Manton Center for Orphan Disease Research
Dr. Alan Beggs was recently named the Sir Edwin and Lady Manton Associate Professor of Pediatrics in the Field of Genetics at Harvard Medical School, as well as the first Director of the new Manton Center for Orphan Disease Research at Children's Hospital. The center supports research and training, and it raises awareness and funding for the broad range of "orphan" diseases that affect people worldwide. For more information on the Manton Center, click below:
Boston Children's Hospital Press Release for the Manton Center
Beggs Lab Annual Newsletter
Since 2005, the Beggs Lab has been publishing an annual newsletter. Generally released around the holiday season, it highlights our accomplishments for the previous year. It is mailed to all of our participants, prospective participants and referring physicians without whom our research wouldn't be possible. We hope that the newsletter not only displays our profound gratitude to all who support our research, but that it will also serve to inspire those whose lives have been affected by this family of diseases. Please click on the links below to see the progress our lab has made!
Beggs Lab Newsletter Spring 2013
Beggs Lab Newsletter Winter 2011-2012
Beggs Lab Newsletter Winter 2010-2011
Advancements in Diamond-Blackfan Anemia Research
Current Articles on Diamond-Blackfan Anemia
Below, please find recent Children's News articles discussing Dr. Hanna Gazda's research on the rare disease Diamond-Blackfan Anemia.
Dr. Hanna Gazda's search for answers about Diamond-Blackfan Anemia
More information on Diamond-Blackfan Anemia
Understanding the Mechanisms of Muscle Weakness
How do mutations in the gene affect muscle weakness?
The following articles discuss Dr. Beggs' recent research findings pertaining to Centronuclear Myopathy, as well as web-based animations that display how some genetic mutations affect the muscle's ability to contract in Nemaline Myopathy. The animations also show the basics of muscle contraction/pathology, so that readers can better understand how genetic mutations disrupt a muscle's normal functioning. Please click below for more information:
"Searching for Strength: One Gene at a Time"
"Nemaline Myopathy – Many Paths to Weakness"