Evidence map›Paper›PMID 17606908›Full record

ArticleProceedings of the National Academy of Sciences of the United States of America2007

A ratiometric lectin microarray approach to analysis of the dynamic mammalian glycome.

Kanoelani T Pilobello, Deepika E Slawek, Lara K Mahal

Open access · greenAbstract readComparative StudyValidation Study
In one paragraph

Article in Proceedings of the National Academy of Sciences of the United States of America, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 81 papers.

0numbers the graph read from it
0cells of the map it votes in
81citing papers in PubMed
7.9field-weighted citation impact, top 2% 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

81 citing papers in PubMed, 213 citations in OpenAlex.

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  14. Lectins as versatile tools to explore cellular glycosylation.European journal of histochemistry : EJH · 2024
    Article
  15. Elucidating the glycan-binding specificity and structure ofBeilstein journal of organic chemistry · 2024
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21 more citing papers are in PubMed but not listed here.

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

3 authors at 2 institutions in 2 countries.

Kanoelani T PilobelloDepartment of Chemistry and Biochemistry, University of Texas, 1 University Station, A5300, Austin, TX 78712-0265, USA.
Deepika E Slawek
Lara K Mahal
The University of Texas at Austin · USInstitut de Biologie systémique et synthétique · FR

Funding

Structural Basis of Immune Recognition of Glycosylated AntigensU54GM062116 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI SASISEKHARAN, RAM · 2001 to 2010
$80.3M
NIGMS NIH HHS GM62116NIGMS NIH HHS U54 GM062116
6 · The paper itself

Abstract

Glycosylation creates an intricate and complex code for biological information that plays a role in cell-cell communication, infection, and immunity among many biological events. Dynamic changes in the glycosylation status of cells have been observed in tumor cell metastasis and cell differentiation but have been difficult to analyze because of a lack of high-throughput and facile technologies. Here, we present a method for the rapid evaluation of differences in the glycosylation of heterogeneous mammalian samples using a ratiometric two-color lectin microarray approach. This work represents a significant improvement in glycomics technology and sets the stage for the systematic evaluation of how glycans encode biological information in complex systems.

Indexed as

LectinsProtein Array AnalysisAnimalsCarbohydrate ConformationCell DifferentiationCHO CellsCricetinaeCricetulusGlycolysisGlycosylationHL-60 CellsHumansPolysaccharidesSensitivity and SpecificityLectinsPolysaccharides

Identifiers

PMID17606908
PMCPMC1913879
OpenAlexW2110417357

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.