Ion channel genes and human neurological disease: recent progress, prospects, and challenges. (Q33603836)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

review article

1 reference

title

Ion channel genes and human neurological disease: recent progress, prospects, and challenges (English)

1 reference

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5 December 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

E C Cooper

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

language of work or name

English

0 references

publication date

1 April 1999

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

Proceedings of the National Academy of Sciences of the United States of America

5 December 2019

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

96

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

issue

9

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5 December 2019

page(s)

4759-4766

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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

KCNQ4, a novel potassium channel expressed in sensory outer hair cells, is mutated in dominant deafness

5 December 2019

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Episodic ataxia mutations in Kv1.1 alter potassium channel function by dominant negative effects or haploinsufficiency

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The Structure of the Potassium Channel: Molecular Basis of K+ Conduction and Selectivity

21 June 2018

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21 June 2018

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21 June 2018

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Patch-clamp recordings from cerebellar basket cell bodies and their presynaptic terminals reveal an asymmetric distribution of voltage-gated potassium channels.

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome

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21 June 2018

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21 June 2018

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21 June 2018

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A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy

21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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21 June 2018

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A mutation in the human ryanodine receptor gene associated with central core disease

21 June 2018

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Presynaptic calcium current modulation by a metabotropic glutamate receptor.

21 January 2018

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Neurobiology of the Caenorhabditis elegans genome.

21 January 2018

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Regulation of ion channel expression by cytoplasmic subunits.

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The familial periodic paralyses and nondystrophic myotonias.

21 January 2018

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Modulation of cardiac Na+ channel expression in Xenopus oocytes by beta 1 subunits.

21 January 2018

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The physiology and pharmacology of melatonin in humans

21 January 2018

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Pathophysiological mechanisms of dominant and recessive KVLQT1 K+ channel mutations found in inherited cardiac arrhythmias.

21 January 2018

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Mutations in the ryanodine receptor gene in central core disease and malignant hyperthermia

21 January 2018

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Specific alteration of spontaneous GABAergic inhibition in cerebellar purkinje cells in mice lacking the potassium channel Kv1. 1.

21 January 2018

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30 October 2018

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21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

Benign familial neonatal convulsions: confirmation of genetic heterogeneity and further evidence for a second locus on chromosome 8q

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

DuP 996 (3,3-bis(4-pyrindinylmethyl)-1-phenylindolin-2-one) enhances the stimulus-induced release of acetylcholine from rat brain in vitro and in vivo

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

Hereditary myokymia and periodic ataxia

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

Autosomal dominant episodic ataxia: a heterogeneous syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

Single-channel analysis of a delayed rectifier K+ channel in Xenopus myelinated nerve

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

Hypomyelination alters K+ channel expression in mouse mutants shiverer and Trembler

21 January 2018

1 reference

https://api.crossref.org/works/10.1073%2FPNAS.96.9.4759

21 January 2018

Identifiers

DOI

10.1073/PNAS.96.9.4759

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

0 references

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:10220366%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference