Evidence map›Paper›PMID 10234005›Full record

ArticleThe Journal of neuroscience : the official journal of the Society for Neuroscience1999

Mapping quantitative trait loci for seizure response to a GABAA receptor inverse agonist in mice.

H K Gershenfeld, P E Neumann, X Li, P L St Jean, S M Paul

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of neuroscience : the official journal of the Society for Neuroscience, 1999. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 27% 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

13 citing papers in PubMed, 31 citations in OpenAlex.

  1. Article
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  6. The genetic basis of adrenal gland weight and structure in BXD recombinant inbred mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2011
    Article
  7. Article
  8. Article
  9. Article
  10. Use of chromosome substitution strains to identify seizure susceptibility loci in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
    Article
  11. Fine mapping of a major locus on chromosome 10 for exploratory and fear-like behavior in mice.Mammalian genome : official journal of the International Mammalian Genome Society · 2005
    Article
  12. Identification of a monogenic locus (jams1) causing juvenile audiogenic seizures in mice.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2002
    Article
  13. 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

5 authors at 4 institutions in 2 countries.

H K GershenfeldDepartment of Psychiatry, University of Texas Southwestern Medical Center, Dallas, Texas 75235-8898, USA.
P E Neumann
X Li
P L St Jean
S M Paul
The University of Texas Southwestern Medical Center · USDalhousie University · CAIndiana University – Purdue University Indianapolis · USResearch Triangle Park Foundation · US

Funding

POSITIONAL CLONING OF A PLEIOTROPIC LOCUS FOR BEHAVIORR01MH058882 · NIMH · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · PI GERSHENFELD, HOWARD K · 1998 to 2002
$688k
NIMH NIH HHS R01-MH58882
6 · The paper itself

Abstract

To define the genetic contributions affecting individual differences in seizure threshold, a beta carboline [methyl-beta-carboline-3-carboxylate (beta-CCM)]-induced model of generalized seizures was genetically dissected in mice. beta-CCM is a GABAA receptor inverse agonist and convulsant. By measuring the latency to generalized seizures after beta-CCM administration to A/J and C57BL6/J mice and their progeny, we estimated a heritability of 0.28 +/- 0.10. A genome wide screen in an F2 population of these parental strains (n = 273) mapped quantitative trait loci (QTLs) on proximal chromosome 7 [logarithm of the likelihood for linkage (LOD) = 3.71] and distal chromosome 10 (LOD = 4.29) for seizure susceptibility, explaining approximately 22 and 25%, respectively, of the genetic variance for this seizure trait. The best fitting logistic regression model suggests that the A/J allele at each locus increases the likelihood of seizures approximately threefold. In a subsequent backcross population (n = 223), we mapped QTLs on distal chromosome 4 (LOD = 2.88) and confirmed the distal chromosome 10 QTLs (LOD = 4.36). In the backcross, the C57BL/6J allele of the chromosome 10 QTL decreases the risk of seizures approximately twofold. These QTLs may ultimately lead to the identification of genes influencing individual differences in seizure threshold in mice and the discovery of novel anticonvulsant agents. The colocalization on distal chromosome 10 of a beta-CCM susceptibility QTL and a QTL for open field ambulation and vertical movement suggests the existence of a single, pleiotropic locus, which we have named Exq1.

Indexed as

Chromosome MappingQuantitative Trait, HeritableAnimalsBehavior, AnimalCarbolinesChromosome SegregationConvulsantsFemaleGABA AgonistsGenetic LinkageGenetic Predisposition to DiseaseHumansLod ScoreMaleMiceMice, Inbred Strainsbeta-carboline-3-carboxylic acid methyl esterCarbolinesConvulsantsGABA Agonists

Identifiers

PMID10234005
PMCPMC6782732
OpenAlexW1642899901

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.