Evidence map›Paper›PMID 42213769›Full record

ArticleSTAR protocols2026

Protocol for generating endogenous degron tags in essential transcription factors in human iPSCs via CRISPR-Cas9.

Ziwei Li, Arthur Roberts, Utkal Nimse, Lucas Vu, Jia Fei

Abstract read
In one paragraph

Article in STAR protocols, 2026. 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. CRISPR Gene Tagging for Illuminating Endogenous Protein Dynamics.International journal of molecular sciences · 2026
    Review
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

5 authors.

Ziwei LiDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA. Electronic address: ziwei.li@rutgers.edu.
Arthur RobertsRutgers Cancer Institute, New Brunswick, NJ, USA.
Utkal NimseDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.
Lucas VuDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA.
Jia FeiDepartment of Molecular Biology and Biochemistry, Rutgers University, Piscataway, NJ, USA; Rutgers Cancer Institute, New Brunswick, NJ, USA. Electronic address: jia.fei@rutgers.edu.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Precise genome engineering in human pluripotent stem cells remains inefficient, limiting endogenous fluorescent tagging needed to study phase-separated membraneless nuclear compartments. Here, we present a protocol for generating precise knockin alleles of essential genes in human induced pluripotent stem cells (iPSCs) via CRISPR-Cas9 editing. We describe steps for combining transient p53 inhibition, optimized transfection conditions, and fluorescence-activated cell sorting. This protocol enables recovery of viable edited clones that would otherwise be lost due to editing-induced stress or essential gene perturbation. For complete details on the use and execution of this protocol, please refer to Li et al.

Indexed as

CRISPR-Cas SystemsGene EditingInduced Pluripotent Stem CellsTranscription FactorsDegronsGene Knock-In TechniquesHumansTumor Suppressor Protein p53Transcription FactorsTumor Suppressor Protein p53Cell BiologyGenomicsMolecular Biology

Identifiers

PMID42213769
PMCPMC13241723

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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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.