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Petar Marinković - Publications

Affiliations: 
Ludwig-Maximilians-Universität München, München, Bayern, Germany 
Area:
axonal transport
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7 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2019 Marinković P, Blumenstock S, Goltstein PM, Korzhova V, Peters F, Knebl A, Herms J. In vivo imaging reveals reduced activity of neuronal circuits in a mouse tauopathy model. Brain : a Journal of Neurology. PMID 30847469 DOI: 10.1093/Brain/Awz035  0.392
2016 Zhu K, Xiang X, Filser S, Marinković P, Dorostkar MM, Crux S, Neumann U, Shimshek DR, Rammes G, Haass C, Lichtenthaler SF, Gunnersen JM, Herms J. Beta-Site Amyloid Precursor Protein Cleaving Enzyme 1 Inhibition Impairs Synaptic Plasticity via Seizure Protein 6. Biological Psychiatry. PMID 28129943 DOI: 10.1016/J.Biopsych.2016.12.023  0.372
2015 Marinković P, Godinho L, Misgeld T. Generation and Screening of Transgenic Mice with Neuronal Labeling Controlled by Thy1 Regulatory Elements. Cold Spring Harbor Protocols. 2015: pdb.top087668. PMID 26430261 DOI: 10.1101/Pdb.Top087668  0.622
2015 Marinković P, Godinho L, Misgeld T. Generation of Thy1 Constructs for Pronuclear Injection. Cold Spring Harbor Protocols. 2015: pdb.prot087676. PMID 26430258 DOI: 10.1101/Pdb.Prot087676  0.595
2015 Marinković P, Godinho L, Misgeld T. Imaging Acute Neuromuscular Explants from Thy1 Mouse Lines. Cold Spring Harbor Protocols. 2015: pdb.prot087692. PMID 26330628 DOI: 10.1101/Pdb.Prot087692  0.633
2015 Marinković P, Godinho L, Misgeld T. Generation of Tissue Sections for Screening Thy1 Mouse Lines. Cold Spring Harbor Protocols. 2015: pdb.prot087684. PMID 26330627 DOI: 10.1101/Pdb.Prot087684  0.63
2012 Marinkovic P, Reuter MS, Brill MS, Godinho L, Kerschensteiner M, Misgeld T. Axonal transport deficits and degeneration can evolve independently in mouse models of amyotrophic lateral sclerosis. Proceedings of the National Academy of Sciences of the United States of America. 109: 4296-301. PMID 22371592 DOI: 10.1073/Pnas.1200658109  0.48
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