Literature DB >> 15239894

ENU mutagenesis in the mouse: application to human genetic disease.

Patrick M Nolan1, Alison Hugill, Roger D Cox.   

Abstract

Genetic approaches in model organisms provide a powerful means by which to examine the biological basis of human diseases as well as the physiological processes that are affected by them. Although not without its drawbacks, the mouse has become the mammalian species of choice in studying the molecular basis of disease. Targeted mutagenesis approaches in the mouse have led to dramatic increases in our understanding of human disease processes. As a complement to these gene-driven studies, three developments have led to the reassessment of a phenotype-driven approach in the mouse--the accumulation of information that has emerged from human and mouse genome sequencing projects, the use of high-efficiency point mutagens such as N-ethyl-N-nitrosourea (ENU) and the application of systematic hierarchical screening protocols for the mouse. In this paper, progress with existing phenotypic screening programmes is discussed and opportunities for the development of new mouse disease models are presented.

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Year:  2002        PMID: 15239894     DOI: 10.1093/bfgp/1.3.278

Source DB:  PubMed          Journal:  Brief Funct Genomic Proteomic        ISSN: 1473-9550


  11 in total

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Review 4.  Examining diabetic nephropathy through the lens of mouse genetics.

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5.  A mouse forward genetics screen identifies LISTERIN as an E3 ubiquitin ligase involved in neurodegeneration.

Authors:  Jessie Chu; Nancy A Hong; Claudio A Masuda; Brian V Jenkins; Keats A Nelms; Christopher C Goodnow; Richard J Glynne; Hua Wu; Eliezer Masliah; Claudio A P Joazeiro; Steve A Kay
Journal:  Proc Natl Acad Sci U S A       Date:  2009-02-05       Impact factor: 11.205

6.  Simulation and estimation of gene number in a biological pathway using almost complete saturation mutagenesis screening of haploid mouse cells.

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Journal:  BMC Genomics       Date:  2014-11-24       Impact factor: 3.969

7.  Inner ear morphology is perturbed in two novel mouse models of recessive deafness.

Authors:  Kerry A Miller; Louise H Williams; Elizabeth Rose; Michael Kuiper; Hans-Henrik M Dahl; Shehnaaz S M Manji
Journal:  PLoS One       Date:  2012-12-12       Impact factor: 3.240

8.  ENU-induced phenovariance in mice: inferences from 587 mutations.

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Journal:  BMC Res Notes       Date:  2012-10-24

9.  Unlocking the bottleneck in forward genetics using whole-genome sequencing and identity by descent to isolate causative mutations.

Authors:  Katherine R Bull; Andrew J Rimmer; Owen M Siggs; Lisa A Miosge; Carla M Roots; Anselm Enders; Edward M Bertram; Tanya L Crockford; Belinda Whittle; Paul K Potter; Michelle M Simon; Ann-Marie Mallon; Steve D M Brown; Bruce Beutler; Christopher C Goodnow; Gerton Lunter; Richard J Cornall
Journal:  PLoS Genet       Date:  2013-01-31       Impact factor: 5.917

10.  A new Otogelin ENU mouse model for autosomal-recessive nonsyndromic moderate hearing impairment.

Authors:  Carole El Hakam Kamareddin; Laetitia Magnol; Veronique Blanquet
Journal:  Springerplus       Date:  2015-11-25
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