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Excavating the Genome: Large-Scale Mutagenesis Screening for the Discovery of New Mouse Models.
Sundberg, John P; Dadras, Soheil S; Silva, Kathleen A; Kennedy, Victoria E; Murray, Stephen A; Denegre, James M; Schofield, Paul N; King, Lloyd E; Wiles, Michael V; Pratt, C Herbert.
Affiliation
  • Sundberg JP; Departments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
  • Dadras SS; Division of Dermatology, Department of Medicine, Vanderbilt University, Nashville, Tennessee, USA.
  • Silva KA; Department of Dermatology, University of Connecticut, Farmington, Connecticut, USA.
  • Kennedy VE; Department of Genetics and Developmental Biology, University of Connecticut, Farmington, Connecticut, USA.
  • Murray SA; Departments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
  • Denegre JM; Departments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
  • Schofield PN; Department of Genetic Resources Science, The Jackson Laboratory, Bar Harbor, Maine, USA.
  • King LE; Department of Genetic Resources Science, The Jackson Laboratory, Bar Harbor, Maine, USA.
  • Wiles MV; Departments of Research and Development, The Jackson Laboratory, Bar Harbor, Maine, USA.
  • Pratt CH; Department of Physiology Development and Neuroscience, University of Cambridge, Cambridge, UK.
J Investig Dermatol Symp Proc ; 17(2): 27-9, 2015 Nov.
Article de En | MEDLINE | ID: mdl-26551941
ABSTRACT
Technology now exists for rapid screening of mutated laboratory mice to identify phenotypes associated with specific genetic mutations. Large repositories exist for spontaneous mutants and those induced by chemical mutagenesis, many of which have never been fully studied or comprehensively evaluated. To supplement these resources, a variety of techniques have been consolidated in an international effort to create mutations in all known protein coding genes in the mouse. With targeted embryonic stem cell lines now available for almost all protein coding genes and more recently CRISPR/Cas9 technology, large-scale efforts are underway to create further novel mutant mouse strains and to characterize their phenotypes. However, accurate diagnosis of skin, hair, and nail diseases still relies on careful gross and histological analysis, and while not automated to the level of the physiological phenotyping, histopathology still provides the most direct and accurate diagnosis and correlation with human diseases. As a result of these efforts, many new mouse dermatological disease models are being characterized and developed.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Analyse de mutations d'ADN / Modèles animaux de maladie humaine / Pelade Type d'étude: Diagnostic_studies / Screening_studies Limites: Animals / Humans Langue: En Journal: J Investig Dermatol Symp Proc Sujet du journal: DERMATOLOGIA Année: 2015 Type de document: Article Pays d'affiliation: États-Unis d'Amérique

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Analyse de mutations d'ADN / Modèles animaux de maladie humaine / Pelade Type d'étude: Diagnostic_studies / Screening_studies Limites: Animals / Humans Langue: En Journal: J Investig Dermatol Symp Proc Sujet du journal: DERMATOLOGIA Année: 2015 Type de document: Article Pays d'affiliation: États-Unis d'Amérique