Wissenschaftliche Publikationen

28. Oktober 2020 / J Genet Genomics

Phosphatidylinositol 4 kinase-β mutations cause non-syndromic sensorineural deafness and inner ear malformation

Use of the human MDR1 promoter for heat-inducible expression of therapeutic genes

Polyglutamine expansion and Huntington's disease

HAP1-huntingtin interactions do not contribute to the molecular pathology in Huntington's disease transgenic mice

Formation of neuronal intranuclear inclusions underlies the neurological dysfunction in mice transgenic for the HD mutation

Detection of polyglutamine aggregation in mouse models

Huntingtin aggregation monitored by dynamic light scattering

Inhibition of huntingtin fibrillogenesis by specific antibodies and small molecules: implications for Huntington's disease therapy

IRS-PCR-based genetic mapping of the huntingtin interacting protein gene (HIP1) on mouse chromosome 5

Aggregation of truncated GST-HD exon 1 fusion proteins containing normal range and expanded glutamine repeats