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  1. Jeffrey Chamberlain PhD. Neurology, Biochemistry, Medicine/Medical Genetics Councilor, Representing ISCRM’s Senior Faculty Leadership McCaw Chair in Muscular Dystrophy and Professor. Email: jsc5@uw.edu | Phone: 206.616.6645.

  2. Jeff Chamberlain is a cinematic director and vfx supervisor at Blizzard Entertainment. A veritable veteran of the cinematics department, Jeff has been part of most of the cinematics they've created over the last couple decades.

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  4. The Chamberlain laboratory is led by Dr. Jeffrey Chamberlain, a professor and director of the Muscular Dystrophy Cooperative Research Center of Seattle. The laboratory focuses on the Duchenne muscular dystrophy (DMD) and LGMD2I genes and their expression and function in muscle, and on the development of gene therapy vectors and methods for muscle wasting disorders.

  5. Mar 3, 2024 · Jeff Chamberlain, PhD, a leading professor in gene therapy focused on Duchenne muscular dystrophy, shared his reaction to being named the recipient of the 2024 MDA Legacy Award, as well as the state of the DMD field currently.

    • Marco Meglio
  6. Jeff Chamberlain was born on January 5, 1954 in Fort Ord, California, USA. He was an actor and producer, known for Black Rain (1989), The Mine (2012) and Pump Up the Volume (1990). He was previously married to Lachelle Chamberlain. He died on September 16, 2020 in Midway, Utah, USA.

    • January 5, 1954 in Fort Ord, California, USA
    • 5' 11" (1.8 m)
    • September 16, 2020 in Midway, Utah, USA
  7. Jan 30, 2024 · The Muscular Dystrophy Association (MDA) today announced Jeffrey Chamberlain, Ph.D., a leading professor in gene therapy focused on Duchenne muscular dystrophy (DMD) at the UW Institute for Stem Cell and Regenerative Medicine, will receive the 2024 MDA Legacy Award for Achievement in Research, for his achievements in translational research.

  8. Jeffrey Chamberlain, PhD. President (2023-2024) My career has focused on muscle biology, diseases, and therapeutics. These activities span basic research on muscle gene structure and function to developing vectors for gene therapy of Duchenne muscular dystrophy (DMD).

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