Evidence map›Paper›PMID 26500224›Full record

ArticleBiology open2015

Hox11 genes regulate postnatal longitudinal bone growth and growth plate proliferation.

Kyriel M Pineault, Ilea T Swinehart, Kayla N Garthus, Edward Ho, Qing Yao, Ernestina Schipani, Kenneth M Kozloff, Deneen M Wellik

Open access · goldAbstract read
In one paragraph

Article in Biology open, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.5field-weighted citation impact, top 17% 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

16 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. The Lung Elastin Matrix Undergoes Rapid Degradation Upon Adult Loss ofFrontiers in cell and developmental biology · 2021
    Article
  6. Mechanisms of bone development and repair.Nature reviews. Molecular cell biology · 2020
    Review
  7. Proceedings of the National Academy of Sciences of the United States of America · 2020
    Article
  8. Review
  9. Article
  10. Proceedings of the National Academy of Sciences of the United States of America · 2018
    Article
  11. Article
  12. Hox11 Function Is Required for Region-Specific Fracture Repair.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2017
    Article
  13. Hox genes in the adult skeleton: Novel functions beyond embryonic development.Developmental dynamics : an official publication of the American Association of Anatomists · 2017
    Review
  14. Article
  15. Article
  16. Hox genes and evolution.F1000Research · 2016
    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

8 authors at 1 institution in 1 country.

Kyriel M PineaultProgram in Cell and Developmental Biology, University of Michigan, Ann Arbor, MI 48109-2200, USA.
Ilea T SwinehartDepartment of Internal Medicine, Division of Molecular Medicine and Genetics, University of Michigan, Ann Arbor, MI 48109-2200, USA.
Kayla N GarthusDepartment of Internal Medicine, Division of Molecular Medicine and Genetics, University of Michigan, Ann Arbor, MI 48109-2200, USA.
Edward HoDepartment of Internal Medicine, Division of Molecular Medicine and Genetics, University of Michigan, Ann Arbor, MI 48109-2200, USA.
Qing YaoDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI 48109, USA.
Ernestina SchipaniDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI 48109, USA.
Kenneth M KozloffDepartment of Orthopaedic Surgery, University of Michigan, Ann Arbor, MI 48109, USA.
Deneen M WellikDepartment of Internal Medicine, Division of Molecular Medicine and Genetics, University of Michigan, Ann Arbor, MI 48109-2200, USA dwellik@umich.edu.
University of Michigan–Ann Arbor · US

Funding

XenograftP30CA046592 · NCI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI THEODORE S LAWRENCE · 1988 to 2026
$178.2M
Tissue Engineering and RegenerationT32DE007057 · NIDCR · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI DAVID H. KOHN · 1985 to 2026
$17.3M
CELLULAR AND MOLECULAR BIOLOGY AT MICHIGANT32GM007315 · NIGMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI PUTHENVEEDU, MANOJKUMAR A · 1985 to 2021
$12.8M
Role of Hox Genes in Integration of the Musculoskeletal System in Development R01AR061402 · NIAMS · UNIVERSITY OF WISCONSIN-MADISON · PI WELLIK, DENEEN M · 2011 to 2021
$3.3M
HIF-1alpha, a Survival and Differentiation Factor for CartilageR01AR065403 · NIAMS · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI SCHIPANI, ERNESTINA · 2013 to 2017
$1.7M
NCI NIH HHS P30 CA046592NIAMS NIH HHS R01 AR061402NIAMS NIH HHS R01 AR065403NIDCR NIH HHS T32 DE007057NIGMS NIH HHS T32 GM007315
6 · The paper itself

Abstract

Hox genes are critical regulators of skeletal development and Hox9-13 paralogs, specifically, are necessary for appendicular development along the proximal to distal axis. Loss of function of both Hoxa11 and Hoxd11 results in severe malformation of the forelimb zeugopod. In the radius and ulna of these mutants, chondrocyte development is perturbed, growth plates are not established, and skeletal growth and maturation fails. In compound mutants in which one of the four Hox11 alleles remains wild-type, establishment of a growth plate is preserved and embryos develop normally through newborn stages, however, skeletal phenotypes become evident postnatally. During postnatal development, the radial and ulnar growth rate slows compared to wild-type controls and terminal bone length is reduced. Growth plate height is decreased in mutants and premature growth plate senescence occurs along with abnormally high levels of chondrocyte proliferation in the reserve and proliferative zones. Compound mutants additionally develop an abnormal curvature of the radius, which causes significant distortion of the carpal elements. The progressive bowing of the radius appears to result from physical constraint caused by the disproportionately slower growth of the ulna than the radius. Collectively, these data are consistent with premature depletion of forelimb zeugopod progenitor cells in the growth plate of Hox11 compound mutants, and demonstrate a continued function for Hox genes in postnatal bone growth and patterning.

Indexed as

ChondrocyteGrowth plateHox genesPostnatal skeletal development

Identifiers

PMID26500224
PMCPMC4728342
OpenAlexW2293398355

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.