Evidence map›Paper›PMID 29237481›Full record

ArticleActa neuropathologica communications2017

Retraction Note: Transgenic mice overexpressing the ALS-linked protein Matrin 3 develop a profound muscle phenotype.

Christina Moloney, Sruti Rayaprolu, John Howard, Susan Fromholt, Hilda Brown, Matt Collins, Mariela Cabrera, Colin Duffy, Zoe Siemienski, Dave Miller and 4 more

RetractedOpen access · goldAbstract readRetraction Notice
In one paragraph

Article in Acta neuropathologica communications, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It has been retracted, and should not be counted. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.2field-weighted citation impact, top 41% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

14 authors at 1 institution in 1 country.

Christina MoloneyCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Sruti RayaproluCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
John HowardCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Susan FromholtCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Hilda BrownCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Matt CollinsCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Mariela CabreraCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Colin DuffyCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Zoe SiemienskiCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Dave MillerCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
Maurice S SwansonDepartment of Molecular Genetics and Microbiology, Center for NeuroGenetics and the Genetics Institute, University of Florida, College of Medicine, Gainesville, FL, USA.
Lucia NotterpekCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA.
David R BorcheltCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA. drb1@ufl.edu.
Jada LewisCenter for Translational Research in Neurodegenerative Disease, University of Florida, Gainesville, FL, USA. jada.lewis@ufl.edu.
University of Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The authors are retracting this article. The article describes mice expressing wild-type human MATR3. However, since publication the authors have become aware that all of the lines of mice described express human MATR3 containing the F115C mutation. Transgenic mice expressing wild-type and mutant Matrin were created simultaneously in their laboratory and, at a crucial stage of generating the DNA for embryo injection, as confirmed by an investigation by the University of Florida, the DNA preparations were accidentally mislabelled. All of the founders created were mosaic, requiring extensive breeding to isolate stable lines. Mice mislabelled as expressing wild-type MATR3 were the first to produce lines that stably transmitted the transgene and thus were the first to be characterized. However, as lines of mice that were mislabelled as expressing the mutant (F115C) MATR3 were ultimately established, the data began to suggest that an error had been made. Sequence analysis of amplified tail DNA from mice descended from the lines reported in the article have revealed that they express the F115C variant. The data described are therefore an accurate description of the pathology of mice that express the F115C variant of MATR3, but not of mice expressing wild-type MATR3. The authors are preparing a new manuscript reporting data from both mice expressing the F115C variant of MATR3 and mice expressing wild-type MATR3.

Identifiers

PMID29237481
PMCPMC5728013
OpenAlexW2773656222

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.