(Q51963281)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:11580756%20AND%20SRC:MED&resulttype=core&format=json

11 November 2019

title

Loss of the potassium channel beta-subunit gene, KCNAB2, is associated with epilepsy in patients with 1p36 deletion syndrome (English)

1 reference

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11 November 2019

10

1 reference

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11 November 2019

author name string

H A Heilstedt

1

1 reference

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11 November 2019

D L Burgess

2

1 reference

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11 November 2019

A E Anderson

3

1 reference

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11 November 2019

A Chedrawi

4

1 reference

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11 November 2019

B Tharp

5

1 reference

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11 November 2019

O Lee

6

1 reference

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11 November 2019

C D Kashork

7

1 reference

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11 November 2019

D E Starkey

8

1 reference

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11 November 2019

Y Q Wu

9

1 reference

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11 November 2019

L G Shaffer

11

1 reference

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11 November 2019

S K Shapira

12

1 reference

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11 November 2019

publication date

1 September 2001

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11 November 2019

1 reference

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11 November 2019

volume

42

1 reference

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11 November 2019

issue

9

1 reference

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11 November 2019

page(s)

1103-1111

1 reference

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Chromosome 1p36 deletions: the clinical phenotype and molecular characterization of a common newly delineated syndrome

11 November 2019

cites work

1 reference

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Molecular mechanisms for constitutional chromosomal rearrangements in humans

21 January 2018

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Molecular refinement of the 1p36 deletion syndrome reveals size diversity and a preponderance of maternally derived deletions

21 January 2018

1 reference

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Localization of two potassium channel beta subunit genes, KCNA1B and KCNA2B.

21 January 2018

1 reference

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Cloned potassium channels from eukaryotes and prokaryotes

21 January 2018

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Inactivation properties of voltage-gated K+ channels altered by presence of beta-subunit

21 January 2018

1 reference

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Determination of the subunit stoichiometry of a voltage-activated potassium channel

21 January 2018

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Subunit stoichiometry of a mammalian K+ channel determined by construction of multimeric cDNAs.

21 January 2018

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Images of purified Shaker potassium channels

21 January 2018

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Distinct functional stoichiometry of potassium channel beta subunits

21 January 2018

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Auxiliary subunits of voltage-gated ion channels

21 January 2018

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Beta subunits promote K+ channel surface expression through effects early in biosynthesis

21 January 2018

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Altered synaptic transmission in Drosophila hyperkinetic mutants.

21 January 2018

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Molecular characterization of Shaker, a Drosophila gene that encodes a potassium channel

21 January 2018

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Genetics and molecular biology of ionic channels in Drosophila

21 January 2018

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Benign familial neonatal convulsions linked to genetic markers on chromosome 20.

21 January 2018

1 reference

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A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns

21 January 2018

1 reference

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A pore mutation in a novel KQT-like potassium channel gene in an idiopathic epilepsy family

21 January 2018

1 reference

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KCNQ2 and KCNQ3 potassium channel subunits: molecular correlates of the M-channel

21 January 2018

1 reference

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Moderate loss of function of cyclic-AMP-modulated KCNQ2/KCNQ3 K+ channels causes epilepsy

21 January 2018

1 reference

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A novel mutation in the human voltage-gated potassium channel gene (Kv1.1) associates with episodic ataxia type 1 and sometimes with partial epilepsy

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.08801.X

Clinical, genetic, and expression studies of mutations in the potassium channel gene KCNA1 reveal new phenotypic variability

21 January 2018

1 reference

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Deletion of the K(V)1.1 potassium channel causes epilepsy in mice.

21 January 2018

1 reference

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Developmental seizure susceptibility of kv1.1 potassium channel knockout mice

21 January 2018

1 reference

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A region of consistent deletion in neuroblastoma maps within human chromosome 1p36.2-36.3

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.08801.X

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.08801.X

A KCNQ2 splice site mutation causing benign neonatal convulsions in a Scottish family

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.08801.X

Molecular diversity of K+ channels

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1528-1157.2001.08801.X

Functional and molecular aspects of voltage-gated K+ channel beta subunits

21 January 2018

1 reference

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Presynaptic A-current based on heteromultimeric K+ channels detected in vivo

21 January 2018

1 reference

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Heteromultimeric K+ channels in terminal and juxtaparanodal regions of neurons

21 January 2018

1 reference

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beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain

21 January 2018

1 reference

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The inactivation behaviour of voltage-gated K-channels may be determined by association of alpha- and beta-subunits.

21 January 2018

1 reference

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Shaker K+ channel beta subunits belong to an NAD(P)H-dependent oxidoreductase superfamily.

21 January 2018

1 reference

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Functional characterization of Kv channel beta-subunits from rat brain

21 January 2018

1 reference

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Structure of a voltage-dependent K+ channel beta subunit

21 January 2018

1 reference

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

21 January 2018

1 reference

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The long QT syndromes: genetic basis and clinical implications

21 January 2018

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Coexpression of the KCNA3B gene product with Kv1.5 leads to a novel A-type potassium channel

21 January 2018

1 reference

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