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10.1038/nrg3116

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suck abstract from ncbi


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pmid22179716
      Nat+Rev+Genet 2011 ; 13 (1 ): 14-20
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  • Genomically humanized mice: technologies and promises #MMPMID22179716
  • Devoy A ; Bunton-Stasyshyn RK ; Tybulewicz VL ; Smith AJ ; Fisher EM
  • Nat Rev Genet 2011[Dec]; 13 (1 ): 14-20 PMID22179716 show ga
  • Mouse models have become an invaluable tool for understanding human health and disease owing to our ability to manipulate the mouse genome exquisitely. Recent progress in genomic analysis has led to an increase in the number and type of disease-causing mutations detected and has also highlighted the importance of non-coding regions. As a result, there is increasing interest in creating 'genomically' humanized mouse models, in which entire human genomic loci are transferred into the mouse genome. The technical challenges towards achieving this aim are large but are starting to be tackled with success.
  • |*Gene Transfer Techniques [MESH]
  • |Animals [MESH]
  • |Chromosomes, Artificial, Mammalian/*genetics [MESH]
  • |Disease Models, Animal [MESH]
  • |Gene Targeting/*methods [MESH]
  • |Genetic Diseases, Inborn/genetics [MESH]
  • |Genome-Wide Association Study/methods [MESH]
  • |Humans [MESH]
  • |Mice [MESH]
  • |Mice, Transgenic/*genetics [MESH]
  • |Promoter Regions, Genetic [MESH]
  • |Recombination, Genetic [MESH]
  • |Regulatory Elements, Transcriptional [MESH]


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