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Targeting Cre recombinase to specific neuron populations with bacterial artificial chromosome constructs.

Shiaoching Gong | Martin Doughty | Carroll R Harbaugh | Alexander Cummins | Mary E Hatten | Nathaniel Heintz | Charles R Gerfen
The Journal of neuroscience : the official journal of the Society for Neuroscience | 2007

Transgenic mouse lines are characterized with Cre recombinase driven by promoters of CNS-specific genes using bacterial artificial chromosome (BAC) constructs. BAC-Cre constructs for 10 genes (Chat, Th, Slc6a4, Slc6a2, Etv1, Ntsr1, Drd2, Drd1, Pcp2, and Cmtm5) produced 14 lines with Cre expression in specific neuronal and glial populations in the brain. These Cre driver lines add functional utility to the >500 BAC-EGFP (enhanced green fluorescent protein) transgenic mouse lines that are part of the Gene Expression Nervous System Atlas Project.

Pubmed ID: 17855595

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: N01 NS-0-2331
  • Agency: NINDS NIH HHS, United States
    Id: N01 NS-7-2370
  • Agency: Intramural NIH HHS, United States

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Mutant Mouse Resource and Research Center (biomaterial supply resource)

RRID:SCR_002953

National public repository system for mutant mice. Archives and distributes scientifically valuable spontaneous and induced mutant mouse strains and ES cell lines for use by biomedical research community. Includes breeding/distribution facilities and information coordinating center. Mice strains are cryopreserved, unless live colony must be established. Live mice are supplied from production colony, from colony recovered from cryopreservation, or via micro-injection of cell line into host blastocysts. MMRRC member facilities also develop technologies to improve handling of mutant mice, including advances in assisted reproductive techniques, cryobiology, genetic analysis, phenotyping and infectious disease diagnostics.

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