Evidence map›Paper›PMID 24648903›Full record

ArticleBiomedical reports2013

An efficient method for high-fidelity messenger RNA amplification from a small amount of total RNA.

Mitsuru Chiba, Saya Asari, Misako Kimura, Toshiya Nakamura

Abstract read
In one paragraph

Article in Biomedical reports, 2013. 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

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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

4 authors.

Mitsuru ChibaDepartment of Biomedical Sciences, Division of Medical Life Sciences; ; Research Center for Biomedical Sciences;
Saya AsariDepartment of Medical Technology, Hirosaki University Graduate School of Health Sciences, Hirosaki, Aomori 036-8564, Japan.
Misako KimuraDepartment of Medical Technology, Hirosaki University Graduate School of Health Sciences, Hirosaki, Aomori 036-8564, Japan.
Toshiya NakamuraDepartment of Biomedical Sciences, Division of Medical Life Sciences; ; Research Center for Biomedical Sciences;

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Comprehensive analyses of gene expression have been carried out by the development of microarrays and deep sequencers. However, it is difficult to obtain comprehensive information on gene expression from a small amount of ribonucleic acid (RNA). Therefore, we investigated the reproducibility and application of T7 RNA polymerase-mediated transcription, adaptor ligation and polymerase chain reaction (PCR) amplification, followed by T7 transcription (TALPAT), an efficient method for amplifying poly (A)-positive RNA, such as messenger RNA (mRNA). When amplified complementary RNA (cRNA) was electrophoresed, a large number of amplified cRNA was detected in the size of 0.2-0.5 kb. This indicates that the region up to 0.2-0.5 kb from the 3' end of the original mRNA was amplified by the TALPAT method. Seven housekeeping genes, glyceraldehyde-3-phosphate dehydrogenase (

Indexed as

adaptor ligationcomplementary ribonucleic acid synthesismRNA amplificationreal-time polymerase chain reactionT7 in vitro transcription

Identifiers

PMID24648903
PMCPMC3956878

What OpenQuestion holds

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Registered trials

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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.