CATEGORIES: CMT Update | Featured

Scientific Advisory Board Meeting

by | Mar 9, 2015 | 0 comments

FullSizeRender (2)On the 7th of November we convened our scientific advisory board meeting at the HNF offices in NY. Our meeting included Renée JG Arnold, PharmD, RPh (President & CEO, Arnold Consultancy & Technology LLC), Robert Burgess, PhD (Faculty of The Jackson Laboratory in Bar Harbor, Maine), Joel Freundlich, PhD (Associate Professor of Pharmacology & Physiology and Medicine at Rutgers University–New Jersey Medical School), Steven J. Gray, PhD (Research Assistant Professor Dept. of Ophthalmology, U. of N. Carolina at Chapel Hill), Joseph J Higgins, MD, FAAN (Director of Neurology Quest Diagnostics, Athena Brand, Marlborough, MA), Brett Langley, PhD (Director of Neural Epigenetics at the Burke Medical Research Institute, Assistant Professor of Neurology and Neuroscience at Weill Medical College of Cornell University), Jun Li, MD, PhD (Associate Professor, Department of Neurology, Director of Charcot-Marie-Tooth Clinic, Faculty Member in Vanderbilt Brain Institute and Faculty Member in the Center for Human Genetics Research at the School of Medicine, Vanderbilt University.) Nadia Litterman, PhD (Collaborations Director at Collaborative Drug Discovery (CDD)), Lucia Notterpek, PhD (William T. and Janice M. Neely Professor and Chair, Department of Neuroscience at the University of Florida, Gainesville), David Pleasure, MD (Professor of Neurology and Pediatrics, Director of Research, Shriner’s Hospital for Children, Director, Institute for Pediatric Regenerative Medicine and Distinguished Professor, UC Davis), Michael Sereda, MD, PhD (Professor of Neurology and Group leader in the Department of Neurogenetics, Max Planck Institute (MPI) of Experimental Medicine, Göttingen, Germany), and Dianna E. Willis, PhD (Head of the Laboratory for Axonal and RNA Biology, Director of the Center for Pain Research at the Burke Medical Research Institute and an Assistant Professor of Neuroscience at Weill Cornell Medical College). In addition Barbara Handelin, PhD from the Biopontis Alliance was in attendance.

After a welcome from Allison Moore (CEO, HNF), I presented a brief overview of the work HNF had funded to date and our goals. Each scientist gave an overview of their latest research related to CMT or related areas of study, whether it was funded by HNF or not, and described the challenges and opportunities. For example Dr. Sereda updated us on his recent work that described how Neuregulin 1 looked promising for reversing CMT1A. Dr. Notterpek described her miRNA project for CMT1A. Dr Li presented how MRI technology was used to see changes in the peripheral nerves which correlates with CMT and hence may be used as a measure of the disease. Dr Pleasure updated us on the CMT2A mouse characterization. Dr. Willis and Dr. Langley described their research which covered the MFN2 mouse and HDAC6 inhibitors, respectively. Dr. Burgess works with various mouse models and focused on characterizing the CMT2D mouse. Dr. Gray outlined his work on gene therapy, including the research on gigaxonin for Giant Axonal Neuropathy (which should be going to clinical trial in the next few weeks). Dr. Higgins summarized his recent publication which analyzed the frequency of gene mutations in 17,377 patients with CMT and showed that just 4 genes can be used to capture most patients with CMT. Dr. Litterman summarized published work on the use of stem cells and how collaboration could have an important role in making the research process more efficient. Dr. Freundlich described how as researchers are generating high throughput screening data, they could be learning from it with computer models and at the same time understanding what molecules should be avoided. Dr. Arnold stressed how patient reported outcomes were instrumental in getting drugs approved as companies increasingly have to show an increase in quality of life to justify the cost of treatment. This led us very nicely into a discussion of what we should be funding in the future and where the gaps are that will impact upcoming clinical trials. We have written a detailed review that has been published and captures all of the discussion and make this freely available to the scientific community.

Learn more on this topic

Related Blog Posts

Accepting Myself for Who I Am

Growing up, I always knew I was different than my friends. I couldn’t run fast, tripped often (the scars on my knees are a reminder), was lousy at any sports-related activity, and was generally weak and uncoordinated.

The Long Road to Diagnosis Renews Dedication to Advocacy

The Long Road to Diagnosis Renews Dedication to Advocacy

Growing up we called it “Steffi disorder.” My friends and family were as baffled as my expert neurologists. I had been diagnosed with typical Spiral Muscular Atrophy (SMA) as a toddler but never followed its progression; I never seemed to get weaker. My myriad of symptoms was distinctly different than anyone else’s I had ever met in a lifetime living in the neuromuscular community. I thought I might never find my true diagnosis, let alone others who share it with me.

A New Mouse Model for Charcot-Marie-Tooth (CMT2)

We were recently informed that The Jackson Laboratory (JAX, a nonprofit biomedical research institution headquartered in Bar Harbor, Maine) had taken delivery and will be distributing a newly generated CMT-related mouse model. The new model expresses mutant mitofusin 2, a mitochondrial membrane protein involved in mitochondrial fusion and regulation of vascular smooth muscle cell proliferation.

Sixth Annual Card Party Brunch

On January 23, 2015 dedicated H.E.L.P. (Help Elliot Live Proud) Fund supporters participated in the 6th Annual Card Party Brunch and Boutique at Broken Sound County Club, Boca Raton, Florida. Record numbers flocked into the picturesque country club for a day filled with gourmet food, raffles, cards and a silent auction! HNF Board member Iris Adler increased this event by 50 new faces this year!

Join the conversation

Leave a Comment

0 Comments

Submit a Comment

Your email address will not be published. Required fields are marked *

Newsletter

Join for notifications on events, campaigns, & news