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Therapeutic Efficacy, Biomarker Signatures and Translatability of Semaglutide in the Liver Biopsy-Confirmed GAN DIO-MASH Mouse Model (study 7/9)

GSE301751 Mus musculus (mouse) RNA-seq (gene expression) 53 samples Submitted 2026/04/14 Platform GPL19057
At a glance

RNA-seq (gene expression) · mouse · 53 samples

What it is
RNA-seq (gene expression)Gene activity measured by sequencing. The summary does not mention single-cell work, so this is most likely bulk: one average per sample, the usual starting point for comparing groups.
Organism
Mus musculus (mouse)
Samples
53 samples: 6 conditions, mostly with about 10 replicates eachGroups are read from the sample names, not from the paper. Check the list below.
Data you can get
A processed table (series matrix) and supplementary files from NCBI; the raw sequencing reads from ENA. Which of these hold counts depends on the study, so check the file list.
Paper
Therapeutic efficacy, biomarker signatures, and translatability of semaglutide in the liver biopsy-confirmed GAN DIO-MASH mouse modelAmerican journal of physiology. Gastrointestinal and liver physiology · 2026
Summary (written by the submitters)
To investigate the effect of treatment duration on therapeutic efficacy, semaglutide was administered in the GAN-DIO MASH mice. Endpoints included body weight, plasma biochemistry as well as liver histological and transcriptome assessments.
Published in
Therapeutic efficacy, biomarker signatures, and translatability of semaglutide in the liver biopsy-confirmed GAN DIO-MASH mouse model
Kristensen JB, Nøhr-Meldgaard J, Pors SE et al. · American journal of physiology. Gastrointestinal and liver physiology 2026 · PMID 41973550 · doi:10.1152/ajpgi.00011.2026
This dataset
Download · which file do I need?

Direct links to NCBI and ENA, no account and no request form. Pick by what you want to do: take the small processed table to look, the supplementary files to re-analyse, or the original raw data to start over.

1 · Just have a look

Processed table

The series matrix: one table of values per sample as the submitters processed it. The smallest download, and it opens in Excel or R. Start here to see what the data look like.

2 · Re-analyse it

Supplementary files

The count tables and other files the authors uploaded. Take only the samples you need, or the whole study as GSE301751_RAW.tar (it can run to tens of gigabytes).

3 · Start from the raw reads

Raw sequencing reads

The original FASTQ files, straight from the sequencer, held at ENA. Large, and you align them yourself, so only choose this if you need to re-process the study from scratch.

What the files usually look like: For RNA-seq the counts are usually a table among the supplementary files (look for 'counts', 'expression', 'FPKM' or 'TPM' in the file name). The series matrix of a sequencing study is sometimes nearly empty.

Also filed as BioProject PRJNA1287526 and SRA study SRP599233. Searching any of these in the dataset finder brings you back here.

Study design
6 conditions, mostly with about 10 replicates each
Liver, Chow Vehicle 12 w, ×10 Liver, DIO-MASH Vehicle 12 w, ×10 Liver, Semaglutide 12 w, ×9 Liver, Chow Vehicle 24 w, ×8 Liver, Semaglutide 24 w, ×8 Liver, DIO-MASH Vehicle 24 w, ×7 Liver, Semaglutide 12 w ×1

Supports a between-group comparison across 52 samples.

How we read this: 6 replicated groups read from 53 sample titles; they account for 52 of them. These groups are guessed from the sample names, not taken from the paper, so check them against the sample list below before relying on them.

Samples in this study

+ 13 more — browse all 53 samples with per-sample file links →

Datasets on a similar topic

Search all mouse RNA-seq datasets in GEO →

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Metadata from NCBI GEO, cached and refreshed periodically — the NCBI page above is authoritative. Downloads link straight to NCBI/ENA; nothing is proxied through BioTransfer.