Evidence map›Paper›PMID 27373927›Full record

ArticleStem cell reports2016

Potential Pitfalls of the Mx1-Cre System: Implications for Experimental Modeling of Normal and Malignant Hematopoiesis.

Talia Velasco-Hernandez, Petter Säwén, David Bryder, Jörg Cammenga

Abstract read
In one paragraph

Article in Stem cell reports, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 43 papers.

0numbers the graph read from it
0cells of the map it votes in
43citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

43 citing papers in PubMed.

  1. Article
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  10. Humanized mouse models in MDS.Cell death & disease · 2025
    Review
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  15. RNA mGenes & diseases · 2024
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  16. Article
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  19. Article
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Talia Velasco-HernandezDivision of Molecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund 22184, Sweden; Division of Molecular Hematology, Lund Stem Cell Center, Lund University, Lund 22184, Sweden. Electronic address: talia.velasco@med.lu.se.
Petter SäwénDivision of Molecular Hematology, Lund Stem Cell Center, Lund University, Lund 22184, Sweden.
David BryderDivision of Molecular Hematology, Lund Stem Cell Center, Lund University, Lund 22184, Sweden.
Jörg CammengaDivision of Molecular Medicine and Gene Therapy, Lund Stem Cell Center, Lund University, Lund 22184, Sweden; Division of Molecular Hematology, Lund Stem Cell Center, Lund University, Lund 22184, Sweden; Department of Hematology, Skanes University Hospital, Lund 22184, Sweden; Department of Hematology, Linköping University Hospital, Linköping 58183, Sweden; Department of Clinical and Experimental Medicine, Linköping University, Linköping 58183, Sweden. Electronic address: jorg.cammenga@med.lu.se.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Conditional knockout mice are commonly used to study the function of specific genes in hematopoiesis. Different promoters that drive Cre expression have been utilized, with the interferon-inducible Mx1-Cre still being the most commonly used "deleter strain" in experimental hematology. However, different pitfalls associated with this system could lead to misinterpretation in functional studies. We present here two of these issues related to the use of Mx1-Cre: first, a high spontaneous recombination rate when applying commonly used techniques in experimental hematology, and second, undesired short-term consequences of the use of polyinosinic:polycytidylic acid, including changes in cellular phenotypes that, however, resolve within days. Our studies emphasize therefore that proper controls are crucial when modeling gene deletion using the Mx1-Cre transgene.

Indexed as

AnimalsGene DeletionHematopoiesisIntegrasesInterferonsMiceMyxovirus Resistance ProteinsRecombination, GeneticTransgenesCre recombinaseIntegrasesInterferonsMx1 protein, mouseMyxovirus Resistance Proteins

Identifiers

PMID27373927
PMCPMC4945592

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.