Evidence map›Paper›PMID 21082689›Full record

ArticleMuscle & nerve2011

Hindlimb skeletal muscle function in myostatin-deficient mice.

Bettina A Gentry, J Andries Ferreira, Charlotte L Phillips, Marybeth Brown

Open access · bronzeAbstract readComparative Study
In one paragraph

Article in Muscle & nerve, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

34 citing papers in PubMed, 63 citations in OpenAlex.

  1. Article
  2. Article
  3. Sexual dimorphisms in skeletal muscle: current concepts and research horizons.Journal of applied physiology (Bethesda, Md. : 1985) · 2024
    Review
  4. Article
  5. Review
  6. Article
  7. Sex Differences in Inflammation and Muscle Wasting in Aging and Disease.International journal of molecular sciences · 2023
    Review
  8. Combinatorial Inhibition of Myostatin and Activin A Improves Femoral Bone Properties in the G610C Mouse Model of Osteogenesis Imperfecta.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2022
    Article
  9. Review
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Decreasing maternal myostatin programs adult offspring bone strength in a mouse model of osteogenesis imperfecta.Proceedings of the National Academy of Sciences of the United States of America · 2016
    Article
  20. Myostatin deficiency partially rescues the bone phenotype of osteogenesis imperfecta model mice.Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA · 2016
    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

4 authors at 1 institution in 1 country.

Bettina A GentryDepartment of Veterinary Pathobiology, University of Missouri, Columbia, Missouri, USA.
J Andries Ferreira
Charlotte L Phillips
Marybeth Brown
University of Missouri · US

Funding

POSTDOCTORAL TRAINING IN LABORATORY ANIMAL MEDICINET32RR007004 · NCRR · UNIVERSITY OF MISSOURI-COLUMBIA · PI BRYDA, ELIZABETH C, FRANKLIN, CRAIG L · 1985 to 2011
$3.3M
Estrogen Effects on Atrophic Skeletal MuscleR21HD058834 · NICHD · UNIVERSITY OF MISSOURI-COLUMBIA · PI BROWN, MARYBETH NONE · 2008 to 2009
$402k
NCRR NIH HHS T32 RR007004NICHD NIH HHS HD058834NICHD NIH HHS R21 HD058834
6 · The paper itself

Abstract

Absence of functional myostatin (MSTN) during fetal development results in adult skeletal muscle hypertrophy and hyperplasia. To more fully characterize MSTN loss in hindlimb muscles, the morphology and contractile function of the soleus, plantaris, gastrocnemius, tibialis anterior, and quadriceps muscles in male and female null (Mstn(-/-)), heterozygous (Mstn(+/-)), and wild-type (Mstn(+/+)) mice were investigated. Muscle weights of Mstn(-/-) mice were greater than those of Mstn(+/+) and Mstn(+/-) mice. Fiber cross-sectional area (CSA) was increased in female Mstn(-/-) soleus and gastrocnemius muscles and in the quadriceps of male Mstn(-/-) mice; peak tetanic force in Mstn(-/-) mice did not parallel the increased muscle weight or CSA. Male Mstn(-/-) muscle exhibited moderate degeneration. Visible pathology in male mice and decreased contractile strength relative to increased muscle weight suggest MSTN loss results in muscle impairment, which is dose-, sex-, and muscle-dependent.

Indexed as

AnimalsDisease Models, AnimalFemaleGene DosageHindlimbMaleMiceMice, Inbred C57BLMice, KnockoutMuscle ContractionMuscle Fibers, SkeletalMuscle, SkeletalMuscle WeaknessMuscular AtrophyMyostatinOrgan SizeMstn protein, mouseMyostatin

Identifiers

PMID21082689
PMCPMC3052792
OpenAlexW2034828790

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.