Evidence mapPaperPMID 42136557Full record

ReviewToxicologic pathology2026

Select Histochemical and Immunohistochemical Methods to Investigate the Cell and Tissue Composition of the Mouse Placenta and Metrial Gland.

Susan A Elmore, Robert Z Cochran, Charan Ganta, Heather Jensen, Beth A Lubeck, Beth Mahler, David Sabio, Greg Stamper, Brad Bolon

Abstract readReview
In one paragraph

Review in Toxicologic pathology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Susan A ElmoreExperimental Pathology Laboratories, Inc., Research Triangle Park, North Carolina, USA.ORCID 0000-0002-1680-9176
Robert Z CochranU.S. National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.ORCID 0000-0003-3138-7861
Charan GantaInotiv, Research Triangle Park, North Carolina, USA.
Heather JensenU.S. National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.
Beth A LubeckU.S. National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.ORCID 0000-0003-3241-2723
Beth MahlerExperimental Pathology Laboratories, Inc., Research Triangle Park, North Carolina, USA.ORCID 0009-0004-5823-0172
David SabioExperimental Pathology Laboratories, Inc., Research Triangle Park, North Carolina, USA.
Greg StamperU.S. National Institute of Environmental Health Sciences, Research Triangle Park, North Carolina, USA.
Brad BolonGEMpath Inc., Longmont, Colorado, USA.ORCID 0000-0002-6065-1492

Funding

Intramural NIH HHS Z99 ES999999Intramural NIH HHS ZIC ES103329
6 · The paper itself

Abstract

Mice as model organisms play a vital role in translational research for developmental biology by aiding our understanding of embryonic and placental evolution in health and various disease states. The close similarity between mouse and human placentas is a great asset in reproductive translational research, making the mouse one of the more prominent model organisms in this field. Mice are routinely used to investigate mechanisms of embryonic and placental development, often through experimental manipulations involving engineered or spontaneous genetic mutations and/or xenobiotic treatments. A crucial aspect of fully appreciating the mouse as a model organism for placental research is understanding the anatomy and physiology of the major embryonic (chorion, labyrinth, junctional zone, and yolk sac) and maternal (decidua basalis and metrial gland) placenta components, including knowledge of the specific cell types active during each gestational stage. This paper discusses histochemical and immunohistochemical (IHC) methods that highlight specific tissue layers and cell types present during normal development of the mouse placenta and maternal metrial gland. Altered numbers and/or locations of these common cell types have been demonstrated in embryonic lethal phenotypes, indicating that placental assessments must examine not only the tissue organization but also affected cell populations when determining the cause of early pregnancy loss.

Indexed as

CK18IBA1Ki67metrial glandPECAM-1perforinplacenta

Identifiers

PMID42136557
PMCPMC13182992

What Socratic holds

Textmetadata
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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 Socratic graph.