Evidence map›Paper›PMID 42230965›Full record

ArticleMolecular psychiatry2026

Sex-specific regulation of angiogenin in Alzheimer's disease.

Marko Jörg, Lukas Walz, Sebastian Nathal, Marco Kristen, Christine Lietz, Max Müller, Vu Thu Thuy Nguyen, Nicolas Ruffini, Marie-Luise Winz, Susanne Gerber and 3 more

Abstract read
In one paragraph

Article in Molecular psychiatry, 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

13 authors.

Marko JörgInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany. marjoerg@uni-mainz.de.ORCID http://orcid.org/0009-0004-5799-1172
Lukas WalzInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.
Sebastian NathalInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.
Marco KristenInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.
Christine LietzInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.
Max MüllerInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.ORCID http://orcid.org/0009-0009-7673-1559
Vu Thu Thuy NguyenDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.
Nicolas RuffiniInstitute of Human Genetics, University Medical Center Johannes Gutenberg University, Mainz, Germany.ORCID http://orcid.org/0000-0003-3342-6756
Marie-Luise WinzInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.ORCID http://orcid.org/0000-0003-0740-8618
Susanne GerberInstitute of Human Genetics, University Medical Center Johannes Gutenberg University, Mainz, Germany.ORCID http://orcid.org/0000-0001-9513-0729
Kristina EndresDepartment of Psychiatry and Psychotherapy, University Medical Center of the Johannes Gutenberg University, Mainz, Germany.ORCID http://orcid.org/0000-0002-1099-8287
Mark HelmInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany.
Kristina FriedlandInstitute of Pharmaceutical and Biomedical Sciences, Johannes Gutenberg University, Mainz, Germany. kfriedla@uni-mainz.de.ORCID http://orcid.org/0000-0001-8603-5957

Funding

Deutsche Forschungsgemeinschaft (German Research Foundation) TRR319 RMaP (Project Id 439669440) TP A05Deutsche Forschungsgemeinschaft (German Research Foundation) TRR319 RMaP (Project Id 439669440) TPB05
6 · The paper itself

Abstract

Alzheimer's disease (AD) is a heterogeneous neurodegenerative disorder, highlighting the need to identify novel molecular regulators for effective treatment development. Angiogenin (ANG), a stress-responsive ribonuclease that inhibits apoptosis by generating 5'-tRNA fragments, is a candidate whose expression and regulation in AD is not understood. Here, we investigated ANG expression and regulation using AD cell and animal models, postmortem human brain tissue, and transcriptomic datasets (n = 645). We found that ANG is dysregulated in AD in a sex-dependent manner, altering downstream levels of 5'-tiRNA

Indexed as

Alzheimer DiseaseRibonuclease, PancreaticAnimalsApoptosisBrainDisease Models, AnimalFemaleHumansInflammationMaleMiceNeuronsangiogeninRibonuclease, Pancreatic

Identifiers

PMID42230965
PMCPMC13569426

What OpenQuestion holds

Textmetadata
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.