Literature DB >> 11065339

Effect of the genetic background on the phenotype of mouse mutations.

X Montagutelli1.   

Abstract

An increasing number of scientific articles report that the phenotype of a given single gene mutation in mice is modulated by the genetic background of the inbred strain in which the mutation is maintained. This effect is attributable to so-called modifier genes, which act in combination with the causative gene. The modulation of the phenotype can be major, as exemplified in the case of several mouse models of polycystic kidney disease. Because of the existence of inbred strains and the possibility of developing congenic strains, the effect of the genetic background can be analyzed in mice, including the identification of major modifier genes. Furthermore, by transferring a given mutation into different genetic backgrounds, mouse models can be manipulated with the aim of more accurately mimicking specific features of human diseases.

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Year:  2000        PMID: 11065339

Source DB:  PubMed          Journal:  J Am Soc Nephrol        ISSN: 1046-6673            Impact factor:   10.121


  60 in total

1.  Telomerase immortalization of principal cells from mouse collecting duct.

Authors:  Stacy L Steele; Yongren Wu; Robert J Kolb; Monika Gooz; Courtney J Haycraft; Kent T Keyser; Lisa Guay-Woodford; Hai Yao; P Darwin Bell
Journal:  Am J Physiol Renal Physiol       Date:  2010-10-06

2.  Bulk segregation mapping of mutations in closely related strains of mice.

Authors:  Yu Xia; Sungyong Won; Xin Du; Pei Lin; Charles Ross; Diantha La Vine; Sean Wiltshire; Gabriel Leiva; Silvia M Vidal; Belinda Whittle; Christopher C Goodnow; James Koziol; Eva Marie Y Moresco; Bruce Beutler
Journal:  Genetics       Date:  2010-10-05       Impact factor: 4.562

3.  Targeted disruption of the gene for the PAK5 kinase in mice.

Authors:  Xiaofan Li; Audrey Minden
Journal:  Mol Cell Biol       Date:  2003-10       Impact factor: 4.272

4.  Disruption of ZAS3 in mice alters NF-kappaB and AP-1 DNA binding and T-cell development.

Authors:  Carl E Allen; John Richards; Natarajan Muthusamy; Herbert Auer; Yang Liu; Michael L Robinson; John A Barnard; Lai-Chu Wu
Journal:  Gene Expr       Date:  2007

Review 5.  Interpreting genetic effects through models of cardiac electromechanics.

Authors:  S A Niederer; S Land; S W Omholt; N P Smith
Journal:  Am J Physiol Heart Circ Physiol       Date:  2012-10-05       Impact factor: 4.733

6.  Rearing and Double-stranded RNA-mediated Gene Knockdown in the Hide Beetle, Dermestes maculatus.

Authors:  Jie Xiang; Katie Reding; Leslie Pick
Journal:  J Vis Exp       Date:  2016-12-28       Impact factor: 1.355

7.  Genetic susceptibility to toxicologic lung responses among inbred mouse strains following exposure to carbon nanotubes and profiling of underlying gene networks.

Authors:  Evan A Frank; Vinicius S Carreira; Kumar Shanmukhappa; Mario Medvedovic; Daniel R Prows; Jagjit S Yadav
Journal:  Toxicol Appl Pharmacol       Date:  2017-04-19       Impact factor: 4.219

8.  Lack of guanylate cyclase C results in increased mortality in mice following liver injury.

Authors:  Elizabeth A Mann; Kumar Shanmukhappa; Mitchell B Cohen
Journal:  BMC Gastroenterol       Date:  2010-08-02       Impact factor: 3.067

9.  Determination of reference genes for circadian studies in different tissues and mouse strains.

Authors:  Rok Kosir; Jure Acimovic; Marko Golicnik; Martina Perse; Gregor Majdic; Martina Fink; Damjana Rozman
Journal:  BMC Mol Biol       Date:  2010-08-16       Impact factor: 2.946

10.  Level of expression of the nonmutant Ferrochelatase allele is a determinant of biochemical phenotype in a mouse model of erythropoietic protoporphyria.

Authors:  Joseph Bloomer; Yongming Wang; Dongquan Chen
Journal:  Gene Regul Syst Bio       Date:  2008-05-29
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