Evidence map›Paper›PMID 42382945›Full record

ArticleMolecular therapy. Advances2026

CRISPR-Cas9 screening reveals

Sungje Park, Seunghyeon Shin, Gyucheol Han, Yubin Won, Sang Yoon Lee, David Razafsky, Henry George, Gyun Min Lee

Abstract read
In one paragraph

Article in Molecular therapy. 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

8 authors.

Sungje ParkDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.
Seunghyeon ShinDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.
Gyucheol HanGraduate School of Engineering Biology, KAIST, Daejeon, Republic of Korea.
Yubin WonGraduate School of Engineering Biology, KAIST, Daejeon, Republic of Korea.
Sang Yoon LeeDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.
David RazafskyMilliporeSigma, St. Louis, MO, USA.
Henry GeorgeMilliporeSigma, St. Louis, MO, USA.
Gyun Min LeeDepartment of Biological Sciences, KAIST, Daejeon, Republic of Korea.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inherent tendency of human embryonic kidney (HEK) cells to aggregate in suspension culture poses a significant obstacle to the large-scale production of adeno-associated virus (AAV) vectors for gene therapy. To overcome this, we employed a virus-free CRISPR-Cas9 single gene knockout (KO) library in HEK293T cells to systematically identify key genetic regulators of cell aggregation. By serially passaging the KO library and selectively sub-culturing only the suspended (non-aggregated) cells, we enriched for genotypes that reduce aggregation. Next-generation sequencing identified

Indexed as

adeno-associated viruscell aggregationCRISPR-Cas9 knockout libraryHEK293suspension culture

Identifiers

PMID42382945
PMCPMC13316624

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.