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Gruppiert nach: Dokumententyp | Veröffentlichungsdatum
Anzahl der Publikationen: 25

Zeitschriftenartikel

Gasparoni, Gilles; Bultmann, Sebastian; Lutsik, Pavlo; Kraus, Theo F. J.; Sordon, Sabrina; Vlcek, Julia; Dietinger, Vanessa; Steinmaurer, Martina; Haider, Melanie; Mulholland, Christopher B.; Arzberger, Thomas; Röber, Sigrun; Riemenschneider, Matthias; Kretzschmar, Hans A.; Giese, Armin; Leonhardt, Heinrich und Walter, Jörn (2018): DNA methylation analysis on purified neurons and glia dissects age and Alzheimer's disease-specific changes in the human cortex. In: Epigenetics & Chromatin 11:41 [PDF, 6MB]

Kraus, Theo F. J.; Haider, Melanie; Spanner, Judith; Steinmaurer, Martina; Dietinger, Vanessa und Kretzschmar, Hans A. (2017): Altered Long Noncoding RNA Expression Precedes the Course of Parkinson's Disease-a Preliminary Report. In: Molecular Neurobiology, Bd. 54, Nr. 4: S. 2869-2877

Kraus, Theo F. J.; Kilinc, Selma; Steinmaurer, Martina; Stieglitz, Marc; Guibourt, Virginie und Kretzschmar, Hans A. (2016): Profiling of methylation and demethylation pathways during brain development and ageing. In: Journal of Neural Transmission, Bd. 123, Nr. 3: S. 189-203

Krasnianski, Anna; Heinemann, Uta; Ponto, Claudia; Kortt, Jasmine; Kallenberg, Kai; Varges, Daniela; Schulz-Schaeffer, Walter J.; Kretzschmar, Hans A. und Zerr, Inga (2016): Clinical findings and diagnosis in genetic prion diseases in Germany. In: European Journal of Epidemiology, Bd. 31, Nr. 2: S. 187-196

Kraus, Theo F. J.; Greiner, Andrea; Guibourt, Virginie; Lisec, Kristina und Kretzschmar, Hans A. (2015): Identification of Stably Expressed lncRNAs as Valid Endogenous Controls for Profiling of Human Glioma. In: Journal of Cancer, Bd. 6, Nr. 2: S. 111-119 [PDF, 1MB]

Kraus, Theo F. J.; Greiner, Andrea; Steinmaurer, Martina; Dietinger, Vanessa; Guibourt, Virginie und Kretzschmar, Hans A. (2015): Genetic Characterization of Ten-Eleven-Translocation Methylcytosine Dioxygenase Alterations in Human Glioma. In: Journal of Cancer, Bd. 6, Nr. 9: S. 832-842 [PDF, 1MB]

Kouri, Naomi; Ross, Owen A.; Dombroski, Beth; Younkin, Curtis S.; Serie, Daniel J.; Soto-Ortolaza, Alexandra; Baker, Matthew; Finch, Ni Cole A.; Yoon, Hyejin; Kim, Jungsu; Fujioka, Shinsuke; McLean, Catriona A.; Ghetti, Bernardino; Spina, Salvatore; Cantwell, Laura B.; Farlow, Martin R.; Grafman, Jordan; Huey, Edward D.; Han, Mi Ryung; Beecher, Sherry; Geller, Evan T.; Kretzschmar, Hans A.; Roeber, Sigrun; Gearing, Marla; Juncos, Jorge L.; Vonsattel, Jean Paul G.; Deerlin, Vivianna M. van; Grossman, Murray; Hurtig, Howard I.; Gross, Rachel G.; Arnold, Steven E.; Trojanowski, John Q.; Lee, Virginia M.; Wenning, Gregor K.; White, Charles L.; Hoeglinger, Gunter U.; Mueller, Ulrich; Devlin, Bernie; Golbe, Lawrence I.; Crook, Julia; Parisi, Joseph E.; Boeve, Bradley F.; Josephs, Keith A.; Wszolek, Zbigniew K.; Uitti, Ryan J.; Graff-Radford, Neill R.; Litvan, Irene; Younkin, Steven G.; Wang, Li-San; Ertekin-Taner, Niluefer; Rademakers, Rosa; Hakonarsen, Hakon; Schellenberg, Gerard D. und Dickson, Dennis W. (2015): Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy. In: Nature Communications, Bd. 6, 7247 [PDF, 729kB]

Krasnianski, A.; Sanchez Juan, P.; Ponto, Claudia; Bartl, M.; Heinemann, U.; Varges, D.; Schulz-Schaeffer, W. J.; Kretzschmar, Hans A. und Zerr, I. (2014): A proposal of new diagnostic pathway for fatal familial insomnia. In: Journal of neurology, neurosurgery, and psychiatry, Bd. 85, Nr. 6: S. 654-659 [PDF, 815kB]

Schelzke, Gabi; Stoeck, Katharina; Eigenbrod, Sabina; Grasbon-Frodl, Eva; Raddatz, Lena M.; Ponto, Claudia; Kretzschmar, Hans A. und Zerr, Inga (2013): Report about Four Novel Mutations in the Prion Protein Gene. In: Dementia and Geriatric Cognitive Disorders, Nr. 3-4: S. 229-237 [PDF, 661kB]

Oeckl, Patrick; Steinacker, Petra; Lehnert, Stefan; Jesse, Sarah; Kretzschmar, Hans A.; Ludolph, Albert C.; Otto, Markus und Ferger, Boris (2012): CSF concentrations of cAMP and cGMP are lower in patients with Creutzfeldt-Jakob disease but not Parkinson's disease and amyotrophic lateral sclerosis.
In: PLOS ONE 7(3), e32664 [PDF, 279kB]

Schön, Christian; Hoffmann, Nadine A.; Ochs, Simon M.; Burgold, Steffen; Filser, Severin; Steinbach, Sonja; Seeliger, Mathias W.; Arzberger, Thomas; Goedert, Michel; Kretzschmar, Hans A.; Schmidt, Boris und Herms, Jochen (2012): Long-term in vivo imaging of fibrillar tau in the retina of P301S transgenic mice.
In: PLOS ONE 7(12), e53547 [PDF, 7MB]

Jesse, Sarah; Lehnert, Stefan; Jahn, Olaf; Parnetti, Lucilla; Soininen, Hilkka; Herukka, Sanna-Kaisa; Steinacker, Petra; Tawfik, Saskia; Tumani, Hayrettin; Arnim, Christine A. F. von; Neumann, Manuela; Kretzschmar, Hans A.; Kulaksiz, Hasan; Lenter, Martin; Wiltfang, Jens; Ferger, Boris; Hengerer, Bastian und Otto, Markus (2012): Differential sialylation of serpin A1 in the early diagnosis of Parkinson's disease dementia.
In: PLOS ONE 7(11), e48783 [PDF, 775kB]

Thon, Niklas; Eigenbrod, Sabina; Grasbon-Frodl, Eva M.; Lutz, Jürgen; Kreth, Simone; Popperl, Gabriele; Belka, Claus; Kretzschmar, Hans A.; Tonn, Jörg-Christian und Kreth, Friedrich-Wilhelm (April 2011): Predominant influence of MGMT methylation in non-resectable glioblastoma after radiotherapy plus temozolomide. In: Journal of neurology, neurosurgery, and psychiatry, Bd. 82, Nr. 4: S. 441-446 [PDF, 184kB]

Kreth, Simone; Thon, Niklas; Eigenbrod, Sabina; Lutz, Juergen; Ledderose, Carola; Egensperger, Rupert; Tonn, Joerg C.; Kretzschmar, Hans A.; Hinske, Ludwig C. und Kreth, Friedrich-Wilhelm (2011): O-methylguanine-DNA methyltransferase (MGMT) mRNA expression predicts outcome in malignant glioma independent of MGMT promoter methylation.
In: PLOS ONE 6(2), e17156 [PDF, 387kB]

Tang, Yue; Xiang, Wei; Terry, Linda; Kretzschmar, Hans A. und Windl, Otto (2010): Transcriptional analysis implicates endoplasmic reticulum stress in bovine spongiform encephalopathy.
In: PLOS ONE 5(12), e14207 [PDF, 595kB]

Wüllner, U.; Schmitt, I.; Kammal, M.; Kretzschmar, Hans A. und Neumann, Manuela (2009): Definite multiple system atrophy in a German family. In: Journal of Neurology, Neurosurgery & Psychiatry, Bd. 80, Nr. 4: S. 449-450 [PDF, 636kB]

Pflanz, Heike; Vana, Karen; Mitteregger, Gerda; Renner-Müller, Ingrid; Pace, Claudia; Küchenhoff, Helmut ORCID logoORCID: https://orcid.org/0000-0002-6372-2487; Kretzschmar, Hans A.; Wolf, Eckhard und Weiss, Stefan (2009): Scrapie-infected transgenic mice expressing a laminin receptor decoy mutant reveal a prolonged incubation time associated with low levels of prpres. In: Journal of Molecular Biology, Bd. 388, Nr. 4: S. 721-729

Roeber, Sigrun; Grasbon-Frodl, Eva-Maria; Windl, Otto; Krebs, Bjarne; Xiang, Wei; Vollmert, Caren; Illig, Thomas; Schröter, Andreas; Arzberger, Thomas; Weber, Petra; Zerr, Inga und Kretzschmar, Hans A. (14. Mai 2008): Evidence for a pathogenic role of different mutations at codon 188 of PRNP.
In: PLOS ONE 3(5), e2147 [PDF, 310kB]

Cepek, Lukas; Brechlin, Peter; Steinacker, Petra; Mollenhauer, Brit; Klingebiel, Enrico; Bibl, Mirko; Kretzschmar, Hans A.; Wiltfang, Jens und Otto, Markus (2007): Proteomic analysis of the cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. In: Dementia and Geriatric Cognitive Disorders, Nr. 1: S. 22-28 [PDF, 205kB]

Mollenhauer, Brit; Steinacker, Petra; Bahn, Erik; Bibl, Mirko; Brechlin, Peter; Schlossmacher, Michael G.; Locascio, Joseph J.; Wiltfang, Jens; Kretzschmar, Hans A.; Poser, Sigrid; Trenkwalder, Claudia und Otto, Markus (2007): Serum heart-type fatty acid-binding protein and cerebrospinal fluid tau: Marker candidates for dementia with Lewy bodies. In: Neurodegenerative Diseases, Nr. 5: S. 366-375 [PDF, 221kB]

Boesenberg-Grosse, Constanze; Schulz-Schaeffer, Walter J.; Bodemer, Monika; Ciesielczyk, Barbara; Meissner, Bettina; Krasnianski, Anna; Bartl, Mario; Heinemann, Uta; Varges, Daniela; Eigenbrod, Sabina; Kretzschmar, Hans A.; Green, Alison und Zerr, Inga (2006): Brain-derived proteins in the CSF, do they correlate with brain pathology in CJD? In: BMC Neurology 6:35 [PDF, 1MB]

Vollmert, C.; Windl, O.; Xiang, W.; Rosenberger, A.; Zerr, I.; Wichmann, Heinz-Erich; Bickeböller, H.; Illig, T. und Kretzschmar, Hans A. (2006): Significant association of a M129V independent polymorphism in the 5\prime UTR of the PRNP gene with sporadic Creutzfeldt-Jakob disease in a large German case-control study. In: Journal of Medical Genetics, Bd. 43, Nr. 10, e53 [PDF, 211kB]

Cepek, Lukas; Steinacker, Petra; Mollenhauer, Brit; Wiese, Birgitt; Ciesielczyk, Barbara; Bibl, Mirko; Wiltfang, Jens; Zerr, Inga; Schulz-Schaeffer, Walter J.; Kretzschmar, Hans A.; Poser, Sigrid und Otto, Markus (2005): Follow-up investigations of tau protein and S-100B levels in cerebrospinal fluid of patients with Creutzfeldt-Jakob disease. In: Dementia and Geriatric Cognitive Disorders, Nr. 5-6: S. 376-382 [PDF, 154kB]

Mollenhauer, Brit; Cepek, Lukas; Bibl, Mirko; Wiltfang, Jens; Schulz-Schaeffer, Walter J.; Ciesielczyk, Barbara; Neumann, Manuela; Steinacker, Petra; Kretzschmar, Hans A.; Poser, Sigrid; Trenkwalder, Claudia und Otto, Markus (2005): Tau protein, A beta 42 and S-100B protein in cerebrospinal fluid of patients with dementia with Lewy bodies. In: Dementia and Geriatric Cognitive Disorders, Nr. 2-3: S. 164-170 [PDF, 111kB]

Bleich, S.; Otto, Markus; Zerr, Inga; Kropp, S.; Kretzschmar, Hans A. und Wiltfang, Jens (2005): Creutzfeldt-Jakob disease and homocysteine levels in plasma and cerebrospinal fluid. In: Gerontology, Nr. 2: S. 142-144 [PDF, 66kB]

Diese Liste wurde am Sat Apr 20 18:44:02 2024 CEST erstellt.