Hereditary Disease Foundation
Click here
for ways of
giving to HDF
Donate NOW to HDF
3960 Broadway, 6th Floor – New York, NY 10032
phone: 212.928.2121, fax: 212.928.2172

cures@hdfoundation.org

GRANTS FUNDED in 2006

1996 1997 1998 1999 2000 2001 2002 2003 2004 2005 2006 2007 2008 2009 2010 2011 2012


Recent Science Funding Provided by the Hereditary Disease Foundation

Click here to begin your search for research updates by HDF-funded scientists and others.

PubMed, a service of the National Library of Medicine, provides access to over 12 million MEDLINE citations back to the mid-1960's and additional life science journals.

PubMed includes links to many sites providing full text articles and other related resources.

Hereditary Disease Foundation grants, postdoctoral fellowships and research contracts are helping identify routes to the development of cures and treatments for Huntington’s disease and other similar hereditary disorders. With your support, the HDF’s Scientific Advisory Board, comprised of world-renowned experts in genetics, neurology, neuroscience, and therapy development, has funded groundbreaking research. The following projects were recently funded in 2006:

RESEARCH GRANTS

Jocelyne Caboche
Universite Pierre et Marie Curie, Paris, France.
Restoration of mitogen and stress-activated kinase as a therapeutic approach in HD.

Yury Chernoff
Georgia Institute of Technology, Atlanta, GA.
Understanding the role of molecular chaperones and the ubiquitin system in polyglutamine aggregation and toxicity.

Nico Dantuma
Karolinska Institute, Stockholm, Sweden.
How does mutant huntingtin disrupt normal protein degradation and how can this be prevented?

Mate Dobrossy
Cardiff University, Cardiff, United Kingdom.
How does cell replacement therapy work in rodent models of Huntington’s disease?

Angela Hodges
King’s College, London, United Kingdom.
How does Dictyostelium tolerate the burden of polyglutamine-containing proteins?

Albert LaSpada
University of Washington, Seattle WA.
Elucidating the mechanism of energy disruption in Huntington’s disease.

Eric Reits
University of Amsterdam, Amsterdam, The Netherlands.
Enhancing polyglutamine degradation as a treatment for Huntington’s disease.

 

POSTDOCTORAL FELLOWSHIPS

Dena Cohen
Massachusetts Institute of Technology, Cambridge, MA.
Mentor: Leonard Guarente
Modulation of SirT1, a longevity gene, as a treatment for Huntington’s disease.

Xueyi Li
Massachusetts General Hospital, Boston, MA.
Mentor: Marian DiFiglia
Understanding and preventing the disruption of endocytosis by mutant huntingtin protein.

 

RESEARCH CONTRACTS

Ron Kopito
Stanford University, Palo Alto, CA.
Cataloging disruptions of protein degradation machinery in the brains of HD mice.

Alexander Osmand
University of Tennessee School of Medicine, Knoxville, TN.
Understanding the early steps in polyglutamine aggregation in the HD brains.

 

Hereditary Disease Foundation
     

This site is copyrighted © 2008 Hereditary Disease Foundation. All rights reserved.
Site Maintained by  DorriOlds.com
.