Torthaí cuardaigh - Weishaupt, Jochen
- 1 - 20 toradh as 70 á dtaispeáint
- Téigh chuig an gcéad leathanach eile
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Gene specific therapies – the next therapeutic milestone in neurology de réir Brenner, David, Ludolph, Albert C., Weishaupt, Jochen H.
Foilsithe / Cruthaithe 2020Téacs -
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Reduction of Potassium Currents and Phosphatidylinositol 3-Kinase-Dependent Akt Phosphorylation by Tumor Necrosis Factor-α Rescues Axotomized Retinal Ganglion Cells from Retrograde... de réir Diem, Ricarda, Meyer, Roman, Weishaupt, Jochen H., Bähr, Mathias
Foilsithe / Cruthaithe 2001Téacs -
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Elevated mRNA-levels of distinct mitochondrial and plasma membrane Ca(2+) transporters in individual hypoglossal motor neurons of endstage SOD1 transgenic mice de réir Mühling, Tobias, Duda, Johanna, Weishaupt, Jochen H., Ludolph, Albert C., Liss, Birgit
Foilsithe / Cruthaithe 2014Téacs -
6
Commentary: alpha-synuclein interacts with SOD1 and promotes its oligomerization de réir Helferich, Anika M., McLean, Pamela J., Weishaupt, Jochen H., Danzer, Karin M.
Foilsithe / Cruthaithe 2016Téacs -
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Brain-Derived Neurotrophic Factor-Mediated Neuroprotection of Adult Rat Retinal Ganglion Cells In Vivo Does Not Exclusively Depend on Phosphatidyl-Inositol-3′-Kinase/Protein Kinase... de réir Klöcker, Nikolaj, Kermer, Pawel, Weishaupt, Jochen H., Labes, Monika, Ankerhold, Richard, Bähr, Mathias
Foilsithe / Cruthaithe 2000Téacs -
9
Commentary: Effects of ALS-associated TANK binding kinase 1 mutations on protein-protein interactions and kinase activity de réir Freischmidt, Axel, Brenner, David, Ludolph, Albert C., Andersen, Peter M., Weishaupt, Jochen H.
Foilsithe / Cruthaithe 2020Téacs -
10
Quadruple genetic variants in a sporadic ALS patient de réir Yilmaz, Rüstem, Weishaupt, Kanchi, Valkadinov, Ivan, Knehr, Antje, Brenner, David, Weishaupt, Jochen H.
Foilsithe / Cruthaithe 2022Téacs -
11
CNS-Expressed Cathepsin D Prevents Lymphopenia in a Murine Model of Congenital Neuronal Ceroid Lipofuscinosis de réir Shevtsova, Zinayida, Garrido, Manuel, Weishaupt, Jochen, Saftig, Paul, Bähr, Mathias, Lühder, Fred, Kügler, Sebastian
Foilsithe / Cruthaithe 2010Téacs -
12
Current knowledge and recent insights into the genetic basis of amyotrophic lateral sclerosis de réir Volk, Alexander E., Weishaupt, Jochen H., Andersen, Peter M., Ludolph, Albert C., Kubisch, Christian
Foilsithe / Cruthaithe 2018Téacs -
13
In vivo histopathological staging in C9orf72-associated ALS: A tract of interest DTI study de réir Müller, Hans-Peter, Del Tredici, Kelly, Lulé, Dorothée, Müller, Kathrin, Weishaupt, Jochen H., Ludolph, Albert C., Kassubek, Jan
Foilsithe / Cruthaithe 2020Téacs -
14
T-cell dysregulation is associated with disease severity in Parkinson’s Disease de réir Bhatia, Divisha, Grozdanov, Veselin, Ruf, Wolfgang P., Kassubek, Jan, Ludolph, Albert C., Weishaupt, Jochen H., Danzer, Karin M.
Foilsithe / Cruthaithe 2021Téacs -
15
Proteasome impairment by α-synuclein de réir Zondler, Lisa, Kostka, Marcus, Garidel, Patrick, Heinzelmann, Udo, Hengerer, Bastian, Mayer, Benjamin, Weishaupt, Jochen H., Gillardon, Frank, Danzer, Karin M.
Foilsithe / Cruthaithe 2017Téacs -
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Sublethal Oxygen–Glucose Deprivation Alters Hippocampal Neuronal AMPA Receptor Expression and Vulnerability to Kainate-Induced Death de réir Ying, Howard S., Weishaupt, Jochen H., Grabb, Margaret, Canzoniero, Lorella M. T., Sensi, Stefano L., Sheline, Christian T., Monyer, Hannah, Choi, Dennis W.
Foilsithe / Cruthaithe 1997Téacs -
17
Both systemic and local application of Granulocyte-colony stimulating factor (G-CSF) is neuroprotective after retinal ganglion cell axotomy de réir Frank, Tobias, Schlachetzki, Johannes CM, Göricke, Bettina, Meuer, Katrin, Rohde, Gundula, Dietz, Gunnar PH, Bähr, Mathias, Schneider, Armin, Weishaupt, Jochen H
Foilsithe / Cruthaithe 2009Téacs -
18
Age Increases Monocyte Adhesion on Collagen de réir Khalaji, Samira, Zondler, Lisa, KleinJan, Fenneke, Nolte, Ulla, Mulaw, Medhanie A., Danzer, Karin M., Weishaupt, Jochen H., Gottschalk, Kay-E.
Foilsithe / Cruthaithe 2017Téacs -
19
Acute TBK1/IKK-ε Inhibition Enhances the Generation of Disease-Associated Microglia-Like Phenotype Upon Cortical Stab-Wound Injury de réir Rehman, Rida, Tar, Lilla, Olamide, Adeyemi Jubril, Li, Zhenghui, Kassubek, Jan, Böckers, Tobias, Weishaupt, Jochen, Ludolph, Albert, Wiesner, Diana, Roselli, Francesco
Foilsithe / Cruthaithe 2021Téacs -
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FUS mutations dominate TBK1 mutations in FUS/TBK1 double-mutant ALS/FTD pedigrees de réir Brenner, David, Müller, Kathrin, Lattante, Serena, Yilmaz, Rüstem, Knehr, Antje, Freischmidt, Axel, Ludolph, Albert C., Andersen, Peter M., Weishaupt, Jochen H.
Foilsithe / Cruthaithe 2021Téacs