Structure and Topology of the Huntingtin 1–17 Membrane Anchor by a Combined Solution and Solid-State NMR Approach

Author:

Michalek Matthias,Salnikov Evgeniy S.,Bechinger Burkhard

Publisher

Elsevier BV

Subject

Biophysics

Reference83 articles.

1. Polyglutamine pathogenesis: emergence of unifying mechanisms for Huntington’s disease and related disorders;Ross;Neuron,2002

2. Phenotypic characterization of individuals with 30-40 CAG repeats in the Huntington disease (HD) gene reveals HD cases with 36 repeats and apparently normal elderly individuals with 36-39 repeats;Rubinsztein;Am. J. Hum. Genet.,1996

3. Identification of an HD patient with a (CAG)180 repeat expansion and the propagation of highly expanded CAG repeats in lambda phage;Sathasivam;Hum. Genet.,1997

4. The relationship between CAG repeat length and age of onset differs for Huntington’s disease patients with juvenile onset or adult onset;Andresen;Ann. Hum. Genet.,2007

5. Early mitochondrial calcium defects in Huntington’s disease are a direct effect of polyglutamines;Panov;Nat. Neurosci.,2002

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