Evidence map›Paper›PMID 34516793›Full record

ArticleScience (New York, N.Y.)2021

A P(V) platform for oligonucleotide synthesis.

Yazhong Huang, Kyle W Knouse, Shenjie Qiu, Wei Hao, Natalia M Padial, Julien C Vantourout, Bin Zheng, Stephen E Mercer, Javier Lopez-Ogalla, Rohan Narayan and 6 more

Abstract read
In one paragraph

Article in Science (New York, N.Y.), 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 32 papers.

0numbers the graph read from it
0cells of the map it votes in
32citing 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

32 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
  4. Review
  5. Article
  6. Review
  7. Article
  8. Conception and Synthesis of Sequence-Coded Morpholinos.Chemistry (Weinheim an der Bergstrasse, Germany) · 2025
    Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
  16. Article
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  18. Article
  19. Article
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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

16 authors.

Yazhong Huang *Small Molecule Drug Discovery, Bristol Myers Squibb, Cambridge, MA 02142, USA.ORCID 0000-0001-5551-2423
Kyle W Knouse *Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.ORCID 0000-0001-9688-0513
Shenjie Qiu *Elsie Biotechnologies, San Diego, CA 92121, USA.ORCID 0000-0002-9341-3749
Wei Hao *Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.ORCID 0000-0001-9493-6894
Natalia M Padial *Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.ORCID 0000-0001-6067-3360
Julien C Vantourout *Department of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.ORCID 0000-0002-0602-069X
Bin ZhengElsie Biotechnologies, San Diego, CA 92121, USA.
Stephen E MercerSmall Molecule Drug Discovery, Bristol Myers Squibb, Cambridge, MA 02142, USA.ORCID 0000-0003-4211-9002
Javier Lopez-OgallaDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.ORCID 0000-0002-7061-0088
Rohan NarayanDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.
Richard E OlsonSmall Molecule Drug Discovery, Bristol Myers Squibb, Cambridge, MA 02142, USA.
Donna G BlackmondDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.
Martin D EastgateElsie Biotechnologies, San Diego, CA 92121, USA.ORCID 0000-0002-6487-3121
Michael A SchmidtElsie Biotechnologies, San Diego, CA 92121, USA.ORCID 0000-0002-4880-2083
Ivar M McDonaldSmall Molecule Drug Discovery, Bristol Myers Squibb, Cambridge, MA 02142, USA.ORCID 0000-0001-7500-7133
Phil S BaranDepartment of Chemistry, The Scripps Research Institute, La Jolla, CA 92037, USA.ORCID 0000-0001-9193-9053

Funding

Scalable Synthesis and New Bond DisconnectionsR35GM118176 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI BARAN, PHIL S · 2016 to 2025
$11.5M
Preparative Radical Chemistry for Biomedical ResearchR01GM106210 · NIGMS · SCRIPPS RESEARCH INSTITUTE, THE · PI BARAN, PHIL S · 2013 to 2016
$2.1M
NIGMS NIH HHS R01 GM106210NIGMS NIH HHS R35 GM118176
6 · The paper itself

Abstract

The promise of gene-based therapies is being realized at an accelerated pace, with more than 155 active clinical trials and multiple U.S. Food and Drug Administration approvals for therapeutic oligonucleotides, by far most of which contain modified phosphate linkages. These unnatural linkages have desirable biological and physical properties but are often accessed with difficulty using phosphoramidite chemistry. We report a flexible and efficient [P(V)]–based platform that can install a wide variety of phosphate linkages at will into oligonucleotides. This approach uses readily accessible reagents and can install not only stereodefined or racemic thiophosphates but any combination of (

Indexed as

OligonucleotidesOligonucleotides

Identifiers

PMID34516793
PMCPMC8579956

What OpenQuestion holds

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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.