Evidence map›Paper›PMID 22245420›Full record

ArticleJournal of proteomics2012

Proteomic changes at 8 weeks after infection are associated with chronic liver pathology in experimental schistosomiasis.

Bhagyashree Manivannan, T William Jordan, W Evan Secor, Anne Camille La Flamme

Open access · greenAbstract read
In one paragraph

Article in Journal of proteomics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 37% 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

4 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. PNAS nexus · 2024
    Article
  3. Profiling the serum proteome duringFrontiers in immunology · 2022
    Article
  4. 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

4 authors at 2 institutions in 2 countries.

Bhagyashree ManivannanCentre for Biodiscovery and School of Biological Sciences, Victoria University of Wellington, Wellington, 6140 New Zealand.
T William Jordan
W Evan Secor
Anne Camille La Flamme
Victoria University of Wellington · NZCenters for Disease Control and Prevention · US

Funding

IL 6 DURING ACUTE SCHISTOMIASISF32AI010151 · NIAID · CORNELL UNIVERSITY ITHACA · PI LA FLAMME, ANNE C · 1998 to 2000
$25k
Intramural CDC HHS CC999999NIAID NIH HHS F32 AI010151
6 · The paper itself

Abstract

Chronic Schistosoma mansoni infection can present as a moderate or severe disease, termed intestinal or hepatosplenic schistosomiasis, respectively. Similarly, either moderate splenomegaly or hypersplenomegaly syndrome develops in CBA/J mice by 20weeks of infection and is similar to intestinal or hepatosplenic schistosomiasis respectively. Using this mouse model and two-dimensional differential in gel electrophoresis, the liver proteomic signatures of uninfected mice and mice infected for 6, 8, 12, or 20weeks were compared, and significant protein spots identified using mass spectrometry. We found the greatest number of changes at 12weeks suggesting that this period represents the peak time of change. Pathway analysis identified specific proteins and pathways that correlated to the pathological changes indicative of severe disease, and these pathways were involved as early as 8weeks after infection. These findings provide insight into the development of severe liver pathology in schistosomiasis and may aid in developing biomarkers for hepatosplenic schistosomiasis.

Indexed as

ProteomicsAnimalsDisease ProgressionHepatomegalyMaleMetabolic Networks and PathwaysMiceMice, Inbred CBASchistosomiasis mansoniSplenomegaly

Identifiers

PMID22245420
PMCPMC11367832
OpenAlexW1973431308

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.