Evidence map›Paper›PMID 29563231›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2018

Genetic mapping of species differences via in vitro crosses in mouse embryonic stem cells.

Stefano Lazzarano, Marek Kučka, João P L Castro, Ronald Naumann, Paloma Medina, Michael N C Fletcher, Rebecka Wombacher, Joost Gribnau, Tino Hochepied, Marc Van Montagu and 2 more

Open access · bronzeAbstract read
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
0.6field-weighted citation impact, top 33% of its field
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

10 citing papers in PubMed, 13 citations in OpenAlex.

  1. Deconstruction ofbioRxiv : the preprint server for biology · 2026
    Article
  2. Article
  3. Article
  4. Article
  5. Genetic studies of human-chimpanzee divergence using stem cell fusions.Proceedings of the National Academy of Sciences of the United States of America · 2021
    Article
  6. Dissecting Trait Variation across Species Barriers.Trends in ecology & evolution · 2019
    Review
  7. Article
  8. Article
  9. Wild-derived mice: from genetic diversity to variation in immune responses.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
  10. Using the inbred mouse strain SPRET/EiJ to provide novel insights in inflammation and infection research.Mammalian genome : official journal of the International Mammalian Genome Society · 2018
    Review
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

12 authors at 4 institutions in 3 countries.

Stefano LazzaranoFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany.
Marek KučkaFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany.
João P L CastroFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany.
Ronald NaumannMax Planck Institute of Cell Biology and Genetics, 01307 Dresden, Germany.
Paloma MedinaFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany.
Michael N C FletcherFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany.
Rebecka WombacherFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany.
Joost GribnauDepartment of Reproduction and Development, Erasmus University Medical Center, 3015 CE Rotterdam, The Netherlands.
Tino HochepiedDepartment of Biomedical Molecular Biology, Ghent University, 9052 Ghent, Belgium.
Marc Van MontaguDepartment of Plant Biotechnology and Bioinformatics, Ghent University, 9052 Ghent, Belgium; marc.vanmontagu@ugent.vib.be frank.chan@tue.mpg.de.
Claude LibertDepartment of Biomedical Molecular Biology, Ghent University, 9052 Ghent, Belgium.
Yingguang Frank ChanFriedrich Miescher Laboratory of the Max Planck Society, 72076 Tübingen, Germany; marc.vanmontagu@ugent.vib.be frank.chan@tue.mpg.de.ORCID 0000-0001-6292-9681
Max Planck Society · DEVlaams Instituut voor Biotechnologie · BEErasmus MC · NLMax Planck Institute of Molecular Cell Biology and Genetics · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Discovering the genetic changes underlying species differences is a central goal in evolutionary genetics. However, hybrid crosses between species in mammals often suffer from hybrid sterility, greatly complicating genetic mapping of trait variation across species. Here, we describe a simple, robust, and transgene-free technique to generate "in vitro crosses" in hybrid mouse embryonic stem (ES) cells by inducing random mitotic cross-overs with the drug ML216, which inhibits the DNA helicase Bloom syndrome (BLM). Starting with an interspecific F1 hybrid ES cell line between the

Indexed as

Crosses, GeneticQuantitative Trait LociAnimalsAntimetabolites, AntineoplasticBiological EvolutionCells, CulturedChromosome MappingDrug ResistanceFemaleHybridization, GeneticIn Vitro TechniquesMiceMice, Inbred C57BLMouse Embryonic Stem CellsPhenotypePregnancyAntimetabolites, AntineoplasticBloom syndrome proteinRecQ HelicasesThioguanineevolutiongeneticsinterspecific hybridsmitotic recombinationQTL mapping

Identifiers

PMID29563231
PMCPMC5889640
OpenAlexW2622859909

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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.