Astrid Lunkes
Max Delbrück Center(DE)Helmholtz Zentrum München(DE)
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Mitochondrial Function and Pathology, DNA Repair Mechanisms, Neurological disorders and treatments, Hereditary Neurological Disorders
Most-Cited Works
- → Moderate expansion of a normally biallelic trinucleotide repeat in spinocerebellar ataxia type 2(1996)1,123 cited
- → Proteases Acting on Mutant Huntingtin Generate Cleaved Products that Differentially Build Up Cytoplasmic and Nuclear Inclusions(2002)416 cited
- → Chromosomal assignment of the second locus for autosomal dominant cerebellar ataxia (SCA2) to chromosome 12q23–24.1(1993)288 cited
- → A cellular model that recapitulates major pathogenic steps of Huntington's disease(1998)191 cited
- → A Gene for Autosomal Dominant Paroxysmal Choreoathetosis/Spasticity (CSE) Maps to the Vicinity of a Potassium Channel Gene Cluster on Chromosome 1p, Probably within 2 cM between D1S443 and D1S197(1996)165 cited
- → The biosocial genome?(2017)121 cited
- → Unstable triplet repeat and phenotypic variability of spinocerebellar ataxia type 1(1996)97 cited
- → SCA2 trinucleotide expansion in German SCA patients(1997)88 cited
- → Gal80 Proteins of Kluyveromyces lactis and Saccharomyces cerevisiae Are Highly Conserved but Contribute Differently to Glucose Repression of the Galactose Regulon(1993)53 cited
- → Polyglutamines, nuclear inclusions and neurodegeneration(1997)52 cited