Evidence map›Paper›PMID 33490906›Full record

ArticleiScience2021

Behavior of glycolylated sialoglycans in the binding pockets of murine and human CD22.

Cristina Di Carluccio, Rosa Ester Forgione, Marco Montefiori, Monica Civera, Sara Sattin, Giovanni Smaldone, K Fukase, Y Manabe, Paul R Crocker, Antonio Molinaro and 2 more

Open access · goldAbstract read
In one paragraph

Article in iScience, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
0.8field-weighted citation impact, top 30% 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

7 citing papers in PubMed, 14 citations in OpenAlex.

  1. JACS Au · 2025
    Article
  2. Article
  3. Review
  4. Article
  5. Conformationally Constrained Sialyl Analogues as New Potential Binders of h-CD22.Chembiochem : a European journal of chemical biology · 2022
    Article
  6. Review
  7. 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

12 authors at 5 institutions in 3 countries.

Cristina Di CarluccioDipartimento di Scienze Chimiche, Complesso Universitario Monte Sant'Angelo, Università di Napoli Federico II, Via Cintia 4, 80126 Napoli, Italy.
Rosa Ester ForgioneDipartimento di Scienze Chimiche, Complesso Universitario Monte Sant'Angelo, Università di Napoli Federico II, Via Cintia 4, 80126 Napoli, Italy.
Marco MontefioriDipartimento di Chimica, Università Degli Studi di Milano, Via Golgi, 19, 20133 Milano, Italy.
Monica CiveraDipartimento di Chimica, Università Degli Studi di Milano, Via Golgi, 19, 20133 Milano, Italy.
Sara SattinDipartimento di Chimica, Università Degli Studi di Milano, Via Golgi, 19, 20133 Milano, Italy.
Giovanni SmaldoneIRCCS SDN, Via E. Gianturco 113, Napoli, Italy.
K FukaseDepartment of Chemistry, Graduate School of Science, Osaka University, Suita, Japan.
Y ManabeDepartment of Chemistry, Graduate School of Science, Osaka University, Suita, Japan.
Paul R CrockerDivision of Cell Signalling and Immunology, School of Life Sciences, University of Dundee, Dundee, United Kingdom.
Antonio MolinaroDipartimento di Scienze Chimiche, Complesso Universitario Monte Sant'Angelo, Università di Napoli Federico II, Via Cintia 4, 80126 Napoli, Italy.
Roberta MarchettiDipartimento di Scienze Chimiche, Complesso Universitario Monte Sant'Angelo, Università di Napoli Federico II, Via Cintia 4, 80126 Napoli, Italy.
Alba SilipoDipartimento di Scienze Chimiche, Complesso Universitario Monte Sant'Angelo, Università di Napoli Federico II, Via Cintia 4, 80126 Napoli, Italy.
Istituto Nazionale di Fisica Nucleare, Sezione di Napoli · ITUniversity of Milan · ITThe University of Osaka · JPSDN Istituto di Ricerca Diagnostica e Nucleare · ITUniversity of Dundee · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Siglecs (sialic acid binding immunoglobulin (Ig)-like lectins) constitute a group of 15 human and 9 murine cell-surface transmembrane receptors belonging to the I-type lectin family, mostly expressed on innate immune cells and characterized by broadly similar structural features. Here, the prominent inhibitory CD22 (Siglec-2), well known in maintaining tolerance and preventing autoimmune responses on B cells, is studied in its human and murine forms in complex with sialoglycans. In detail, the role of the

Indexed as

BiochemistryImmunologyStructural Biology

Identifiers

PMID33490906
PMCPMC7811138
OpenAlexW3114065842

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.