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We are analyzing https://link.springer.com/article/10.1007/s11248-007-9100-4.

Title:
Excision of the Frt-flanked neo R cassette from the CD19cre knock-in transgene reduces Cre-mediated recombination | Transgenic Research
Description:
Intercross of mice transgenic for Flp-recombinase with the CD19cre mouse strain leads to excision of the Frt-flanked neo R cassette from the CD19cre knock-in transgene. This significantly reduces the expression level of Cre by the CD19cre transgene and consequently decreases the extent of Cre-mediated recombination of loxP-flanked alleles, most likely due to the fact that this neo R cassette contains polyoma enhancer sequences. We wish to draw attention to this finding, since the Flp-deleter mouse strain is commonly used to remove Frt-flanked selection cassettes in vivo from conditional alleles. Therefore conditional alleles have to be separated from the Flp-deleter transgene by breeding before crosses with CD19cre mice are initiated. In addition our findings suggest that gene expression from the CD19 locus can be increased by the insertion of exogenous enhancer sequences, without compromising B cell specificity.
Website Age:
28 years and 1 months (reg. 1997-05-29).

Matching Content Categories {πŸ“š}

  • Education
  • Telecommunications
  • Science

Content Management System {πŸ“}

What CMS is link.springer.com built with?

Custom-built

No common CMS systems were detected on Link.springer.com, and no known web development framework was identified.

Traffic Estimate {πŸ“ˆ}

What is the average monthly size of link.springer.com audience?

🌠 Phenomenal Traffic: 5M - 10M visitors per month


Based on our best estimate, this website will receive around 5,000,016 visitors per month in the current month.

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How Does Link.springer.com Make Money? {πŸ’Έ}

We can't see how the site brings in money.

While profit motivates many websites, others exist to inspire, entertain, or provide valuable resources. Websites have a variety of goals. And this might be one of them. Link.springer.com might be making money, but it's not detectable how they're doing it.

Keywords {πŸ”}

article, pubmed, google, scholar, cell, cas, rajewsky, cdcre, gene, research, mice, cells, privacy, cookies, cassette, transgene, cremediated, recombination, schmidtsupprian, content, publish, search, transgenic, frtflanked, neo, mouse, conditional, access, author, data, information, log, journal, excision, knockin, reduces, marc, thomas, wunderlich, klaus, alleles, flpdeleter, discover, targeting, rickert, nature, download, springer, essential, function,

Topics {βœ’οΈ}

t-cell-dependent b-cell responses conditional gene-targeted mutation month download article/chapter gene targeting flp-deleter mouse strain cre-mediated recombination article schmidt-supprian marc schmidt-supprian frt-flanked neo gene expression site-directed mutagenesis full article pdf privacy choices/manage cookies cre-mediated mutagenesis polyoma enhancer sequences author information authors flp-deleter transgene b-1 cell development loxp-flanked alleles flp-deleter mice thomas wunderlich targeted insertion european economic area exogenous enhancer sequences diphtheria toxin fragment c-myc-deficient induced cell death pax5/bsap maintains ikappab kinase signaling nih grant ai057947 harvard medical school conditions privacy policy check access instant access schmidt-supprian cd19-deficient mice accepting optional cookies cell depletion due c-myc function author correspondence main content log biomedical research article log journal finder publish hagan rc cd19cre transgene significantly reduces article cite normal cells mice transgenic

Schema {πŸ—ΊοΈ}

WebPage:
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         headline:Excision of the Frt-flanked neo R cassette from the CD19cre knock-in transgene reduces Cre-mediated recombination
         description:Intercross of mice transgenic for Flp-recombinase with the CD19cre mouse strain leads to excision of the Frt-flanked neo R cassette from the CD19cre knock-in transgene. This significantly reduces the expression level of Cre by the CD19cre transgene and consequently decreases the extent of Cre-mediated recombination of loxP-flanked alleles, most likely due to the fact that this neo R cassette contains polyoma enhancer sequences. We wish to draw attention to this finding, since the Flp-deleter mouse strain is commonly used to remove Frt-flanked selection cassettes in vivo from conditional alleles. Therefore conditional alleles have to be separated from the Flp-deleter transgene by breeding before crosses with CD19cre mice are initiated. In addition our findings suggest that gene expression from the CD19 locus can be increased by the insertion of exogenous enhancer sequences, without compromising B cell specificity.
         datePublished:2007-06-01T00:00:00Z
         dateModified:2007-06-01T00:00:00Z
         pageStart:657
         pageEnd:660
         sameAs:https://doi.org/10.1007/s11248-007-9100-4
         keywords:
             CD19cre mouse stain
            Conditional gene targeting efficiency
            B cells
            Frt-site flanked neomycin resistance gene cassette
            Animal Genetics and Genomics
            Plant Genetics and Genomics
            Transgenics
            Biomedical Engineering/Biotechnology
            Genetic Engineering
            Molecular Medicine
         image:
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            name:Transgenic Research
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               name:Marc Schmidt-Supprian
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                        name:The CBR Institute for Biomedical Research, Harvard Medical School, Boston, USA
                        type:PostalAddress
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               email:[email protected]
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               name:F. Thomas Wunderlich
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                     name:University of Cologne
                     address:
                        name:Institute for Genetics, University of Cologne, Cologne, Germany
                        type:PostalAddress
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               name:Klaus Rajewsky
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      headline:Excision of the Frt-flanked neo R cassette from the CD19cre knock-in transgene reduces Cre-mediated recombination
      description:Intercross of mice transgenic for Flp-recombinase with the CD19cre mouse strain leads to excision of the Frt-flanked neo R cassette from the CD19cre knock-in transgene. This significantly reduces the expression level of Cre by the CD19cre transgene and consequently decreases the extent of Cre-mediated recombination of loxP-flanked alleles, most likely due to the fact that this neo R cassette contains polyoma enhancer sequences. We wish to draw attention to this finding, since the Flp-deleter mouse strain is commonly used to remove Frt-flanked selection cassettes in vivo from conditional alleles. Therefore conditional alleles have to be separated from the Flp-deleter transgene by breeding before crosses with CD19cre mice are initiated. In addition our findings suggest that gene expression from the CD19 locus can be increased by the insertion of exogenous enhancer sequences, without compromising B cell specificity.
      datePublished:2007-06-01T00:00:00Z
      dateModified:2007-06-01T00:00:00Z
      pageStart:657
      pageEnd:660
      sameAs:https://doi.org/10.1007/s11248-007-9100-4
      keywords:
          CD19cre mouse stain
         Conditional gene targeting efficiency
         B cells
         Frt-site flanked neomycin resistance gene cassette
         Animal Genetics and Genomics
         Plant Genetics and Genomics
         Transgenics
         Biomedical Engineering/Biotechnology
         Genetic Engineering
         Molecular Medicine
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            1573-9368
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            Periodical
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         name:Springer Netherlands
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      author:
            name:Marc Schmidt-Supprian
            affiliation:
                  name:Harvard Medical School
                  address:
                     name:The CBR Institute for Biomedical Research, Harvard Medical School, Boston, USA
                     type:PostalAddress
                  type:Organization
            email:[email protected]
            type:Person
            name:F. Thomas Wunderlich
            affiliation:
                  name:University of Cologne
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                     name:Institute for Genetics, University of Cologne, Cologne, Germany
                     type:PostalAddress
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            name:Klaus Rajewsky
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                  name:Harvard Medical School
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         name:Institute for Genetics, University of Cologne, Cologne, Germany
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         name:The CBR Institute for Biomedical Research, Harvard Medical School, Boston, USA
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            name:University of Cologne
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               name:Institute for Genetics, University of Cologne, Cologne, Germany
               type:PostalAddress
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      name:Klaus Rajewsky
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            name:Harvard Medical School
            address:
               name:The CBR Institute for Biomedical Research, Harvard Medical School, Boston, USA
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      name:The CBR Institute for Biomedical Research, Harvard Medical School, Boston, USA
      name:Institute for Genetics, University of Cologne, Cologne, Germany
      name:The CBR Institute for Biomedical Research, Harvard Medical School, Boston, USA
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