Evidence map›Paper›PMID 35620073›Full record

ArticleSTAR protocols2022

Targeted LC-MS/MS-based metabolomics and lipidomics on limited hematopoietic stem cell numbers.

Katharina Schönberger, Michael Mitterer, Joerg M Buescher, Nina Cabezas-Wallscheid

Abstract read
In one paragraph

Article in STAR protocols, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Multi-omics to study chronic respiratory diseases and viral infections.European respiratory review : an official journal of the European Respiratory Society · 2026
    Review
  2. Article
  3. Review
  4. Review
  5. Review
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

4 authors.

Katharina SchönbergerMax Planck Institute of Immunobiology and Epigenetics, Department of Cellular and Molecular Immunology, Stübeweg 51, 79108 Freiburg, Germany.
Michael MittererMax Planck Institute of Immunobiology and Epigenetics, Metabolomics Core Facility, Stübeweg 51, 79108 Freiburg, Germany.
Joerg M BuescherMax Planck Institute of Immunobiology and Epigenetics, Metabolomics Core Facility, Stübeweg 51, 79108 Freiburg, Germany.
Nina Cabezas-WallscheidMax Planck Institute of Immunobiology and Epigenetics, Department of Cellular and Molecular Immunology, Stübeweg 51, 79108 Freiburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Metabolism is important for the regulation of hematopoietic stem cells (HSCs) and drives cellular fate. Due to the scarcity of HSCs, it has been technically challenging to perform metabolome analyses gaining insight into HSC metabolic regulatory networks. Here, we present two targeted liquid chromatography-mass spectrometry approaches that enable the detection of metabolites after fluorescence-activated cell sorting when sample amounts are limited. One protocol covers signaling lipids and retinoids, while the second detects tricarboxylic acid cycle metabolites and amino acids. For complete details on the use and execution of this protocol, please refer to Schönberger et al. (2022).

Indexed as

LipidomicsTandem Mass SpectrometryChromatography, LiquidHematopoietic Stem CellsMetabolomicsMass SpectrometryMetabolomicsStem Cells

Identifiers

PMID35620073
PMCPMC9127697

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.