Evidence map›Paper›PMID 21328530›Full record

ArticleJournal of experimental zoology. Part B, Molecular and developmental evolution2011

Developmental and genetic origins of murine long bone length variation.

Thomas J Sanger, Elizabeth A Norgard, L Susan Pletscher, Michael Bevilacqua, Victoria R Brooks, Linda J Sandell, James M Cheverud

Abstract read
In one paragraph

Article in Journal of experimental zoology. Part B, Molecular and developmental evolution, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 24 papers.

0numbers the graph read from it
0cells of the map it votes in
24citing papers in PubMed
–field-weighted citation impact
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

24 citing papers in PubMed.

  1. Microevolutionary divergence and plasticity of laryngeal shape in the house mouse (American journal of physiology. Regulatory, integrative and comparative physiology · 2025
    Article
  2. Article
  3. BMP3 Affects Cortical and Trabecular Long Bone Development in Mice.International journal of molecular sciences · 2022
    Article
  4. Article
  5. Sex-specific effects of neonatal oral sucrose treatment on growth and liver choline and glucocorticoid metabolism in adulthood.American journal of physiology. Regulatory, integrative and comparative physiology · 2021
    Article
  6. Article
  7. Article
  8. A NaFrontiers in cell and developmental biology · 2021
    Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Alterations to the Gut Microbiome Impair Bone Strength and Tissue Material Properties.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  15. Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. 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

7 authors.

Thomas J SangerDepartment of Organismic and Evolutionary Biology and Museum of Comparative Zoology, Harvard University, Cambridge, Massachusetts 02138, USA. tsanger@oeb.harvard.edu
Elizabeth A Norgard
L Susan Pletscher
Michael Bevilacqua
Victoria R Brooks
Linda J Sandell
James M Cheverud

Funding

The Role of the Osteoblast Secretome in Bone FormationP30AR057235 · NIAMS · WASHINGTON UNIVERSITY · PI SILVA, MATTHEW J · 2009 to 2018
$5.7M
FUNCTION AND REGULATION OF CD/RAPR01AR045550 · NIAMS · WASHINGTON UNIVERSITY · PI SANDELL, LINDA J · 1998 to 2013
$4.1M
GENETIC VARIATION IN MURINE LONG BONE GROWTH AND DEVELOPMENTR01AR053224 · NIAMS · WASHINGTON UNIVERSITY · PI CHEVERUD, JAMES M · 2006 to 2010
$1.6M
NIAMS NIH HHS P30 AR057235NIAMS NIH HHS R01 AR045550NIAMS NIH HHS R01 AR053224
6 · The paper itself

Abstract

If we wish to understand whether development influences the rate or direction of morphological evolution, we must first understand the developmental bases of morphological variation within species. However, quantitative variation in adult morphology is the product of molecular and cellular processes unfolding from embryonic development through juvenile growth to maturity. The Atchley-Hall model provides a useful framework for dissecting complex morphologies into their component parts as a way of determining which developmental processes contribute to variation in adult form. We have examined differences in postnatal allometry and the patterns of genetic correlation between age-specific traits for ten recombinant inbred strains of mice generated from an intercross of LG/J and SM/J. Long bone length is closely tied to body size, but variation in adult morphology is more closely tied to differences in growth rate between 3 and 5 weeks of age. These analyses show that variation generated during early development is overridden by variation generated later in life. To more precisely determine the cellular processes generating this variation we then examined the cellular dynamics of long bone growth plates at the time of maximum elongation rate differences in the parent strains. Our analyses revealed that variation in long bone length is the result of faster elongation rates of the LG/J stain. The developmental bases for these differences in growth rate involve the rate of cell division and chondrocyte hypertrophy in the growth plate.

Indexed as

AnimalsAnimals, NewbornBone and BonesBone DevelopmentCohort StudiesCrosses, GeneticFemaleGenetic VariationGrowth PlateMaleMiceMice, Inbred StrainsStatistics, Nonparametric

Identifiers

PMID21328530
PMCPMC3160521

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.