Evidence map›Paper›PMID 35320532›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2022

Investigation of Galectins in Frozen Tissue and Mammalian Cell Culture Using Confocal Miccroscopy.

Daniel Giuliano Cerri, Lilian Cataldi Rodrigues, Marise Lopes Fermino, Marcelo Papoti, Richard D Cummings, Sean R Stowell, Marcelo Dias-Baruffi

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
1.2field-weighted citation impact, top 24% 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

0 citing papers in PubMed, 2 citations in OpenAlex.

No citing paper in PubMed yet.

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

7 authors at 3 institutions in 2 countries.

Daniel Giuliano CerriDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas da Faculdade de Ciências Farmacênuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil.
Lilian Cataldi RodriguesDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas da Faculdade de Ciências Farmacênuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil.
Marise Lopes FerminoDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas da Faculdade de Ciências Farmacênuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil.
Marcelo PapotiEscola de Educação Física e Esporte de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil.
Richard D CummingsDepartment of Surgery, National Center for Functional Glycomics, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Sean R StowellDepartment of Pathology, Harvard Medical School, Brigham and Women's Hospital, Boston, MA, USA.
Marcelo Dias-BaruffiDepartamento de Análises Clínicas, Toxicológicas e Bromatológicas da Faculdade de Ciências Farmacênuticas de Ribeirão Preto, Universidade de São Paulo, Ribeirão Preto, São Paulo, Brasil. mdbaruff@fcfrp.usp.br.
Universidade de São Paulo · BRBeth Israel Deaconess Medical Center · USHarvard University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Galectins are multifunctional glycan-binding proteins present in various tissues that participate in multiple physiological and pathological processes and are considered as not only biomarkers of human diseases but also molecular targets for treating cancer and inflammatory illnesses in many organs. In the glycobiology field, it is crucial to determine the pattern of galectin expression and location in cells and tissues. Confocal microscopy is a powerful imaging technology that represents a unique approach to investigate the expression and location of biomolecules in various tissues and cells. The confocal microscope acquires images of the specimen through the reflected or fluorescent light from the objective's focal plane, using laser light focused on a small spot inside the tissue or cell. This technique provides high-resolution and high-contrast images without artifacts generated by conventional microscopy and enables reconstruction of virtual tridimensional images by acquiring multiple sections from several focal planes, which makes it possible to obtain the precise spatial location of any cellular structure or molecule. Furthermore, confocal microscopy is a non-invasive tissue imaging strategy used in clinical practices. We describe herein the immunofluorescence confocal method for examining galectins in frozen tissue sections and mammalian cell culture.

Indexed as

GalectinsImmunologic TestsAnimalsCell Culture TechniquesFluorescent Antibody TechniqueHumansMammalsMicroscopy, ConfocalGalectinsConfocal microscopyGalectinsImmunofluorescenceTissue and cell culture

Identifiers

PMID35320532
OpenAlexW4220820864

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.