Evidence map›Paper›PMID 24504478›Full record

ArticleNature protocols2014

Optimized axolotl (Ambystoma mexicanum) husbandry, breeding, metamorphosis, transgenesis and tamoxifen-mediated recombination.

Shahryar Khattak, Prayag Murawala, Heino Andreas, Verena Kappert, Maritta Schuez, Tatiana Sandoval-Guzmán, Karen Crawford, Elly M Tanaka

Abstract read
PubMed Publisher
In one paragraph

Article in Nature protocols, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 59 papers.

0numbers the graph read from it
0cells of the map it votes in
59citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

59 citing papers in PubMed, 133 citations in OpenAlex.

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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

8 authors at 3 institutions in 1 country.

Shahryar Khattak1] Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany. [2] Technische Universität Dresden, Deutsche Forschungsgemeinschaft (DFG) Center for Regenerative Therapies, Dresden, Germany.
Prayag MurawalaTechnische Universität Dresden, Deutsche Forschungsgemeinschaft (DFG) Center for Regenerative Therapies, Dresden, Germany.ORCID 0000000206071059
Heino AndreasMax Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany.
Verena KappertMax Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany.
Maritta Schuez1] Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany. [2] Technische Universität Dresden, Deutsche Forschungsgemeinschaft (DFG) Center for Regenerative Therapies, Dresden, Germany.
Tatiana Sandoval-Guzmán1] Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany. [2] Technische Universität Dresden, Deutsche Forschungsgemeinschaft (DFG) Center for Regenerative Therapies, Dresden, Germany.
Karen Crawford1] Technische Universität Dresden, Deutsche Forschungsgemeinschaft (DFG) Center for Regenerative Therapies, Dresden, Germany. [2] St. Mary's College of Maryland, St. Mary's City, Maryland, USA.
Elly M Tanaka1] Max Planck Institute of Molecular Cell Biology and Genetics (MPI-CBG), Dresden, Germany. [2] Technische Universität Dresden, Deutsche Forschungsgemeinschaft (DFG) Center for Regenerative Therapies, Dresden, Germany.
Center for Systems Biology Dresden · DEMax Planck Institute of Molecular Cell Biology and Genetics · DETechnische Universität Dresden · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The axolotl (Mexican salamander, Ambystoma mexicanum) has become a very useful model organism for studying limb and spinal cord regeneration because of its high regenerative capacity. Here we present a protocol for successfully mating and breeding axolotls in the laboratory throughout the year, for metamorphosing axolotls by a single i.p. injection and for axolotl transgenesis using I-SceI meganuclease and the mini Tol2 transposon system. Tol2-mediated transgenesis provides different features and advantages compared with I-SceI-mediated transgenesis, and it can result in more than 30% of animals expressing the transgene throughout their bodies so that they can be directly used for experimentation. By using Tol2-mediated transgenesis, experiments can be performed within weeks (e.g., 5-6 weeks for obtaining 2-3-cm-long larvae) without the need to establish germline transgenic lines (which take 12-18 months). In addition, we describe here tamoxifen-induced Cre-mediated recombination in transgenic axolotls.

Indexed as

Gene Transfer TechniquesModels, AnimalAmbystoma mexicanumAnimal HusbandryAnimalsBreedingDeoxyribonucleases, Type II Site-SpecificMetamorphosis, BiologicalRecombination, GeneticSaccharomyces cerevisiae ProteinsTamoxifenTransposasesDeoxyribonucleases, Type II Site-SpecificSaccharomyces cerevisiae ProteinsSCEI protein, S cerevisiaeTamoxifenTransposases

Identifiers

PMID24504478
OpenAlexW2070353993

What OpenQuestion holds

Textmetadata
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.