Evidence map›Paper›PMID 40418471›Full record

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

Nonradiolabeled Radioresistant DNA Synthesis and S-Phase Checkpoint Analysis.

Takamitsu A Kato

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.

Takamitsu A KatoDepartment of Environmental and Radiological Health Sciences, Colorado State University, Fort Collins, CO, USA. tkato@rams.colostate.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

DNA damage activates cell cycle checkpoints and repairs damages during cell cycle arrest. Radiation-induced S-phase arrest occurs in normal cells, but cells from ataxia telangiectasia (AT) patients present radioresistant DNA synthesis (RDS). AT-derived cells proceed DNA synthesis with DNA damage. Upon detection of radiation-induced DSBs, ATM becomes activated and initiates a signaling cascade that triggers multiple cellular responses aimed to repair the damaged DNA. One of them is the S-phase checkpoint to stop DNA synthesis. Originally, RDS was detected using pulse chase of two radiolabeled thymidines. This chapter introduces modified nonradiolabeled RDS assay using dual labeling of EdU and BrdU and detection of thymidine analogous by specific antibody and Click reaction.

Indexed as

DNADNA ReplicationRadiation ToleranceS Phase Cell Cycle CheckpointsAtaxia TelangiectasiaAtaxia Telangiectasia Mutated ProteinsBromodeoxyuridineDeoxyuridineDNA DamageHumans5-ethynyl-2'-deoxyuridineAtaxia Telangiectasia Mutated ProteinsBromodeoxyuridineDeoxyuridineDNAATMBrdUEdURadioresistant DNA synthesis

Identifiers

What OpenQuestion holds

Textmetadata
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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.