Evidence map›Paper›PMID 15619674›Full record

ArticleJournal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research2005

Quantitative trait loci analysis of structural and material skeletal phenotypes in C57BL/6J and DBA/2 second-generation and recombinant inbred mice.

Dean H Lang, Neil A Sharkey, Holly A Mack, George P Vogler, David J Vandenbergh, David A Blizard, Joseph T Stout, Gerald E McClearn

Open access · greenAbstract read
In one paragraph

Article in Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
5.5field-weighted citation impact, top 4% 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

28 citing papers in PubMed, 55 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Rare coding variants in ALPL are associated with low serum alkaline phosphatase and low bone mineral density.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2012
    Article
  7. Whole bone mechanics and bone quality.Clinical orthopaedics and related research · 2011
    Review
  8. Article
  9. Genetically determined phenotype covariation networks control bone strength.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2010
    Article
  10. Article
  11. Article
  12. Bone, muscle, and physical activity: structural equation modeling of relationships and genetic influence with age.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2009
    Article
  13. Replication of long-bone length QTL in the F9-F10 LG,SM advanced intercross.Mammalian genome : official journal of the International Mammalian Genome Society · 2009
    Article
  14. Phenotypic integration among trabecular and cortical bone traits establishes mechanical functionality of inbred mouse vertebrae.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2009
    Article
  15. Identification of quantitative trait loci affecting murine long bone length in a two-generation intercross of LG/J and SM/J Mice.Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research · 2008
    Article
  16. Article
  17. Article
  18. Article
  19. Article
  20. Fine mapping dissects pleiotropic growth quantitative trait locus into linked loci.Mammalian genome : official journal of the International Mammalian Genome Society · 2007
    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

8 authors at 1 institution in 1 country.

Dean H LangThe Center for Locomotion Studies, The Pennsylvania State University, University Park, Pennsylvania 16802, USA.
Neil A Sharkey
Holly A Mack
George P Vogler
David J Vandenbergh
David A Blizard
Joseph T Stout
Gerald E McClearn
Pennsylvania State University · US

Funding

QUANTITATIVE TRAIT LOCI AND LONGEVITYP01AG014731 · NIA · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI MCCLEARN, GERALD E · 1999 to 2003
$6.1M
TRAINING IN GENETICS OF COMPLEX BEHAVIORS IN AGINGT32AG000276 · NIA · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI VOGLER, GEORGE P · 2000 to 2009
$1.2M
BONE QUALITY: A COMPOSITE OF COMPLEX PHENOTYPIC TRAITSR01AG021559 · NIA · PENNSYLVANIA STATE UNIVERSITY-UNIV PARK · PI SHARKEY, NEIL A · 2002 to 2007
$812k
NIA NIH HHS AG00276NIA NIH HHS P01 AG014731NIA NIH HHS P01 AG14731NIA NIH HHS R01 AG021559NIA NIH HHS R01 AG021559-01NIA NIH HHS R01 AG021559-02NIA NIH HHS R01 AG21559NIA NIH HHS T32 AG000276
6 · The paper itself

Abstract

unlabelledQTL analyses identified several chromosomal regions influencing skeletal phenotypes of the femur and tibia in BXD F2 and BXD RI populations of mice. QTLs for skeletal traits co-located with each other and with correlated traits such as body weight and length, adipose mass, and serum alkaline phosphatase.

introductionPast research has shown substantial genetic influence on bone quality, and the impact of reduced bone mass on our aging population has heightened the interest in skeletal genetic research. MATERIALS AND

methodsQuantitative trait loci (QTL) analyses were performed on morphologic measures and structural and material properties of the femur and tibia in 200-day-old C57BL/6J x DBA/2 (BXD) F2 (second filial generation; n = 400) and BXD recombinant inbred (RI; n = 23 strains) populations of mice. Body weight, body length, adipose mass, and serum alkaline phosphatase were correlated phenotypes included in the analyses.

resultsSkeletal QTLs for morphologic bone measures such as length, width, cortical thickness, and cross-sectional area mapped to nearly every chromosome. QTLs for both structural properties (ultimate load, yield load, or stiffness) and material properties (stress and straincharacteristics and elastic modulus) mapped to chromosomes 4, 6, 9, 12, 13, 15, and 18. QTLs that were specific to structural properties were identified on chromosomes 1, 2, 3, 7, 8, and 17, and QTLs that were specific to skeletal material properties were identified on chromosomes 5, 11, 16, and 19. QTLs for body size (body weight, body length, and adipose mass) often mapped to the same chromosomal regions as those identified for skeletal traits, suggesting that several QTLs identified as influencing bone could be mediated through body size.

conclusionNew QTLs, not previously reported in the literature, were identified for structural and material properties and morphological measures of the mouse femur and tibia. Body weight and length, adipose mass, and serum alkaline phosphatase were correlated phenotypes that mapped in close proximity of skeletal chromosomal loci. The more specific measures of bone quality included in this investigation enhance our understanding of the functional significance of previously identified QTLs.

Indexed as

PhenotypeAnimalsChromosome MappingFemaleFemurMaleMiceMice, Inbred C57BLMice, Inbred DBAQuantitative Trait LociTibia

Identifiers

PMID15619674
PMCPMC1201529
OpenAlexW2017966093

What OpenQuestion holds

Textmetadata
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.