Muscular Dystrophy Center Focus: tissue banks, cell culture and diagnostics

Who could benefit from this research

What this research studies

If you or a family member has muscular dystrophy or a related neuromuscular condition, this program helps researchers by providing well-characterized muscle tissues, fibroblasts, and diagnostic services. The core maintains a large repository of patient samples and cells and makes them available to scientists to study disease mechanisms and test potential therapies. It also develops and validates new diagnostic tests that could eventually be used in clinical laboratories. The work is closely linked with the University of Iowa Hospital to ensure clinical relevance and quality control. Participation may involve providing samples or contributing to studies that use existing patient tissues or cells.

Why it matters

Where this research is happening

• University of Iowa
  Iowa City, United States Active

Researchers

• Principal investigator: Moore, Steven a — University of Iowa
• Study coordinator: Moore, Steven a

Related research

Other NIH-funded projects on the same topics.

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• Understanding why Duchenne Muscular Dystrophy worsens and how to stop it

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  NIH research University of Southern California · Los Angeles, UNITED STATES · NIH-11502706

• Endocrine role of intramuscular fat in muscular dystrophy

  This grant studies how fat that builds up inside muscles in Duchenne and Becker muscular dystrophy may release hormones that affect overall health, especially metabolism.

  NIH research University of Florida · Gainesville, United States · NIH-11460264

• Stopping steroid-related muscle and bone wasting in Duchenne muscular dystrophy

  Researchers are testing ways to protect muscles and bones in people with Duchenne muscular dystrophy who take long-term steroid medicines.

  NIH research Univ of Arkansas for Med Scis · Little Rock, United States · NIH-11458914

• Curation of muscular dystrophy genes to improve diagnosis and care

  A grant to help doctors better interpret genetic tests for muscular dystrophy and myopathy so patients get clearer diagnoses and faster access to therapies.

  NIH research Washington University · Saint Louis, United States · NIH-11417940

• MR clues to how nNOS affects energy use and blood flow in Becker and Duchenne muscular dystrophy

  This project looks at how advanced MRI tests can track muscle energy and blood flow changes in people with Becker and Duchenne muscular dystrophy as new gene therapies are explored.

  NIH research University of Florida · Gainesville, United States · NIH-11413866

About this research

1. This is an active NIH-funded research project — typically early-stage science, not a clinical trial accepting patient enrollment.
2. Some NIH-funded labs run parallel clinical studies or seek volunteers for related work. To check, contact the principal investigator or institution listed above.
3. For full project details, budget, and progress reports, visit the official NIH RePORTER page.