Evidence map›Paper›PMID 26142958›Full record

ArticleJournal of lipid research2015

Apprehending ganglioside diversity: a comprehensive methodological approach.

Elodie A Y Masson, Estelle Sibille, Lucy Martine, Fanny Chaux-Picquet, Lionel Bretillon, Olivier Berdeaux

Open access · hybridAbstract read
In one paragraph

Article in Journal of lipid research, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
1.2field-weighted citation impact, top 21% of its field
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

9 citing papers in PubMed, 26 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Deciphering the Action of Neuraminidase in Glioblastoma Models.International journal of molecular sciences · 2023
    Article
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  6. Review
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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

6 authors at 3 institutions in 1 country.

Elodie A Y MassonCNRS, UMR6265 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France INRA, UMR1324 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France Université de Bourgogne Franche-Comté UMR Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France.
Estelle SibilleCNRS, UMR6265 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France INRA, UMR1324 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France Université de Bourgogne Franche-Comté UMR Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France.
Lucy MartineCNRS, UMR6265 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France INRA, UMR1324 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France Université de Bourgogne Franche-Comté UMR Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France.
Fanny Chaux-PicquetInstitut de Chimie Moléculaire de l'Université de Bourgogne, UMR 6302 CNRS, Université de Bourgogne Franche-Comté, F-21000 Dijon, France.
Lionel BretillonCNRS, UMR6265 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France INRA, UMR1324 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France Université de Bourgogne Franche-Comté UMR Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France.
Olivier BerdeauxCNRS, UMR6265 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France INRA, UMR1324 Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France Université de Bourgogne Franche-Comté UMR Centre des Sciences du Goût et de l'Alimentation, F-21000 Dijon, France.
Centre des Sciences du Goût et de l'Alimentation · FRCentre National de la Recherche Scientifique · FRInstitut de Chimie Moléculaire de l'Université de Bourgogne

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Gangliosides (GGs) make a wide family of glycosphingolipids ubiquitously expressed in mammalian tissues and particularly abundant in the brain and nervous system. They exhibit a huge diversity due to structural variations in both their oligosaccharidic chain and ceramide moiety, which represent a real analytical challenge. Since their discovery in the 1940s, methods have persistently improved until the emergence of LC/MS, which offers a high level of specificity and sensitivity and is suitable with high-throughput profiling studies. We describe here a comprehensive approach relying on various techniques and aiming at fully characterizing GGs in biological samples. First, total GG content was determined by a biochemical assay. Second, GG class composition was assessed by high-performance thin-layer chromatography followed by colorimetric revelation. Then, ceramide types of GG classes were identified, and their relative quantification was performed thanks to the development of a powerful and reliable LC/MS method. Finally, ceramides were structurally characterized, and minor and less common GG classes were identified using high-resolution MS. These methods were applied to the rat retina to provide an exhaustive description of its GG composition, giving the base for a better understanding of the precise roles of GGs in this tissue.

Indexed as

AnimalsBrainBrain ChemistryCeramidesChromatography, LiquidGangliosidesGlycosphingolipidsNervous SystemRatsRetinaSpectrometry, Mass, Electrospray IonizationCeramidesGangliosidesGlycosphingolipidsglycosphingolipidsliquid chromatographymolecular speciesretina

Identifiers

PMID26142958
PMCPMC4548786
OpenAlexW2150112127

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.