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Name/Symbol
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Strain Name
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Transgene/
Promoter and Regulatory Elements
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Genetic Background
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Behavioral
Phenotype
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Neurological
Characteristics
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Patents/
Availability
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Primary Citation
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Psen2-EGFP
Posted 1/23/09
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STOCK Tg(Psen2-EGFP)244Gsat/Mmcd
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Modified BAC containing inserted EGFP upstream of targeted gene injected into pronuclei
of FVB/N fertilized oocytes/ founder line DF244.
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Background: FVB/N-Swiss Webster hybrid, Generation: N1F2.
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MMRRC Cryopreserved stock# 011154-UCD. For non-profit only.
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Gong et al., 2003
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NSE-hPS2(N141I) and hPS2wt
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pNSE-CAT promoter and hPS2(N141I) inserted in pUHD10-3/microinjected BDF1
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Origin C57BL/6 x DBA/2, Background C57BL/6, Backcross 5 generations
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Behavior dysfunction in water maze
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Levels of hPS2, Aβ-42, caspase-3, and Cox-2 expression were modulated in tg
and wt. No AD phenotype seen between mutant and wt.
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Patent filing date 11/4/02
Contact: Yong K Kim
kimyongkyu@hanmail.net
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Hwang et al., 2002
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PS2N141I
Symbol: PS2
Posted 6/10/05
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Tg.Prp-huPS2.30H
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Human FAD mutation N141I inserted into PS2 cDNA/ murine prion protein genomic fragment
(pPrnpHG) promoter/microinjection into pronuclei B6D2F1 zygotes.
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Origin C57BL/6, DBA/2. Backcrossed C57BL/6 for 3N, then intercrossed F8
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14% mortality before weaning.
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Contact: Laurence Ozmen
Laurence.ozmen@roche.com
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Richards et al., 2003
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PS2 N141I
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Human PS2 cDNA with N141I/
chicken b-actin promoter
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C57BL/6 (B6)J or DBF1 females and B6N males
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N/A
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Age-dependent increase in Aβ42, higher level of insoluble Aβ
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Unpatented
Contact Yasuo Ihara
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Oyama et al
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PS2 null
Updated 1/23/09
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B6.129P-Psen2tm1Bdes/J
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Exon 5 was replaced by a hygromycin cassette under the control of the PGK promoter
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C57B6/J black x 129Sv
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Viable and fertile no behavioral abnormalities.
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No abnormal pathology, develop only mild pulmonary fibrosis and hemorrhage with
age.
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The Jackson Lab,
cryopreserved, stock #005617. Use by companies or for-profit entities requires a
license prior to shipping.
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Herreman et al., 1999.
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PS2 null
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Ablated PS2 gene created by the deletion of exon 5 and insertion of the neomycin
resistance gene disrupted translation of the mouse gene in ES cells.
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129sv/ev x C57/blk6
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No behavioral abnormalities
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No abnormal pathology
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Unpatented
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Steiner H et al.
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