Evidence map›Paper›PMID 24009271›Full record

ArticleVeterinary pathology2014

Phenotypic characterization of the KK/HlJ inbred mouse strain.

A Berndt, B A Sundberg, K A Silva, V E Kennedy, M A Richardson, Q Li, R T Bronson, J Uitto, J P Sundberg

Abstract read
In one paragraph

Article in Veterinary pathology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
1.2field-weighted citation impact, top 18% 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

15 citing papers in PubMed, 18 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
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  7. ABCC6, Pyrophosphate and Ectopic Calcification: Therapeutic Solutions.International journal of molecular sciences · 2021
    Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Article
  14. Genetic determinants of fibro-osseous lesions in aged inbred mice.Experimental and molecular pathology · 2016
    Article
  15. 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

9 authors at 3 institutions in 1 country.

A BerndtDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
B A SundbergThe Jackson Laboratory, Bar Harbor, ME, USA.
K A SilvaThe Jackson Laboratory, Bar Harbor, ME, USA.
V E KennedyThe Jackson Laboratory, Bar Harbor, ME, USA.
M A RichardsonDepartment of Medicine, University of Pittsburgh, Pittsburgh, PA, USA.
Q LiDepartment of Dermatology and Cutaneous Biology, Jefferson Medical College, Philadelphia, PA, USA.
R T BronsonThe Jackson Laboratory, Bar Harbor, ME, USA.
J UittoDepartment of Dermatology and Cutaneous Biology, Jefferson Medical College, Philadelphia, PA, USA.
J P SundbergThe Jackson Laboratory, Bar Harbor, ME, USA john.sundberg@jax.org.
Jackson Laboratory · USJefferson College · USUniversity of Pittsburgh · US

Funding

Shared Resource ManagementP30CA034196 · NCI · JACKSON LABORATORY · PI William Carl Skarnes · 1985 to 2026
$61.9M
BIOCHEMISTRY AND MORPHOLOGY OF CONNECTIVE TISSUESR01AR028450 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI UITTO, JOUNI · 1986 to 2019
$6.5M
Shock Center for Aging Research at The Jackson Laborato*P30AG025707 · NIA · JACKSON LABORATORY · PI HARRISON, DAVID E · 2005 to 2009
$4.1M
Model Systems for PXER01AR055225 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI UITTO, JOUNI · 2008 to 2017
$3.2M
Modifier Genes for Ectopic MineralizationK01AR064766 · NIAMS · THOMAS JEFFERSON UNIVERSITY · PI LI, QIAOLI · 2014 to 2018
$634k
NCI NIH HHS CA34196NCI NIH HHS P30 CA034196NIAMS NIH HHS K01 AR064766NIAMS NIH HHS R01 AR028450NIAMS NIH HHS R01 AR055225NIA NIH HHS AG25707NIA NIH HHS P30 AG025707
6 · The paper itself

Abstract

Detailed histopathological diagnoses of inbred mouse strains are important for interpreting research results and defining novel models of human diseases. The aim of this study was to histologically detect lesions affecting the KK/HlJ inbred strain. Mice were examined at 6, 12, and 20 months of age and near natural death (ie, moribund mice). Histopathological lesions were quantified by percentage of affected mice per age group and sex. Predominant lesions were mineralization, hyperplasia, and fibro-osseous lesions. Mineralization was most frequently found in the connective tissue dermal sheath of vibrissae, the heart, and the lung. Mineralization was also found in many other organs but to a lesser degree. Hyperplasia was found most commonly in the pancreatic islets, and fibro-osseous lesions were observed in several bones. The percentage of lesions increased with age until 20 months. This study shows that KK/HlJ mice demonstrate systemic aberrant mineralization, with greatest frequency in aged mice. The detailed information about histopathological lesions in the inbred strain KK/HlJ can help investigators to choose the right model and correctly interpret the experimental results.

Indexed as

Models, AnimalPhenotypeAge FactorsAnimalsCalcinosisMiceMice, Inbred StrainsSex FactorsVibrissaeectopic mineralizationKK/HlJ micePXE modelsystemic mineralizationvibrissae dermal sheath

Identifiers

PMID24009271
PMCPMC4037397
OpenAlexW2161320860

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.