Evidence map›Paper›PMID 23652855›Full record

ArticleScientific reports2013

Destruction of tissue, cells and organelles in type 1 diabetic rats presented at macromolecular resolution.

Raimond B G Ravelli, Ruby D Kalicharan, M Cristina Avramut, Klaas A Sjollema, Joachim W Pronk, Freark Dijk, Abraham J Koster, Jeroen T J Visser, Frank G A Faas, Ben N G Giepmans

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 33 papers.

0numbers the graph read from it
0cells of the map it votes in
33citing papers in PubMed
6.4field-weighted citation impact, top 3% 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

33 citing papers in PubMed, 53 citations in OpenAlex.

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  4. Morphomics via next-generation electron microscopy.Journal of molecular cell biology · 2024
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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

10 authors at 3 institutions in 2 countries.

Raimond B G RavelliDept. Molecular Cell Biology, Leiden University Medical Center, P. O. Box 9600, 2300 RC, Leiden, The Netherlands.
Ruby D Kalicharan
M Cristina Avramut
Klaas A Sjollema
Joachim W Pronk
Freark Dijk
Abraham J Koster
Jeroen T J Visser
Frank G A Faas
Ben N G Giepmans
Leiden University · NLUniversity Medical Center Groningen · NLUniversity of Groningen · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Finding alternatives for insulin therapy and making advances in etiology of type 1 diabetes benefits from a full structural and functional insight into Islets of Langerhans. Electron microscopy (EM) can visualize Islet morphology at the highest possible resolution, however, conventional EM only provides biased snapshots and lacks context. We developed and employed large scale EM and compiled a resource of complete cross sections of rat Islets during immuno-destruction to provide unbiased structural insight of thousands of cells at macromolecular resolution. The resource includes six datasets, totalling 25.000 micrographs, annotated for cellular and ultrastructural changes during autoimmune diabetes. Granulocytes are attracted to the endocrine tissue, followed by extravasation of a pleiotrophy of leukocytes. Subcellullar changes in beta cells include endoplasmic reticulum stress, insulin degranulation and glycogen accumulation. Rare findings include erythrocyte extravasation and nuclear actin-like fibers. While we focus on a rat model of autoimmune diabetes, our approach is general applicable.

Indexed as

AnimalsCell NucleolusDiabetes Mellitus, ExperimentalDiabetes Mellitus, Type 1Disease ProgressionEndocrine CellsEndoplasmic Reticulum StressErythrocytesGlycogenGranulocytesInsulinInsulin-Secreting CellsIslets of LangerhansLeukocytesMicroscopy, ElectronRatsGlycogenInsulin

Identifiers

PMID23652855
PMCPMC3647201
OpenAlexW2068042284

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-SA
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.