Evidence map›Paper›PMID 38542660›Full record

ArticleMicromachines2024

Droplets for Gene Editing Using CRISPR-Cas9 and Clonal Selection Improvement Using Hydrogels.

Camilo Pérez-Sosa, Maximiliano S Pérez, Alexander Paolo Vallejo-Janeta, Shekhar Bhansali, Santiago Miriuka, Betiana Lerner

Abstract read
In one paragraph

Article in Micromachines, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. Review
  2. Nanoparticle Carriers: A New Era of Precise CRISPR/Cas9 Gene Editing.MicroRNA (Shariqah, United Arab Emirates) · 2025
    Review
  3. Review
  4. 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

6 authors.

Camilo Pérez-SosaIREN Center, National Technological University, Buenos Aires B1706EAH, Argentina.
Maximiliano S PérezIREN Center, National Technological University, Buenos Aires B1706EAH, Argentina.
Alexander Paolo Vallejo-JanetaIREN Center, National Technological University, Buenos Aires B1706EAH, Argentina.
Shekhar BhansaliDepartment of Electrical and Computer Engineering, Florida International University, Miami, FL 33174, USA.
Santiago MiriukaNational Council for Scientific and Technical Research-Foundation for the Fight against Neurological Diseases of Childhood, (LIAN-CONICET-FLENI), FLENI Sede Escobar, Ruta 9 Km 53, Belén de Escobar, Buenos Aires B1625XAF, Argentina.
Betiana LernerIREN Center, National Technological University, Buenos Aires B1706EAH, Argentina.ORCID 0000-0003-3341-5686

Funding

Consejo Nacional de Investigaciones Científicas y Técnicas PICT STARTUP 2020_0017, PIP 2021-2023, PIP 2021-2023 , PICT 2021 CAT I 00058
6 · The paper itself

Abstract

Gene editing tools have triggered a revolutionary transformation in the realms of cellular and molecular physiology, serving as a fundamental cornerstone for the evolution of disease models and assays in cell culture reactions, marked by various enhancements. Concurrently, microfluidics has emerged over recent decades as a versatile technology capable of elevating performance and reducing costs in daily experiments across diverse scientific disciplines, with a pronounced impact on cell biology. The amalgamation of these groundbreaking techniques holds the potential to amplify the generation of stable cell lines and the production of extracellular matrix hydrogels. These hydrogels, assuming a pivotal role in isolating cells at the single-cell level, facilitate a myriad of analyses. This study presents a novel method that seamlessly integrates CRISPR-Cas9 gene editing techniques with single-cell isolation methods in induced pluripotent stem cell (hiPSC) lines, utilizing the combined power of droplets and hydrogels. This innovative approach is designed to optimize clonal selection, thereby concurrently reducing costs and the time required for generating a stable genetically modified cell line. By bridging the advancements in gene editing and microfluidic technologies, our approach not only holds significant promise for the development of disease models and assays but also addresses the crucial need for efficient single-cell isolation. This integration contributes to streamlining processes, making it a transformative method with implications for enhancing the efficiency and cost-effectiveness of stable cell line generation. As we navigate the intersection of gene editing and microfluidics, our study marks a significant stride toward innovative methodologies in the dynamic landscape of cellular and molecular physiology research.

Indexed as

clone selectionCRISPR-Cas9dropletsmicrofluidicssingle cell

Identifiers

PMID38542660
PMCPMC10972466

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.