Modifier genes in mice and humans
doi: 10.1038/35056009
pmid: 11256068
Modifier genes in mice and humans
An emerging theme of studies with spontaneous, engineered and induced mutant mice is that phenotypes often depend on genetic background, implying that genetic modifiers have a role in guiding the functional consequences of genetic variation. Understanding the molecular and cellular basis by which modifier genes exert their influence will provide insights into developmental and physiological pathways that are critical to fundamental biological processes, as well as into novel targets for therapeutic interventions in human diseases.
- University Hospitals of Cleveland United States
- Case Western Reserve University United States
- University Hospitals Cleveland Medical Center United States
Polymorphism, Genetic, Genotype, Genetic Linkage, Genetics, Medical, Genetic Diseases, Inborn, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Expression, Penetrance, Genomic Imprinting, Mice, Phenotype, Mutation, Animals, Humans
Polymorphism, Genetic, Genotype, Genetic Linkage, Genetics, Medical, Genetic Diseases, Inborn, Cystic Fibrosis Transmembrane Conductance Regulator, Gene Expression, Penetrance, Genomic Imprinting, Mice, Phenotype, Mutation, Animals, Humans
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