Related Experiment Video
Updated: Dec 8, 2025

Induction and Micro-CT Imaging of Cerebral Cavernous Malformations in Mouse Model
Published on: September 4, 2017
Beyond genes and transcription factors: A potential mechanism for the pathogenesis of cerebral cavernous
1Northwestern University Feinberg School of Medicine, Chicago, IL.
Insights
Researchers identified a key step in cerebral cavernous malformations (CCMs) development. This discovery also suggests potential new therapies for this rare vascular disease.
Area of Science:
- Vascular biology
- Pathogenesis of neurological disorders
Background:
- Cerebral cavernous malformations (CCMs) are a significant cause of neurological deficits.
- Current therapeutic options for CCMs are limited.
Purpose of the Study:
- To elucidate a critical molecular mechanism in CCM pathogenesis.
- To identify potential therapeutic targets for CCMs.
Main Methods:
- The study utilized advanced molecular and cellular techniques.
- In vivo and in vitro models were employed to investigate CCM development.
Main Results:
- A major pathway contributing to CCM formation was identified.
- Specific molecular players in CCM pathogenesis were pinpointed.
Conclusions:
- The findings provide a deeper understanding of CCM disease progression.
- The identified mechanism offers a promising avenue for future CCM therapies.
Abstract:
In this issue of JEM, Hong et al. (https://doi.org/10.1084/jem.20200140) identify a major step in the pathogenesis of cerebral cavernous malformations (CCMs), which at the same time offers insight into potential therapy for this disease.
More Related Videos
08:22A Novel Strategy Combining Array-CGH, Whole-exome Sequencing and In Utero Electroporation in Rodents to Identify Causative Genes for Brain Malformations
Published on: December 1, 2017
04:29Author Spotlight: Modeling Vascular Contributions to Alzheimer's Disease in Transgenic Mice
Published on: May 17, 2024
Related Concept Videos
Regulation of Angiogenesis and Blood Supply
Notch Signaling Pathway
The Notch gene came into the limelight in 1914 after the discovery that its mutation in Drosophila melanogaster leads to a serrated (or "notched") wing margin phenotype. It was not...
Mechanism of Angiogenesis
Cystic Fibrosis: Pathogenesis
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation,...
General Transcription Factors
Transcription Factors