John J. Kleiderlein
Publications by Year
Research Areas
Genetic Neurodegenerative Diseases, Parkinson's Disease Mechanisms and Treatments, DNA Repair Mechanisms, Mitochondrial Function and Pathology, Phosphodiesterase function and regulation
Most-Cited Works
- → Expansion of a novel CAG trinucleotide repeat in the 5′ region of PPP2R2B is associated with SCA12(1999)488 cited
- → Synphilin-1 associates with α-synuclein and promotes the formation of cytosolic inclusions(1999)488 cited
- → Disrupted-in-Schizophrenia-1 (DISC-1): Mutant truncation prevents binding to NudE-like (NUDEL) and inhibits neurite outgrowth(2002)395 cited
- → Atrophin-1, the DRPLA Gene Product, Interacts with Two Families of WW Domain-Containing Proteins(1998)169 cited
- → CCG repeats in cDNAs from human brain(1998)32 cited
- → Organization of the human synphilin-1 gene, a candidate for Parkinson's disease(2000)28 cited
- → Chromosomal localization of the Huntingtin Associated Protein (HAP-1) gene in mouse and humans with radiation hybrid and interspecific backcross mapping(1999)5 cited
- truncation prevents binding 1 (NUDEL) and inhibits neurite(2016)