Evidence map›Paper›PMID 20860919›Full record

ReviewCurrent opinion in pharmacology2010

Animal models of IBD: linkage to human disease.

Atsushi Mizoguchi, Emiko Mizoguchi

Abstract readReview
In one paragraph

Review in Current opinion in pharmacology, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 50 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
50citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

50 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Trial
  3. IL-22 synergizes with IL-17 to promote mucosal inflammation and bone loss.Journal of immunology (Baltimore, Md. : 1950) · 2026
    Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Antibiotics for inflammatory bowel disease: Current status.Indian journal of gastroenterology : official journal of the Indian Society of Gastroenterology · 2024
    Review
  10. Article
  11. Article
  12. Article
  13. Article
  14. Article
  15. Review
  16. Review
  17. Article
  18. Article
  19. Review
  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

2 authors.

Atsushi MizoguchiMolecular Pathology Unit, Massachusetts General Hospital, Boston, MA, USA. amizoguchi@partners.org
Emiko Mizoguchi

Funding

Role of Mammalian Chitinases in Inflammatory Bowel DiseaseR01DK080070 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MIZOGUCHI, EMIKO · 2009 to 2013
$1.6M
Role of Galectin-4 in ColitisR01DK064351 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MIZOGUCHI, ATSUSHI · 2004 to 2008
$1.5M
Endoscopic Theranostics SystemRC1DK086242 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MIZOGUCHI, ATSUSHI, YUN, SEOK-HYUN ANDY · 2009 to 2010
$965k
TNF Receptors of Colonic Epithelial Cells in IBDK08DK064289 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MIZOGUCHI, EMIKO · 2003 to 2007
$637k
Regulatory Role of TNFR1 in Inflammatory Bowel DiseaseR03DK074454 · NIDDK · MASSACHUSETTS GENERAL HOSPITAL · PI MIZOGUCHI, EMIKO · 2006 to 2007
$172k
NIDDK NIH HHS DK64289NIDDK NIH HHS DK74454NIDDK NIH HHS DK80070NIDDK NIH HHS K08 DK064289NIDDK NIH HHS R01 DK064351NIDDK NIH HHS R01DK064351NIDDK NIH HHS R01 DK080070NIDDK NIH HHS R03 DK074454NIDDK NIH HHS RC1 DK086242NIDDK NIH HHS RC1DK086242
6 · The paper itself

Abstract

Spontaneous development of intestinal inflammation in many different kinds of genetically engineered mice as well as the presence of numerous susceptibility genes in humans suggests that inflammatory bowel disease (IBD) is mediated by more complicated mechanisms than previously predicted. The human genetic studies implicate some major pathways in the pathogenesis of IBD, including epithelial defense against commensal microbiota, the IL-23/Th17 axis, and immune regulation. Murine IBD models, which are genetically engineered to lack some susceptibility genes, have been generated, and have provided useful insights into the therapeutic potential of targeting the susceptibility genes directly or their downstream pathways indirectly for IBD. This review summarizes current information related to the function of IBD-associated genes as derived from genetically engineered mouse models.

Indexed as

Disease Models, AnimalAnimalsHumansImmunity, MucosalInflammatory Bowel DiseasesIntestinal MucosaMiceMice, TransgenicMutation

Identifiers

PMID20860919
PMCPMC3176311

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.