Evidence map›Paper›PMID 41927756›Full record

ArticleScientific reports2026

Laboratory-based cellular-level correlative visible-light and X-ray microscopy for 3D evaluation of mouse kidney biopsy.

Naoki Kunishima, Raita Hirose, Yoshihiro Takeda, Koichiro Ito, Kengo Furuichi, Kazuhiko Omote

Abstract read
In one paragraph

Article in Scientific reports, 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
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0citing papers in PubMed
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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

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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

6 authors.

Naoki KunishimaX-Ray Research Laboratory, Rigaku Corporation, 3-9-12 Matsubara-Cho, Akishima, Tokyo, 196-8666, Japan. kunisima@rigaku.co.jp.
Raita HiroseX-Ray Research Laboratory, Rigaku Corporation, 3-9-12 Matsubara-Cho, Akishima, Tokyo, 196-8666, Japan.
Yoshihiro TakedaX-Ray Research Laboratory, Rigaku Corporation, 3-9-12 Matsubara-Cho, Akishima, Tokyo, 196-8666, Japan.
Koichiro ItoNew Market Development Office, Rigaku Corporation, 3-9-12 Matsubara-Cho, Akishima, Tokyo, 196-8666, Japan.
Kengo FuruichiDepartment of Nephrology, School of Medicine, Kanazawa Medical University, 1-1 Daigaku, Uchinada, Kahoku, Ishikawa, 920-0293, Japan. furuichi@kanazawa-med.ac.jp.
Kazuhiko OmoteX-Ray Research Laboratory, Rigaku Corporation, 3-9-12 Matsubara-Cho, Akishima, Tokyo, 196-8666, Japan.

Funding

Japan Society for the Promotion of Science 24K11398
6 · The paper itself

Abstract

X-ray microscopy (XRM) is an emerging technology for nondestructive evaluation of bio-specimen. We previously reported that paraffin, which is used for normal histology, acts as a tissue contrast enhancement agent in XRM, thereby enabling cellular-level 3D visualization of unstained biological samples. In this work, a new form of correlative visible-light and X-ray microscopy (CLXM) was introduced, where a kidney biopsy sample was first observed by laboratory-based XRM with paraffin-mediated contrast enhancement, and the same sample was then observed by visible-light microscopy (LM) at the same measurement point, to compare images from these two modalities precisely. This laboratory-based cellular-level CLXM was applied to a kidney biopsy from a 5/6 nephrectomy model mouse to evaluate glomerular hypercellularity lesions. The image comparison identified high-opacity particles in XRM images as cell nuclei in various parts of the nephron including glomeruli and tubules. A complementary approach using both LM and XRM images allowed us to identify/segment three lesions as aggregations of mesangial cells. It was found that one mesangial cell occupied a volume of about 100 μm

Indexed as

Imaging, Three-DimensionalKidneyMicroscopyAnimalsBiopsyKidney GlomerulusMiceComputed tomographyGlomerulusHypercellularityMesangial cellNondestructive

Identifiers

PMID41927756
PMCPMC13187297

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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.