Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

In-vitro Mutagenesis01:16

In-vitro Mutagenesis

To learn more about the function of a gene, researchers can observe what happens when the gene is inactivated or “knocked out,” by creating genetically engineered knockout animals. Knockout mice have been particularly useful as models for human diseases such as cancer, Parkinson’s disease, and diabetes.

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

Feeder-free yet still naïve: improved method for capturing human pluripotent stem cells.

The EMBO journal·2026
Same author

Post-replicative chromatin accessibility predicts cell fate change.

Stem cell reports·2026
Same author

Morphomechanic tuning of ERK by actin-TFII-IΔ regulates cell identity.

bioRxiv : the preprint server for biology·2026
Same author

Modulation of Nudt21 levels reveals dose-dependent roles of alternative polyadenylation in tissue regeneration.

Nature communications·2026
Same author

Metformin inhibits nuclear egress of chromatin fragments in senescence and aging.

Nature aging·2026
Same author

T follicular helper cells transiently unlock a plasticity state in germinal centre B cells during the humoral immune response.

Nature cell biology·2025

Related Experiment Video

Updated: Jun 17, 2026

Reprogramming Mouse Embryonic Fibroblasts with Transcription Factors to Induce a Hemogenic Program
11:00

Reprogramming Mouse Embryonic Fibroblasts with Transcription Factors to Induce a Hemogenic Program

Published on: December 16, 2016

A reprogrammable mouse strain from gene-targeted embryonic stem cells.

Matthias Stadtfeld1, Nimet Maherali, Marti Borkent

  • 1Massachusetts General Hospital Cancer Center and Center for Regenerative Medicine, Harvard Stem Cell Institute, Boston, Massachusetts, USA.

Nature Methods
|December 17, 2009
PubMed
Summary
This summary is machine-generated.

Researchers developed

More Related Videos

CRISPR/Cas9-Mediated Highly Efficient Gene Targeting in Embryonic Stem Cells for Developing Gene-Manipulated Mouse Models
10:57

CRISPR/Cas9-Mediated Highly Efficient Gene Targeting in Embryonic Stem Cells for Developing Gene-Manipulated Mouse Models

Published on: August 24, 2022

Generation of Mice Derived from Induced Pluripotent Stem Cells
11:56

Generation of Mice Derived from Induced Pluripotent Stem Cells

Published on: November 29, 2012

Related Experiment Videos

Last Updated: Jun 17, 2026

Reprogramming Mouse Embryonic Fibroblasts with Transcription Factors to Induce a Hemogenic Program
11:00

Reprogramming Mouse Embryonic Fibroblasts with Transcription Factors to Induce a Hemogenic Program

Published on: December 16, 2016

CRISPR/Cas9-Mediated Highly Efficient Gene Targeting in Embryonic Stem Cells for Developing Gene-Manipulated Mouse Models
10:57

CRISPR/Cas9-Mediated Highly Efficient Gene Targeting in Embryonic Stem Cells for Developing Gene-Manipulated Mouse Models

Published on: August 24, 2022

Generation of Mice Derived from Induced Pluripotent Stem Cells
11:56

Generation of Mice Derived from Induced Pluripotent Stem Cells

Published on: November 29, 2012

Area of Science:

  • Stem cell biology
  • Genetics
  • Molecular biology

Background:

  • Induced pluripotent stem cells (iPSCs) are typically generated using viral methods.
  • Viral delivery can pose risks and limitations in reprogramming somatic cells.

Purpose of the Study:

  • To create a novel genetic tool for studying cellular reprogramming.
  • To develop a safer and more efficient method for generating iPSCs.

Main Methods:

  • Gene targeting was employed to create a mouse model.
  • A single-copy inducible, polycistronic reprogramming cassette was integrated into the mouse genome.
  • This allows for controlled induction of pluripotency in various somatic cell types.

Main Results:

  • A new strain of 'reprogrammable mice' was successfully generated.
  • The system allows for the induction of pluripotency in diverse somatic cells.
  • These mice are easily bred, facilitating further research.

Conclusions:

  • The developed 'reprogrammable mice' offer a valuable, non-viral tool for studying reprogramming mechanisms.
  • This genetic approach simplifies the generation and study of iPSCs.
  • The model system aids in understanding the fundamental processes of cellular reprogramming.