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Pathway-driven discovery of epilepsy genes.
scientific article published on 24 February 2015
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Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
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1 March 2020
review article
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Europe PubMed Central
title
Pathway-driven discovery of epilepsy genes
(English)
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Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
author
Jeffrey L. Noebels
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Jeffrey Noebels
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Europe PubMed Central
PMC publication ID
4852130
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
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1 March 2020
language of work or name
English
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publication date
24 February 2015
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Europe PubMed Central
PMC publication ID
4852130
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
published in
Nature Neuroscience
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Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
volume
18
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Europe PubMed Central
PMC publication ID
4852130
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https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
issue
3
1 reference
stated in
Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
page(s)
344-350
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Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
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1 March 2020
exact match
https://scigraph.springernature.com/pub.10.1038/nn.3933
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29 September 2017
beta subunit reshuffling modifies N- and P/Q-type Ca2+ channel subunit compositions in lethargic mouse brain
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PubMed Central
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29 September 2017
Overexpression of a Shaker-type potassium channel in mammalian central nervous system dysregulates native potassium channel gene expression.
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PubMed Central
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29 September 2017
Radicals r'aging
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PubMed Central
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29 September 2017
A novel potassium channel gene, KCNQ2, is mutated in an inherited epilepsy of newborns
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4852130
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29 September 2017
A missense mutation in the neuronal nicotinic acetylcholine receptor alpha 4 subunit is associated with autosomal dominant nocturnal frontal lobe epilepsy
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29 September 2017
Sequence of a probable potassium channel component encoded at Shaker locus of Drosophila
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29 September 2017
Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation
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PubMed Central
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4852130
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29 September 2017
Generating genetically modified mice using CRISPR/Cas-mediated genome engineering
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27 June 2018
Transcriptional and electrophysiological maturation of neocortical fast-spiking GABAergic interneurons
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27 June 2018
Febrile seizures and generalized epilepsy associated with a mutation in the Na+-channel beta1 subunit gene SCN1B.
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27 June 2018
Clinical features of early-onset Alzheimer disease in a large kindred with an E280A presenilin-1 mutation.
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27 June 2018
Drosophila mutants with opposing effects on nerve excitability: genetic and spatial interactions in repetitive firing
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27 June 2018
Dominant-negative effects of KCNQ2 mutations are associated with epileptic encephalopathy.
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4 September 2018
The neuron identity problem: form meets function.
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4 September 2018
Genome-wide analysis of A-to-I RNA editing by single-molecule sequencing in Drosophila.
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4 September 2018
SCN1A testing for epilepsy: application in clinical practice.
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4 September 2018
Masking epilepsy by combining two epilepsy genes.
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4 September 2018
Selective localization of cardiac SCN5A sodium channels in limbic regions of rat brain.
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https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4852130
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4 September 2018
Applying tensor-based morphometry to parametric surfaces can improve MRI-based disease diagnosis
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21 January 2018
Missense mutations in the sodium-gated potassium channel gene KCNT1 cause severe autosomal dominant nocturnal frontal lobe epilepsy
1 reference
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Crossref
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21 January 2018
Cardiac I(to), KCNE2, and Brugada syndrome: promiscuous subunit interactions, or what happens in HEK cells stays in HEK cells?
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12 December 2020
based on heuristic
inferred from PubMed ID database lookup
Identifiers
DOI
10.1038/NN.3933
1 reference
stated in
Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
PMC publication ID
4852130
1 reference
stated in
Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
PubMed publication ID
25710836
1 reference
stated in
Europe PubMed Central
PMC publication ID
4852130
reference URL
https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25710836%20AND%20SRC:MED&resulttype=core&format=json
retrieved
1 March 2020
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