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on page 1 showing 20 out of 58 results from 1 sources

Cite this (NSRRC Cat# 0014, RRID:NSRRC_0014)

Source Database: NSRRC, catalog # 0014
Genetic Background: inbred
Affected Genes: N/A
Genomic Alteration: wildtype
Availability: Available
Reference: PMID:137560
Notes: homozygous at MHC SLA c/c Application: research in the areas of immune system, and xenotransplantation

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Cite this (NSRRC Cat# 0013, RRID:NSRRC_0013)

Source Database: NSRRC, catalog # 0013
Genetic Background: inbred
Affected Genes: N/A
Genomic Alteration: wildtype
Availability: Available
Reference: PMID:137560
Notes: homozygous at MHC SLA g/g Application: research in the areas of immune system, and xenotransplantation

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Cite this (NSRRC Cat# 0055, RRID:NSRRC_0055)

Source Database: NSRRC, catalog # 0055
Genetic Background: outbred
Affected Genes: PROM1
Genomic Alteration: Transgene: wild type human PROML1
Availability: Available
Reference:
Notes: Stargard Disease 4 Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0010, RRID:NSRRC_0010)

Source Database: NSRRC, catalog # 0010
Genetic Background: outbred
Affected Genes: N/A
Genomic Alteration: Transgene: CAG promoter driving eGFP
Availability: Available
Reference: PMID:11808633
Notes: express enhanced green fluorescent protein Application: Cell tracking

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Cite this (NSRRC Cat# 0037, RRID:NSRRC_0037)

Source Database: NSRRC, catalog # 0037
Genetic Background: Minnesota Mini
Affected Genes: GGTA1 and CD55
Genomic Alteration: GGTA1 knockout with a transgene for human decay-accelerating factor (CD55) inserted into GGTA1
Availability: Available
Reference:
Notes: Application: Xenotransplantation studies

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Cite this (NSRRC Cat# 0052, RRID:NSRRC_0052)

Source Database: NSRRC, catalog # 0052
Genetic Background: outbred
Affected Genes: ELOVL4
Genomic Alteration: Transgene: ELOVL4 Y270X with the enhanced yellow fluorescent protein
Availability: Available
Reference: PMID:21873315
Notes: Stargard Disease 3 Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0011, RRID:NSRRC_0011)

Source Database: NSRRC, catalog # 0011
Genetic Background: outbred
Affected Genes: FAT1
Genomic Alteration: Transgene: expression of hFAT1
Availability: Available
Reference: PMID:16565727
Notes: altered N6/N3 fatty acid ratio Application: research in the areas of reproduction, cardiovascular, immune system, depression and cancer

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Cite this (NSRRC Cat# 0059, RRID:NSRRC_0059)

Source Database: NSRRC, catalog # 0059
Genetic Background: outbred
Affected Genes: Enhanced Yellow Fluorescent Protein
Genomic Alteration: Transgene: male germ cell (STR8) tissue specific expression of enhance yellow fluroescent protein (EYFP)
Availability: Available
Reference: PMID:21826492
Notes: EYFP expression in male germ cells Application: Cell tracking

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Cite this (NSRRC Cat# 0002, RRID:NSRRC_0002)

Source Database: NSRRC, catalog # 0002
Genetic Background: outbred
Affected Genes: N/A
Genomic Alteration: wildtype
Availability: Available
Reference:
Notes: Application: Background for genetic modification

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Cite this (NSRRC Cat# 0015, RRID:NSRRC_0015)

Source Database: NSRRC, catalog # 0015
Genetic Background: inbred
Affected Genes: N/A
Genomic Alteration: wildtype
Availability: Available
Reference: PMID:137560
Notes: homozygous at MHC SLA a/a Application: research in the areas of immune system, and xenotransplantation

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Cite this (NSRRC Cat# 0034, RRID:NSRRC_0034)

Source Database: NSRRC, catalog # 0034
Genetic Background: Yucatan
Affected Genes: DMD
Genomic Alteration: Deletion of Exon 42 of DMD
Availability: Available
Reference:
Notes: potentially muscle tissue abnormalities Application: Becker muscular dystrophy 

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Cite this (NSRRC Cat# 0051, RRID:NSRRC_0051)

Source Database: NSRRC, catalog # 0051
Genetic Background: outbred
Affected Genes: ELOVL4
Genomic Alteration: Transgene: ELOVL4 Y270X with the enhanced yellow fluorescent protein
Availability: Available
Reference: PMID:21873315
Notes: Stargard Disease 3 Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0048, RRID:NSRRC_0048)

Source Database: NSRRC, catalog # 0048
Genetic Background: outbred
Affected Genes: ELOVL4
Genomic Alteration: Transgene: ELOVL4 Y270X with the enhanced yellow fluorescent protein
Availability: Available
Reference: PMID:21873315
Notes: Stargard Disease 3 Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0028, RRID:NSRRC_0028)

Source Database: NSRRC, catalog # 0028
Genetic Background: outbred
Affected Genes: CDA
Genomic Alteration: Transgene: Alpha fetoprotein (AFP) promoter driving cytidine deaminase (CDA)
Availability: Available
Reference:
Notes: Tissue specific expression of cytosine deaminase Application: Liver Research

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Cite this (NSRRC Cat# 0021, RRID:NSRRC_0021)

Source Database: NSRRC, catalog # 0021
Genetic Background: Yucatan
Affected Genes: NOS3
Genomic Alteration: Transgene: Tie2 promoter driving endothelial Nitrate Oxide Synthase (NOS3)
Availability: Available
Reference: PMID:17080303
Notes: Express endothetial cell specific nitric oxide synthase (NOS3) Application: Cardiovascular, Exercise Physiology

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Cite this (NSRRC Cat# 0009, RRID:NSRRC_0009)

Source Database: NSRRC, catalog # 0009
Genetic Background: inbred
Affected Genes: CD55 and GGTA1
Genomic Alteration: GGTA1 knockout and CD55 transgene
Availability: Available
Reference: PMID:7518135
Notes: Application: Xenotransplantation research- has the Cozzi integration of CD55

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Cite this (NSRRC Cat# 0053, RRID:NSRRC_0053)

Source Database: NSRRC, catalog # 0053
Genetic Background: outbred
Affected Genes: PROM1
Genomic Alteration: Transgene: R373C mutation of human PROM1
Availability: Available
Reference:
Notes: Stargard Disease 4 Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0057, RRID:NSRRC_0057)

Source Database: NSRRC, catalog # 0057
Genetic Background: outbred
Affected Genes: C1QTNF5 (CTRP)
Genomic Alteration: Transgene: S163R mutation of pig CTRP (C1QTNF5)
Availability: Available
Reference:
Notes: Age related macular degeneration Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0058, RRID:NSRRC_0058)

Source Database: NSRRC, catalog # 0058
Genetic Background: outbred
Affected Genes: C1QTNF5 (CTRP)
Genomic Alteration: Transgene: S163R mutation of pig CTRP (C1QTNF5)
Availability: Available
Reference:
Notes: Age related macular degeneration Application: Study of Eye Disorders

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Cite this (NSRRC Cat# 0025, RRID:NSRRC_0025)

Source Database: NSRRC, catalog # 0025
Genetic Background: outbred
Affected Genes: GGTA1, CD39, CD55, CD59
Genomic Alteration: GGTA1 knockout; with three randomly integrated transgenes: human decay-accelerating factor (CD55); CD39; CD59 and thrombomodulin
Availability: Available
Reference:
Notes: Lack of expression of GGTA1 and expression of CD55, CD39, CD59 and Thrombomodulin Application: Xenotransplantation

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