Literature DB >> 11471049

Trans-NIH neuroscience initiatives on mouse phenotyping and mutagenesis.

S O Moldin1, M E Farmer, H R Chin, J F Battey .   

Abstract

In the post-genomic era, the laboratory mouse will excel as a premier mammalian system to study normal and disordered biological processes, in part because of low cost, but largely because of the rich opportunities that exist for exploiting genetic tools and technologies in the mouse to systematically determine mammalian gene function. Many robust models of human disease may therefore be developed, and these in turn will provide critical clues to understanding gene function. The full potential of the mouse for understanding many of the neural and behavioral phenotypes of relevance to neuroscientists has yet to be realized. With the full anatomy of the mouse genome at hand, researchers for the first time will be able to move beyond traditional gene-by-gene approaches and take a global view of gene expression patterns crucial for neurobiological processes. In response to an action plan for mouse genomics developed on the basis of recommendations from the scientific community, seven institutes of the National Institutes of Health (NIH) initiated in 1999 a mouse genetics research program that specifically focused on neurobiology and complex behavior. The specific goals of these neuroscience initiatives are to develop high-throughput phenotyping assays and to initiate genome-wide mutagenesis projects to identify hundreds of mutant strains with heritable abnormalities of high relevance to neuroscientists. Assays and mutants generated in these efforts will be made widely available to the scientific community, and such resources will provide neuroscientists unprecedented opportunities to elucidate the molecular mechanisms of neural function and complex behavior. Such research tools ultimately will permit the manipulation and analysis of the mouse genome, as a means of gaining insight into the genetic bases of the mammalian nervous system and its complex disorders.

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Mesh:

Year:  2001        PMID: 11471049     DOI: 10.1007/s00335-001-4005-7

Source DB:  PubMed          Journal:  Mamm Genome        ISSN: 0938-8990            Impact factor:   2.957


  10 in total

1.  Changes in behaviors of male C57BL/6J mice across adult life span and effects of dietary restriction.

Authors:  Andreas Fahlström; Hugo Zeberg; Brun Ulfhake
Journal:  Age (Dordr)       Date:  2011-10-12

2.  Identification of mutations from phenotype-driven ENU mutagenesis in mouse chromosome 7.

Authors:  Cymbeline T Culiat; Mitchell L Klebig; Zhaowei Liu; Heidi Monroe; Beverly Stanford; Jayashree Desai; Samvit Tandan; Lori Hughes; Marilyn K Kerley; Donald A Carpenter; Dabney K Johnson; Eugene M Rinchik; Qingbo Li
Journal:  Mamm Genome       Date:  2005-08       Impact factor: 2.957

3.  ENU mutagenesis in mice identifies candidate genes for hypogonadism.

Authors:  Jeffrey Weiss; Lisa A Hurley; Rebecca M Harris; Courtney Finlayson; Minghan Tong; Lisa A Fisher; Jennifer L Moran; David R Beier; Christopher Mason; J Larry Jameson
Journal:  Mamm Genome       Date:  2012-01-19       Impact factor: 2.957

4.  Neurobehavioral mutants identified in an ENU-mutagenesis project.

Authors:  Melloni N Cook; Jonathan P Dunning; Ronald G Wiley; Elissa J Chesler; Dabney K Johnson; Darla R Miller; Dan Goldowitz
Journal:  Mamm Genome       Date:  2007-07-15       Impact factor: 2.957

5.  Forward genetic screens to identify circadian rhythm mutants in mice.

Authors:  Sandra M Siepka; Joseph S Takahashi
Journal:  Methods Enzymol       Date:  2005       Impact factor: 1.600

6.  Role of Environment and Experimenter in Reproducibility of Behavioral Studies With Laboratory Mice.

Authors:  Martina Nigri; Johanna Åhlgren; David P Wolfer; Vootele Voikar
Journal:  Front Behav Neurosci       Date:  2022-02-18       Impact factor: 3.558

Review 7.  Finding new clock components: past and future.

Authors:  Joseph S Takahashi
Journal:  J Biol Rhythms       Date:  2004-10       Impact factor: 3.182

Review 8.  Large-scale mutagenesis and phenotypic screens for the nervous system and behavior in mice.

Authors:  Martha Hotz Vitaterna; Lawrence H Pinto; Joseph S Takahashi
Journal:  Trends Neurosci       Date:  2006-03-07       Impact factor: 13.837

9.  The optokinetic reflex as a tool for quantitative analyses of nervous system function in mice: application to genetic and drug-induced variation.

Authors:  Hugh Cahill; Jeremy Nathans
Journal:  PLoS One       Date:  2008-04-30       Impact factor: 3.240

10.  Corticotropin releasing factor-overexpressing mouse is a model of chronic stress-induced muscle atrophy.

Authors:  Wesuk Kang; Tao Tong; Taesun Park
Journal:  PLoS One       Date:  2020-02-12       Impact factor: 3.240

  10 in total

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