Spectrum of phenotypes and genotypes in Parkinson's diseaseRIESS, Olaf; KRÜGER, Rejko; SCHULZ, Jörg B et al.Journal of neurology. Supplement. 2002, Vol 249, Num 3, issn 0939-1517, III/15-III/20Article

Automated home cage assessment shows behavioral changes in a transgenic mouse model of spinocerebellar ataxia type 17PORTAL, Esteban; RIESS, Olaf; NGUYEN, Huu Phuc et al.Behavioural brain research. 2013, Vol 250, pp 157-165, issn 0166-4328, 9 p.Article

14-3-3 Proteins in the nervous systemBERG, Daniela; HOLZMANN, Carsten; RIESS, Olaf et al.Nature reviews. Neuroscience (Print). 2003, Vol 4, Num 9, pp 752-762, issn 1471-003X, 11 p.Article

B-Raf and Ha-ras mutations in chemically induced mouse liver tumorsJAWORSKI, Maike; BUCHMANN, Albrecht; BAUER, Peter et al.Oncogene (Basingstoke). 2005, Vol 24, Num 7, pp 1290-1295, issn 0950-9232, 6 p.Article

Autophagy induction reduces mutant ataxin-3 levels and toxicity in a mouse model of spinocerebellar ataxia type 3MENZIES, Fiona M; HUEBENER, Jeannette; RENNA, Maurizio et al.Brain. 2010, Vol 133, pp 93-104, issn 0006-8950, 12 p., 1Article

Association between genetic variants of IL-1β, IL-6 and TNF-α cytokines and cognitive performance in the elderly general population of the MEMO-studyBAUNE, Bernhard T; PONATH, Gerald; ROTHERMUNDT, Matthias et al.Psychoneuroendocrinology. 2008, Vol 33, Num 1, pp 68-76, issn 0306-4530, 9 p.Article

Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutationBAUER, Andreas; ZILLES, Karl; MATUSCH, Andreas et al.Journal of neurochemistry. 2005, Vol 94, Num 3, pp 639-650, issn 0022-3042, 12 p.Article

Neurofilament L gene is not a genetic factor of sporadic and familial Parkinson's diseaseRAHNER, Nils; HOLZMANN, Carsten; KRÜGER, Rejko et al.Brain research. 2002, Vol 951, Num 1, pp 82-86, issn 0006-8993Article

High-throughput resequencing in the diagnosis of BRCA1/2 mutations using oligonucleotide resequencing microarraysSCHROEDER, Christopher; STUTZMANN, Fanny; WEBER, Bernhard H. F et al.Breast cancer research and treatment. 2010, Vol 122, Num 1, pp 287-297, issn 0167-6806, 11 p.Article

Interstitial 3p25.3―p26.1 Deletion in a Patient With Intellectual DisabilityRIESS, Angelika; GRASSHOFF, Ute; SCHÄFERHOFF, Karin et al.American journal of medical genetics. Part A. 2012, Vol 158, Num 10, pp 2587-2590, issn 1552-4825, 4 p.Article

Therapeutic strategies for Parkinson's disease based on data derived from genetic researchRIESS, Olaf; BERG, Daniela; KRÜGER, Rejko et al.Journal of neurology. Supplement. 2003, Vol 250, Num 1, pp 3-10, issn 0939-1517, 8 p.Article

Functional characterization of the human Huntington's disease gene promoterHOLZMANN, Carsten; SCHMIDT, Thorsten; THIEL, Gerald et al.Molecular brain research. 2001, Vol 92, Num 1-2, pp 85-97, issn 0169-328XArticle

Adult neural precursor cells unaffected in animal models of DYT1 dystoniaREGENSBURGER, Martin; KOHL, Zacharias; GRUNDMANN, Kathrin et al.Neuroreport (Oxford). 2009, Vol 20, Num 17, pp 1529-1533, issn 0959-4965, 5 p.Article

Motor function and dopamine release measurements in transgenic Huntington's disease model ratsORTIZ, Andrea N; OSTERHAUS, Gregory L; LAUDERDALE, Kelli et al.Brain research. 2012, Vol 1450, pp 148-156, issn 0006-8993, 9 p.Article

Stem Cell Quiescence in the Hippocampal Neurogenic Niche Is Associated With Elevated Transforming Growth Factor-β Signaling in an Animal Model of Huntington DiseaseKANDASAMY, Mahesh; COUILLARD-DESPRES, Sebastien; BOGDAHN, Ulrich et al.Journal of neuropathology and experimental neurology. 2010, Vol 69, Num 7, pp 717-728, issn 0022-3069, 12 p.Article

Dissecting the role of the mitochondrial chaperone mortalin in Parkinson's disease: functional impact of disease-related variants on mitochondrial homeostasisBURBULLA, Lena F; SCHELLING, Carina; JUNG, Stephan et al.Human molecular genetics (Print). 2010, Vol 19, Num 22, pp 4437-4452, issn 0964-6906, 16 p.Article

Long-Term Course and Mutational Spectrum of spatacsin-Linked Spastic ParaplegiaHEHR, Ute; BAUER, Peter; HEHR, Andreas et al.Annals of neurology. 2007, Vol 62, Num 6, pp 656-665, issn 0364-5134, 10 p.Article

Progression-specific genes identified by expression profiling of matched ductal carcinomas in situ and invasive breast tumors, combining laser capture microdissection and oligonucleotide microarray analysisSCHUETZ, Christina S; BONIN, Michael; KUREK, Raffael et al.Cancer research (Baltimore). 2006, Vol 66, Num 10, pp 5278-5286, issn 0008-5472, 9 p.Article

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonismKLEIN, Christine; DJARMATI, Ana; WINKLER, Susen et al.European journal of human genetics. 2005, Vol 13, Num 9, pp 1086-1093, issn 1018-4813, 8 p.Article

Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's diseaseMARX, Frank P; HOLZMANN, Carsten; ENGELENDER, Simone et al.Human molecular genetics (Print). 2003, Vol 12, Num 11, pp 1223-1231, issn 0964-6906, 9 p.Article

Screening for mutations of the ferritin light and heavy genes in Parkinson's disease patients with hyperechogenicity of the substantia nigraFELLETSCHIN, Bettina; BAUER, Peter; BERG, Daniela et al.Neuroscience letters. 2003, Vol 352, Num 1, pp 53-56, issn 0304-3940, 4 p.Article

N-terminal ataxin-3 causes neurological symptoms with inclusions, endoplasmic reticulum stress and ribosomal dislocationHÜBENER, Jeannette; VAUTI, Franz; ARNOLD, Hans-Henning et al.Brain. 2011, Vol 134, pp 1925-1942, issn 0006-8950, 18 p., 7Article

Genome-wide association study reveals genetic risk underlying Parkinson's diseaseSIMON-SANCHEZ, Javier; SCHULTE, Claudia; KRÜGER, Rejko et al.Nature genetics. 2009, Vol 41, Num 12, pp 1308-1312, issn 1061-4036, 5 p.Article

Sex differences in a transgenic rat model of Huntington's disease : decreased 17β-estradiol levels correlate with reduced numbers of DARPP32⁺ neurons in malesBODE, Felix J; STEPHAN, Michael; SJOBERG, Charlotte et al.Human molecular genetics (Print). 2008, Vol 17, Num 17, pp 2595-2609, issn 0964-6906, 15 p.Article

Screening for mutations of the HFE gene in Parkinson's disease patients with hyperechogenicity of the substantia nigraAKBAS, Nilgtin; HOCHSTRASSER, Helmine; DEPLAZES, Joelle et al.Neuroscience letters. 2006, Vol 407, Num 1, pp 16-19, issn 0304-3940, 4 p.Article