Evidence map›Paper›PMID 42170085›Full record

ArticleRSC advances2026

Combinatorial and rational synthesis of complex, base-modified aptamer libraries on microarrays.

Erika Schaudy, Jory Lietard

Abstract read
In one paragraph

Article in RSC advances, 2026. 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

2 authors.

Erika SchaudyInstitute of Inorganic Chemistry, University of Vienna Vienna 1090 Austria erika.schaudy@univie.ac.at.ORCID https://orcid.org/0000-0002-2803-6684
Jory LietardInstitute of Inorganic Chemistry, University of Vienna Vienna 1090 Austria erika.schaudy@univie.ac.at.ORCID https://orcid.org/0000-0003-4523-6001

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Chemically modifying the backbone, sugar, or nucleobase moieties of nucleic acids greatly expands their functional repertoire. Nucleobase modifications have received particular attention for their proven ability to generate a greater diversity of intra- and intermolecular interactions. This broader interaction landscape has facilitated advances in the identification of aptamers with high affinity to different target molecules, including proteins. As common practice, SELEX (Systematic Evolution of Ligands by EXponential enrichment) is used to select the best binders from a large pool of random oligonucleotides. However, the combinatorial space of SELEX is usually limited to

Identifiers

PMID42170085
PMCPMC13187762

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.