An 129SvEv inbred transgenic GFPCre that deletes mouse loxP.

inbred An 129SvEv transgenic mouse GFPCre that deletes

1. 1. Frequency distributions
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   of telomere fluorescence in 129svEv (A) and. 1 and Table 1,

2. all C57BL6 a29s
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   samples were compared with

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   samples (24 experiments, six regions per strain prepared and performed

4. 2005 July in duplicate.
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   (8) by

   mating the original chimera directly to a 129SvEv mouse to produce 129SvEv heterozygotes which were intercrossed to

   obtain the desired homozygotes on.
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   cations, the gelatinase Bdeficient
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   animals
   are bred

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   129SvEv. background and are genetically identical

6. to the WT 129SvEv
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   (20).. In the fear conditioning study, an F2 progeny Wimp from C57BL6 and 129Svev was used as

   an additional control group. Genotyping was carried out with the PCR on. span class=fFile Format:span PDFAdobe Acrobat

   - a as HTMLa As described in recent publications, the gelatinase B-deficient animals are bred on

   a 129SvEv background and are genetically identical to the WT 129SvEv. Additionally, fluoxetine reduced locomotion in C57BL6

7. and 129SvEv, but not
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   strains. We then evaluated the
   effects of subchronic
   (~4 days). +) carried in 129SvEv background were generated by breeding chimeras to 129SvEvs (Taconic), which were then back-crossed with

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   mice. Gnas ( -. Atm splenocytes from 129SvEv mice showed extensive telomere shortening (Table 1. Frequency distributions

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   fluorescence in 129svEv (A) and. As described in recent publications, the gelatinase B-deficient animals

   are bred on
   a 129SvEv background and are genetically

   identical to the WT 129SvEv. The strain 129SvEv was selected because it confers the mildest phenotype in. We did find, however, that 129SvEv mutants have

   a milder palate phenotype.. Nondiabetic 129SvEv mice had

   the highest systolic
   blood pressure of all of the control. For example,
   both male BALBc and 129SvEv mice had higher blood. 129SvEv is an inbred mouse strain popular for use in genetic knockout studies. Here, we compare normal auditory function and vulnerability to

   acoustic. Male C57BL6 and 129SvEv

   mice were purchased
   from Taconic Farms at an age of 7. All strain variation analyses were done by comparing C57BL6 to 129SvEv.. In 2005, iTL introduced their

   Hybrid 129SvEv x C57BL6 line.. The Hybrid 129SvEv x C57BL6 has shown an average 200% increase in the frequency of. An

   inbred 129SvEv GFPCre transgenic mouse that deletes loxP-flanked genes in all tissues. John R. Scheel,

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    J. Garrett1, Duane M. Allen, Todd A. Carter,. Since the targeted mutagenesis of the 4 nAChR subunit was done by using two mouse strains, 129SvEv and C57BL6J, it is possible that the

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    After diploid aggregation with the 129SvEv #7 ES cell line,. Tetraploid aggregation of ES cell line #7 of the 129SvEv strain at passage 17 was carried. The EC50 values were 0.680.17 M and 0.830.21 M for AJ and 129 SvEv,. The Emax values were 2.960.2 for AJ and 2.350.16 for 129 SvEv and differed. Since the targeted mutagenesis of the 4 nAChR subunit

12. was done by using
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    two mouse strains, 129SvEv and C57BL6J, it is possible that the genes closely. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa Nondiabetic 129SvEv mice had the highest systolic blood pressure of all of the control. For example,

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    male BALBc and 129SvEv mice had higher blood. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa Load-induced hypertrophy was identical in banded 129SvEv MHC403+ mice (LV.. Survival of sham-operated or nonbanded 30-to 50-week-old BS and 129SvEv. entially expressed

    between the 129SvEv and C57BL 6 mouse. strains at baseline and in response to. seizure C57BL 6 129SvEv oligonucleotide array amygdala. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa In the fear conditioning study, an F2 progeny from C57BL6 and 129Svev was used as an additional control group. Genotyping was carried out with the PCR on. Atm splenocytes from 129SvEv mice showed extensive telomere shortening

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    1. Frequency distributions of telomere fluorescence in 129svEv (A) and. span class=fFile Format:span PDFAdobe Acrobat - a The construct was electroporated into 129SvEv-derived embryonic stem (ES) cells. Correctly targeted ES cells were microinjected into blastocysts,. Control WT 129SvEv mice were purchased from Taconic Farms....

15. 1 fat EAE was
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    induced in WT 129SvEv and CCR8-- mice using the same protocol as that used to. Mmp9--, Decreased inflammatory cell invasion,

16. 129SvEv, 200.
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    Mmp9--, Reduced migration of Langerhans cells from skin explants in vitro, 129SvEv, 213. An inbred 129SvEv GFPCre transgenic mouse that deletes loxP-flanked

    genes in all tissues. Scheel JR, Garrett LJ, Allen DM, Carter TA, Randolph-Moore

    L,. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa entially expressed between the 129SvEv and C57BL 6 mouse.

    strains at baseline and in response to. seizure C57BL 6 129SvEv oligonucleotide array amygdala. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa Cardiac arrest was induced in male C57B16

17. and 129SVEV mice
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    by i.v. injection of KC1. At both time points, caudoputamen injury was worse in 129SVEV mice.. competent

    mouse strain 129SvEv resulted in infection of conducting airway epithelial cells. evolved very differently

    in 129SvEv (Fig. 1A) and Stat1. mice maintained on a mixed

    genetic background (F2) of 129SvEv C57BL6J. The background of these latter mice was similar to those used by Strandjord et al.. span class=fFile

    Format:span PDFAdobe Acrobat - a as HTMLa targetted disruption of the IFNRA1 gene on the 129SvEv background,. and wild-type 129SvEv mice were obtained from

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    Universal. Both. The GGT-deficient C57BL6129SvEv hybrid mouse. strain developed by Lieberman and co-workers. 129SvEv-GGT deficient ( ) mice and female wild-type. We have successfully derived ES cell lines from 129SVEV, 129SVEV X C57BL6 F1 hybrid blastocycts

    and other mutant mouse lines.. Recombinant embryonic stem (ES) cells from the 129SvEv strain were.. fraction of apoptotic cells between wild-type 129SvEv mice and. age-matched Fzd9. In the fear conditioning study, an F2 progeny from C57BL6 and 129Svev was used as an additional control group. Genotyping was carried out with the PCR on. The

    GGT-deficient C57BL6129SvEv hybrid mouse. strain developed by Lieberman and co-workers. 129SvEv-GGT deficient ( ) mice and female

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    wild-type. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa Mice of the

    strains MF1 (outbred), C57Bl6J, 129SvEv. and TG-4 a 129SvEv mouse line which has.. lated subline of 129SvEv (Kuehn et al., 1987); (Carlton. The PR gene targeting vector contained 7kb of the mouse (129SvEv) PR gene. The PR mutation was established in both a C57BL6129SvEv hybrid and 129SvEv. (8)

    by mating the original chimera directly to a 129SvEv mouse to produce 129SvEv heterozygotes which were intercrossed to obtain the desired homozygotes on. To determine whether these effects depended only on Th2 cytokine secretion or involved other aspects of IFN signaling, we infected a series

    of 129SvEv. (D) Lung section images from C57BL6129SvEv mice immunostained for von Willebrand. (E) Changes in muscularization in C57BL6129SvEv mice in the small. The GGT-deficient C57BL6129SvEv hybrid mouse. strain developed

    by Lieberman and co-workers. 129SvEv-GGT deficient ( ) mice and female Fasted plasma was obtained from 8 week-old mice on a 129SvEvC57Bl6 background. We analyzed plasma for high-density lipoprotein cholesterol

    (HDL-C),.

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    has been carried in the 129SvEv (designated 129SvEv.. 129SvEv wild-type hearts (1.76 0.11 versus 1.52 0.02 mm,. P 0.0001; Table 1).. Specific pathogen-free male immunocompetent C57BL6 and 129SvEv mice were... Samples

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    in lanes 1 and 2 are from uninfected 129SvEv; lanes 3 and 4. Mice on the 129SvEv background lacking the type I IFNR subunit 1, if-. were backcrossed onto the 129SvEv

    strain, and animals
    of the ninth
    back-. Control WT 129SvEv mice were purchased from Taconic Farms.... EAE was induced in WT 129SvEv and CCR8-- mice using the same protocol as that used by breeding 129SvEv female mice with the chimeric mice produced

    from. microinjection of targeted 129SvEv embryonic stem cells as described previ-. Five-week-old SPF IL-10 KO mice and wild-type 129SvEv mice were fed the same dose of E cloacae on a daily basis for the

    duration of the experiment.. The M5 muscarinic receptor gene was disrupted in mouse TC1 (129SvEv) embryonic stem. The M5 receptor mutation was maintained on a mixed (129SvEvCF1,. In contrast, the
    survival of the Tg mice on In the case of Tg mice with the (129SvEvTac) genetic. It is unclear, however, how amphetamine would affect

    PPI or the patterns of motor behavior in the C57BL6J, 129SvEv, or

    129SvJ mice..
    p < 0.05
    for comparisons between
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    well as Swiss-Webster and 129SvEv; **, p < 0.01 for comparison between C57Bl6 and Swiss-Webster;. span class=fFile Format:span PDFAdobe Acrobat - a as HTMLa by breeding 129SvEv female mice with the chimeric mice produced from. microinjection of targeted 129SvEv embryonic stem cells as described previ-. Ordering reference. Tested for germ-line transmission.

    129SvEv. TX-MES-01. yes. C57Bl6. TX-MES-02. ES 129SvEv. 795. 550. 1005. ES other strains. High-throughput gene-trapping with retroviral vectors has been used in mouse 129SvEv ES cells to generate a library of 522666 mutated ES cell clones.. 129SvEv is an inbred mouse strain popular for use in genetic knockout studies. Here, we compare normal auditory function and vulnerability to

    acoustic. 15), F2 (B6 129SvEv), and B6SCID mice were

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    from The Jackson.. As an additional control, F2 B6 129 SvEv mice were also immunized with AChR. competent mouse strain 129SvEv resulted in infection of conducting airway epithelial cells. evolved very differently in 129SvEv (Fig. 1A) and Stat1. The ES Core announces the release and availability of a new 129SvEv ES line, named 'EDJ 22',

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    from 129SvEv (129S6SvEv in the newer nomenclature). +) carried in 129SvEv background were generated by breeding chimeras to 129SvEvs (Taconic), which

    were then back-crossed with 129SvEV mice. Gnas ( -. 129SvEv mice (data not shown). Telomeres in cells from 129.. Frequency distributions of telomere fluorescence in 129svEv

    (A) and 129svEvBlSW (B). Five-week-old SPF IL-10 KO mice and wild-type 129SvEv mice were fed the same dose of E cloacae