Resultats de la cerca - Thomas Ströbel
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Creutzfeldt–Jakob disease and inclusion body myositis: Abundant disease‐associated prion protein in muscle per Gábor G. Kovács, Elisabeth Lindeck‐Pozza, Leila Chimelli, Abelardo Araújo, Alberto A. Gabbai, Thomas Ströbel, Markus Glatzel, Adriano Aguzzi, Herbert Budka
Publicat 2003Artigo -
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Genetically Engineered Microvesicles Carrying Suicide mRNA/Protein Inhibit Schwannoma Tumor Growth per Arda Mizrak, Mehmet Fatih Bolukbasi, Gokhan Baris Ozdener, Gary J. Brenner, Sibylle Madlener, Erdoğan Pekcan Erkan, Thomas Ströbel, Xandra O. Breakefield, Okay Saydam
Publicat 2012Artigo -
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Tau pathology in Creutzfeldt‐Jakob disease revisited per Gábor G. Kovács, Jasmin Rahimi, Thomas Ströbel, Mirjam I. Lutz, Günther Regelsberger, Nathalie Streichenberger, Armand Perret‐Liaudet, Romana Höftberger, Paweł P. Liberski, Herbert Budka, Beata Sikorska
Publicat 2016Artigo -
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Dura mater is a potential source of Aβ seeds per Gábor G. Kovács, Mirjam I. Lutz, Gerda Ricken, Thomas Ströbel, Romana Höftberger, Matthias Preusser, Günther Regelsberger, Selma Hönigschnabl, Angelika Reiner, Peter Fischer, Herbert Budka, Johannes A. Hainfellner
Publicat 2016Artigo -
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A case of variably protease-sensitive prionopathy treated with doxycyclin per Hamid Assar, Raffi Topakian, Serge Weis, Jasmin Rahimi, Johannes Trenkler, Romana Höftberger, Fahmy Aboulenein-Djamshidian, Thomas Ströbel, Herbert Budka, Helen Yull, Mark Head, James W. Ironside, Gábor G. Kovács
Publicat 2015Carta -
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Effects of Formalin Fixation, Paraffin Embedding, and Time of Storage on DNA Preservation in Brain Tissue: A BrainNet Europe Study per Isidró Ferrer, Judith Armstrong, Sabina Capellari, Piero Parchi, Thomas Arzberger, Jeanne E. Bell, Herbert Budka, Thomas Ströbel, Giorgio Giaccone, Giacomina Rossi, Nenad Bogdanović, Peter Fakai, Andrea Schmitt, Peter Riederers, Safa Al‐Sarraj, Rivka Ravid, Hans A. Kretzschmar
Publicat 2007Artigo -
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The DNA methylation landscape of glioblastoma disease progression shows extensive heterogeneity in time and space per Johanna Klughammer, Barbara Kiesel, Thomas Roetzer-Pejrimovsky, Nikolaus Fortelny, Amelie Nemc, Karl‐Heinz Nenning, Julia Furtner, Nathan C. Sheffield, Paul Datlinger, Nadine Peter, Martha Nowosielski, Marco Augustin, Mario Mischkulnig, Thomas Ströbel, Donát Alpár, Bekir Ergüner, Martin Senekowitsch, Patrizia Moser, Christian F. Freyschlag, Johannes Kerschbaumer, Claudius Thomé, Astrid Grams, Günther Stockhammer, Melitta Kitzwoegerer, Stefan Oberndorfer, Franz Marhold, Serge Weis, Johannes Trenkler, Johanna Buchroithner, Josef Pichler, Johannes Haybaeck, Stefanie Krassnig, Kariem Mahdy Ali, Gord von Campe, Franz Payer, Camillo Sherif, Julius Preiser, Thomas Hauser, Peter Winkler, Waltraud Kleindienst, Franz Würtz, Tanisa Brandner-Kokalj, Martin Stultschnig, Stefan Schweiger, Karin Dieckmann, Matthias Preusser, Georg Langs, Bernhard Baumann, Engelbert Knosp, Georg Widhalm, Christine Marosi, Johannes A. Hainfellner, Adelheid Wöehrer, Christoph Bock
Publicat 2018Artigo -
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Rare mutations in SQSTM1 modify susceptibility to frontotemporal lobar degeneration per Julie van der Zee, Tim Van Langenhove, Gábor G. Kovács, Lubina Dillen, William Deschamps, Sebastiaan Engelborghs, Radoslav Matěj, Mathieu Vandenbulcke, Anne Sieben, Bart Dermaut, Katrien Smets, Philip Van Damme, Céline Merlin, Annelies Laureys, Marleen Van den Broeck, Maria Mattheijssens, Karin Peeters, Luisa Benussi, Giuliano Binetti, Roberta Ghidoni, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Pau Pástor, Cristina Razquín, Sara Ortega‐Cubero, Isabel Hernández, Merçé Boada, Agustı́n Ruiz, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Frederico Simões do Couto, Sandro Sorbi, Benedetta Nacmias, Silvia Bagnoli, Caroline Graff, Huei-Hsin Chiang, Håkan Thonberg, Robert Perneczky, Janine Diehl‐Schmid, Panagiotis Alexopoulos, Giovanni B. Frisoni, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Tobias B. Haack, Tim M. Strom, Holger Prokisch, Oriol Dols‐Icardo, Jordi Clarimón, Alberto Lleó, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Michael T. Heneka, Frank Jessen, Alfredo Ramı́rez, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Eva Parobková, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Thomas Ströbel, Patrick Santens, Wim Robberecht, Peter De Jonghe, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Kristel Sleegers, Christine Van Broeckhoven
Publicat 2014Artigo -
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A Pan‐<scp>E</scp>uropean Study of the<i>C9orf72</i>Repeat Associated with<scp>FTLD</scp>: Geographic Prevalence, Genomic Instability, and Intermediate Repeats per Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Sebastiaan Engelborghs, Stéphanie Philtjens, Mathieu Vandenbulcke, Kristel Sleegers, Anne Sieben, Veerle Bäumer, Githa Maes, Ellen Corsmit, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Alexandre de Mendonça, Gábriel Miltenberger-Miltényi, Sónia Pereira, José Pimentel, Benedetta Nacmias, Silvia Bagnoli, Sandro Sorbi, Caroline Graff, Huei‐Hsin Chiang, Marie Westerlund, Raquel Sánchez‐Valle, Albert Lladó, Ellen Gelpí, Isabel Santana, Maria Rosário Almeida, Beatriz Santiago, Giovanni B. Frisoni, Orazio Zanetti, Cristian Bonvicini, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen, Lüdger Schöls, Michael T. Heneka, Frank Jessen, Radoslav Matěj, Eva Parobková, Gábor G. Kovács, Thomas Ströbel, Stayko Sarafov, Ivailo Tournev, Albena Jordanova, Adrian Danek, Thomas Arzberger, Gian Maria Fabrizi, Silvia Testi, Éric Salmon, Patrick Santens, Jean‐Jacques Martin, Patrick Cras, Rik Vandenberghe, Peter Paul De Deyn, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Jessie Theuns, Stéphanie Philtjens, Kristel Sleegers, Veerle Bäumer, Githa Maes, Ellen Corsmit, Marc Cruts, Christine Van Broeckhoven, Julie van der Zee, Ilse Gijselinck, Lubina Dillen, Tim Van Langenhove, Stéphanie Philtjens, Jessie Theuns, Kristel Sleegers, Veerle Bäumer, Githa Maes, Marc Cruts, Christine Van Broeckhoven, Sebastiaan Engelborghs, Peter P. De Deyn, Patrick Cras, Sebastiaan Engelborghs, Peter P. De Deyn, Mathieu Vandenbulcke, Mathieu Vandenbulcke, Barbara Borroni, Alessandro Padovani, Silvana Archetti, Robert Perneczky, Janine Diehl‐Schmid, Matthis Synofzik, Walter Maetzler, Jennifer Müller vom Hagen
Publicat 2012Revisão
Eines de cerca:
Matèries relacionades
Biology
Genetics
Gene
Medicine
Pathology
Disease
Biochemistry
Cancer research
Cell biology
DNA
Molecular biology
Alzheimer's disease
Anatomy
Computational biology
Dementia
Immunohistochemistry
Internal medicine
Messenger RNA
Microvesicles
Neurodegeneration
Neuroscience
Prion protein
Tauopathy
microRNA
AP endonuclease
AP site
Allele
Antibiotics
Apolipoprotein E
Apoptosis