Dr. rer. nat. Carsten Holzmann
Dr. rer. nat. Carsten Holzmann
Universitätsmedizin Rostock
Verified email at - Homepage
Cited by
Cited by
14-3-3 proteins in the nervous system
D Berg, C Holzmann, O Riess
Nature Reviews Neuroscience 4 (9), 752-762, 2003
Transgenic rat model of Huntington's disease
S von Hörsten, I Schmitt, HP Nguyen, C Holzmann, T Schmidt, T Walther, ...
Human molecular genetics 12 (6), 617-624, 2003
Neurodegeneration and motor dysfunction in a conditional model of Parkinson's disease
S Nuber, E Petrasch-Parwez, B Winner, J Winkler, S von Hörsten, ...
Journal of Neuroscience 28 (10), 2471-2484, 2008
Identification and functional characterization of a novel R621C mutation in the synphilin-1 gene in Parkinson's disease
FP Marx, C Holzmann, KM Strauss, L Li, O Eberhardt, E Gerhardt, ...
Human molecular genetics 12 (11), 1223-1231, 2003
Behavioral abnormalities precede neuropathological markers in rats transgenic for Huntington's disease
HP Nguyen, P Kobbe, H Rahne, T Wörpel, B Jäger, M Stephan, R Pabst, ...
Human Molecular Genetics 15 (21), 3177-3194, 2006
Reversibility of symptoms in a conditional mouse model of spinocerebellar ataxia type 3
J Boy, T Schmidt, H Wolburg, A Mack, S Nuber, M Böttcher, I Schmitt, ...
Human molecular genetics 18 (22), 4282-4295, 2009
Lifelong caloric restriction increases working memory in mice
A Kuhla, S Lange, C Holzmann, F Maass, J Petersen, B Vollmar, A Wree
PloS one 8 (7), e68778, 2013
14-3-3 protein is a component of Lewy bodies in Parkinson’s disease—Mutation analysis and association studies of 14-3-3 eta
A Ubl, D Berg, C Holzmann, R Krüger, K Berger, T Arzberger, ...
Molecular brain research 108 (1-2), 33-39, 2002
Selective striatal neuron loss and alterations in behavior correlate with impaired striatal function in Huntington's disease transgenic rats
O Kántor, Y Temel, C Holzmann, K Raber, HP Nguyen, C Cao, ...
Neurobiology of disease 22 (3), 538-547, 2006
A transgenic mouse model of spinocerebellar ataxia type 3 resembling late disease onset and gender-specific instability of CAG repeats
J Boy, T Schmidt, U Schumann, U Grasshoff, S Unser, C Holzmann, ...
Neurobiology of disease 37 (2), 284-293, 2010
Extended mutation analysis and association studies of Nurr1 (NR4A2) in Parkinson disease
R Hering, S Petrovic, EM Mietz, C Holzmann, D Berg, P Bauer, D Woitalla, ...
Neurology 62 (7), 1231-1232, 2004
Polymorphisms of the α-synuclein promoter: expression analyses and association studies in Parkinson's disease
C Holzmann, R Krüger, AMMV Saecker, I Schmitt, L Schöls, K Berger, ...
Journal of neural transmission 110, 67-76, 2003
Regional and subtype selective changes of neurotransmitter receptor density in a rat transgenic for the Huntington's disease mutation
A Bauer, K Zilles, A Matusch, C Holzmann, O Riess, S Von Hörsten
Journal of neurochemistry 94 (3), 639-650, 2005
Current challenges in understanding the cellular and molecular mechanisms in Niemann–Pick disease type C1
AU Bräuer, A Kuhla, C Holzmann, A Wree, M Witt
International Journal of Molecular Sciences 20 (18), 4392, 2019
Effects of intrastriatal botulinum neurotoxin A on the behavior of Wistar rats
C Holzmann, D Dräger, E Mix, A Hawlitschka, V Antipova, R Benecke, ...
Behavioural brain research 234 (1), 107-116, 2012
Combined therapy with cyclodextrin/allopregnanolone and miglustat improves motor but not cognitive functions in Niemann–Pick Type C1 mice
M Hovakimyan, F Maass, J Petersen, C Holzmann, M Witt, J Lukas, ...
Neuroscience 252, 201-211, 2013
The ε4 genotype of apolipoprotein E and white matter integrity in Alzheimer's disease
V Kljajevic, P Meyer, C Holzmann, M Dyrba, E Kasper, ALW Bokde, ...
Alzheimer's & Dementia 10 (3), 401-404, 2014
Expression mapping of tetracycline-responsive prion protein promoter: digital atlasing for generating cell-specific disease models
J Boy, TB Leergaard, T Schmidt, F Odeh, U Bichelmeier, S Nuber, ...
Neuroimage 33 (2), 449-462, 2006
Isolation and characterization of the rat huntingtin promoter
Biochemical Journal 336 (1), 227-234, 1998
Cytogenetically normal uterine leiomyomas without MED12-mutations – a source to identify unknown mechanisms of the development of uterine smooth muscle …
C Holzmann, DN Markowski, D Koczan, W Küpker, BM Helmke, ...
Molecular Cytogenetics 7, 1-8, 2014
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