Evidence map›Paper›PMID 15389317›Full record

ArticleMammalian genome : official journal of the International Mammalian Genome Society2004

Genetic and phenotypic analysis of seizure susceptibility in PL/J mice.

Toshimori Kitami, Sheila Ernest, Laura Gallaugher, Lee Friedman, Wayne N Frankel, Joseph H Nadeau

Abstract read
PubMed Publisher
In one paragraph

Article in Mammalian genome : official journal of the International Mammalian Genome Society, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
0.4field-weighted citation impact, top 48% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 15 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Szt2, a novel gene for seizure threshold in mice.Genes, brain, and behavior · 2009
    Article
  5. Fine mapping of an epilepsy modifier gene on mouse Chromosome 19.Mammalian genome : official journal of the International Mammalian Genome Society · 2009
    Article
  6. Article
  7. Genetic modifiers affecting severity of epilepsy caused by mutation of sodium channel Scn2a.Mammalian genome : official journal of the International Mammalian Genome Society · 2005
    Article
  8. Development of a new genetic model for absence epilepsy: spike-wave seizures in C3H/He and backcross mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2005
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 5 institutions in 1 country.

Toshimori KitamiDepartment of Genetics, Case Western Reserve University School of Medicine, Cleveland, Ohio 44106, USA.
Sheila Ernest
Laura Gallaugher
Lee Friedman
Wayne N Frankel
Joseph H Nadeau
Case Western Reserve University · USDiscovery Institute · USJackson Laboratory · USLouis Stokes Cleveland VA Medical Center · USUniversity School · US

Funding

GENETIC DETERMINANTS OF EPILEPSY IN MURINE SYSTEMSR01NS031348 · NINDS · JACKSON LABORATORY · PI SANDS, TRISTAN T · 1993 to 2025
$11.5M
Genetic Determinants of Epilepsy in Murine SystemsR37NS031348 · NINDS · JACKSON LABORATORY · PI FRANKEL, WAYNE N. · 2014 to 2020
$5.8M
SLEEP AND ENTRAINMENT OF SCN FUNCTIONR01HL064278 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI STROHL, KINGMAN PERKINS · 1999 to 2002
$871k
GENETIC CONTROL OF HOMOCYSTEINE METABOLISM IN MICER01HL058982 · NHLBI · CASE WESTERN RESERVE UNIVERSITY · PI NADEAU, JOSEPH H. · 1998 to 2000
$389k
NHLBI NIH HHS HL58982NHLBI NIH HHS HL64278NINDS NIH HHS NS31348
6 · The paper itself

Abstract

Epilepsy is one of the most common but genetically complex neurological disorders in humans. Identifying animal models that recapitulate human epilepsies is important for pharmacological studies of anticonvulsants, dissection of molecular and biochemical pathogenesis of epilepsy, and discovery of epilepsy susceptibility genes. We discovered that the PL/J inbred mouse strain is susceptible to handling- and rhythmic tossing-induced seizure. The tonic-clonic and generalized seizures observed after induction were accompanied by abnormal EEGs, similar to seizures observed in EL and SWXL-4 mice. PL/J mice also had an extremely low threshold to electroconvulsive seizures compared to other strains and showed variable sensitivity to pentylenetetrazole-induced seizures. Gross neurostructural abnormalities were not found in PL/J mice. Crosses with the seizure-resistant C57BL/6 J strain revealed semidominant inheritance of the rhythmic tossing seizure trait with low penetrance. F2 progeny indicated that the genetic inheritance of seizure susceptibility in PL/J is non-Mendelian. We crossed DBA/2 J mice, which are resistant to rhythmic tossing seizure but susceptible to audiogenic seizures, to PL/J. We found that seizure penetrance in (DBA/2 J x PL/J)F1 mice was similar to the penetrance in (C57BL/6 J x PL/J)F1 mice but the severity and frequency of seizure were higher in (DBA/2 J x PL/J)F1 mice. The PL/J strain serves as an interesting new model for studying the genetics, neurobiology, and pharmacology of epilepsy.

Indexed as

AnimalsConvulsantsCrosses, GeneticDisease Models, AnimalElectroencephalographyElectroshockEpilepsyFemaleGenetic Predisposition to DiseaseMaleMiceMice, Inbred C57BLMice, Inbred DBAMice, Neurologic MutantsPentylenetetrazoleSeizuresConvulsantsPentylenetetrazole

Identifiers

PMID15389317
OpenAlexW2067658528

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.