancing agonist binding affinity

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Mutation in the M1 domain of the acetylcholine receptor alpha subunit decreases the rate of agonist dissociation

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Single-channel activations and concentration jumps: comparison of recombinant NR1a/NR2A and NR1a/NR2D NMDA receptors

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Activation of recombinant mouse acetylcholine receptors by acetylcholine, carbamylcholine and tetramethylammonium

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Active calcium accumulation underlies severe weakness in a panel of mice with slow-channel syndrome.

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464449

29 August 2018

Slow-channel myasthenic syndrome caused by enhanced activation, desensitization, and agonist binding affinity attributable to mutation in the M2 domain of the acetylcholine receptor alpha subunit

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=1464449

29 August 2018

Joint distributions of apparent open and shut times of single-ion channels and maximum likelihood fitting of mechanisms

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

The distributions of the apparent open times and shut times in a single channel record when brief events cannot be detected

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

Asymptotic distributions of apparent open times and shut times in a single channel record allowing for the omission of brief events

1 reference

https://api.crossref.org/works/10.1113%2FJPHYSIOL.2004.081497

21 January 2018

A newly recognized congenital myasthenic syndrome attributed to a prolonged open time of the acetylcholine-induced ion channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/15731194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Burst kinetics of single calcium-activated potassium channels in cultured rat muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/15731194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Substance P reduces acetylcholine-induced currents in isolated bovine chromaffin cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/15731194

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1113/JPHYSIOL.2004.081497

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

PMC publication ID

0 references

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

20 September 2017

ResearchGate publication ID

0 references

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