Evidence map›Paper›PMID 28335860›Full record

ReviewCurrent topics in developmental biology2017

"Muscling" Throughout Life: Integrating Studies of Muscle Development, Homeostasis, and Disease in Zebrafish.

Michelle F Goody, Erin V Carter, Elisabeth A Kilroy, Lisa Maves, Clarissa A Henry

Open access · greenAbstract readReview
In one paragraph

Review in Current topics in developmental biology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
7.0field-weighted citation impact, top 2% 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

17 citing papers in PubMed, 34 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Article
  6. Review
  7. Experimental models of Barth syndrome.Journal of inherited metabolic disease · 2022
    Review
  8. Review
  9. Article
  10. Article
  11. Skeletal muscle in health and disease.Disease models & mechanisms · 2020
    Review
  12. Article
  13. Article
  14. Review
  15. Review
  16. Article
  17. 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

5 authors at 2 institutions in 1 country.

Michelle F GoodySchool of Biology and Ecology, University of Maine, Orono, ME, United States.
Erin V CarterGraduate School of Biomedical Sciences and Engineering, University of Maine, Orono, ME, United States.
Elisabeth A KilroyGraduate School of Biomedical Sciences and Engineering, University of Maine, Orono, ME, United States.
Lisa MavesCenter for Developmental Biology and Regenerative Medicine, Seattle Children's Research Institute, Seattle, WA, United States; Division of Cardiology, University of Washington, Seattle, WA, United States.
Clarissa A HenrySchool of Biology and Ecology, University of Maine, Orono, ME, United States; Graduate School of Biomedical Sciences and Engineering, University of Maine, Orono, ME, United States. Electronic address: Clarissa_Henry@umit.maine.edu.
University of Maine · USSeattle Children's Hospital · US

Funding

Novel Mechanisms of Extracellular Matrix Regulation During DevelopmentR15HD088217 · NICHD · UNIVERSITY OF MAINE ORONO · PI HENRY, CLARISSA A · 2016 to 2016
$355k
Mechanisms underlying Paxillin-mediated amelioration of muscle degenerationR03HD077545 · NICHD · UNIVERSITY OF MAINE ORONO · PI HENRY, CLARISSA A · 2013 to 2014
$141k
NICHD NIH HHS R03 HD077545NICHD NIH HHS R15 HD088217
6 · The paper itself

Abstract

The proper development and function of skeletal muscle is vital for health throughout the lifespan. Skeletal muscle function enables posture, breathing, and locomotion; and also impacts systemic processes-such as metabolism, thermoregulation, and immunity. Diseases of skeletal muscle (myopathies, muscular dystrophies) and even some neurological, age-related, and metabolic diseases compromise muscle function and negatively affect health span and quality of life. There have been numerous, recent examples of studies on skeletal muscle development with exciting, therapeutic implications for muscle diseases. The zebrafish (Danio rerio) is a vertebrate model organism well accepted for developmental biology and biomedical research and thus an ideal system in which to elucidate the translational implications of mechanisms regulating skeletal muscle development and homeostasis. Muscle fiber types (slow- vs fast-twitch) are spatially segregated in zebrafish allowing for the opportunity to identify distinct mechanisms regulating fiber type specification during development as well as observe fiber type-specific effects in zebrafish models of muscle diseases. Accessible genetics coupled with transparent zebrafish embryos has enabled in vivo cell biology experiments allowing for the visualization and understanding of never-before-seen cellular processes occurring in muscle development, regeneration, and disease. In addition, high-throughput drug screening provides a platform for efficient drug discovery. The purpose of this chapter is to review the studies in zebrafish that significantly contributed to our understanding of cellular and molecular mechanisms regulating skeletal muscle development, homeostasis, or disease in vertebrates, with a particular emphasis on the basic developmental biology studies with promising therapeutic implications.

Indexed as

HomeostasisMuscle DevelopmentAnimalsDisease Models, AnimalMuscle, SkeletalMuscular DiseasesZebrafishHomeostasisMorphogenesisMuscleMuscular dystrophyMyogenesisMyopathyZebrafish

Identifiers

PMID28335860
PMCPMC8629151
OpenAlexW2739657592

What OpenQuestion holds

Textmetadata
LicenceTDM
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.