Differential expression of kcnq2 splice variants: implications to m current function during neuronal development (Q28143016)

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12 May 2020

author name string

J S Smith

1

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12 May 2020

C A Iannotti

2

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12 May 2020

P Dargis

3

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12 May 2020

E P Christian

4

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12 May 2020

J Aiyar

5

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12 May 2020

language of work or name

English

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publication date

15 February 2001

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published in

Journal of Neuroscience

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12 May 2020

volume

21

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issue

4

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12 May 2020

page(s)

1096-1103

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A reduced K current due to a novel mutation in KCNQ2 causes neonatal convulsions

12 May 2020

cites work

1 reference

12 December 2020

Molecular cloning and functional expression of KCNQ5, a potassium channel subunit that may contribute to neuronal M-current diversity

1 reference

12 December 2020

A trafficking checkpoint controls GABA(B) receptor heterodimerization

1 reference

12 December 2020

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

1 reference

12 December 2020

The expression of two splice variants of the Kv3.1 potassium channel gene is regulated by different signaling pathways

1 reference

12 December 2020

Reconstitution of muscarinic modulation of the KCNQ2/KCNQ3 K( ) channels that underlie the neuronal M current

1 reference

12 December 2020

Modulation of the electrical differentiation of neurons by interactions with glia and other non-neuronal cells.

1 reference

12 December 2020

Muscarinic suppression of a novel voltage-sensitive K current in a vertebrate neurone

1 reference

12 December 2020

A new ER trafficking signal regulates the subunit stoichiometry of plasma membrane K(ATP) channels

1 reference

12 December 2020

1 reference

12 December 2020

KQT2, a new putative potassium channel family produced by alternative splicing. Isolation, genomic structure, and alternative splicing of the putative potassium channels

1 reference

12 December 2020

The role of glial cells in synaptic function

1 reference

12 December 2020

The KCNQ2 potassium channel: splice variants, functional and developmental expression. Brain localization and comparison with KCNQ3

1 reference

12 December 2020

Colocalization and coassembly of two human brain M-type potassium channel subunits that are mutated in epilepsy

1 reference

12 December 2020

Identification and cloning of neuroblastoma-specific and nerve tissue-specific genes through compiled expression profiles

1 reference

12 December 2020

Coassembly of K(V)LQT1 and minK (IsK) proteins to form cardiac I(Ks) potassium channel

1 reference

12 December 2020

Mutations in the KCNQ4 gene are responsible for autosomal dominant deafness in four DFNA2 families.

1 reference

12 December 2020

Surface expression and single channel properties of KCNQ2/KCNQ3, M-type K channels involved in epilepsy

1 reference

12 December 2020

Potassium channels from NG108-15 neuroblastoma-glioma hybrid cells. Primary structure and functional expression from cDNAs

1 reference

12 December 2020

A constitutively open potassium channel formed by KCNQ1 and KCNE3

1 reference

12 December 2020

The new voltage gated potassium channel KCNQ5 and neonatal convulsions

1 reference

12 December 2020

Cloned potassium channels from eukaryotes and prokaryotes

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12 December 2020

ATP-sensitive K( )-channel run-down is Mg2 dependent

1 reference

12 December 2020

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

1 reference

12 December 2020

Rapid amplification of cDNA ends

1 reference

12 December 2020

A potassium channel mutation in neonatal human epilepsy

1 reference

12 December 2020

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

1 reference

12 December 2020

Positional cloning of a novel potassium channel gene: KVLQT1 mutations cause cardiac arrhythmias

1 reference

12 December 2020

Overexpression of a potassium channel gene perturbs neural differentiation.

1 reference

12 December 2020

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

1 reference

12 December 2020

Endogenous voltage-gated potassium channels in human embryonic kidney (HEK293) cells

1 reference

12 December 2020

Functional expression of two KvLQT1-related potassium channels responsible for an inherited idiopathic epilepsy

1 reference

12 December 2020

Alternative splicing contributes to K channel diversity in the mammalian central nervous system

1 reference

12 December 2020

Overexpression of potassium channel RNA: in vivo development rescues neurons from suppression of morphological differentiation in vitro

1 reference

12 December 2020

Eight potassium channel families revealed by the C. elegans genome project

1 reference

12 December 2020

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

1 reference

12 December 2020

Characterization of primary human fetal dissociated central nervous system cultures with an emphasis on microglia

1 reference

12 December 2020

A new twist in the saga of charge movement in voltage-dependent ion channels

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12 December 2020

K(V)LQT1 and lsK (minK) proteins associate to form the I(Ks) cardiac potassium current

1 reference

12 December 2020

Potassium currents in developing neurons.

1 reference

12 December 2020

Induction of neurite outgrowth in the IMR-32 human neuroblastoma cell line by nerve growth factor.

1 reference

12 December 2020

Structural and mutational analysis of KCNQ2, the major gene locus for benign familial neonatal convulsions

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12 December 2020

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

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12 December 2020

10.1523/JNEUROSCI.21-04-01096.2001

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=PMCID:PMC6762257&resulttype=core&format=json

12 May 2020

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12 May 2020

PubMed publication ID

11160379

1 reference