Evidence map›Paper›PMID 39702715›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Temporal Expression Analysis to Unravel Gene Regulatory Dynamics by microRNAs.

Ranjan Kumar Maji, Marcel H Schulz

Abstract read
PubMed Publisher
In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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.

Ranjan Kumar MajiGoethe University Frankfurt, Institute for Computational Genomic Medicine & Institute for Cardiovascular Regeneration, Frankfurt, Germany.
Marcel H SchulzGoethe University Frankfurt, Institute for Computational Genomic Medicine & Institute for Cardiovascular Regeneration, Frankfurt, Germany. marcel.schulz@em.uni-frankfurt.de.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are a class of small non-coding RNAs (sncRNAs) of length 21-25 nucleotides. These sncRNAs hybridize to repress their target genes and inhibit protein translation, thereby controlling regulatory functions in the cell. Integration of time-series matched small and RNA-seq data enables investigation of dynamic gene regulation through miRNAs during development or in response to a stimulus, such as stress. Here we summarize analysis strategies, such as probabilistic and regression-based models, that take advantage of the temporal dimension to investigate the complexity of miRNA regulation.

Indexed as

Gene Expression RegulationMicroRNAsAnimalsComputational BiologyGene Expression ProfilingGene Regulatory NetworksHumansMicroRNAsmiRNA regulationMulti-omicsProbabilistic modelsRNA-seqSmall RNA-seqTime series

Identifiers

What OpenQuestion 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 OpenQuestion graph.