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NAD-dependent redox control enables endothelial quiescence and vascular stabilization during angiogenesis

GSE318549 Homo sapiens (human) RNA-seq (gene expression) 15 samples Submitted 2026/04/30 Platform GPL24676
At a glance

RNA-seq (gene expression) · human · 15 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
Homo sapiens (human)
Samples
15 samples: 5 conditions, mostly in triplicateGroups 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
NAD-dependent redox control enables endothelial quiescence and vascular stabilization during angiogenesisCell metabolism · 2026
Summary (written by the submitters)
The process of angiogenesis requires endothelial cells (ECs) to toggle between states of quiescence versus high replication, migration, and tissue invasion. Little is known regarding how ECs return to quiescence during this process. This project aims to understand the role of NAD in endothelial cell proliferation and the transition of from proliferation to quiescence.
Published in
NAD-dependent redox control enables endothelial quiescence and vascular stabilization during angiogenesis
Zhao W, Zhu W, Thome T et al. · Cell metabolism 2026 · PMID 42061402 · doi:10.1016/j.cmet.2026.04.004
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 GSE318549_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 PRJNA1419213 and SRA study SRP674920. Searching any of these in the dataset finder brings you back here.

Study design
5 conditions, mostly in triplicate
CTL-D2 ×3 FK-D2 ×3 CTL-D5 ×3 FK-D5 ×3 FK-NMN-D5 ×3

Supports a between-group comparison across 15 samples.

How we read this: 5 replicated groups read from 15 sample titles; they account for 15 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
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