Evidence map›Paper›PMID 31855104›Full record

ArticleSLAS discovery : advancing life sciences R & D2020

Forced Self-Modification Assays as a Strategy to Screen MonoPARP Enzymes.

Tim J Wigle, W David Church, Christina R Majer, Kerren K Swinger, Demet Aybar, Laurie B Schenkel, Melissa M Vasbinder, Arne Brendes, Claudia Beck, Martin Prahm and 3 more

Open access · hybridAbstract read
In one paragraph

Article in SLAS discovery : advancing life sciences R & D, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
2.0field-weighted citation impact, top 11% 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

11 citing papers in PubMed, 23 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

13 authors at 2 institutions in 2 countries.

Tim J WigleRibon Therapeutics Inc., Cambridge, MA, USA.
W David ChurchRibon Therapeutics Inc., Cambridge, MA, USA.
Christina R MajerRibon Therapeutics Inc., Cambridge, MA, USA.
Kerren K SwingerRibon Therapeutics Inc., Cambridge, MA, USA.
Demet AybarRibon Therapeutics Inc., Cambridge, MA, USA.
Laurie B SchenkelRibon Therapeutics Inc., Cambridge, MA, USA.
Melissa M VasbinderRibon Therapeutics Inc., Cambridge, MA, USA.
Arne BrendesEvotec SE, Hamburg, Germany.
Claudia BeckEvotec SE, Hamburg, Germany.
Martin PrahmEvotec SE, Hamburg, Germany.
Dennis WegenerEvotec SE, Hamburg, Germany.
Paul ChangRibon Therapeutics Inc., Cambridge, MA, USA.
Kevin W KuntzRibon Therapeutics Inc., Cambridge, MA, USA.
Ribon Therapeutics (United States) · USEvotec (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mono(ADP-ribosylation) (MARylation) and poly(ADP-ribosylation) (PARylation) are posttranslational modifications found on multiple amino acids. There are 12 enzymatically active mono(ADP-ribose) polymerase (monoPARP) enzymes and 4 enzymatically active poly(ADP-ribose) polymerase (polyPARP) enzymes that use nicotinamide adenine dinucleotide (NAD

Indexed as

High-Throughput Screening AssaysAdenosine Diphosphate RiboseADP Ribose TransferasesADP-RibosylationEnzyme InhibitorsHumansNADPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) PolymerasesPoly ADP RibosylationProtein Processing, Post-TranslationalSubstrate SpecificityAdenosine Diphosphate RiboseADP Ribose TransferasesEnzyme InhibitorsNADPoly(ADP-ribose) Polymerase InhibitorsPoly(ADP-ribose) Polymerasesdissociation-enhanced lanthanide fluorescence immunoassay (DELFIA)mono(ADP-ribosylation) (MARylation)nicotinamide adenine dinucleotide (NAD+)poly(ADP-ribose) polymerase (PARP)self-modification

Identifiers

PMID31855104
PMCPMC7036481
OpenAlexW2995386570

What OpenQuestion holds

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LicenceCC BY-NC
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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.