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Content archived on 2024-05-14

Effective reagents to detect and prevent HD, SCA1 and SBMA in presymptomatic humans and to stop progress in afflicted people

Objective



Antiobodies directed against proteins encoded by genes complementary to the regions which encode the (CAG) repeat on the huntington gene, the ataxin 1 gene and the androgen receptor gene will be prepared and humanised. Each antisense protein contains an unstable, expandable polyleucine tract within a plasma membrane spanning helix and is a putative causative factor of the biochemical characteristics of Huntington's disease, spinocerebellar ataxia type 1 and spino bulbar muscular atrophy. The antibodies will be evaluated for use as accurate diagnostic reagents to detect initiation of the disease before clinical symptoms are discernible, to confer passive immunity to the disease and to prevent further progressive neurodegeneration in people afflicted with these diseases.

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Funding Scheme

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EAW - Exploratory awards

Coordinator

Provebec Inc. AG
EU contribution
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Address
22,Mörikestraße 22
22587 Hamburg
Germany

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Total cost

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