(Q41720371)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

review article

1 reference

title

Epilepsy genetics: an abundance of riches for biologists (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

author name string

J O McNamara

series ordinal

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

language of work or name

English

0 references

publication date

1 February 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

volume

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

page(s)

R168-70

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

Proposal for revised classification of epilepsies and epileptic syndromes. Commission on Classification and Terminology of the International League Against Epilepsy

10 November 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Sodium/hydrogen exchanger gene defect in slow-wave epilepsy mutant mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Targeting epilepsy genes

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Growth factors induce phosphorylation of the Na+/H+ antiporter, glycoprotein of 110 kD

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Autoradiographic maps of regional brain glucose consumption in resting, awake rats using [14c] 2-deoxyglucose

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

The regulation and modulation of pH in the nervous system

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Acidosis of rat dorsal vagal neurons in situ during spontaneous and evoked activity.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Knock-out mice reveal a critical antiepileptic role for neuropeptide Y.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Essential functions of synapsins I and II in synaptic vesicle regulation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Epilepsy and exacerbation of brain injury in mice lacking the glutamate transporter GLT-1

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Mice devoid of gamma-aminobutyrate type A receptor beta3 subunit have epilepsy, cleft palate, and hypersensitive behavior

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Early-onset epilepsy and postnatal lethality associated with an editing-deficient GluR-B allele in mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Eating disorder and epilepsy in mice lacking 5-HT2c serotonin receptors

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

A potassium channel mutation in weaver mice implicates membrane excitability in granule cell differentiation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Absence epilepsy in tottering mutant mice is associated with calcium channel defects

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Mutation of the Ca2+ channel beta subunit gene Cchb4 is associated with ataxia and seizures in the lethargic (lh) mouse

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Limbic epilepsy in transgenic mice carrying a Ca2+/calmodulin-dependent kinase II alpha-subunit mutation

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Ataxia and epileptic seizures in mice lacking type 1 inositol 1,4,5-trisphosphate receptor.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Overexpression of the neural growth-associated protein GAP-43 induces nerve sprouting in the adult nervous system of transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Mice lacking p35, a neuronal specific activator of Cdk5, display cortical lamination defects, seizures, and adult lethality

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Epilepsy and brain abnormalities in mice lacking the Otx1 gene

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Epileptic seizures caused by inactivation of a novel gene, jerky, related to centromere binding protein-B in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Mice lacking tissue non-specific alkaline phosphatase die from seizures due to defective metabolism of vitamin B-6.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Exon 1 of the HD gene with an expanded CAG repeat is sufficient to cause a progressive neurological phenotype in transgenic mice

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Deficiency of a protein-repair enzyme results in the accumulation of altered proteins, retardation of growth, and fatal seizures in mice.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Mice lacking both subunits of lysosomal beta-hexosaminidase display gangliosidosis and mucopolysaccharidosis

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Jimpy mutant mouse: a 74-base deletion in the mRNA for myelin proteolipid protein and evidence for a primary defect in RNA splicing

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

Ectopically expressed CAG repeats cause intranuclear inclusions and a progressive late onset neurological phenotype in the mouse.

1 reference

https://api.crossref.org/works/10.1016%2FS0960-9822%2898%2970102-2

7 January 2021

10.1016/S0960-9822(98)70102-2

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9501059%20AND%20SRC:MED&resulttype=core&format=json

10 November 2019

1 reference