Evidence map›Paper›PMID 37034664›Full record

ArticlebioRxiv : the preprint server for biology2023

TNF-NFkB-p53 axis restricts

Tae Wan Kim, So Yeon Koo, Markus Riessland, Hyunwoo Cho, Fayzan Chaudhry, Benjamin Kolisnyk, Marco Vincenzo Russo, Nathalie Saurat, Sanjoy Mehta, Ralph Garippa and 2 more

Abstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

12 authors.

So Yeon Koo
Markus Riessland
Hyunwoo Cho
Fayzan Chaudhry
Benjamin Kolisnyk
Marco Vincenzo Russo
Nathalie Saurat
Sanjoy Mehta
Ralph Garippa
Doron Betel

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Ongoing, first-in-human clinical trials illustrate the feasibility and translational potential of human pluripotent stem cell (hPSC)-based cell therapies in Parkinson's disease (PD). However, a major unresolved challenge in the field is the extensive cell death following transplantation with <10% of grafted dopamine neurons surviving. Here, we performed a pooled CRISPR/Cas9 screen to enhance survival of postmitotic dopamine neurons Highlights:

Identifiers

PMID37034664
PMCPMC10081262

What OpenQuestion holds

Textmetadata
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.