Evidence map›Paper›PMID 30727784›Full record

ArticleJournal of enzyme inhibition and medicinal chemistry2019

Development of a novel, high-affinity ssDNA trypsin inhibitor.

Stanislaw Malicki, Miroslaw Ksiazek, Pawel Majewski, Aleksandra Pecak, Piotr Mydel, Przemyslaw Grudnik, Grzegorz Dubin

Open access · goldAbstract read
In one paragraph

Article in Journal of enzyme inhibition and medicinal chemistry, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

4 citing papers in PubMed, 7 citations in OpenAlex.

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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 2 institutions in 3 countries.

Stanislaw Malickia Malopolska Centre of Biotechnology , Jagiellonian University , Krakow , Poland.
Miroslaw Ksiazeka Malopolska Centre of Biotechnology , Jagiellonian University , Krakow , Poland.
Pawel Majewskib Department of Microbiology, Faculty of Biochemistry , Biophysics and Biotechnology, Jagiellonian University , Krakow , Poland.
Aleksandra Pecaka Malopolska Centre of Biotechnology , Jagiellonian University , Krakow , Poland.
Piotr Mydelb Department of Microbiology, Faculty of Biochemistry , Biophysics and Biotechnology, Jagiellonian University , Krakow , Poland.
Przemyslaw Grudnika Malopolska Centre of Biotechnology , Jagiellonian University , Krakow , Poland.
Grzegorz Dubina Malopolska Centre of Biotechnology , Jagiellonian University , Krakow , Poland.
Jagiellonian University · PLUniversity of Bergen · NO

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Inhibitors of serine proteases are not only extremely useful in the basic research but are also applied extensively in clinical settings. Using Systematic Evolution of Ligands by Exponential Enrichment (SELEX) approach we developed a family of novel, single-stranded DNA aptamers capable of specific trypsin inhibition. Our most potent candidate (T24) and its short version (T59) were thoroughly characterised in terms of efficacy. T24 and T59 efficiently inhibited bovine trypsin with K

Indexed as

AnimalsAptamers, NucleotideCattleDNA, Single-StrandedDose-Response Relationship, DrugHumansStructure-Activity RelationshipSwineTrypsinTrypsin InhibitorsAptamers, NucleotideDNA, Single-StrandedTrypsinTrypsin InhibitorsAptamerprotease inhibitorssDNAtrypsin

Identifiers

PMID30727784
PMCPMC6366424
OpenAlexW2913511461

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.