Evidence map›Paper›PMID 24710205›Full record

ArticlePloS one2014

Noninvasive imaging of in vivo MuRF1 expression during muscle atrophy.

Wei Li, Mark D Claypool, Annabelle M Friera, John McLaughlin, Kristen A Baltgalvis, Ira J Smith, Taisei Kinoshita, Kathy White, Wayne Lang, Guillermo Godinez and 2 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 42% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Skeletal muscle atrophy and the E3 ubiquitin ligases MuRF1 and MAFbx/atrogin-1.American journal of physiology. Endocrinology and metabolism · 2014
    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 1 institution in 1 country.

Wei LiDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Mark D ClaypoolDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Annabelle M FrieraDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
John McLaughlinDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Kristen A BaltgalvisDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Ira J SmithDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Taisei KinoshitaDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Kathy WhiteDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Wayne LangDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Guillermo GodinezDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Donald G PayanDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Todd M KinsellaDiscovery Research, Rigel Pharmaceuticals Inc., South San Francisco, California, United States of America.
Rigel (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Numerous human diseases can lead to atrophy of skeletal muscle, and loss of this tissue has been correlated with increased mortality and morbidity rates. Clinically addressing muscle atrophy remains an unmet medical need, and the development of preclinical tools to assist drug discovery and basic research in this effort is important for advancing this goal. In this report, we describe the development of a bioluminescent gene reporter rat, based on the zinc finger nuclease-targeted insertion of a bicistronic luciferase reporter into the 3' untranslated region of a muscle specific E3 ubiquitin ligase gene, MuRF1 (Trim63). In longitudinal studies, we noninvasively assess atrophy-related expression of this reporter in three distinct models of muscle loss (sciatic denervation, hindlimb unloading and dexamethasone-treatment) and show that these animals are capable of generating refined detail on in vivo MuRF1 expression with high temporal and anatomical resolution.

Indexed as

AnimalsFemaleGenes, ReporterHindlimb SuspensionLuminescent MeasurementsMuscle ProteinsMuscle, SkeletalMuscular AtrophyRatsTripartite Motif ProteinsUbiquitin-Protein LigasesMuscle ProteinsTrim63 protein, ratTripartite Motif ProteinsUbiquitin-Protein Ligases

Identifiers

PMID24710205
PMCPMC3977994
OpenAlexW1966707015

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.