Evidence map›Paper›PMID 40572156›Full record

ArticleMicroorganisms2025

Real-Time PCR Assay to Quantify Moloney Murine Leukemia Virus in Mouse Cells.

Jiwon Choi, Amaiya Murphy, Takayuki Nitta

Abstract read
In one paragraph

Article in Microorganisms, 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

3 authors.

Jiwon ChoiDepartment of Biology, Savannah State University, Savannah, GA 31404, USA.ORCID 0009-0008-5664-3415
Amaiya MurphyDepartment of Biology, Savannah State University, Savannah, GA 31404, USA.
Takayuki NittaDepartment of Biology, Savannah State University, Savannah, GA 31404, USA.ORCID 0000-0003-3625-4398

Funding

SSU MARC U-STAR ProgramT34GM100832 · NIGMS · SAVANNAH STATE UNIVERSITY · PI JONES, CECIL LAVERNE · 2012 to 2022
$1.8M
NIGMS NIH HHS T34 GM100832NIH HHS 2T34GM100832-06A1United States Department of Defense W911NF1810405United States Department of Education Title III Part-F (1012-525)U.S. National Science Foundation 1800683U.S. National Science Foundation 2011969
6 · The paper itself

Abstract

Murine leukemia viruses (MuLVs) are retroviruses that cause various diseases in mice and have served as a model for retrovirus replication and pathogenesis. MuLVs are separated into infectious exogenous retroviruses (XRVs) and endogenous retroviruses (ERVs) that are remnants of ancient infectious XRVs. Detection of XRVs in the original host cells has some difficulties because of the high similarity in sequence between ERVs and XRVs and expression of some ERV genes. There are some techniques available for monitoring retroviral replication, but each comes with limitations in terms of labor intensity, detection range, cost, and phases after infection. This study developed a novel quantitative PCR (qPCR) method for assessing replication of Moloney MuLV (M-MuLV) in mouse cells. The method amplified the region in packaging signal and

Indexed as

endogenous retrovirusexogenous retrovirusfocal immunofluorescence assaymurine leukemia virusquantitative PCRviral DNA

Identifiers

PMID40572156
PMCPMC12194895

What OpenQuestion holds

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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.