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 Experiment Videos

Microarray analysis of normal and dystrophic skeletal muscle.

Judith N Haslett1, Louis M Kunkel

  • 1Department of Genetics, Harvard Medical School, Boston, MA, USA. haslett@enders.tch.harvard.edu

International Journal of Developmental Neuroscience : the Official Journal of the International Society for Developmental Neuroscience
|August 15, 2002
PubMed
Summary

DNA microarrays enable comprehensive RNA expression analysis, revolutionizing molecular pathology. This technology reveals complex biological pathways, particularly advancing our understanding of muscular dystrophy molecular mechanisms.

Related Concept Videos

You might also read

Related Articles

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

Sort by
Same author

Missense variants in TUBA4A cause myo-tubulinopathies.

Brain : a journal of neurology·2026
Same author

Conditional Dmd ablation in muscle and brain causes profound effects on muscle function and neurobehavior.

Communications biology·2025
Same author

Muscle-specific increased expression of <i>JAG1</i> improves the skeletal muscle phenotype in dystrophin-deficient mice.

Proceedings of the National Academy of Sciences of the United States of America·2025
Same author

Missense variants in <i>TUBA4A</i> cause myo-tubulinopathies.

medRxiv : the preprint server for health sciences·2025
Same author

Identifying kinematic biomarkers of the dystrophic phenotype in a zebrafish model of Duchenne muscular dystrophy.

Skeletal muscle·2025
Same author

Muscle-specific increased expression of <i>JAG1</i> improves skeletal muscle phenotype in dystrophin-deficient mice.

bioRxiv : the preprint server for biology·2025

Area of Science:

  • Molecular Pathology
  • Genomics
  • Biotechnology

Background:

  • Traditional molecular studies focused on individual genes, limiting understanding of complex biological pathways.
  • DNA microarrays allow simultaneous measurement of thousands of transcripts, overcoming previous technical limitations.
  • This technology facilitates a holistic approach to studying biological processes and their interconnections.

Purpose of the Study:

  • To review the application of DNA microarray technology in interrogating muscular gene expression.
  • To highlight how differential gene expression analysis in muscular dystrophy contributes to understanding disease pathophysiology.
  • To explore the impact of microarrays on molecular pathology research.

Main Methods:

  • Utilizing DNA microarrays for high-density arrangements of nucleic acid spots.

Related Experiment Videos

  • Performing comprehensive RNA expression analysis.
  • Conducting differential expression analysis on dystrophic and normal skeletal muscle tissue.
  • Main Results:

    • Microarray technology enables rapid measurement of thousands of distinct transcripts simultaneously.
    • Data from differential expression analysis provides insights into molecular pathophysiological pathways.
    • The study of muscular gene expression using microarrays has significantly advanced understanding of muscular dystrophy.

    Conclusions:

    • DNA microarrays have substantially impacted molecular pathology by enabling global gene expression analysis.
    • Microarray technology allows for the examination of biological pathways in their full complexity.
    • Differential expression analysis of skeletal muscle using microarrays is crucial for understanding muscular dystrophy.