Evidence map›Paper›PMID 8209253›Full record

ReviewScience (New York, N.Y.)1994

Forward and reverse genetic approaches to behavior in the mouse.

J S Takahashi, L H Pinto, M H Vitaterna

Abstract readReview
In one paragraph

Review in Science (New York, N.Y.), 1994. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 55 papers.

0numbers the graph read from it
0cells of the map it votes in
55citing papers in PubMed
13.5field-weighted citation impact, top 1% 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

55 citing papers in PubMed, 251 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. An inherited life-threatening arrhythmia model established by screening randomly mutagenized mice.Proceedings of the National Academy of Sciences of the United States of America · 2024
    Article
  6. Article
  7. A missense mutation inProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  8. Article
  9. Article
  10. The 50th anniversary of the Konopka and Benzer 1971 paper in PNAS: "Clock Mutants ofProceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  11. Molecular Evolution of clock Genes in Vertebrates.Journal of molecular evolution · 2021
    Article
  12. Review
  13. Review
  14. Tissue-specific FAH deficiency alters sleep-wake patterns and results in chronic tyrosinemia in mice.Proceedings of the National Academy of Sciences of the United States of America · 2019
    Article
  15. Review
  16. Article
  17. Review
  18. Review
  19. A mutagenesis-derivedMolecular vision · 2017
    Article
  20. Molecular components of the circadian clock in mammals.Diabetes, obesity & metabolism · 2015
    Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

3 authors at 1 institution in 1 country.

J S TakahashiDepartment of Neurobiology and Physiology, Northwestern University, Evanston, IL 60208.
L H Pinto
M H Vitaterna
U.S. National Science Foundation · US

Funding

TRAINING IN SENSORY PHYSIOLOGY AND PSYCHOPHYSICST32DC000015 · NIDCD · NORTHWESTERN UNIVERSITY · PI PETERSON, BARRY W · 1989 to 2002
$400k
MELATONIN SYNTHESIS IN RETINAL &RETINOBLASTOMA CELLSR01EY008467 · NEI · NORTHWESTERN UNIVERSITY · PI TAKAHASHI, JOSEPH S · 1990 to 1994
–
CELLULAR ANALYSIS OF VERTEBRATE CIRCADIAN PACEMAKERSR01MH039592 · NIMH · NORTHWESTERN UNIVERSITY · PI TAKAHASHI, JOSEPH S · 1985 to 1986
–
CIRCADIAN REGULATION OF IMMEDIATE-EARLY GENES IN SCNR01MH049241 · NIMH · NORTHWESTERN UNIVERSITY · PI TAKAHASHI, JOSEPH S · 1993 to 1995
–
CELLULAR ANALYSIS OF VERTEBRATE CIRCADIAN PACEMAKERR37MH039592 · NIMH · NORTHWESTERN UNIVERSITY · PI TAKAHASHI, JOSEPH S · 1988 to 1997
–
Howard Hughes Medical InstituteNEI NIH HHS EY08467NIDCD NIH HHS T32 DC000015NIMH NIH HHS MH39592NIMH NIH HHS MH49241
6 · The paper itself

Abstract

Modern molecular genetic and genomic approaches are revolutionizing the study of behavior in the mouse. "Reverse genetics" (from gene to phenotype) with targeted gene transfer provides a powerful tool to dissect behavior and has been used successfully to study the effects of null mutations in genes implicated in the regulation of long-term potentiation and spatial learning in mice. In addition, "forward genetics" (from phenotype to gene) with high-efficiency mutagenesis in the mouse can uncover unknown genes and has been used to isolate a behavioral mutant of the circadian system. With the recent availability of high-density genetic maps and physical mapping resources, positional cloning of virtually any mutation is now feasible in the mouse. Together, these approaches permit a molecular analysis of both known and previously unknown genes regulating behavior.

Indexed as

Behavior, AnimalGenetic TechniquesAnimalsCircadian RhythmFemaleGenetics, BehavioralLearningLong-Term PotentiationMaleMiceMice, Inbred StrainsMice, KnockoutMutagenesis

Identifiers

PMID8209253
PMCPMC3830945
OpenAlexW1980485998

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.