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

Genetic Screens02:46

Genetic Screens

5.8K
Genetic screens are tools used to identify genes and mutations responsible for phenotypes of interest. Genetic screens help identify individuals or a group of people at risk of developing  genetic diseases and help them with early intervention, targeted therapy, and reproductive options.
Forward genetic screens
Forward or “classical” genetic screens involve creating random mutations in an organism’s DNA using radiation, mutagens, or insertion of additional bases, which...
5.8K

You might also read

Related Articles

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

Sort by
Same author

A Cascade Enzyme System Based on the Catalase-like Activity of Co-MQDs for Enhanced Visualized Tumor Combination Therapy.

ACS applied materials & interfaces·2026
Same author

Habitat context affects sediment nitrogen burial by restored Eastern Oyster reefs.

PloS one·2026
Same author

A self-energized photodynamic therapy agent based on persistent luminescence nanoparticles.

Biomaterials science·2026
Same author

Intermolecular Cyclization of Alkyl Chains of Ketones for Constructing <i>ortho</i>-Diacylbenzenes.

Journal of the American Chemical Society·2026
Same author

Mac-/Lactosylceramide regulates intestinal homeostasis and secretory cell fate commitment by facilitating Notch signaling.

eLife·2025
Same author

Evaluating the efficacy of compound probiotics as an antibiotic alternative: A comprehensive analysis of growth performance and intestinal health via feed and water routes.

Animal nutrition (Zhongguo xu mu shou yi xue hui)·2025

Related Experiment Video

Updated: Feb 19, 2026

A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening
07:18

A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening

Published on: May 12, 2017

6.8K

Phenotypic Screen Identifies a Small Molecule Modulating ERK2 and Promoting Stem Cell Proliferation.

Chang Yin1,2, Temesgen Fufa1,3, Gayathri Chandrasekar1,4

  • 1Department of Microbiology, Tumor and Cell Biology, Karolinska Institutet, Stockholm, Sweden.

Frontiers in Pharmacology
|November 9, 2017
PubMed
Summary

Researchers identified a small molecule that enhances stem cell proliferation using integrated phenotypic drug discovery (PDD) models. This approach combines in vitro and in vivo methods for improved hit identification and reproducibility in drug discovery.

Keywords:
PDDmousephenotypesmall moleculesstem cellszebrafish

More Related Videos

An Efficient Protocol to Assess ERK Activity Modulation in Early Zebrafish Noonan Syndrome Models via Live FRET Microscopy and Immunofluorescence
09:58

An Efficient Protocol to Assess ERK Activity Modulation in Early Zebrafish Noonan Syndrome Models via Live FRET Microscopy and Immunofluorescence

Published on: May 2, 2025

718
Identification of Kinase-substrate Pairs Using High Throughput Screening
11:13

Identification of Kinase-substrate Pairs Using High Throughput Screening

Published on: August 29, 2015

8.6K

Related Experiment Videos

Last Updated: Feb 19, 2026

A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening
07:18

A Simple Method to Identify Kinases That Regulate Embryonic Stem Cell Pluripotency by High-throughput Inhibitor Screening

Published on: May 12, 2017

6.8K
An Efficient Protocol to Assess ERK Activity Modulation in Early Zebrafish Noonan Syndrome Models via Live FRET Microscopy and Immunofluorescence
09:58

An Efficient Protocol to Assess ERK Activity Modulation in Early Zebrafish Noonan Syndrome Models via Live FRET Microscopy and Immunofluorescence

Published on: May 2, 2025

718
Identification of Kinase-substrate Pairs Using High Throughput Screening
11:13

Identification of Kinase-substrate Pairs Using High Throughput Screening

Published on: August 29, 2015

8.6K

Area of Science:

  • Stem cell biology
  • Pharmacology
  • Drug discovery

Background:

  • Stem cells possess unique proliferation controls distinct from somatic cells.
  • Understanding these mechanisms is crucial for advancing drug discovery and translational applications.
  • Phenotype-based drug discovery (PDD) offers an unbiased route to novel biological insights.

Purpose of the Study:

  • To identify small molecules that promote stem cell proliferation.
  • To evaluate an integrated phenotypic screening approach using combined in vitro and in vivo models.
  • To characterize the mechanism of action for identified compounds.

Main Methods:

  • Employed an integrated phenotypic screening approach combining in vitro and in vivo PDD models.
  • Utilized cell viability and colony size measurements for phenotype assessment.
  • Performed structure-activity relationship studies on the lead molecule.

Main Results:

  • The integrated PDD approach improved hit identification and reproducibility across models.
  • A novel small molecule was identified that significantly increases stem cell proliferation.
  • The molecule was found to inhibit ERK2 phosphorylation, a key pathway in cell proliferation.

Conclusions:

  • An integrated PDD strategy using combinatorial models effectively identifies compounds promoting stem cell proliferation.
  • This approach enhances the discovery of molecules with potential therapeutic applications in regenerative medicine.
  • The identified small molecule targeting ERK2 phosphorylation represents a promising candidate for further investigation.