Evidence map›Paper›PMID 16337774›Full record

ArticleJournal of autoimmunity2006

The mitochondrial and kidney disease phenotypes of kd/kd mice under germfree conditions.

Troy M Hallman, Min Peng, Ray Meade, Wayne W Hancock, Michael P Madaio, David L Gasser

Open access · greenAbstract read
In one paragraph

Article in Journal of autoimmunity, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

22 citing papers in PubMed, 36 citations in OpenAlex.

  1. Review
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  12. Review
  13. Genetics of coenzyme q10 deficiency.Molecular syndromology · 2014
    Article
  14. Article
  15. Tissue-specific oxidative stress and loss of mitochondria in CoQ-deficient Pdss2 mutant mice.FASEB journal : official publication of the Federation of American Societies for Experimental Biology · 2013
    Article
  16. Article
  17. TNFR2 interposes the proliferative and NF-κB-mediated inflammatory response by podocytes to TNF-α.Laboratory investigation; a journal of technical methods and pathology · 2011
    Article
  18. Renal mitochondrial cytopathies.International journal of nephrology · 2011
    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

6 authors at 2 institutions in 1 country.

Troy M HallmanUniversity Laboratory Animal Resources, University of Pennsylvania School of Medicine, Philadelphia, PA 19104, USA.
Min Peng
Ray Meade
Wayne W Hancock
Michael P Madaio
David L Gasser
University of Pennsylvania · USPhiladelphia University · US

Funding

TRANSGENIC AND CHIMERIC MOUSE COREP30DK050306 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI Ken Hashigiwa Cadwell · 1997 to 2026
$32.5M
SPONTANEOUS TUBULOINTERSTITAL NEPHRITIS IN KDKD MICER01DK055852 · NIDDK · UNIVERSITY OF PENNSYLVANIA · PI GASSER, DAVID L · 2000 to 2012
$4.5M
USE OF SCID &IMMUNOCOMPETENT MICE TO ANALYZE PATHOGENESIS OF ORAL LISTERIOSISP01RR012211 · NCRR · UNIVERSITY OF PENNSYLVANIA · PI ROZMIAREK, HARRY NMN · 1998 to 2002
$863k
NCRR NIH HHS P01 RR012211NCRR NIH HHS RR12211NIDDK NIH HHS DK 55852NIDDK NIH HHS P30 DK050306NIDDK NIH HHS P30-DK 50306NIDDK NIH HHS R01 DK055852
6 · The paper itself

Abstract

Interstitial nephritis occurs spontaneously in kd/kd mice, but the mechanisms leading to this disease have not been fully elucidated. The earliest manifestation of a phenotype is the appearance of ultrastructural defects in the mitochondria of mice as young as 42 days of age. To examine the influence of the environment on the phenotype, homozygous B6.kd/kd mice were transferred from specific pathogen-free (SPF) conditions to a germfree (GF) environment, and the development of the disease was observed. The GF state resulted in a highly significant reduction in the frequency of tubulointerstitial nephritis. In addition, GF conditions markedly reduced the appearance of the mitochondrial phenotype, with no sign of mitochondrial abnormalities in GF mice of up to 155 days of age. These results suggest that environmental factors are involved in the progression of all known manifestations of this disease phenotype.

Indexed as

Germ-Free LifeAnimalsKidneyMiceMice, Mutant StrainsMitochondriaNephritis, InterstitialPhenotypeSpecific Pathogen-Free Organisms

Identifiers

PMID16337774
PMCPMC2254222
OpenAlexW2026317851

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.