Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation. (Q52535337)

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scientific article published in June 1999

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English	Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation.	scientific article published in June 1999

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scholarly article

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10366610%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

Activation and inactivation of the voltage-gated sodium channel: role of segment S5 revealed by a novel hyperkalaemic periodic paralysis mutation (English)

1 reference

Europe PubMed Central

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10366610%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

periodic paralysis

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author name string

S Bendahhou

1

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8 December 2019

T R Cummins

2

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8 December 2019

R Tawil

3

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8 December 2019

S G Waxman

4

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8 December 2019

L J Ptácek

5

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8 December 2019

language of work or name

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publication date

1 June 1999

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8 December 2019

Journal of Neuroscience

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8 December 2019

19

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8 December 2019

12

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8 December 2019

4762-4771

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8 December 2019

A new technique for the assay of infectivity of human adenovirus 5 DNA

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Human sodium channel myotonia: slowed channel inactivation due to substitutions for a glycine within the III-IV linker

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A cluster of hydrophobic amino acid residues required for fast Na(+)-channel inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role of transmembrane segment S5 on gating of voltage-dependent K+ channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional expression of the Ile693Thr Na+ channel mutation associated with paramyotonia congenita in a human cell line

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hyperkalemic periodic paralysis with cardiac dysrhythmia: A novel sodium channel mutation?

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A mutation in segment I-S6 alters slow inactivation of sodium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Primary structure of Electrophorus electricus sodium channel deduced from cDNA sequence

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Persistent sodium currents through brain sodium channels induced by G protein betagamma subunits

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Impaired slow inactivation in mutant sodium channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Phenotype variation and newcomers in ion channel disorders

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional expression of sodium channel mutations identified in families with periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow inactivation differs among mutant Na channels associated with myotonia and periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role in fast inactivation of the IV/S4-S5 loop of the human muscle Na+ channel probed by cysteine mutagenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow sodium channel inactivation in mammalian muscle: a possible role in regulating excitability

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Novel mutations in families with unusual and variable disorders of the skeletal muscle sodium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Functional consequences of a Na+ channel mutation causing hyperkalemic periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channel mutations in paramyotonia congenita uncouple inactivation from activation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channel mutations in acetazolamide-responsive myotonia congenita, paramyotonia congenita, and hyperkalemic periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Segmental exchanges define 4-aminopyridine binding and the inner mouth of K+ pores

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A critical role for the S4-S5 intracellular loop in domain IV of the sodium channel alpha-subunit in fast inactivation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Defective fast inactivation recovery and deactivation account for sodium channel myotonia in the I1160V mutant

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Insertion of a SNS-specific tetrapeptide in S3-S4 linker of D4 accelerates recovery from inactivation of skeletal muscle voltage-gated Na channel mu1 in HEK293 cells

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Role in fast inactivation of conserved amino acids in the IV/S4-S5 loop of the human muscle Na+ channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow Na+ channel inactivation must be disrupted to evoke prolonged depolarization-induced paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Serine-1321-independent regulation of the mu 1 adult skeletal muscle Na+ channel by protein kinase C

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Mutations in an S4 segment of the adult skeletal muscle sodium channel cause paramyotonia congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A defect in skeletal muscle sodium channel deactivation exacerbates hyperexcitability in human paramyotonia congenita

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Improved patch-clamp techniques for high-resolution current recording from cells and cell-free membrane patches

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Alterations in activation gating of single Shaker A-type potassium channels by the Sh5 mutation

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Sodium channel mutations in paramyotonia congenita exhibit similar biophysical phenotypes in vitro

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Structural parts involved in activation and inactivation of the sodium channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A role for hydrophobic residues in the voltage-dependent gating of Shaker K+ channels

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A Met-to-Val mutation in the skeletal muscle Na+ channel alpha-subunit in hyperkalaemic periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identification of a mutation in the gene causing hyperkalemic periodic paralysis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

N-type inactivation and the S4-S5 region of the Shaker K+ channel

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A novel sodium channel mutation causing a hyperkalemic paralytic and paramyotonic syndrome with variable clinical expressivity

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The "megaprimer" method of site-directed mutagenesis

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Slow sodium channel inactivation in rat fast-twitch muscle

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A proposed mutation, Val781Ile, associated with hyperkalemic periodic paralysis and cardiac dysrhythmia is a benign polymorphism

1 reference

https://pubmed.ncbi.nlm.nih.gov/10366610

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1523/JNEUROSCI.19-12-04762.1999

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10366610%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

PMC publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10366610%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

PubMed publication ID

1 reference

Europe PubMed Central

PMC publication ID

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10366610%20AND%20SRC:MED&resulttype=core&format=json

8 December 2019

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