Evidence map›Paper›PMID 40016458›Full record

ArticleMethods in molecular biology (Clifton, N.J.)2025

Determination of Binding and Endocytosis of Rhinovirus by Flow Cytometry.

Umadevi Sajjan

Abstract read
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In one paragraph

Article in Methods in molecular biology (Clifton, N.J.), 2025. 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
–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

0 citing papers in PubMed.

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

1 author.

Umadevi SajjanCentre for Inflammation and Lung Research, Lewis Katz Medical School, Temple University, Philadelphia, PA, USA. uma.sajjan@temple.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Viruses are dependent on their host cells for replication. The first step in viral infection is the binding of the virus to the host cell membrane, followed by internalization or endocytosis of the virus. Rhinoviruses utilize several cellular membrane receptors to cross the plasma membrane by endocytosis. Three major glycoprotein receptors that are utilized by rhinoviruses to gain entry into the cells are intracellular adhesion molecules, low-density lipoprotein receptor family members, and cadherin-related family member-3. Rhinovirus is endocytosed by a clathrin- or dynamin-dependent mechanism. Upon uptake into an acidic endosomal environment, rhinovirus uncoats and injects its genome into the cytoplasm, where the viral replication begins. It is often difficult to differentiate between bound and the endocytosed rhinovirus in the cells. Here, we describe a method to quantify bound and endocytosed virus by flow cytometry.

Indexed as

EndocytosisFlow CytometryRhinovirusVirus AttachmentCell LineClathrinDynaminsHumansReceptors, VirusVirus UncoatingClathrinDynaminsReceptors, VirusEndosomesImmunofluorescenceRhinovirus antibody

Identifiers

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.